胶体
量子点
钝化
钙钛矿(结构)
能量转换效率
碘化物
材料科学
兴奋剂
卤化物
吸收(声学)
太阳能电池
纳米颗粒
化学物理
离子
纳米技术
结晶学
化学
光电子学
无机化学
物理化学
复合材料
有机化学
图层(电子)
作者
Chenghao Bi,Xuejiao Sun,Xin Huang,Shixun Wang,Jifeng Yuan,Jun Xi Wang,Tõnu Pullerits,Jianjun Tian
标识
DOI:10.1021/acs.chemmater.0c01750
摘要
All inorganic halide perovskites in the form of colloidal quantum dots (QDs) have come into people's view as one of the potential materials for the high-efficiency solar cells; nevertheless, the high surface trap density and poor stability of QDs restrict the performance improvement and application. Here, we obtain colloidal inorganic perovskite CsPb1–xZnxI3 QDs by the hot-injection synthesis process with the addition of ZnCl2. Synchrotron-based X-ray absorption fine structures demonstrate that the guest Zn2+ ions are doped into the CsPbI3 structure to improve the local ordering of the lattice of the perovskite, reducing the octahedral distortions. The increase of the Goldschmidt tolerance factor and the Pb–I bond energy also enhance the stability of the perovskite structure. Furthermore, the Cl– ions from ZnCl2 occupy the iodide vacancies of the perovskite to decrease the nonradiative recombination. The synergistic effect of doping and defect passivation makes for stable colloidal CsPb0.97Zn0.03I3 QDs with ultralow density of trap states. The champion solar cell based on the QDs shows a power conversion efficiency of 14.8% and a largely improved stability under ambient conditions.
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