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    Всероссийская конференция "Комбинационное рассеяние - 85 лет исследований" и 4-й Сибирский семинар "Спектроскопия комбинационного рассеяния света" : тезисы докл. / Рос. акад. наук ; сопредс. прогр. ком.: В. Ф. Шабанов, В. С. Горелик ; чл. орг. ком.: А. Н. Втюрин [и др.]. - Красноярск : ИФ СО РАН, 2013. - 70 с. - Авт. указ. - Адреса участников. - 100 экз. - Б. ц.
    Содержание:
Архипкин, Василий Григорьевич. Оптический транзистор на основе фотонного кристалла с рамановски усиливающим дефектом / В. Г. Архипкин, С. А. Мысливец. - С .26-27
Зиненко, Виктор Иванович. Динамика решетки, упругие и пьезоэлектрические свойства кристаллов HoFe3(BO3) / В. И. Зиненко. - С .40-41
Орешонков, Александр Сергеевич. Исследование структуры кристалла Ca2Al3O6 методами рентгеноструктурного анализа и колебательной спектроскопии / А. С. Орешонков [и др.]. - С .16-17
Другие авторы: Втюрин А. Н., Zhiguo Xia, Молокеев, Максим Сергеевич, Атучин В.В.
Орешонков, Александр Сергеевич. Исследование структуры кристалла Ca2Al3O6F методами рентгеноструктурного анализа и колебательной спектроскопии / А. С. Орешонков [и др.]. - С .16-17
Другие авторы: Втюрин А. Н., Zhiguo Xia, Молокеев, Максим Сергеевич, Атучин В. В.
Ершов, Александр Андреевич. Колебательные спектры кристалла MnGeO3 группы пироксена / А. А. Ершов [и др.]. - С .16
Другие авторы: Орешонков А. С., Герасимова Ю. В., Крылов, Александр Сергеевич, Иваненко, Александр Анатольевич, Шайхутдинов, Кирилл Александрович, Терентьев К. Ю., Михашонок Н.В., Втюрин, Александр Николаевич
Крылова, Светлана Николаевна. Исследования фазовых переходов, индуцированных гидростатическим давлением во фторсодержащих эльпасолитах / С. Н. Крылова [и др.]. - С .18
Другие авторы: Крылов А. С., Горяйнов С. В., Орешонков, Александр Сергеевич, Втюрин, Александр Николаевич
Герасимова, Юлия Валентиновна. Спектральные исследования углеродной структуры природных импактных алмазов Попигайской астроблемы / Ю. В. Герасимова [и др.]. - С .50
Другие авторы: Крылов А. С., Иваненко А. А., Втюрин, Александр Николаевич, Елисеев А. П., Александровский, Александр Сергеевич, Афанасьев В. П., Исакова, Алина Алексеевна
Герасимова, Юлия Валентиновна. Спектральные исследования углеродной структуры природных импактных алмазов Попигайской астроблемы / Ю. В. Герасимова [и др.]. - С .50
Другие авторы: Крылов А. С., Иваненко А. А., Втюрин, Александр Николаевич, Елисеев А. П., Александровский, Александр Сергеевич, Афанасьев В. П., Исакова А. А.
Корец, Анатолий Яковлевич. Использование оптических методов для исследования структуры алмазосодержащих частиц детонационного синтеза, подвергнутых механохимическому и тепловому воздействиям / А. Я. Корец [и др.]. - С .53
Другие авторы: Королькова И. В., Крылов А. С., Миронов Е. В., Рабчевский Е. В.
Втюрин, Александр Николаевич. Комбинационное рассеяние и фазовые переходы во фторидах со структурой эльпасолита / А. Н. Втюрин [и др.]. - С .14
Другие авторы: Крылов А. С., Крылова С. Н., Орешонков, Александр Сергеевич, Воронов, Владимир Николаевич
Крылов, Александр Сергеевич. Исследование фазового перехода в кристалле Rb2KMoO3F3: эффект управляемого беспорядка / А. С. Крылов [и др.]. - С .21-22
Другие авторы: Колесникова Е. М., Крылова С. Н., Втюрин, Александр Николаевич
Горяйнов, Сергей Владимирович. Сверхгидратация микропористых алюмосиликатных структур при высоких давлениях водной среды / С. В. Горяйнов [и др.]. - С .12
Другие авторы: Крылов А. С., Лихачева А. Ю., Втюрин, Александр Николаевич
Александровский, Александр Сергеевич. Luminescence spectra of Ho3+ in a monoclinic elpasolite / А. С. Александровский, А. С. Крылов, А. В. Малаховский [и др.] ; A. S. Aleksandrovsky [и др.]. - С .13
Другие авторы: Крылов А. С., Малаховский А. В., Voronov V. N., Molokeev M. S.

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Держатели документа:
Институт физики им. Л.В. Киренского СО РАН

Доп.точки доступа:
Шабанов, Василий Филиппович \сопредс. прогр. ком.\; Shabanov, V. F.; Горелик, Владимир Семенович \сопредс. прогр. ком.\; Втюрин, Александр Николаевич \чл. орг. ком.\; Vtyurin, A. N.; Крылов, Александр Сергеевич \чл. орг. ком.\; Krylov, A. S.; Крылова, Светлана Николаевна \чл. орг. ком.\; Krylova, S. N.; Герасимова, Юлия Валентиновна \чл. орг. ком.\; Gerasimova, J. V.; Орешонков, Александр Сергеевич \чл. орг. ком.\; Oreshonkov, A. S.; Колесникова, Евгения Михайловна \чл. орг. ком.\; Kolesnikova, E. M.; Ершов, Александр Андреевич \чл. орг. ком.\; Ershov, A. A.; Руденко, Людмила Михайловна \чл. орг. ком.\; Втюрин, Александр Николаевич; Елисеев, Александр Павлович; Александровский, Александр Сергеевич; Афанасьев, В. П.; Исакова, Алина Алексеевна; Воронов, Владимир Николаевич; Molokeev, M. S.; Орешонков, Александр Сергеевич; Крылов, Александр Сергеевич; Иваненко, Александр Анатольевич; Шайхутдинов, Кирилл Александрович; Терентьев, Константин Юрьевич; Михашенок, Наталья Владимировна; Атучин, Виктор Валерьевич; Миронов, Е. В.; Рабчевский, Е. В.; Российская академия наук; Научный совет по физике конденсированных сред РАН; Научный совет по спектроскопии атомов и молекул РАН; Сибирское отделение РАН; Объединенный ученый совет по физическим наукам СО РАН; Институт физики им. Л.В. Киренского Сибирского отделения РАН; Сибирский семинар по спектроскопии комбинационного рассеяния света (4 ; 2013 ; авг. ; 26-29 ; Красноярск); "Спектроскопия комбинационного рассеяния света", сибирский семинар (4 ; 2013 ; авг. ; 26-29 ; Красноярск)
Свободных экз. нет}
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    Всероссийская конференция "Комбинационное рассеяние - 85 лет исследований" и 4-й Сибирский семинар "Спектроскопия комбинационного рассеяния света" : Тезисы докл. / Рос. акад. наук [и др.] ; сопредс. прогр. ком.: В. Ф. Шабанов, В. С. Горелик ; чл. орг. ком. А. Н. Втюрин [и др.]. - Красноярск : ИФ СО РАН, 2013. - 70 с. - Авт. указ. - Адреса участников. - 100 экз. - ISBN 978-5-904603-02-1 : Б. ц.
    Содержание:
Архипкин, Василий Григорьевич. Оптический транзистор на основе фотонного кристалла с рамановски усиливающим дефектом / В. Г. Архипкин, С. А. Мысливец. - С .26-27
Зиненко, Виктор Иванович. Динамика решетки, упругие и пьезоэлектрические свойства кристаллов HoFe3(BO3) / В. И. Зиненко. - С .40-41
Aleksandrovsky, A. S. Luminescence spectra of Ho3+ in a monoclinic elpasolite / A. S. Aleksandrovsky [и др.]. - С .13
Другие авторы: Krylov A. S., Malakhovskii A.V., Voronov V.N., Molokeev M.S.
Орешонков, Александр Сергеевич. Исследование структуры кристалла Ca2Al3O6 методами рентгеноструктурного анализа и колебательной спектроскопии / А. С. Орешонков [и др.]. - С .16-17
Другие авторы: Втюрин А. Н., Zhiguo Xia, Молокеев, Максим Сергеевич, Атучин В. В.
Орешонков, Александр Сергеевич. Исследование структуры кристалла Ca2Al3O6F методами рентгеноструктурного анализа и колебательной спектроскопии / А. С. Орешонков [и др.]. - С .16-17
Другие авторы: Втюрин А. Н., Zhiguo Xia, Молокеев, Максим Сергеевич, Атучин В. В.
Ершов, Александр Андреевич. Колебательные спектры кристалла MnGeO3 группы пироксена / А. А. Ершов [и др.]. - С .16
Другие авторы: Орешонков А. С., Герасимова Ю. В., Крылов, Александр Сергеевич, Иваненко, Александр Анатольевич, Шайхутдинов, Кирилл Александрович, Терентьев К. Ю., Михашонок Н.В., Втюрин, Александр Николаевич
Крылова, Светлана Николаевна. Исследования фазовых переходов, индуцированных гидростатическим давлением во фторсодержащих эльпасолитах / С. Н. Крылова [и др.]. - С .18
Другие авторы: Крылов А. С., Горяйнов С. В., Орешонков, Александр Сергеевич, Втюрин, Александр Николаевич
Герасимова, Юлия Валентиновна. Спектральные исследования углеродной структуры природных импактных алмазов Попигайской астроблемы / Ю. В. Герасимова [и др.]. - С .50
Другие авторы: Крылов А. С., Иваненко А. А., Втюрин, Александр Николаевич, Елисеев А.П., Александровский, Александр Сергеевич, Афанасьев В.П., Исакова А. А.
Герасимова, Юлия Валентиновна. Спектральные исследования углеродной структуры природных импактных алмазов Попигайской астроблемы / Ю. В. Герасимова [и др.]. - С .50
Другие авторы: Крылов А. С., Иваненко А. А., Втюрин, Александр Николаевич, Елисеев А.П., Александровский, Александр Сергеевич, Афанасьев В. П., Исакова А. А.
Корец, Анатолий Яковлевич. Использование оптических методов для исследования структуры алмазосодержащих частиц детонационного синтеза, подвергнутых механохимическому и тепловому воздействиям / А. Я. Корец [и др.]. - С .53
Другие авторы: Королькова И.В., Крылов А. С., Миронов Е.В., Рабчевский Е.В.
Втюрин, Александр Николаевич. Комбинационное рассеяние и фазовые переходы во фторидах со структурой эльпасолита / А. Н. Втюрин [и др.]. - С .14
Другие авторы: Крылов А. С., Крылова С. Н., Орешонков, Александр Сергеевич, Воронов, Владимир Николаевич
Крылов, Александр Сергеевич. Исследование фазового перехода в кристалле Rb2KMoO3F3: эффект управляемого беспорядка / А. С. Крылов [и др.]. - С .21-22
Другие авторы: Колесникова Е. М., Крылова С. Н., Втюрин, Александр Николаевич
Горяйнов, Сергей Владимирович. Сверхгидратация микропористых алюмосиликатных структур при высоких давлениях водной среды / С. В. Горяйнов [и др.]. - С .12
Другие авторы: Крылов А. С., Лихачева А. Ю., Втюрин, Александр Николаевич

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Держатели документа:
Институт физики им. Л.В. Киренского СО РАН

Доп.точки доступа:
Шабанов, Василий Филиппович \сопредс. прогр. ком.\; Shabanov, V. F.; Горелик, В. С. \сопредс. прогр. ком.\; Втюрин, Александр Николаевич \чл. орг. ком.\; Vtyurin, A. N.; Крылов, Александр Сергеевич \чл. орг. ком.\; Krylov, A. S.; Крылова, Светлана Николаевна \чл. орг. ком.\; Krylova, S. N.; Герасимова, Юлия Валентиновна \чл. орг. ком.\; Gerasimova, J. V.; Орешонков, Александр Сергеевич \чл. орг. ком.\; Oreshonkov, A. S.; Колесникова, Евгения Михайловна \чл. орг. ком.\; Kolesnikova, E. M.; Ершов, А. С. \чл. орг. ком.\; Руденко, Людмила Михайловна \чл. орг. ком.\; Втюрин, Александр Николаевич; Елисеев, А. П.; Александровский, Александр Сергеевич; Афанасьев, В. П.; Исакова, А. А.; Voronov, V. N.; Molokeev, M. S.; Орешонков, Александр Сергеевич; Воронов, Владимир Николаевич; Крылов, Александр Сергеевич; Иваненко, Александр Анатольевич; Шайхутдинов, Кирилл Александрович; Терентьев, Константин Юрьевич; Михашенок, Наталья Владимировна; Атучин, В. В.; Миронов, Е. В.; Рабчевский, Е. В.; Российская академия наук; Научный совет по физике конденсированных сред РАН; Научный совет по спектроскопии атомов и молекул РАН; Сибирское отделение РАН; Объединенный ученый совет по физическим наукам СО РАН; Институт физики им. Л.В. Киренского Сибирского отделения РАН; "Комбинационное рассеяние - 85 лет исследований", всероссийская конференция (2013 ; авг. ; 26-29 ; Красноярск); "Спектроскопия комбинационного рассеяния света", сибирский семинар (4 ; 2013 ; авг. ; 26-29 ; Красноярск)
Экземпляры всего: 2
РСФ (2)
Свободны: РСФ (2)}
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    Thermometry and up-conversion luminescence of Ln3+ (Ln = Er, Ho, Tm)-doped double molybdate LiYbMo2O8 / X. Y. Yun, J. Zhou, Y. H. Zhu [et al.] // J. Mater. Sci.: Mater. Electron. - 2020. - Vol. 31, Is. 21. - P. 18370-18380, DOI 10.1007/s10854-020-04382-8. - Cited References: 41. - This work is supported by the National Natural Science Foundation of China (No. 21576002 and 61705003) and Beijing Technology and Business University Research Team Construction Project (No. PXM2019_014213_000007) . - ISSN 0957-4522. - ISSN 1573-482X
   Перевод заглавия: Термометрия и апконверсионная люминесценции двойного молибдата LiYbMo2O8, легированного Ln (3+) (Ln = Er, Ho, Tm)

РУБ Engineering, Electrical & Electronic + Materials Science, Multidisciplinary + Physics, Applied + Physics, Condensed Matter
Рубрики:
TEMPERATURE SENSING BEHAVIOR
   OPTICAL THERMOMETRY
   EMISSION
   PHOSPHOR
Аннотация: The discovery of stable and highly sensitive up-conversion (UC) phosphors using the fluorescence intensity ratio (FIR) is a significant challenge in the field of optical temperature sensor. Er3+/Ho3+/Tm3+-doped LiYbMo2O8 UC phosphors with excellent luminescence properties were successfully synthesized through a high-temperature solid-state reaction, and the crystal structure and UC luminescence properties were discussed in detail. The UC process has been investigated by spectra pump power dependence and further explained via the energy level diagram. All emission processes about Er3+ ions and Ho3+ ions are two-photon processes and the blue emission process about Tm3+ ions is a combination of two-photon process and three-photon process. Thermal sensing performances depended on FIR technology were estimated and the sensitivities of LiYb1−xMo2O8:xLn3+ included absolute sensitivity (Sa) and relative sensitivity (Sr) can produce particular change rules with the temperature, which can serve as excellent candidates for applications in optical temperature sensing. With the increase of temperature, the maximum values of Sr of LiYb1−xMo2O8:xLn3+ are 1.16% K−1 (0.05Er3+), 0.25% K−1 (0.01Ho3+), and 0.51% K−1 (0.01Tm3+), respectively. In addition, the Sa value of LiYb0.95Mo2O8:0.05Er3+ phosphor will reach the maximum (1.08% K−1) at 475 K, while the maximum values of Sa of LiYb0.99Mo2O8:0.01Ho3+ and LiYb0.99Mo2O8:0.01Tm3+ are 0.16% K−1, 0.14% K−1.

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Держатели документа:
Beijing Technol & Business Univ, Sch Sci, Beijing 100048, Peoples R China.
RAS, Fed Res Ctr, Kirensky Inst Phys, Lab Crystal Phys,KSC,SB, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Yun, Xiangyan; Zhou, Jun; Zhu, Yaohui; Molokeev, M. S.; Молокеев, Максим Сергеевич; Jia, Yetong; Wei, Chao; Xu, Denghui; Sun, Jiayue
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    Enhanced cyan emission and optical tuning of Ca3Ga4O9:Bi3+ for high-quality full-spectrum white light-emitting diodes / D. J. Liu, X. H. Yun, G. G. Li [et al.] // Adv. Opt. Mater. - 2020. - Vol. 8, Is. 22. - Ст. 2001037, DOI 10.1002/adom.202001037. - Cited References: 55. - This work was financially supported by the National Natural Science Foundation of China (NSFC No. 51932009, 51720105015, 51672265, 51672266, 51672257 and 51672259), the Key Research Program of Frontier Sciences, CAS (Grant No. YZDY-SSW-JSC018), Science and Technology Cooperation Project between Chinese and Australian Governments (2017YFE0132300), the Jiangmen Innovative Research Team Program (2017), and the Major Program of Basic Research and Applied Research of Guangdong Province (2017KZDXM083) . - ISSN 2195-1071
   Перевод заглавия: Улучшенное голубое излучение и оптическая настройка Ca3Ga4O9:Bi3+ для получения высококачественных белых светодиодов полного спектра

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
ENERGY-TRANSFER
   TUNABLE LUMINESCENCE
   PHOSPHOR
   CRYSTAL
   MODULATION
Кл.слова (ненормированные):
cyan-emitting phosphors -- full-spectrum white lighting -- optical tuning -- single-phased white light-emitting diodes
Аннотация: Highly efficient cyan‐emitting phosphor materials are indispensable for closing the cyan gap in spectra of the traditional phosphor‐converted white light‐emitting diodes (WLEDs) to achieve high‐quality full‐spectrum white lighting. In this work, bright cyan‐emitting Ca3Ga4O9 (CGO):0.02Bi3+,0.07Zn2+ phosphor is developed to bridge the cyan gap. Such a Bi3+,Zn2+ codoping enhances the cyan emission of CGO:0.02Bi3+ by 4.1 times due to the influence of morphology and size of phosphor particles, charge compensation and lattice distortion. Interestingly, codoping La3+ ions into the current system can achieve a photoluminescence tuning of CGO:0.02Bi3+ from cyan to yellowish‐green by crystallographic site engineering. Besides, Bi3+–Eu3+ energy transfer is successfully realized in CGO:0.02Bi3+,0.07Zn2+,nEu3+ phosphors and the emission color tuning from cyan to orange is observed. The investigation of thermal quenching behaviors reveals that the incorporation of Zn2+ and La3+ improves the thermal stability of CGO:0.02Bi3+. Finally, CGO:0.02Bi3+,0.07Zn2+,0.10Eu3+ phosphor is employed to obtain a single‐phased warm WLED device. A full‐spectrum WLED device with remarkable color rendering index (Ra) of 97.4 and high luminous efficiency of 69.72 lm W−1 is generated by utilizing CGO:0.02Bi3+,0.07Zn2+ phosphor. This result suggests the important effect of CGO:0.02Bi3+,0.07Zn2+ phosphor on closing the cyan gap, providing new insights of cyan‐emitting phosphors applied in full‐spectrum white lighting.

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Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Sch Appl Chem & Engn, Hefei 230026, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Engn Res Ctr Nanogeomat, Minist Educ, Wuhan 430074, Peoples R China.
RAS, SB, Lab Crystal Phys, Kirensky Inst Phys,Fed Res Ctr,KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Dept Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Shandong Univ, Sch Mat Sci & Engn, Jinan 266071, Peoples R China.
Wuyi Univ, Sch Appl Phys & Mat, Jiangmen 529020, Guangdong, Peoples R China.

Доп.точки доступа:
Liu, Dongjie; Yun, Xiaohan; Li, Guogang; Dang, Peipei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lian, Hongzhou; Shang, Mengmeng; Lin, Jun
}
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    Solvatochromic photoluminescent effects in all-inorganic manganese(II)-based perovskites by highly selective solvent-induced crystal-to-crystal phase transformations / H. Xiao, P. Dang, X. Yun [et al.] // Angew. Chem. - 2021. - Vol. 133, Is. 7. - P. 3743-3751, DOI 10.1002/ange.202012383. - Cited References: 73. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018) . - ISSN 1521-3757
   Перевод заглавия: Сольватохромные фотолюминесцентные эффекты в полностью неорганическом перовските на основе марганца (II), вызванные высокоселективными фазовыми превращениями кристалла-кристалл, индуцированными растворителем
Кл.слова (ненормированные):
lead-free materials -- low-dimensional perovskites -- luminescence -- manganese -- phase transitions
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.

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Держатели документа:
State Key Laboratory of Rare Earth Resource Utilization, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, 5625 Renmin Street, Changchun, 130022 China
University of Science and Technology of China, Hefei, 230026 China
Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry, China University of Geosciences, Wuhan, 430074 China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, 660036 Krasnoyarsk, Russia
Siberian Federal University, 660041 Krasnoyarsk, Russia
Department of Physics, Far Eastern State Transport University, 680021 Khabarovsk, Russia

Доп.точки доступа:
Xiao, Hui; Dang, Peipei; Yun, Xiaohan; Li, Guogang; Wei, Yi; Xiao, Xiao; Zhao, Yajie; Molokeev, M. S.; Молокеев, Максим Сергеевич; Cheng, Ziyong; Lin, Jun
}
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Synthesis and luminescent properties of (RE0.95Ln0.05)2O2S (RE = La, Y; Ln = Ho, Tm) / E. I. Sal'nikova, Y. G. Denisenko, I. E. Kolesnikov [et al.] // J. Solid State Chem. - 2021. - Vol. 293. - Ст. 121753, DOI 10.1016/j.jssc.2020.121753. - Cited References: 33 . - ISSN 0022-4596
Кл.слова (ненормированные):
Rare earth oxysulfides -- Synthesis -- Rietveld -- Luminescence -- Lifetime -- Quantum yield
Аннотация: Solid solutions of oxysulfides (RE0.95Ln0.05)2O2S (RE = La, Y; Ln = Ho, Tm) were obtained by hydrogen reduction of the co-precipitated sulfates followed by sulfidation of the reaction products. The crystal chemical characteristics of the obtained compounds were refined by the Rietveld method. Morphological certification of particles in the dynamics of synthesis was performed. Most of the particles produced by chemical reactions have a cut that indicates the formation of a compound with a hexagonal syngony with angles of 60 and 120°. This indicates that the thermal effect of gaseous reagents H2, H2S on sulfates leads to heterogeneous reactions of thermal dissociation and the formation of new phases. Steady state luminescence properties displayed characteristic sharp bands corresponding to 4f-4f transitions. Luminescence decay curves of all studied samples showed monoexponential decay with microsecond and hundreds microsecond lifetimes depending on doping ions. Calculated color coordinates of Ho3+ and Tm3+-doped powders make them promising candidates to be used as phosphors.

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Держатели документа:
Department of Inorganic and Physical Chemistry, Tyumen State University, Tyumen, 625003, Russian Federation
Komissarov Department of General Chemistry, Northen Trans-Ural Agricultural University, Tyumen, 625003, Russian Federation
Department of General and Special Chemistry, Industrial University of Tyumen, Tyumen, 625000, Russian Federation
Center for Optical and Laser Materials Research, St. Petersburg State University, St. Petersburg, 199034, Russian Federation
Department of Physics, Lappeenranta University of Technology LUT, Lappeenranta, 53850, Finland
Laboratory of the Chemistry of Rare Earth Compounds, Institute of Solid State Chemistry, UB RAS, Ekaterinburg, 620137, Russian Federation
Laboratory of Electron and Probe Microscopy, Tyumen State University, Tyumen, 625003, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Laboratory of Molecular Spectroscopy, Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Sal'nikova, E. I.; Denisenko, Y. G.; Kolesnikov, I. E.; Lahderanta, E.; Andreev, O. V.; Azarapin, N. O.; Basova, S. A.; Gubin, A. A.; Oreshonkov, A. S.; Орешонков, Александр Сергеевич
}
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    Monoclinic SmAl3(BO3)4: synthesis, structural and spectroscopic properties / A. S. Oreshonkov, N. P. Shestakov, M. S. Molokeev [et al.] // Acta Crystallogr. B. - 2020. - Vol. 76. - P. 654-660, DOI 10.1107/S2052520620008781. - Cited References: 38. - Funding for this research was provided by: Russian Foundation for Basic Research (grant Nos. 18-03-00750, 18-05-00682 and 18-32-20011 to AO) . - ISSN 2052-5206
   Перевод заглавия: Моноклинный SmAl3(BO3)4: синтез, структура и спектроскопические свойства

РУБ Chemistry, Multidisciplinary + Crystallography
Рубрики:
Optical-properties
   Luminescence
   Spectra
   Crystals
   Sm
Кл.слова (ненормированные):
IR spectroscopy -- monoclinic structure -- luminescence -- Raman spectroscopy -- X-ray diffraction -- crystal structure
Аннотация: Single crystals of SmAl3(BO3)4 were synthesized by the group growth on seeds method. The crystal structure was solved using a single-crystal experiment and the purity of the bulk material was proved by the Rietveld method. This borate crystallizes in the monoclinic C2/c space group with unit-cell parameters a = 7.2386 (3), b = 9.3412 (5), c = 11.1013 (4) Å and β = 103.2240 (10)°. IR and Raman spectroscopic analyses confirmed the monoclinic structure of SmAl3(BO3)4. Under 532.1 nm excitation, luminescence spectra exhibit bands assignable to the transitions from 4G5/2 to 6H5/2, 6H7/2, 6H9/2 and 6H11/2. The similarity of the luminescence spectra of the trigonal and monoclinic polymorphs is explained by the minor role of Sm—O bond distortion and the primary role of rotational distortion of SmO6 octahedra. The smaller covalency of the Sm—O bond in alumoborates is deduced in comparison with galloborates. Calorimetric measurements did not reveal high-temperature structural phase transitions up to a temperature of 720 K.

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Держатели документа:
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Mol Spect, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sch Engn & Construct, Krasnoyarsk 660041, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk, Russia.
Siberian Fed Univ, Sch Engn Phys & Radio Elect, Krasnoyarsk 660041, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Coherent Opt, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Nanotechnol Spect & Quantum Chem, Krasnoyarsk 660041, Russia.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Radiospect & Spintron, Krasnoyarsk 660036, Russia.
Russian Acad Sci, Inst Automat & Electrometry, Novosibirsk 630090, Russia.
Fed Res Ctr KSC SB RAS, Dept Mol Elect, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660074, Russia.
Tyumen State Univ, Dept Inorgan & Phys Chem, Tyumen 625003, Russia.
Ind Univ Tyumen, Dept Gen & Special Chem, Tyumen 625000, Russia.

Доп.точки доступа:
Oreshonkov, A. S.; Орешонков, Александр Сергеевич; Shestakov, N. P.; Шестаков, Николай Петрович; Molokeev, M. S.; Молокеев, Максим Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Gudim, I. A.; Гудим, Ирина Анатольевна; Temerov, V. L.; Темеров, Владислав Леонидович; Adichtchev, S. V.; Pugachev, A. M.; Nemtsev, I. V.; Немцев, Иван Васильевич; Pogoreltsev, E. I.; Погорельцев, Евгений Ильич; Denisenko, Y. G.; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [18-03-00750, 18-05-00682, 18-32-20011]
}
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    Improving thermal stability of novel single-component white-light emitting phosphor Ca8MgLu(PO4)7:Tm3+, Dy3+ by back-energy-transfer / F. Xie, D. Xu, Z. Wu [et al.] // J. Lumines. - 2020. - Vol. 227. - Ст. 117516, DOI 10.1016/j.jlumin.2020.117516. - Cited References: 54. - This work was financially supported by grants from the National Natural Science Foundation of China (No. 21771195 and 51972347), the Natural Science Foundation of Guangdong Province (No. 2016A030313118), the Science and Technology program of Huizhou City (No. 2016X0421036), the Department of Education of Guangdong Province (No. 2018KQNCX249), and the Professorial and Doctoral Scientific Research Foundation of Huizhou University (No. 2018JB012) . - ISSN 0022-2313
   Перевод заглавия: Повышение термостойкости нового однокомпонентного люминофора, излучающего белый свет, Ca8MgLu(PO4)7:Tm3+,Dy3+ за счет обратной передачи энергии
Кл.слова (ненормированные):
Single-phase white-light emitting phosphor -- Ca8MgLu(PO4)7:Tm3+,Dy3+ -- Back-energy-transfer -- Highly thermal stability
Аннотация: The light degradation of WLED devices after long-time use has been proved to be mainly caused by thermal quenching of phosphors, therefore, the design of single-component white-light emitting phosphors with high thermal stability remains a huge challenge. A novel single-phase white light-emitting phosphor Ca8MgLu(PO4)7:Tm3+,Dy3+ was designed and prepared in this work. The photoluminescent results show that white light emission from the phosphor can be achieved by controlling the ratio of Tm3+ and Dy3+ to adjust the relative intensity of the emission at 451 nm of Tm3+ and the emissions at 488, 571 and 660 nm of Dy3+. The luminescence decay results reveal that there is energy transfer from Tm3+ to Dy3+ in Ca8MgLu(PO4)7:Tm3+,Dy3+ and the efficiency of energy transfer between the two dopants reaches as much as 55%. Temperature-dependent luminescent analyses suggest the highly stable emission of Ca8MgLu0.76(PO4)7:0.12Tm3+,0.12Dy3+ as the integrated emission intensity of the phosphor at 475 K reduces only about 13% of that at room temperature, which is due to the back-energy-transfer from highly doped Dy3+ to Tm3+ that compensates the luminescence energy. This single-phase white-light emitting phosphor exhibits superior color and luminescence stability and thus may find a potential application in WLEDs.

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School of Chemistry and Materials Engineering, Huizhou University, Huizhou, 516007, China
Key Laboratory of Bioinorganic and Synthetic Chemistry of Ministry of Education, School of Chemistry, Sun Yat-Sen University, Guangzhou, 510275, China
College of Chemistry and Molecular Engineering, Qingdao University of Science &Technology, Qingdao, 266042, China
Kirensky Institute of Physics, SB RAS, Krasnoyarsk, RU 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Xie, F.; Xu, D.; Wu, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Milicevic, B.; Li, H.; Shi, J.
}
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    Synthesis, crystal structure and green luminescence in zero-dimensional tin halide (C8H14N2)2SnBr6 / B. Su, G. Song, M. S. Molokeev [et al.] // Inorg. Chem. - 2020. - Vol. 59, Is. 14. - P. 9962–9968, DOI 10.1021/acs.inorgchem.0c01103. - Cited References: 33. - This work is supported by the National Natural Science Foundation of China (51961145101, 51722202, and 51972118), Fundamental Research Funds for the Central Universities (D2190980), Guangzhou Science & Technology Project (202007020005), and the Guangdong Provincial Science & Technology Project (No. 2018A050506004), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to Research Project No. 19-52-80003 . - ISSN 0020-1669
   Перевод заглавия: Синтез, кристаллическая структура и зеленая люминесценция в нульмерном галогениде олова (C8H14N2)2SnBr6
Аннотация: Organic-inorganic hybrid metal halides with broad-band emission are currently receiving an increasing interest for their unique light emission properties. Here we report a novel lead-free zero-dimensional (0D) tin halide, (C8H14N2)2SnBr6, in which isolated [SnBr6]4- octahedrons are cocrystallized with organic cations, 1,3-bis(aminomethyl)benzene (C8H14N22+). Upon photoexcitation, the bulk crystals exhibit broad-band green emission peaking at 507 nm with a full width at half-maximum (fwhm) of 82 nm (0.395 eV), a Stokes shift of 157 nm (1.09 eV), and a photoluminescence quantum yield (PLQY) of 36 ± 4%. Combined structural analysis and density functional theory (DFT) calculations indicate that the excited state structural distortion of [SnBr6]4- octahedral units account for the formation of this green emission. The relatively small Stokes shift and narrow fwhm of the emission are hence caused by the reduced distortion of [SnBr6]4- octahedrons and rigid molecular structure. The discovery of lead-free (C8H14N2)2SnBr6 and insight into the mechanism of green emission provide an essential platform toward unveiling the relationship between structure and property for 0D metal halide perovskites.

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Держатели документа:
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Technology, South China University of Technology, Guangzhou, 510640, China
Technical Institute of Physics and Chemistry, University of Chinese Academy of Sciences, Beijing, 100190, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, 680021, Russian Federation

Доп.точки доступа:
Su, B.; Song, G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lin, Z.; Xia, Z.
}
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10.

    Two-site Cr3+ occupation in the MgTa2O6:Cr3+ phosphor toward broad-band near-infrared emission for vessel visualization / G. C. Liu, M. S. Molokeev, B. F. Lei, Z. G. Xia // J. Mater. Chem. C. - 2020. - Vol. 8, Is. 27. - P. 9322-9328, DOI 10.1039/d0tc01951h. - Cited References: 52. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51972118, 51961145101 and 51722202), Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science & Technology Project (202007020005), the Guangdong Provincial Science & Technology Project (No. 2018A050506004), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003. . - ISSN 2050-7526. - ISSN 2050-7534
   Перевод заглавия: Заселение Cr3+ двух кристаллографических позиций в люминофоре MgTa2O6:Cr3+ для широкополосного ближнего инфракрасного излучения используемого для визуализации сосудов

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
LIGHT-SOURCES
   PHOSPHOR
   LUMINESCENCE
   PHOTOLUMINESCENCE
Аннотация: Near-infrared (NIR) phosphor-converted light-emitting diodes (pc-LEDs) have great potential in photonic, optoelectronic and biological applications, while the discovery of a broad-band NIR phosphor still remains a challenge. Here, we report a novel Cr3+-activated MgTa2O6 phosphor with an asymmetrical emission band ranging from 700 to 1150 nm and a large full width at half maximum (FWHM) of 140 nm upon 460 nm blue light excitation. The broad spectrum is assigned to the overlap of two bands centered at 910 and 834 nm, which originate from the spin-allowed transition of 4T2 → 4A2 for different Cr3+ ions located in the two six-coordinated crystallographic sites of Mg2+ and Ta5+, respectively. The distribution of blood vessels and bones in human palm and wrist is observed with the assistance of a commercial NIR camera and a fabricated pc-LED, which demonstrates that the MgTa2O6:Cr3+ phosphor is promising in biological applications.

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Держатели документа:
South China Univ Technol, Sch Mat Sci & Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Guangzhou 510640, Peoples R China.
Fed Res Ctr KSC SB RAS, Lab Crystal Phys, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
South China Agr Univ, Coll Mat & Energy, Guangdong Prov Engn Technol Res Ctr Opt Agr, Guangzhou 510642, Peoples R China.

Доп.точки доступа:
Liu, Gaochao; Molokeev, M. S.; Молокеев, Максим Сергеевич; Lei, Bingfu; Xia, Zhiguo
}
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11.

    Bismuth activated full spectral double perovskite luminescence materials by excitation and valence control for future intelligent LED lighting / Y. Wei, H. Yang, Z. Y. Gao [et al.] // Chem. Commun. - 2020. - Vol. 56, Is. 64. - P. 9170-9173, DOI 10.1039/d0cc03975f. - Cited References: 27. - This work was supported by the National Natural Science Foundation of China (Grant No. 51672259) and the Fundamental Research Funds for the National Universities, China University of Geosciences (Wuhan) (No. 1910491T02) . - ISSN 1359-7345. - ISSN 1364-548X
   Перевод заглавия: Активированные висмутом люминесцентные материалы двойных перовскитов, с полным спектром излучения, который получается за счет управления возбуждением и валентностью, для интеллектуального светодиодного освещения в будущем

РУБ Chemistry, Multidisciplinary
Рубрики:
PHOTOLUMINESCENCE
   PHOSPHORS
   Bi3+
   MODULATION
   CRYSTAL
Аннотация: A novel La2Mg1.14Zr0.86O6:Bi3+ double perovskite phosphor with excitation-induced blue/green photoluminescence tuning is reported. By designing Bi3+ → Eu3+ energy transfer, single-composition white light with wide-scale adjustable corrected color temperatures (CCTs) is successfully achieved. This work initiates a new insight to explore phosphors with excitation-induced photoluminescence tuning and wide CCT control for future intelligent LED lighting.

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Держатели документа:
China Univ Geosci, Engn Res Ctr Nanogeomat, Minist Educ, Fac Mat Sci & Chem, Wuhan 430074, Hubei, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Wei, Y.i.; Yang, Hang; Gao, Zhiyu; Xing, Gongcheng; Molokeev, M. S.; Молокеев, Максим Сергеевич; Li, Guogang
}
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12.

    Data-driven photoluminescence tuning in Eu2+-doped phosphors / S. Lai, M. Zhao, J. Qiao [et al.] // J. Phys. Chem. Lett. - 2020. - Vol. 11, Is. 14. - P. 5680-5685, DOI 10.1021/acs.jpclett.0c01471. - Cited References: 34. - The present work was supported by the National Natural Science Foundations of China (Grant No. 51972118, 51961145101 and 51722202), Fundamental Research Funds for the Central Universities (D2190980), Guangzhou Science & Technology Project (202007020005), Guangdong Provincial Science & Technology Project (No. 2018A050506004), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003 . - ISSN 1948-7185
   Перевод заглавия: Настройка фотолюминесценции люминофоров, легированных Eu2+, за счет анализа базы данных
Рубрики:
Phosphors
   Luminescence properties
   Crystal structure
   Ions
   Quantum mechanics
Аннотация: Discovery of rare earth phosphors has generally relied on the chemical intuition and time-intensive trial-and-error synthesis; therefore, finding new materials assisted by data-driven computations is urgent. Herein, we utilize a regression model to predict the emission wavelengths of Eu2+-doped phosphors by revealing the relationships between the crystal structure and luminescence property. The emission wavelengths of [Rb(1–x)K(x)]3LuSi2O7:Eu2+ (0 ≤ x ≤ 1) phosphors, as examples for the data-driven photoluminescence tuning, are successfully predicted on the basis of the existing data of only eight systems, also consistent with the experimental results. These phosphors can be excited by blue light and exhibit broad-band red and near-infrared emission ranging from 619 to 737 nm. These findings in Eu2+-doped silicate phosphors indicate that data-driven computations through the regression mode would have bright application in discovering novel phosphors with a target emission wavelengths.

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Держатели документа:
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Engineering, South China University of Technology, Guangzhou, 510641, China
Beijing Municipal Key Laboratory of New Energy Materials and Technologies, School of Materials Sciences and Engineering, University of Science and Technology BeijingBeijing 100083, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Physics, Far Eastern State Transport University, Russian Federation

Доп.точки доступа:
Lai, S.; Zhao, M.; Qiao, J.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.
}
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13.

Solvatochromic Photoluminescent Effects in All-Inorganic Manganese(II)-Based Perovskites by Highly Selective Solvent-Induced Crystal-to-Crystal Phase Transformations / H. Xiao, P. P. Dang, X. H. Yun [et al.] // Angew. Chem. Int. Edit. - 2021. - Vol. 60, Is. 7. - P. 3699-3707, DOI 10.1002/anie.202012383. - Cited References: 85. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018) . - ISSN 1433-7851. - ISSN 1521-3773

РУБ Chemistry, Multidisciplinary
Рубрики:
LEAD-FREE
   HALIDE PEROVSKITE
   NANOCRYSTALS
   MN2+
   LUMINESCENCE
Кл.слова (ненормированные):
lead-free materials -- low-dimensional perovskites -- luminescence -- manganese -- phase transitions
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.

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Держатели документа:
Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Rare Earth Resource Utilizat, 5625 Renmin St, Changchun 130022, Peoples R China.
Univ Sci & Technol China, Hefei 230026, Peoples R China.
China Univ Geosci, Fac Mat Sci & Chem, Minist Educ, Engn Res Ctr Nanogeomat, Wuhan 430074, Peoples R China.
RAS, SB, Lab Crystal Phys, Kirensky Inst Phys,Fed Res Ctr,KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.

Доп.точки доступа:
Xiao, Hui; Dang, Peipei; Yun, Xiaohan; Li, Guogang; Wei, Y.i.; Xiao, Xiao; Zhao, Yajie; Molokeev, M. S.; Молокеев, Максим Сергеевич; Cheng, Ziyong; Lin, Jun
}
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14.

    Luminescent zero-dimensional hybrid lead thiohalide nanostructures for high quantum yield and broadband excitation / N. N. Golovnev, A. S. Aleksandrovsky, M. A. Gerasimova [et al.] // ACS Appl. Nano Mat. - 2021. - Vol. 4, Is. 4. - P. 3654-3663, DOI 10.1021/acsanm.1c00162. - Cited References: 55. - This work is supported by the RFBR according to the research project No. 19-52-80003. This work is also supported by the National Natural Science Foundation of China (51961145101). V.M. thanks Russian Foundation for Basic Research (project number 19-03-00043) for funding. The use of equipment of Krasnoyarsk Regional Center of Research Equipment of Federal Research Center “Krasnoyarsk Science Center SB RAS” is acknowledged. The authors thank JSCC RAS for providing computational resources . - ISSN 2574-0970
   Перевод заглавия: Наноструктуры люминесцентных нульразмерных гибридных тиогалогенов свинца для высокого квантового выхода и широкополосного спектра возбуждения
Кл.слова (ненормированные):
Zero-dimensional hybrid metal halide -- Luminescence -- Quantum yield -- Mechanochemical synthesis -- X-ray diffraction -- Dimethylthiourea
Аннотация: Luminescent trans-[Pb(DMTU-S)4Cl2] (DMTU: N,N′-dimethylthiourea) was designed and prepared via either mechanochemical or solvothermal methods, and the structures of DMTU and trans-[Pb(DMTU-S)4Cl2] have been resolved using X-ray single-crystal diffraction. Upon excitation over broadband covering the range from 450 to 250 nm, trans-[Pb(DMTU-S)4Cl2] shows yellow-green emission peaking at 549 nm with a spectral width of 110 nm, which is assigned to the triplet–singlet transition of Pb2+ ions within distorted heterogeneous S4Cl2 octahedra. The broadband excitation comprised singlet–singlet transitions of Pb2+ ions and energy transfer from orbitals involving those of organic ligands. Simultaneous analysis of the luminescent bandwidth and Stokes shift gives for Pb2+ ions in S4Cl2 octahedra the value of the Huang–Rhys parameter S = 4.25 and the energy of phonon involved in the formation of the luminescence spectrum of the order of 90 meV. Quantum yield as high as 91% is detected for excitation at 365 nm. This high quantum yield indicates the absence of noticeable concentration quenching at an average distance of 9.4 Å between the Pb2+ ions within the structure of trans-[Pb(DMTU)4Cl2]. The weak spin–orbit intersystem crossing is deduced from a high photoluminescence quantum yield (PLQY) value. Time dependent-density functional theory (TD-DFT) calculations of the nanocluster indicate the red shift of absorption bands in Pb(DMTU)4Cl2 with respect to parent DMTU. The high-performance photoluminescence and stability demonstrated promising applications in photonics.

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Держатели документа:
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Department of Chemistry, Lomonosov Moscow State University, Moscow, 119991, Russian Federation
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Technology, South China University of Technology, Guangzhou, 510641, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center, KSC, SB, RAS, Krasnoyarsk, 660036, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo 650000, Russian Federation

Доп.точки доступа:
Golovnev, N. N.; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич; Gerasimova, M. A.; Tomilin, F. N.; Томилин, Феликс Николаевич; Mironov, V. A.; Demina, A. V.; Xia, Z.; Molokeev, M. S.; Молокеев, Максим Сергеевич
}
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15.

    Role of metal-chloride anions in photoluminescence regulations for hybrid metal halides / B. Su, G. Song, M. S. Molokeev [et al.] // J. Phys. Chem. Lett. - 2021. - Vol. 12, Is. 7. - P. 1918-1925, DOI 10.1021/acs.jpclett.1c00182. - Cited References: 40. - This work is supported by the National Natural Science Foundation of China (51961145101 and 51972118), the Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science & Technology Project (202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). This work is also funded by RFBR according to the research project No. 19-52-80003 . - ISSN 1948-7185
   Перевод заглавия: Роль металл-хлорид-анионов в регуляции фотолюминесценции гибридных галогенидов металлов
Кл.слова (ненормированные):
Intra-molecular hydrogen bonds -- Intramolecular interactions -- Luminescence mechanisms -- Organic-inorganic hybrid -- Photoluminescence properties -- Photoluminescence quantum yields -- Photophysical properties -- Structural diversity -- Metal halides
Аннотация: Organic–inorganic hybrid metal halides with emissive organic cations are of great interest due to their structural diversity and interesting photophysical properties. Here, we assemble emissive organic cations (EnrofloH22+) with different metal–chloride anions (Pb2Cl62– to Bi2Cl104– to SnCl62–) to form the new single crystal phases, and thus the photoluminescence properties of the metal halides, including Stokes shift, full width at half-maximum (FWHM), and photoluminescence quantum yield (PLQY) have been studied accordingly. (EnrofloH2)SnCl6·H2O, as an example, possesses narrow FWHM and high PLQY, which are caused by the strong π–π stacking and inter- and intramolecular hydrogen bonds interactions. Compared with EnrofloH22+ cation in solution, the interactions generate a restraining effect and increase the rigid degree of EnrofloH22+ cation in the bulk single crystals. Our work clarifies the photophysical properties of the EnrofloH22+ organic cations by constructing the inter- and intramolecular interactions and boosts the further study of organic–inorganic hybrid metal halides materials with different luminescence mechanisms.

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Держатели документа:
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Technology, South China University of Technology, Guangzhou, 510640, China
Technical Institute of Physics and Chemistry, University of Chinese Academy of Sciences, Beijing, 100190, China
Center of Materials Science and Optoelectronics Engineering, University of the Chinese Academy of Sciences, Beijing, 100049, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation

Доп.точки доступа:
Su, B.; Song, G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Golovnev, N. N.; Lesnikov, M. K.; Lin, Z.; Xia, Z.
}
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16.

    Rapid synthesis of red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors and the tunable photoluminescence via Sr/Ba substitution / Z. Y. Yang, Y. Y. Zhou, J. W. Qiao [et al.] // Adv. Opt. Mater. - 2021. - Vol. 9. Is. 16. - Ст. 2100131, DOI 10.1002/adom.202100131. - Cited References: 44. - Z.Y. and Y.Z. contributed equally to this work. This research was supported by the National Natural Science Foundations of China (Grant Nos. 51972118 and 51961145101), International Cooperation Project of National Key Research and Development Program of China (No. 2021YFE0105700), Guangzhou Science & Technology Project (No. 202007020005), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (No. 2017BT01x137). This work was also funded by RFBR according to the research Project No. 19-52-80003 . - ISSN 2195-1071
   Перевод заглавия: Синтез люминофоров Sr2Sc0.5Ga1.5O5: Eu2+ с красным излучением и перестраиваемая фотолюминесценция за счет замещения Sr/Ba

РУБ Materials Science, Multidisciplinary + Optics
Рубрики:
LUMINESCENCE PROPERTIES
   THERMAL-STABILITY
   EU2+
   GREEN
   EU3+
   SR
Кл.слова (ненормированные):
Eu2+-doped phosphors -- light-emitting diodes -- photoluminescence -- red emission
Аннотация: Discovering new Eu2+-doped red-emitting phosphors in oxide-based materials is a challenge for white light-emitting diode (WLED) applications. Herein, a highly efficient high-frequency induction heating method is employed to rapidly prepare the red-emitting Sr2Sc0.5Ga1.5O5:Eu2+ phosphors peaking at 614 nm and exhibiting a high photoluminescence quantum yield of 78.4% under the excitation of 440 nm. The structural and spectral analyses suggest that Eu2+ ions tend to enter the [Sc1/Ga1O6] and [Ga2O6] polyhedrons with small coordination numbers, leading to the broadband red emission originated from large crystal field splitting of Eu2+ 5d level. The chemical substitution of Ba in the Sr site enhances the thermal stability and helps to the photoluminescence tuning from 614 to 728 nm in SrBaSc0.5Ga1.5O5:Eu2+. The WLED device fabricated by blending the red Sr1.7Ba0.3Sc0.5Ga1.5O5:Eu2+ and yellow Y3(Al, Ga)5O12:Ce3+ phosphors shows a high color-rendering index (Ra = 91.1), and low color-correlated temperature (CCT = 4750 K). This study aims to provide a new synthesis method and design principle for guiding the development of Eu2+-doped oxide-based red phosphors with low preparation cost; moreover, the photoluminescence tuning strategy via cation substitutions is essential to achieve tunable emission, even the near-infrared luminescence.

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Держатели документа:
South China Univ Technol, State Key Lab Luminescent Mat & Devices, Guangdong Prov Key Lab Fiber Laser Mat & Appl Tec, Sch Mat Sci & Engn,Guangdong Engn Technol Res & D, Guangzhou 510641, Guangdong, Peoples R China.
Fed Res Ctr KSC SB RAS, Kirensky Inst Phys, Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
Kemerovo State Univ, Dept Res & Dev, Kemerovo 650000, Russia.
South China Univ Technol, Sch Phys & Optoelect, Guangzhou 510641, Guangdong, Peoples R China.

Доп.точки доступа:
Yang, Zhiyu; Zhou, Yayun; Qiao, Jianwei; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Zhiguo
}
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17.

CaY2Al4SiO12:Ce3+,Mn2+: a single component phosphor to produce high color rendering index WLEDs with a blue chip / Q. H. Zhang, J. H. Li, W. Jiang [et al.] // J. Mater. Chem. C. - 2021. - Vol. 9, Is. 34. - P. 11292-11298, DOI 10.1039/d1tc01770e. - Cited References: 35. - This work has been financially supported by the National Nature Science Foundation of China (51902063, 51902354, U1801253), the Science and Technology Project of Guangdong Province (2018A050506061), the Science and Technology Project of Guangzhou City (202007020005, 202007020008) and GDAS' Project of Science and Technology Development (2020GDASYL-20200302010, 2018GDASCX-0110). M. G. Brik also thanks the support from the Chongqing Recruitment Program for 100 Overseas Innovative Talents (Grant No. 2015013), the Program for the Foreign Experts (Grant No. W2017011) and Wenfeng High-End Talents Project (Grant No. W2016-01) offered by Chongqing University of Posts and Telecommunications (CQUPT), Estonian Research Council grant PUT PRG111, European Regional Development Fund (TK141) and NCN project 2018/31/B/ST4/00924 . - ISSN 2050-7526. - ISSN 2050-7534

РУБ Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
GARNET PHOSPHOR
   ENERGY-TRANSFER
   RED EMISSION
   LUMINESCENCE PROPERTIES
Аннотация: A high color rendering index white light emitting diode (WLED) is generally produced by combining yellow and red mixed phosphors on a blue chip. Herein we report a single component phosphor based on CaY2Al4SiO12 (CYAS) to achieve warm white light emission with a high color rendering index (Ra), which can be up to 90.5. Ce3+, Mn2+ singly doped and co-doped CYAS phosphors have been synthesized by solid state reactions, respectively, for comparative investigations. The Rietveld X-ray diffraction (XRD) refinements show that the CYAS host crystallizes in a cubic structure with the Ia[3 with combining macron]d space group. The valence states of Ce and Mn inside the CYAS host have been confirmed by XPS and EPR. Ce3+ occupies the Ca2+/Y3+ site and generates a yellow emission band around 543 nm from its characteristic 5d–4f transition. Mn2+ occupies both the dodecahedron Ca2+/Y3+ and octahedral Al3+ sites, emitting red and deep red lights at 616 nm and 750 nm, respectively. These two emission bands are attributed to the 4T1(4G)–6A1(6S) transitions of Mn2+. Upon 460 nm light excitation, both the Ce3+ and Mn2+ characteristic emissions can be obtained, in which the emissions of Mn2+ result from the occurrence of energy transfer from Ce3+ in CYAS. All the results indicate that the prepared CYAS:Ce3+,Mn2+ could be a promising single component phosphor for blue chip WLEDs.

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Держатели документа:
Guangdong Acad Sci, Inst Rare Met, Guangdong Prov Key Lab Rare Earth Dev & Applicat, Guangzhou 510651, Peoples R China.
Chongqing Univ Posts & Telecommun, Coll Sci, Chongqing 400065, Peoples R China.
Chongqing Univ Posts & Telecommun, CQUPT BUL Innovat Inst, Chongqing 400065, Peoples R China.
Univ Tartu, Inst Phys, W Ostwald Str 1, EE-50411 Tartu, Estonia.
Jan Dlugosz Univ, Fac Sci & Technol, Armii Krajowej 13-15, PL-42200 Czestochowa, Poland.
RAS, Fed Res Ctr, KSC SB, Kirensky Inst Phys,Lab Crystal Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Krasnoyarsk 660041, Russia.
Far Eastern State Transport Univ, Dept Phys, Khabarovsk 680021, Russia.
Sun Yat Sen Univ, Sch Marine Sci, Zhuhai 510275, Peoples R China.

Доп.точки доступа:
Zhang, Qiuhong; Li, Junhao; Jiang, Wei; Lin, Litian; Ding, Jianhong; Brik, Mikhail G.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Ni, Haiyong; Wu, Mingmei
}
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18.

    Ultra-broad-band-excitable Cu(I)-based organometallic halide with near-unity emission for light-emitting diode applications / J. Huang, B. Su, E. Song [et al.] // Chem. Mater. - 2021. - Vol. 33, Is. 12. - P. 4382-4389, DOI 10.1021/acs.chemmater.1c00085. - Cited References: 43. - This research was supported by the National Natural Science Foundation of China (Grant Nos. 51961145101 and 51972118), the Fundamental Research Funds for the Central Universities (D2190980), the Guangzhou Science and Technology Project (202007020005), International Cooperation Project of National Key Research and Development Program of China (2021YFE0105700), and the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program (2017BT01X137). The reported study was also funded by RFBR according to research project no. 19-52-80003 . - ISSN 0897-4756
   Перевод заглавия: Металлоорганический галогенид на основе Cu (I) со сверхширокополосным возбуждением и излучением с квантовым выходом близким к единице для применения в светодиодах
Кл.слова (ненормированные):
Crown ethers -- Hybrid materials -- Light -- Luminescence -- Metal halide lamps -- Metal halides -- Organic light emitting diodes (OLED) -- Organometallics -- Sodium compounds -- Application prospect -- Excitation characteristics -- Green emission bands -- High color rendering index -- Luminescence mechanisms -- Luminescent material -- Photoluminescence quantum yields -- White light emitting diodes -- Copper compounds
Аннотация: Low-dimensional hybrid metal halides demonstrate broad-band emission and high photoluminescence quantum yield (PLQY) acting as excellent candidates for a new generation of luminescent materials in lighting fields. However, most luminescent metal halides can only be excited by ultraviolet radiation, and the discovery of high-efficient emitters with broad-band excitation characteristics, especially upon efficient blue light irradiation, is a challenge. Herein, a zero-dimensional (0D) Cu(I)-based organometallic halide (18-crown-6)2Na2(H2O)3Cu4I6 (CNCI) was prepared with a green emission band centered at 536 nm and a near-unity PLQY (91.8%) upon excitation of 450 nm. Importantly, the ultrabroad excitation band covering a 300-500 nm range was observed in CNCI, and the luminescence mechanism has been discussed in detail. A white light-emitting diode (WLED) was fabricated with high luminous efficiency of 156 lm/W and a high color rendering index of 89.6. This work provides guidance for designing high-performance luminescent metal halides with suitable excitation characteristics and also promotes the application prospects of such materials in WLED fields.

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Держатели документа:
The State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Fiber Laser Materials and Applied Techniques, School of Materials Science and Engineering, South China University of Technology, Guangzhou, 510641, China
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation
Research and Development Department, Kemerovo State University, Kemerovo, 650000, Russian Federation

Доп.точки доступа:
Huang, J.; Su, B.; Song, E.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Xia, Z.
}
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19.

Synthesis, structure and photoluminescent properties of Eu:Gd2O3 nanophosphor synthesized by cw CO2 laser vaporization / A. I. Kostyukov, V. N. Snytnikov, V. N. Snytnikov [et al.] // J. Lumines. - 2021. - Vol. 235. - Ст. 118050, DOI 10.1016/j.jlumin.2021.118050. - Cited References: 42. - The TEM studies are conducted using the equipment of the Center of Collective Use « National Center of Catalyst Research». This work is financially supported by the Russian Foundation for Basic Research (RFBR), Project no. 19-32-60027 . - ISSN 0022-2313
Кл.слова (ненормированные):
Photoluminescence -- Eu3+ ions -- Monoclinic Gd2O3 -- Nanophosphors -- Laser vaporization
Аннотация: Europium doped Gd2O3 sphere-like nanoparticles with dm = 9.3 ± 3.5 nm were synthesized by cw CO2 laser vaporization technique in a flowing mixture of argon and oxygen. According to XRD data, the Eu:Gd2O3 nanoparticles crystallize in the monoclinic symmetry class (C2/m space group). High-resolution luminescence spectroscopy study showed that the ultra-narrow 5D0 → 7F0 transition of Eu3+ demonstrates only two peaks corresponding to two inequivalent Cs positions of Eu3+ ion in monoclinic Gd2O3 lattice that is explained by the peculiarities of local environment of Eu3+ ion at these sites. The hypersensitive transition 5D0 → 7F2 dominates in the spectrum and is expanded to the red part of the spectrum in comparison with cubic Eu:Gd2O3 due to intense transitions terminating at higher-lying components of the crystal-field-split 7F2 state. In the luminescence spectrum, an additional weak band with the maximum at 407 nm corresponding to the electronic transitions 4f65 d1(7FJ) → 4f7(8S7/2) of Eu2+ was detected. The obtained values of chromaticity coordinates and absolute quantum yield are (0.644; 0.325) and ca. 1%, respectively. The phase transformations have been investigated using differential scanning calorimetry and thermogravimetry (50–1400 °C). After annealing in air at 700 °C, the monoclinic symmetry class of the Eu:Gd2O3 nanoparticles is preserved and the particle size increases to dm = 17.8 ± 6.1 nm. After annealing, the chromaticity coordinates (0.659; 0.334) and absolute quantum yield (ca. 4%) can be obtained using red phosphor based on monoclinic Gd2O3:Eu3+. The lifetime of the excited 5D0 state of Eu3+ in the annealed nanoparticles is longer than that in the as-synthesized nanoparticles, due to the suppression of nonradiative decay after annealing.

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Держатели документа:
Novosibirsk State University, Pirogova Str. 2, Novosibirsk, 630090, Russian Federation
Boreskov Institute of Catalysis SB RAS, Lavrentieva Ave. 5, Novosibirsk, 630090, Russian Federation
Nikolaev Institute of Inorganic Chemistry SB RAS, Akad. Lavrentiev Ave. 3, Novosibirsk, 630090, Russian Federation
Institute of Laser Physics SB RAS, Lavrentyev Ave. 15b, Novosibirsk, 630090, Russian Federation
Novosibirsk State Technical University, K. Marx Ave. 20, Novosibirsk, 630073, Russian Federation
Kirensky Institute of Physics Federal Research Center KSC SB RAS, Krasnoyarsk, 660036, Russian Federation
Department of Photonics and Laser Technology, Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Kostyukov, A. I.; Snytnikov, V. N.; Rakhmanova, M. I.; Kostyukova, N. Y.; Ishchenko, A. V.; Cherepanova, S. V.; Krylov, A. S.; Крылов, Александр Сергеевич; Aleksandrovsky, A. S.; Александровский, Александр Сергеевич
}
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20.

Peschanskii, A. V.
Spectroscopic study of the TbAl3(BO3)4 single crystal: Raman and luminescence spectroscopy / A. V. Peschanskii, A. Y. Glamazda, I. A. Gudim // Low Temp. Phys. - 2020. - Vol. 46, Is. 12. - P. 1223-1230, DOI 10.1063/10.0002478. - Cited References: 20 . - ISSN 1063-777X. - ISSN 1090-6517

РУБ Physics, Applied
Рубрики:
SCATTERING
GENERATION
ND
Кл.слова (ненормированные):
TbAl3(BO3)4 -- vibrational spectrum -- electronic transitions -- Raman spectroscopy -- luminescence
Аннотация: The vibrational and luminescence properties of the TbAl3(BO3)4 single crystal were studied in the temperature range of 5–300 K. Raman spectra of the single crystal revealed 5 of 7 A1 and all E phonon modes predicted by the group-theory analysis. The splitting energy between the LO and TO components of polar E phonons is determined. A group of intense bands associated with the 5D4 → 7F0 electronic transition was observed in the energy range of 14520–14680 cm−1 of the luminescence spectra. The intensity of these bands decreases upon heating. At the same time, the bands which can be assigned with 5D4 → 7F6, 5D4 → 7F5, and 5D4 → 7F4 transitions were revealed in luminescence spectra at room temperature. The intensity of these bands is comparable to the intensity of the Raman spectrum of TbAl3(BO3)4. The observation of luminescence from the 5D4 multiplet (20600–20750 cm−1) upon excitation at λexc = 632.8 nm (15803 cm−1) and λexc = 532 nm (18797 cm−1) indicates strong nonlinear properties of the studied crystal. The structure of the main 7F6 multiplet of Tb+3 in the TbAl3(BO3)4 single crystal has been studied at 5 K by Raman spectroscopy. The energies of the electronic levels of 7F6 and 5D4 multiplets were determined from the luminescence spectra measured at 300 K.

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Публикация в журнале "Физика низких температур" Peschanskii A. V. Spectroscopic study of the TbAl3(BO3)4 single crystal: Raman and luminescence spectroscopy [Текст] / A. V. Peschanskii, A. Y. Glamazda, I. A. Gudim // Физ. низких температур. - 2020. - Т. 46 Вып. 12.- С.1437-1445

Держатели документа:
Natl Acad Sci Ukraine, B Verkin Inst Low Temp Phys & Engn, UA-61103 Kharkov, Ukraine.
RAS, Siberian Branch, LV Kirensky Inst Phys, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Glamazda, A. Yu.; Gudim, I. A.; Гудим, Ирина Анатольевна
}
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