光致发光
钙钛矿(结构)
量子点
材料科学
三极管
电致发光
发光二极管
量子产额
光电子学
发光
量子效率
吸收(声学)
超快激光光谱学
光谱学
分析化学(期刊)
纳米技术
化学
结晶学
荧光
光学
物理
量子力学
图层(电子)
复合材料
色谱法
作者
Hung‐Chia Wang,Weigao Wang,An‐Cih Tang,Hsinyu Tsai,Zhen Bao,Toshiyuki Ihara,Naoki Yarita,Hirokazu Tahara,Yoshihiko Kanemitsu,Shuming Chen,Ru‐Shi Liu
标识
DOI:10.1002/anie.201706860
摘要
All inorganic CsPbBr3 perovskite quantum dots (QDs) are potential emitters for electroluminescent displays. We have developed a facile hot-injection method to partially replace the toxic Pb2+ with highly stable Sn4+ . Meanwhile, the absolute photoluminescence quantum yield of CsPb1-x Snx Br3 increased from 45 % to 83 % with SnIV substitution. The transient absorption (TA) exciton dynamics in undoped CsPbBr3 and CsPb0.67 Sn0.33 Br3 QDs at various excitation fluences were determined by femtosecond transient absorption, time-resolved photoluminescence, and single-dot spectroscopy, providing clear evidence for the suppression of trion generation by Sn doping. These highly luminescent CsPb0.67 Sn0.33 Br3 QDs emit at 517 nm. A device based on these QDs exhibited a luminance of 12 500 cd m-2 , a current efficiency of 11.63 cd A-1 , an external quantum efficiency of 4.13 %, a power efficiency of 6.76 lm w-1 , and a low turn-on voltage of 3.6 V, which are the best values among reported tin-based perovskite quantum-dot LEDs.
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