TY - JOUR
T1 - Superior thermally-stable narrow-band green emitter from Mn2+-doped zero thermal expansion (ZTE) material
AU - Wang, Wei
AU - Yang, Hang
AU - Fu, Meiqian
AU - Zhang, Xinyang
AU - Guan, Mengyu
AU - Wei, Yi
AU - Lin, Chun Che
AU - Li, Guogang
N1 - Funding Information:
This work was supported by National Natural Science Foundation of China (Grant Nos. 52072349 and 51672259), and the Ministry of Science and Technology of Taiwan (Contract Nos. MOST 109-2113-M-027-004 and MOST 109-2622-M-027-001-CC2).
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/7/1
Y1 - 2021/7/1
N2 - Thermal quenching is still a pivotal challenge for phosphor materials in white light emitting diodes lighting applications. Herein, we propose an effective strategy to design a near zero-thermal-quenching green emission in zero-thermal-expanding Zn4B6O13 host based on unique 3D isotropic cage structure. The integrated emission intensity of Zn4B6O13:Mn2+ could maintain 103% of initial intensity at 150 °C and 98% at 250 °C under blue light excitation. During the low-frequency vibrations, the unchanged bonds and angles induce the zero thermal expansion, and the unaffected lattice and coordination environment contribute the nearly unchanged emission intensity during the heating process. In addition, an efficient self-reduction of activators in the studied system is ascribed to vacancy and interstitial oxygen defects act as donors to provide electrons. This work initiates a novel strategy to construct thermally-stable and self-reductive phosphors for multiple optical applications.
AB - Thermal quenching is still a pivotal challenge for phosphor materials in white light emitting diodes lighting applications. Herein, we propose an effective strategy to design a near zero-thermal-quenching green emission in zero-thermal-expanding Zn4B6O13 host based on unique 3D isotropic cage structure. The integrated emission intensity of Zn4B6O13:Mn2+ could maintain 103% of initial intensity at 150 °C and 98% at 250 °C under blue light excitation. During the low-frequency vibrations, the unchanged bonds and angles induce the zero thermal expansion, and the unaffected lattice and coordination environment contribute the nearly unchanged emission intensity during the heating process. In addition, an efficient self-reduction of activators in the studied system is ascribed to vacancy and interstitial oxygen defects act as donors to provide electrons. This work initiates a novel strategy to construct thermally-stable and self-reductive phosphors for multiple optical applications.
KW - 3D isotropic cage structure
KW - Narrow band green emission
KW - Self-reduction
KW - Superior thermal stability
KW - Zero thermal expansion
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U2 - 10.1016/j.cej.2021.128979
DO - 10.1016/j.cej.2021.128979
M3 - Article
AN - SCOPUS:85101159499
SN - 1385-8947
VL - 415
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
M1 - 128979
ER -