Liao, Jin-Feng, Li, Wen-Guang, Rao, Hua-Shang, Chen, Bai-Xue, Wang, Xu-Dong, Chen, Hong-Yan, and Kuang, Dai-Bin
ABX3-type organic-inorganic hybrid halide perovskite materials have been recognized as promising candidates for optoelectronic applications. However, poor stability of organic-inorganic hybrid perovskite hinders their forward long-term utilization and hence an effective strategy is needed to replace the organic part with an inorganic cation. Herein, all inorganic CsPbI3nanowires with a diameter of 50–100 nm are synthesized on fluorine-doped tin oxide glass via a simple solution-dipping process, which are further transformed into CsPbBr3nanowires through a solution-phase halide exchange method. A phase change from non-perovskite to perovskite structure is observed during the ion substitution process of I−by Br−, which is elaborated by X-ray diffraction, absorption and photoluminescence spectra. We for the first time apply the as-formed CsPbI3and CsPbBr3nanowires into perovskite solar cells, yielding power conversion efficiency of 0.11% and 1.21%, respectively. The inorganic CsPbBr3nanowire solar cell shows impressive stability which still remains 99% of the initial power conversion efficiency even after 5500 h aging. 有机无机杂化钙钛矿因其优异的光电性能受到广泛关注, 但是其对湿度、热的不稳定性会限制钙钛矿电池的进一步发展. 本文通过简单的溶液浸泡法在导电基底上制备了尺寸为50–100 nm的全无机碘化铅铯纳米线, 并通过离子交换法将碘化铅铯置换成溴化铅铯纳米线. 文章通过X射线衍射谱、紫外可见吸收光谱、荧光发光光谱对I离子交换成Br离子过程进行了研究. 结果发现I-Br离子交换过程中伴随着晶体结构的变化, 起初的碘化铅铯为非钙钛矿结构, 离子交换后制备的溴化铅铯为钙钛矿结构. 本文将全无机卤化铅铯纳米线应用在钙钛矿电池器件中, 器件显示出优越的稳定性, 放置5500小时效率几乎未衰减.