钝化
铵
碘化物
三碘化物
热稳定性
钙钛矿(结构)
胺气处理
降级(电信)
化学工程
材料科学
氨
碘化铵
能量转换效率
无机化学
化学
纳米技术
有机化学
物理化学
光电子学
图层(电子)
电信
电极
色素敏化染料
电解质
工程类
计算机科学
作者
Shin-Shin Kao,Ming‐Hsuan Yu,Jin‐Ming Chen,Hao-Wei Yu,Hsin‐Yu Yu,Bi‐Hsuan Lin,I‐Chih Ni,Yi‐Pei Li,Chu‐Chen Chueh
标识
DOI:10.1002/smtd.202400039
摘要
Abstract Additive engineering, with its excellent ability to passivate bulk or surface perovskite defects, has become a common strategy to improve the performance and stability of perovskite solar cells (PVSCs). Among the various additives reported so far, ammonium salts are considered an important branch. It is worth noting that although both ammonium‐based additives (R‐NH 3 + ) and amine‐based additives (R‐NH 2 ) are derivatives of ammonia (NH 3 ), the functions of the two can be easily confused due to their structural similarities. Moreover, there is no comprehensive comparative analysis of them in the literature. Here, the differences between phenethylammonium iodide (PEA + ) and phenethylamine (PEA) additives are revealed experimentally and theoretically. The results clearly show that PEA outperforms PEA + in terms of device performance and stability based on the following three factors: i) PEA's defect passivation capability is superior to that of PEA + ; ii) PEA has better hydrophobicity to hinder water ingress; and iii) PEA completely improves the stability of PVSCs by enhancing thermal stability and inhibiting iodide migration in perovskite more effectively than PEA + . As a result, the power conversion efficiency (PCE) of the inverted methylammonium triiodide (MAPbI 3 ) device using PEA increases by ≈15% to over 21%. More importantly, this device exhibits greater ability to prevent water invasion, thermal‐induce degradation, and inhibit iodide ion migration, resulting in better long‐term stability.
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