卤化物
镱
镧系元素
兴奋剂
原子单位
离子
材料科学
密度泛函理论
化学物理
光电效应
纳米技术
化学
无机化学
光电子学
物理
计算化学
有机化学
量子力学
作者
Wen Feng Xu,J. Liu,Bin Dong,Jindou Huang,Honglong Shi,Xiangxin Xue,Mao Liu
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2023-09-01
卷期号:9 (35)
被引量:30
标识
DOI:10.1126/sciadv.adi7931
摘要
Lanthanide-doped lead halide perovskites have demonstrated great potential for photoelectric applications. However, there is a long-standing controversy about the existence of lanthanide ions, e.g., whether the doping of Ln 3+ is successful or not; the substituting sites of Ln 3+ in lead halide perovskites are unclear. We directly identify the doped Yb 3+ in CsPbCl 3 perovskites by using the state-of-the-art transmission electron microscopy and three-dimensional atom probe tomography at atomic scale. Different from the previous assumptions and/or results, we evidence that Yb 3+ simultaneously replace Pb 2+ and occupy the lattice interstitial sites. Furthermore, we directly observe the cluster phenomenon of CsPbCl 3 single crystal at near atomic scale. Density functional theory modeling further confirms and explains the mechanisms of our findings. Our findings thus provide an atomic-level understanding of the doping mechanism in perovskites and will stimulate a further thinking of the doping effect on the performance of perovskites.
科研通智能强力驱动
Strongly Powered by AbleSci AI