非阻塞I/O
材料科学
氧化镍
能量转换效率
钙钛矿(结构)
光伏
光电流
纳米技术
化学工程
电子迁移率
光电子学
氧化物
光伏系统
催化作用
冶金
电气工程
有机化学
化学
工程类
作者
Fang Cao,Fangwen Cheng,Xiaofeng Huang,Xinfeng Dai,Ziheng Tang,Siqing Nie,Jun Yin,Jing Li,Nanfeng Zheng,Binghui Wu
标识
DOI:10.1002/adfm.202201423
摘要
Abstract As an inorganic hole transport material (HTM), nickel oxide (NiO x ) is widely used in perovskite solar cells (PSCs) due to its low cost and intrinsic stability. However, on account of its poor film formation on perovskite, the low power conversion efficiency (PCE) and stability of regular NiO x ‐based PSCs is a main obstacle for commercialization. Here, a solution‐processed inorganic/organic hybrid hole transporting system is developed to resolve this issue, thereby improving the PCE from 16.0% to 21.2%. Poly(3‐hexylthiophene) (P3HT) is studied as the typical case, revealing that the performance improvement mainly lies in the synergistic interaction between NiO x and P3HT: 1) the introduction of P3HT improves assembly regularity and film uniformity of NiO x ; 2) electron redistribution between P3HT and NiO x increases the Ni 3+ /Ni 2+ ratio for higher hole mobility; 3) the feed‐back impact of NiO x on P3HT enhances molecular orientation of polymer chains in P3HT for better hole transport through polymer framework. Finally, the encapsulated solar cell modules with P3HT‐promoted NiO x maintains 91% of the initial efficiency after 1000 h aging at a harsh 85 °C/85% relative humidity condition. This finding provides a feasible approach for using NiO x ‐based HTMs to realize high‐performance regular PSCs, paving the way for their commercialization.
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