光致发光
钙钛矿(结构)
三极管
量子产额
材料科学
发光
发光二极管
量子点
量子效率
吸收(声学)
超快激光光谱学
光电子学
光谱学
分析化学(期刊)
结晶学
电致发光
化学
纳米技术
荧光
光学
物理
图层(电子)
量子力学
色谱法
复合材料
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/ange.201706860
摘要
Abstract All inorganic CsPbBr 3 perovskite quantum dots (QDs) are potential emitters for electroluminescent displays. We have developed a facile hot‐injection method to partially replace the toxic Pb 2+ with highly stable Sn 4+ . Meanwhile, the absolute photoluminescence quantum yield of CsPb 1− x Sn x Br 3 increased from 45 % to 83 % with Sn IV substitution. The transient absorption (TA) exciton dynamics in undoped CsPbBr 3 and CsPb 0.67 Sn 0.33 Br 3 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 CsPb 0.67 Sn 0.33 Br 3 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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