光催化
材料科学
甲苯
钙钛矿(结构)
八面体
选择性
吸附
二胺
化学工程
光化学
化学
结晶学
催化作用
晶体结构
有机化学
高分子化学
工程类
作者
Zhangjun Bai,Jie Xiong,Yu Mao,Tian Sheng,Binghao Wang,Biao Hu,Xiong Wang,Wei Zhou,Chak Tong Au,Lang Chen,Shuang‐Feng Yin
标识
DOI:10.1016/j.xcrp.2023.101591
摘要
Two-dimensional (2D) perovskites have recently garnered widespread attention for their favorable properties, such as stability. However, their application in photoelectric fields is typically limited by the low mobility of charge carriers. Herein, a range of 2D lead-free double perovskites are fabricated using substituted aliphatic diamine cations. This modification leads to distortions in the octahedral structure of 2D perovskites, enhancing the connectivity of atomic orbitals at band edges. Notably (NH3(CH2)3NH3)2AgBiBr8, with minimized layer spacing compared to reported 2D lead-free double perovskites, shows the highest carrier mobility, surpassing its 3D counterpart. (NH3(CH2)3NH3)2AgBiBr8 displays excellent activity and stability in photocatalytic selective oxidation, achieving a toluene conversion up to 100% with a benzoic acid selectivity of 99% under visible light irradiation. Lower hydrophilicity as well as higher toluene adsorption capacity with the diamine cation substitutions could be responsible for the boosted photocatalytic performances.
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