非阻塞I/O
钙钛矿(结构)
氧化镍
材料科学
能量转换效率
化学工程
氧化物
光电子学
纳米技术
化学
冶金
催化作用
工程类
有机化学
作者
Yuan Yu,Peng Xu,Huitian Du,Qian Zhou,Yukun Wu,Yuying Hao,Junfeng Ren,Zhiyong Pang,Zhaolai Chen,Shenghao Han
出处
期刊:Solar RRL
[Wiley]
日期:2023-01-14
卷期号:7 (6)
被引量:8
标识
DOI:10.1002/solr.202201047
摘要
In recent years, nickel oxide (NiO x ) is widely used as an excellent hole transport layer for the inverted perovskite solar cells (PSCs), due to its decent hole conductivity, easy processability, and low cost. However, the photovoltaic performance and stability of NiO x ‐based PSCs are severely limited by the poor perovskite/NiO x interface. Herein, a versatile coupling agent di(dioctylpyrophosphato) ethylene titanate (NDZ‐311) is introduced to improve the performance of NiO x ‐based inverted PSCs by suppressing nonradiative recombination and strengthening charge transfer at the perovskite/NiO x interface. Moreover, the chemical reaction between NDZ‐311 and NiO x reduces the surface hydroxyl groups of NiO x film and avoids direct contact between perovskite and NiO x film, which mitigate material degradation caused by high‐valence Ni ions and hydroxyl groups. As a result, the average power conversion efficiency (PCE) of inverted PSCs is enhanced from ≈18.01% to ≈19.92% and a maximum PCE of ≈20.39% is obtained. The unencapsulated PSC with NDZ‐311 modification maintains 87.65% of their initial performance after 400 h aging test in air, much better than the control device (49.41% after 400 h). The work demonstrates the potential application of NDZ‐311 for commercial PSCs, considering NDZ‐311 is a cheap industrial material.
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