材料科学
碘化物
钙钛矿(结构)
离子
碘
能量转换效率
载流子寿命
空位缺陷
微晶
离子键合
光化学
光电子学
化学工程
无机化学
结晶学
有机化学
硅
冶金
化学
工程类
作者
Qi Huang,Qiangqiang Zhao,Bingqian Zhang,Xiaofan Du,Dachang Liu,Hongpei Ji,Caiyun Gao,Xiuhong Sun,Yijin Wei,Zhipeng Shao,Jianxu Ding,Xiao Wang,Guanglei Cui,Shuping Pang
标识
DOI:10.1021/acsami.4c00731
摘要
Owing to the ionic bond nature of the Pb–I bond, the iodide at the interface of perovskite polycrystalline films was easily lost during the preparation process, resulting in the formation of a large number of iodine vacancy defects. The presence of iodine vacancy defects can cause nonradiative recombination, provide a pathway for iodide migration, and be harmful to the power conversion efficiency (PCE) and stability of organic–inorganic hybrid perovskite solar cells (HPSCs). Here, in order to increase the robustness of iodides at the interface, a strategy to introduce anion binding effects was developed to stabilize the perovskite films. It was demonstrated that the N,N′-diphenylurea (DPU), characterized by high anionic binding constants and a Y-shaped structure, provides a relatively strong hydrogen bond donor site to effectively reduce the iodine loss during film preparation and inhibits iodide migration in the device working condition. As expected, the reduced iodine loss considerably improves the quality of the perovskite films and suppresses nonradiative recombination. The performance of the device after DPU modification was significantly increased, with the PCE rising from 23.65 to 25.01% with huge stability enhancement as well.
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