卤化物
钙钛矿(结构)
量子点
材料科学
壳体(结构)
光电子学
芯(光纤)
半导体
纳米技术
化学
无机化学
复合材料
结晶学
作者
Xiaosheng Tang,Jie Yang,Shiqi Li,Zhengzheng Liu,Zhiping Hu,Jiongyue Hao,Juan Du,Yuxin Leng,Haiyan Qin,Xing Lin,Yue Lin,Yuxi Tian,Miao Zhou,Qihua Xiong
标识
DOI:10.1002/advs.201900412
摘要
Abstract The further practical applications of halide perovskite quantum dots (QDs) are blocked by problems of instability and nonradiative Auger recombination manifested as photoluminescence blinking. Here, single core/shell structured perovskite semiconductor QDs are successfully fabricated by capping CsPbBr 3 QD core with CdS shell. It is demonstrated that CsPbBr 3 /CdS core/shell QDs exhibit ultrahigh chemical stability and nonblinking photoluminescence with high quantum yield due to the reduced electronic traps within the core/shell structure. Efficiency of amplified spontaneous emission exhibits obvious enhancement compared to that of pure CsPbBr 3 QDs, originating from the mitigated competition between stimulated emission and suppressed nonradiative biexciton Auger recombination. Furthermore, low‐threshold whispering‐gallery‐mode lasing with a high‐quality factor is achieved by incorporating CsPbBr 3 /CdS QDs into microtubule resonators. Density functional theory (DFT)‐based first‐principles calculations are also performed to reveal the atomic interface structure, which supports the existence of CsPbBr 3 /CdS structure. An interesting feature of spatially separated charge density at CsPbBr 3 /CdS interface is found, which may greatly contribute to the suppressed Auger recombination. The results provide a practical approach to improve the stability and suppress the blinking of halide perovskite QDs, which may pave the way for future applications for various optoelectronic devices.
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