Zhou, Lei

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Authority KeyName Variants
orcid::0000-0001-6942-5363
  • Zhou, Lei (6)
Projects
International Postdoctoral Exchange Fellowship Program [20180056] Bilateral project China-Serbia “Highly efficient, thermally stable and moisture-resistant red-emitting Mn4+-activated single crystal phosphors for high performance warm wLEDs"
China-Poland Intergovernmental Science and Technology Cooperation Program [2015[170]/36-13] China Postdoctoral Science Foundation [2017M622848]
European Regional Development Fund [TK141] Government of Guangzhou City for international joint project [201704030020]
Guangdong Basic and Applied Basic Research Foundation [No. 2020A1515011556] Guangdong Province [U1702254, U1301242]
Guangdong Province [U1801253] Physics of amorphous and nanostructural materials
Joint Funds of the National Natural Science Foundation of China (NSFC) and Yunnan Province [U U1702254] Joint Funds of the National Natural Science Foundation of China (NSFC)-Guangdong Provinces [No. U22A20135 and U1801253]
Ministry of Education and Research of Estonia [GLTFY0111PR] Ministry of Education, Science and Technological Development of the Republic of Serbia
National Natural Science Foundation of China (11375278) National Natural Science Foundation of China [21771195]
National Natural Science Foundation of China [51662039, 21661033, 21771195] National Natural Science Foundation of China [51672315]
National Natural Science Foundation of China (NSFC) [21771195] National Natural Science Foundation of China (NSFC) [51902355]
National Natural Science Foundation of China (NSFC) [No. 51802359, 52002411 and 51902355] National Natural Science Foundation of China (NSFC) [U1301242]
National Natural Science Foundation of China (NSFC) [U1702254] National Natural Science Foundation of China (NSFC) [U1801253]
National Natural Science Foundation of China (NSFC)-Yunnan Province (U1301242) National Natural Science Foundation of China (NSFC)-Yunnan Province (U1702254)
National Natural Science Foundation of Guangdong Province [2016A030313305] Natural Science Foundation of Guangdong Province (2016A030313305)
Natural Science Foundation of Guangdong Province [2016A030313305] NSFC (21771195)

Author's Bibliography

The Upconversion Luminescence of Ca3Sc2Si3O12:Yb3+,Er3+ and Its Application in Thermometry

Hong, Junyu; Liu, Feilong; Dramićanin, Miroslav; Zhou, Lei; Wu, Mingmei

(2023)

TY  - JOUR
AU  - Hong, Junyu
AU  - Liu, Feilong
AU  - Dramićanin, Miroslav
AU  - Zhou, Lei
AU  - Wu, Mingmei
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11366
AB  - To develop novel luminescent materials for optical temperature measurement, a series of Yb3+- and Er3+-doped Ca3Sc2Si3O12 (CSS) upconversion (UC) phosphors were synthesized by the sol– gel combustion method. The crystal structure, phase purity, and element distribution of the samples were characterized by powder X-ray diffraction and a transmission electron microscope (TEM). The detailed study of the photoluminescence emission spectra of the samples shows that the addition of Yb3+ can greatly enhance the emission of Er3+ by effective energy transfer. The prepared Yb3+ and Er3+ co-doped CSS phosphors exhibit green emission bands near 522 and 555 nm and red emission bands near 658 nm, which correspond to the 2H11/2→4 I15/2, 4S3/2→4 I15/2, and 4F9/2→4 I15/2 transitions of Er3+, respectively. The temperature-dependent behavior of the CSS:0.2Yb3+,0.02Er3+ sample was carefully studied by the fluorescence intensity ratio (FIR) technique. The results indicate the excellent sensitivity of the sample, with a maximum absolute sensitivity of 0.67% K−1 at 500 K and a relative sensitivity of 1.34% K−1 at 300 K. We demonstrate here that the temperature measurement performance of FIR technology using the CSS:Yb3+,Er3+ phosphor is not inferior to that of infrared thermal imaging thermometers. Therefore, CSS:Yb3+,Er3+ phosphors have great potential applications in the field of optical thermometry.
T2  - Nanomaterials
T1  - The Upconversion Luminescence of Ca3Sc2Si3O12:Yb3+,Er3+ and Its Application in Thermometry
VL  - 13
IS  - 13
SP  - 1910
DO  - 10.3390/nano13131910
ER  - 
@article{
author = "Hong, Junyu and Liu, Feilong and Dramićanin, Miroslav and Zhou, Lei and Wu, Mingmei",
year = "2023",
abstract = "To develop novel luminescent materials for optical temperature measurement, a series of Yb3+- and Er3+-doped Ca3Sc2Si3O12 (CSS) upconversion (UC) phosphors were synthesized by the sol– gel combustion method. The crystal structure, phase purity, and element distribution of the samples were characterized by powder X-ray diffraction and a transmission electron microscope (TEM). The detailed study of the photoluminescence emission spectra of the samples shows that the addition of Yb3+ can greatly enhance the emission of Er3+ by effective energy transfer. The prepared Yb3+ and Er3+ co-doped CSS phosphors exhibit green emission bands near 522 and 555 nm and red emission bands near 658 nm, which correspond to the 2H11/2→4 I15/2, 4S3/2→4 I15/2, and 4F9/2→4 I15/2 transitions of Er3+, respectively. The temperature-dependent behavior of the CSS:0.2Yb3+,0.02Er3+ sample was carefully studied by the fluorescence intensity ratio (FIR) technique. The results indicate the excellent sensitivity of the sample, with a maximum absolute sensitivity of 0.67% K−1 at 500 K and a relative sensitivity of 1.34% K−1 at 300 K. We demonstrate here that the temperature measurement performance of FIR technology using the CSS:Yb3+,Er3+ phosphor is not inferior to that of infrared thermal imaging thermometers. Therefore, CSS:Yb3+,Er3+ phosphors have great potential applications in the field of optical thermometry.",
journal = "Nanomaterials",
title = "The Upconversion Luminescence of Ca3Sc2Si3O12:Yb3+,Er3+ and Its Application in Thermometry",
volume = "13",
number = "13",
pages = "1910",
doi = "10.3390/nano13131910"
}
Hong, J., Liu, F., Dramićanin, M., Zhou, L.,& Wu, M.. (2023). The Upconversion Luminescence of Ca3Sc2Si3O12:Yb3+,Er3+ and Its Application in Thermometry. in Nanomaterials, 13(13), 1910.
https://doi.org/10.3390/nano13131910
Hong J, Liu F, Dramićanin M, Zhou L, Wu M. The Upconversion Luminescence of Ca3Sc2Si3O12:Yb3+,Er3+ and Its Application in Thermometry. in Nanomaterials. 2023;13(13):1910.
doi:10.3390/nano13131910 .
Hong, Junyu, Liu, Feilong, Dramićanin, Miroslav, Zhou, Lei, Wu, Mingmei, "The Upconversion Luminescence of Ca3Sc2Si3O12:Yb3+,Er3+ and Its Application in Thermometry" in Nanomaterials, 13, no. 13 (2023):1910,
https://doi.org/10.3390/nano13131910 . .
1

Hydroquinone-modified Mn4+-activated fluoride red phosphors with improved water-resistance

Liu, Feilong; Yingyuan, Chen; Milićević, Bojana R.; Jiang, Chunyan; Huang, Senchuan; Zhou, Lei; Zhou, Jianbang; Wu, Mingmei

(2023)

TY  - JOUR
AU  - Liu, Feilong
AU  - Yingyuan, Chen
AU  - Milićević, Bojana R.
AU  - Jiang, Chunyan
AU  - Huang, Senchuan
AU  - Zhou, Lei
AU  - Zhou, Jianbang
AU  - Wu, Mingmei
PY  - 2023
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/10605
AB  - A facile strategy to modify the surface of K2SiF6:Mn4+ (KSFM) with commercially available hydrophilic hydroquinone (HQ) has been developed and waterproof stability (moisture resistance) of the KSFM has been significantly improved. It has been demonstrated that there are strong interactions between KSFM and HQ on the interface due to the hydrogen bonds of fluorine in KSFM with hydrogen in HQ. The relative luminous intensity of HQ-modified KSFM (denoted as KSFM-HQ) remained 99.7% of its initial value after immersion in water for 336 h, remarkable higher than that of KSFM which remained only 38.0%. It is proposed that the high water resistance of KSFM-HQ is achieved via two possible mechanisms: in situ decomposition of dark brown manganese (owing to the hydrolysis of [MnF6]2−) on the KSFM crystal surface and consequently the formation of a more protective Mn4+-free layer. The process effectively combines the advantages of transparent organic materials (herein HQ) before immersion in water and durable moisture resistance of inorganic materials (herein K2SiF6) on surface after immersion in water. The importance of HQ loading on moisture-sensitive fluoride phosphors has been further confirmed by using HQ-treated K2GeF6:Mn4+ (KGFM) as an additional example. This strategy provides a one-of-a-kind way to the development of water-resistant Mn4+-doped fluoride phosphors with high luminous stability for potential applications in water-borne fluorescent anti-counterfeiting ink and even warm WLEDs operating in high humidity. © 2023
T2  - Colloids and Surfaces. A: Physicochemical and Engineering Aspects
T1  - Hydroquinone-modified Mn4+-activated fluoride red phosphors with improved water-resistance
VL  - 661
DO  - 10.1016/j.colsurfa.2023.130954
ER  - 
@article{
author = "Liu, Feilong and Yingyuan, Chen and Milićević, Bojana R. and Jiang, Chunyan and Huang, Senchuan and Zhou, Lei and Zhou, Jianbang and Wu, Mingmei",
year = "2023",
abstract = "A facile strategy to modify the surface of K2SiF6:Mn4+ (KSFM) with commercially available hydrophilic hydroquinone (HQ) has been developed and waterproof stability (moisture resistance) of the KSFM has been significantly improved. It has been demonstrated that there are strong interactions between KSFM and HQ on the interface due to the hydrogen bonds of fluorine in KSFM with hydrogen in HQ. The relative luminous intensity of HQ-modified KSFM (denoted as KSFM-HQ) remained 99.7% of its initial value after immersion in water for 336 h, remarkable higher than that of KSFM which remained only 38.0%. It is proposed that the high water resistance of KSFM-HQ is achieved via two possible mechanisms: in situ decomposition of dark brown manganese (owing to the hydrolysis of [MnF6]2−) on the KSFM crystal surface and consequently the formation of a more protective Mn4+-free layer. The process effectively combines the advantages of transparent organic materials (herein HQ) before immersion in water and durable moisture resistance of inorganic materials (herein K2SiF6) on surface after immersion in water. The importance of HQ loading on moisture-sensitive fluoride phosphors has been further confirmed by using HQ-treated K2GeF6:Mn4+ (KGFM) as an additional example. This strategy provides a one-of-a-kind way to the development of water-resistant Mn4+-doped fluoride phosphors with high luminous stability for potential applications in water-borne fluorescent anti-counterfeiting ink and even warm WLEDs operating in high humidity. © 2023",
journal = "Colloids and Surfaces. A: Physicochemical and Engineering Aspects",
title = "Hydroquinone-modified Mn4+-activated fluoride red phosphors with improved water-resistance",
volume = "661",
doi = "10.1016/j.colsurfa.2023.130954"
}
Liu, F., Yingyuan, C., Milićević, B. R., Jiang, C., Huang, S., Zhou, L., Zhou, J.,& Wu, M.. (2023). Hydroquinone-modified Mn4+-activated fluoride red phosphors with improved water-resistance. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 661.
https://doi.org/10.1016/j.colsurfa.2023.130954
Liu F, Yingyuan C, Milićević BR, Jiang C, Huang S, Zhou L, Zhou J, Wu M. Hydroquinone-modified Mn4+-activated fluoride red phosphors with improved water-resistance. in Colloids and Surfaces. A: Physicochemical and Engineering Aspects. 2023;661.
doi:10.1016/j.colsurfa.2023.130954 .
Liu, Feilong, Yingyuan, Chen, Milićević, Bojana R., Jiang, Chunyan, Huang, Senchuan, Zhou, Lei, Zhou, Jianbang, Wu, Mingmei, "Hydroquinone-modified Mn4+-activated fluoride red phosphors with improved water-resistance" in Colloids and Surfaces. A: Physicochemical and Engineering Aspects, 661 (2023),
https://doi.org/10.1016/j.colsurfa.2023.130954 . .
4
3

Structural modulation induced intensity enhancement of full color spectra: A case of Ba3ZnTa2-xNbxO9:Eu3+phosphors

Li, Xiaohui; Zhou, Lei; Hong, Junyu; He, Shiman; Jing, Xiping; Dramićanin, Miroslav; Shi, Jianxin; Wu, Mingmei

(2020)

TY  - JOUR
AU  - Li, Xiaohui
AU  - Zhou, Lei
AU  - Hong, Junyu
AU  - He, Shiman
AU  - Jing, Xiping
AU  - Dramićanin, Miroslav
AU  - Shi, Jianxin
AU  - Wu, Mingmei
PY  - 2020
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/9016
AB  - Modulation of structural order-disorder transition and structural oxygen defects can provide fundamental insights in the optimization of luminescence performances of phosphors. In this study, the luminescence of Ba3ZnTa2O9(BZT) was systematically elucidated, including the emission arising from the charge transfer (Nb5+/Ta5+ O2-) and anti-site oxygen defect emission due to the B-site disordering (defect type: [2ZnNb3-+ 3Vo2+]), as corroborated by the electronic structural calculations and detailed experiments. We present a two-step design for the optimization of luminescence properties of Ba3ZnTa2O9phosphor. In the first step, the B-site equivalent doping (Ta5+substituted by Nb5+) was used to modulate the B-site atomic arrangement, which induced the formation of the cubic phase with B-site full disordering. In the second step, the A-site nonequivalent doping (Ba2+substituted by Eu3+) was used to decrease the oxygen defect concentration. After the two-step optimization, the photoluminescence excitation spectrum of Ba3-yEuyZnNb2O9(y= 0.1) shows a broad band excitation (300-400 nm), which is a good match with the near-UV LED chip emission. Even more importantly, the emission spectrum covers the entire visible spectral region and exhibits a remarkably enhanced emission intensity (a 40 times enhancement when compared to that of the intrinsic BZT). The fabricated LED device comprising an n-UV chip (= 370 nm) and a single-component Ba3-yEuyZnNb2O9(y= 0.1) phosphor coating emits a warm white light with a low correlated color temperature (CCT = 4813 K) and a good color rendering index (Ra= 82.36).
T2  - Journal of Materials Chemistry C
T1  - Structural modulation induced intensity enhancement of full color spectra: A case of Ba3ZnTa2-xNbxO9:Eu3+phosphors
VL  - 8
IS  - 20
SP  - 6715
EP  - 6723
DO  - 10.1039/D0TC01201G
ER  - 
@article{
author = "Li, Xiaohui and Zhou, Lei and Hong, Junyu and He, Shiman and Jing, Xiping and Dramićanin, Miroslav and Shi, Jianxin and Wu, Mingmei",
year = "2020",
abstract = "Modulation of structural order-disorder transition and structural oxygen defects can provide fundamental insights in the optimization of luminescence performances of phosphors. In this study, the luminescence of Ba3ZnTa2O9(BZT) was systematically elucidated, including the emission arising from the charge transfer (Nb5+/Ta5+ O2-) and anti-site oxygen defect emission due to the B-site disordering (defect type: [2ZnNb3-+ 3Vo2+]), as corroborated by the electronic structural calculations and detailed experiments. We present a two-step design for the optimization of luminescence properties of Ba3ZnTa2O9phosphor. In the first step, the B-site equivalent doping (Ta5+substituted by Nb5+) was used to modulate the B-site atomic arrangement, which induced the formation of the cubic phase with B-site full disordering. In the second step, the A-site nonequivalent doping (Ba2+substituted by Eu3+) was used to decrease the oxygen defect concentration. After the two-step optimization, the photoluminescence excitation spectrum of Ba3-yEuyZnNb2O9(y= 0.1) shows a broad band excitation (300-400 nm), which is a good match with the near-UV LED chip emission. Even more importantly, the emission spectrum covers the entire visible spectral region and exhibits a remarkably enhanced emission intensity (a 40 times enhancement when compared to that of the intrinsic BZT). The fabricated LED device comprising an n-UV chip (= 370 nm) and a single-component Ba3-yEuyZnNb2O9(y= 0.1) phosphor coating emits a warm white light with a low correlated color temperature (CCT = 4813 K) and a good color rendering index (Ra= 82.36).",
journal = "Journal of Materials Chemistry C",
title = "Structural modulation induced intensity enhancement of full color spectra: A case of Ba3ZnTa2-xNbxO9:Eu3+phosphors",
volume = "8",
number = "20",
pages = "6715-6723",
doi = "10.1039/D0TC01201G"
}
Li, X., Zhou, L., Hong, J., He, S., Jing, X., Dramićanin, M., Shi, J.,& Wu, M.. (2020). Structural modulation induced intensity enhancement of full color spectra: A case of Ba3ZnTa2-xNbxO9:Eu3+phosphors. in Journal of Materials Chemistry C, 8(20), 6715-6723.
https://doi.org/10.1039/D0TC01201G
Li X, Zhou L, Hong J, He S, Jing X, Dramićanin M, Shi J, Wu M. Structural modulation induced intensity enhancement of full color spectra: A case of Ba3ZnTa2-xNbxO9:Eu3+phosphors. in Journal of Materials Chemistry C. 2020;8(20):6715-6723.
doi:10.1039/D0TC01201G .
Li, Xiaohui, Zhou, Lei, Hong, Junyu, He, Shiman, Jing, Xiping, Dramićanin, Miroslav, Shi, Jianxin, Wu, Mingmei, "Structural modulation induced intensity enhancement of full color spectra: A case of Ba3ZnTa2-xNbxO9:Eu3+phosphors" in Journal of Materials Chemistry C, 8, no. 20 (2020):6715-6723,
https://doi.org/10.1039/D0TC01201G . .
12
10
11

Efficient Luminescence Enhancement of Mg 2 TiO 4 :Mn 4+ Red Phosphor by Incorporating Plasmonic Ag@SiO 2 Nanoparticles

Dolgov, Leonid; Hong, Junyu; Zhou, Lei; Li, Xiaohui; Li, Junhao; Đorđević, Vesna R.; Dramićanin, Miroslav; Shi, Jianxin; Wu, Mingmei

(2019)

TY  - JOUR
AU  - Dolgov, Leonid
AU  - Hong, Junyu
AU  - Zhou, Lei
AU  - Li, Xiaohui
AU  - Li, Junhao
AU  - Đorđević, Vesna R.
AU  - Dramićanin, Miroslav
AU  - Shi, Jianxin
AU  - Wu, Mingmei
PY  - 2019
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/8349
AB  - One of prospective ways for boosting efficiency of luminescent materials is their combination with noble metal nanoparticles. Collective, so-called plasmon, oscillations of surface electrons in a nanoparticle can resonantly interact with incident or fluorescent light and cause an increase in the light absorption cross section or radiative rate for an adjacent emitter. Plasmonic inorganic phosphors require gentle host crystallization at which added noble nanoparticles will not suffer from aggregation or oxidation. The prospective plasmonic Mg2TiO4:Mn4+ phosphor containing core@shell Ag@SiO2 nanoparticles is prepared here by spare low-temperature annealing of a sol-gel host precursor. It is revealed that Mn4+ luminescence nonmonotonously depends on the size and concentration of 40 and 70 nm silver nanoparticles. It is demonstrated that luminescence of the Mg2TiO4:Mn4+ phosphor can be up to a 1.5 times increase when Mn4+ excitation is supported by localized surface plasmon resonance in Ag@SiO2 nanoparticles. © 2019 American Chemical Society.
T2  - ACS Applied Materials and Interfaces
T1  - Efficient Luminescence Enhancement of Mg 2 TiO 4 :Mn 4+ Red Phosphor by Incorporating Plasmonic Ag@SiO 2 Nanoparticles
VL  - 11
IS  - 23
SP  - 21004
EP  - 21009
DO  - 10.1021/acsami.9b05781
ER  - 
@article{
author = "Dolgov, Leonid and Hong, Junyu and Zhou, Lei and Li, Xiaohui and Li, Junhao and Đorđević, Vesna R. and Dramićanin, Miroslav and Shi, Jianxin and Wu, Mingmei",
year = "2019",
abstract = "One of prospective ways for boosting efficiency of luminescent materials is their combination with noble metal nanoparticles. Collective, so-called plasmon, oscillations of surface electrons in a nanoparticle can resonantly interact with incident or fluorescent light and cause an increase in the light absorption cross section or radiative rate for an adjacent emitter. Plasmonic inorganic phosphors require gentle host crystallization at which added noble nanoparticles will not suffer from aggregation or oxidation. The prospective plasmonic Mg2TiO4:Mn4+ phosphor containing core@shell Ag@SiO2 nanoparticles is prepared here by spare low-temperature annealing of a sol-gel host precursor. It is revealed that Mn4+ luminescence nonmonotonously depends on the size and concentration of 40 and 70 nm silver nanoparticles. It is demonstrated that luminescence of the Mg2TiO4:Mn4+ phosphor can be up to a 1.5 times increase when Mn4+ excitation is supported by localized surface plasmon resonance in Ag@SiO2 nanoparticles. © 2019 American Chemical Society.",
journal = "ACS Applied Materials and Interfaces",
title = "Efficient Luminescence Enhancement of Mg 2 TiO 4 :Mn 4+ Red Phosphor by Incorporating Plasmonic Ag@SiO 2 Nanoparticles",
volume = "11",
number = "23",
pages = "21004-21009",
doi = "10.1021/acsami.9b05781"
}
Dolgov, L., Hong, J., Zhou, L., Li, X., Li, J., Đorđević, V. R., Dramićanin, M., Shi, J.,& Wu, M.. (2019). Efficient Luminescence Enhancement of Mg 2 TiO 4 :Mn 4+ Red Phosphor by Incorporating Plasmonic Ag@SiO 2 Nanoparticles. in ACS Applied Materials and Interfaces, 11(23), 21004-21009.
https://doi.org/10.1021/acsami.9b05781
Dolgov L, Hong J, Zhou L, Li X, Li J, Đorđević VR, Dramićanin M, Shi J, Wu M. Efficient Luminescence Enhancement of Mg 2 TiO 4 :Mn 4+ Red Phosphor by Incorporating Plasmonic Ag@SiO 2 Nanoparticles. in ACS Applied Materials and Interfaces. 2019;11(23):21004-21009.
doi:10.1021/acsami.9b05781 .
Dolgov, Leonid, Hong, Junyu, Zhou, Lei, Li, Xiaohui, Li, Junhao, Đorđević, Vesna R., Dramićanin, Miroslav, Shi, Jianxin, Wu, Mingmei, "Efficient Luminescence Enhancement of Mg 2 TiO 4 :Mn 4+ Red Phosphor by Incorporating Plasmonic Ag@SiO 2 Nanoparticles" in ACS Applied Materials and Interfaces, 11, no. 23 (2019):21004-21009,
https://doi.org/10.1021/acsami.9b05781 . .
1
25
18
27

Mn 2+ and Mn 4+ red phosphors: synthesis, luminescence and applications in WLEDs. A review

Zhou, Qiang; Dolgov, Leonid; Srivastava, Alok M; Zhou, Lei; Wang, Zhengliang; Shi, Jianxin; Dramićanin, Miroslav; Brik, Mikhail G.; Wu, Mingmei

(2018)

TY  - JOUR
AU  - Zhou, Qiang
AU  - Dolgov, Leonid
AU  - Srivastava, Alok M
AU  - Zhou, Lei
AU  - Wang, Zhengliang
AU  - Shi, Jianxin
AU  - Dramićanin, Miroslav
AU  - Brik, Mikhail G.
AU  - Wu, Mingmei
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7638
AB  - Transition-metal activated phosphors are an important family of luminescent materials that can produce white light with an outstanding color rendering index and correlated color temperature for use in light-emitting diodes.  In recent years, work in this quite “hot” research field has focused on the development of Mn2+ and Mn4+ activated red phosphors. In this review article, we provide an overview of recent studies on Mn2+ and Mn4+ doped phosphors, including detailed synthesis routes (solid-state reaction and wet-chemical synthesis) and description of luminescence mechanisms and phosphors’ behaviors; discuss their promising applications in white light-emitting diodes; and present an extensive list of references to representative works in this field.
T2  - Journal of Materials Chemistry C
T1  - Mn 2+ and Mn 4+ red phosphors: synthesis, luminescence and applications in WLEDs. A review
VL  - 6
IS  - 11
SP  - 2652
EP  - 2671
DO  - 10.1039/C8TC00251G
ER  - 
@article{
author = "Zhou, Qiang and Dolgov, Leonid and Srivastava, Alok M and Zhou, Lei and Wang, Zhengliang and Shi, Jianxin and Dramićanin, Miroslav and Brik, Mikhail G. and Wu, Mingmei",
year = "2018",
abstract = "Transition-metal activated phosphors are an important family of luminescent materials that can produce white light with an outstanding color rendering index and correlated color temperature for use in light-emitting diodes.  In recent years, work in this quite “hot” research field has focused on the development of Mn2+ and Mn4+ activated red phosphors. In this review article, we provide an overview of recent studies on Mn2+ and Mn4+ doped phosphors, including detailed synthesis routes (solid-state reaction and wet-chemical synthesis) and description of luminescence mechanisms and phosphors’ behaviors; discuss their promising applications in white light-emitting diodes; and present an extensive list of references to representative works in this field.",
journal = "Journal of Materials Chemistry C",
title = "Mn 2+ and Mn 4+ red phosphors: synthesis, luminescence and applications in WLEDs. A review",
volume = "6",
number = "11",
pages = "2652-2671",
doi = "10.1039/C8TC00251G"
}
Zhou, Q., Dolgov, L., Srivastava, A. M., Zhou, L., Wang, Z., Shi, J., Dramićanin, M., Brik, M. G.,& Wu, M.. (2018). Mn 2+ and Mn 4+ red phosphors: synthesis, luminescence and applications in WLEDs. A review. in Journal of Materials Chemistry C, 6(11), 2652-2671.
https://doi.org/10.1039/C8TC00251G
Zhou Q, Dolgov L, Srivastava AM, Zhou L, Wang Z, Shi J, Dramićanin M, Brik MG, Wu M. Mn 2+ and Mn 4+ red phosphors: synthesis, luminescence and applications in WLEDs. A review. in Journal of Materials Chemistry C. 2018;6(11):2652-2671.
doi:10.1039/C8TC00251G .
Zhou, Qiang, Dolgov, Leonid, Srivastava, Alok M, Zhou, Lei, Wang, Zhengliang, Shi, Jianxin, Dramićanin, Miroslav, Brik, Mikhail G., Wu, Mingmei, "Mn 2+ and Mn 4+ red phosphors: synthesis, luminescence and applications in WLEDs. A review" in Journal of Materials Chemistry C, 6, no. 11 (2018):2652-2671,
https://doi.org/10.1039/C8TC00251G . .
1
513
317
505

Broad-band emission of A3B′B′′2O9 complex perovskites (A = Ba, Sr; B′ = Zn; B′′ = Ta, Nb) realized by structural variations of the B site order–disorder

Li, Xiaohui; Zhou, Lei; Dramićanin, Miroslav; Tang, Qiang; Jing, Xiping; Shi, Jianxin; Xu, Yiqin; Wu, Mingmei

(2018)

TY  - JOUR
AU  - Li, Xiaohui
AU  - Zhou, Lei
AU  - Dramićanin, Miroslav
AU  - Tang, Qiang
AU  - Jing, Xiping
AU  - Shi, Jianxin
AU  - Xu, Yiqin
AU  - Wu, Mingmei
PY  - 2018
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/7987
AB  - Broad emission with a full and continuous color spectrum realized by crystal engineering is extensively desired to simulate natural sunlight and improve the white color quality. Herein, new insight into the modulation of B site order-disorder and intrinsic oxygen defects for complex perovskite (A(3)BB(2)O(9)) Sr3-xScxZnNb2O9 (0 x 0.1) phosphors is demonstrated for broad-band emission via crystal engineering. We elucidate that the spectrum of Sr3ZnNb2O9 synthesized at an optimal temperature exhibits two emission bands under near-ultraviolet excitation ((ex) = 374 nm) which is readily available from near ultraviolet chips. The two broad emission bands can be ascribed to charge transfer from the empty 4d (t(2g))-orbitals of Nb5+ ions to the filled 2p-orbitals of O2- ions and the intrinsic oxygen defects. Further, as a proposed strategy to optimize the luminescence property of Sr3ZnNb2O9 (SZN), we realized A-site nonequivalent doping to induce B-site disordering and cancel the luminescence quenching which results from B site ordering. The A-site nonequivalent doping efficiently offsets intrinsic oxygen defects, as validated by systematic analyses of experiments and DFT calculations. Consequently, the novel phosphor Sr3-xScxZnNb2O9 (x = 0.1) shows a high color rendering index (R-a = 82.2) and negligible color shift. In addition, its emission intensity is enhanced by approximate to 70 times as compared to the pristine Sr3ZnNb2O9.
T2  - Journal of Materials Chemistry C
T1  - Broad-band emission of A3B′B′′2O9 complex perovskites (A = Ba, Sr; B′ = Zn; B′′ = Ta, Nb) realized by structural variations of the B site order–disorder
VL  - 6
IS  - 46
SP  - 12566
EP  - 12574
DO  - 10.1039/C8TC04874F
ER  - 
@article{
author = "Li, Xiaohui and Zhou, Lei and Dramićanin, Miroslav and Tang, Qiang and Jing, Xiping and Shi, Jianxin and Xu, Yiqin and Wu, Mingmei",
year = "2018",
abstract = "Broad emission with a full and continuous color spectrum realized by crystal engineering is extensively desired to simulate natural sunlight and improve the white color quality. Herein, new insight into the modulation of B site order-disorder and intrinsic oxygen defects for complex perovskite (A(3)BB(2)O(9)) Sr3-xScxZnNb2O9 (0 x 0.1) phosphors is demonstrated for broad-band emission via crystal engineering. We elucidate that the spectrum of Sr3ZnNb2O9 synthesized at an optimal temperature exhibits two emission bands under near-ultraviolet excitation ((ex) = 374 nm) which is readily available from near ultraviolet chips. The two broad emission bands can be ascribed to charge transfer from the empty 4d (t(2g))-orbitals of Nb5+ ions to the filled 2p-orbitals of O2- ions and the intrinsic oxygen defects. Further, as a proposed strategy to optimize the luminescence property of Sr3ZnNb2O9 (SZN), we realized A-site nonequivalent doping to induce B-site disordering and cancel the luminescence quenching which results from B site ordering. The A-site nonequivalent doping efficiently offsets intrinsic oxygen defects, as validated by systematic analyses of experiments and DFT calculations. Consequently, the novel phosphor Sr3-xScxZnNb2O9 (x = 0.1) shows a high color rendering index (R-a = 82.2) and negligible color shift. In addition, its emission intensity is enhanced by approximate to 70 times as compared to the pristine Sr3ZnNb2O9.",
journal = "Journal of Materials Chemistry C",
title = "Broad-band emission of A3B′B′′2O9 complex perovskites (A = Ba, Sr; B′ = Zn; B′′ = Ta, Nb) realized by structural variations of the B site order–disorder",
volume = "6",
number = "46",
pages = "12566-12574",
doi = "10.1039/C8TC04874F"
}
Li, X., Zhou, L., Dramićanin, M., Tang, Q., Jing, X., Shi, J., Xu, Y.,& Wu, M.. (2018). Broad-band emission of A3B′B′′2O9 complex perovskites (A = Ba, Sr; B′ = Zn; B′′ = Ta, Nb) realized by structural variations of the B site order–disorder. in Journal of Materials Chemistry C, 6(46), 12566-12574.
https://doi.org/10.1039/C8TC04874F
Li X, Zhou L, Dramićanin M, Tang Q, Jing X, Shi J, Xu Y, Wu M. Broad-band emission of A3B′B′′2O9 complex perovskites (A = Ba, Sr; B′ = Zn; B′′ = Ta, Nb) realized by structural variations of the B site order–disorder. in Journal of Materials Chemistry C. 2018;6(46):12566-12574.
doi:10.1039/C8TC04874F .
Li, Xiaohui, Zhou, Lei, Dramićanin, Miroslav, Tang, Qiang, Jing, Xiping, Shi, Jianxin, Xu, Yiqin, Wu, Mingmei, "Broad-band emission of A3B′B′′2O9 complex perovskites (A = Ba, Sr; B′ = Zn; B′′ = Ta, Nb) realized by structural variations of the B site order–disorder" in Journal of Materials Chemistry C, 6, no. 46 (2018):12566-12574,
https://doi.org/10.1039/C8TC04874F . .
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