钙钛矿(结构)
材料科学
分解水
钙钛矿太阳能电池
光电子学
能量转换效率
卤化物
化学工程
纳米技术
无机化学
化学
催化作用
光催化
生物化学
工程类
作者
Juwon Yun,Hyungsoo Lee,Young Sun Park,Wooyong Jeong,Chang‐Seop Jeong,Junwoo Lee,Jeongyoub Lee,Jeiwan Tan,Seohee Ma,Gyumin Jang,Chan Uk Lee,Subin Moon,Hayoung Im,Soo‐Bin Lee,D. S. Yee,Ji‐Hee Kim,Jooho Moon
标识
DOI:10.1002/aenm.202301693
摘要
Abstract Recently, lead halide perovskites have attracted significant attention as promising absorber materials for photoelectrochemical (PEC) solar water splitting. However, charge‐accumulation‐induced ion migration at the interface causes perovskite degradation and efficiency loss. To suppress the charge accumulation and improve the PEC performance of the perovskite photoanode, a simple interface engineering is proposed by decorating the SnO 2 /perovskite interface with a mixture of polyethylenimine ethoxylated (PEIE) and chlorobenzenesulfonic acid (CBSA). The mixed CBSA+PEIE treatment effectively passivates the oxygen vacancies in SnO 2 and adjusts the band alignment between SnO 2 and the perovskite. The synergistic effects of the mixture treatment facilitate an effective carrier extraction at the SnO 2 /perovskite interface, enhance the PEC performance, and improve the stability of the device. The perovskite photoanode exhibits an impressive applied bias photon‐to‐current efficiency of 12.9% with an outstanding durability for 225 h. Furthermore, an unbiased solar water splitting is achieved using all the perovskite photoelectrodes, resulting in a remarkable unassisted solar‐to‐hydrogen efficiency of 10.9% and a continuous 22 h stable operation.
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