材料科学
结晶
钙钛矿(结构)
能量转换效率
化学工程
Crystal(编程语言)
沉积(地质)
碘化物
溴化物
部分
晶体生长
光电子学
无机化学
结晶学
有机化学
化学
程序设计语言
计算机科学
生物
工程类
沉积物
古生物学
作者
Wei You,Zhu Ma,Zhuowei Du,Yi Chen,Junbo Yang,Qiang Yang,Zhangfeng Huang,Shanyue Hou,Yanlin Li,Qian Zhang,Hao Du,Yixian Li,Fuchun Gou,Zhuo Lv,Hong Yu,Yan Xiang,Cheng Huang,Jian Yu,Yaohua Mai,Fangdan Jiang
标识
DOI:10.1021/acsami.4c05880
摘要
The two-step sequential deposition strategy has been widely recognized in promoting the research and application of perovskite solar cells, but the rapid reaction of organic salts with lead iodide inevitably affects the growth of perovskite crystals, accompanied by the generation of more defects. In this study, the regulation of crystal growth was achieved in a two-step deposition method by mixing 1-naphthylmethylammonium bromide (NMABr) with organic salts. The results show that the addition of NMABr effectively delays the aggregation and crystallization behavior of organic salts; thereby, the growth of the optimal crystal (001) orientation of perovskite is promoted. Based on this phenomenon of delaying the crystallization process of perovskite, the “slow-release effect assisted crystallization” is defined. Moreover, the incorporation of the Br element expands the band gap of perovskite and mitigates material defects as nonradiative recombination centers. Consequently, the power conversion efficiency (PCE) of the enhanced perovskite solar cells (PSCs) reaches 20.20%. It is noteworthy that the hydrophobic nature of the naphthalene moiety in NMABr can enhance the humidity resistance of PSCs, and the perovskite phase does not decompose for more than 3000 h (30–40% RH), enabling it to retain 90% of its initial efficiency even after exposure to a nitrogen environment for 1200 h.
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