乙醛
醋酸
溴化氢
钙钛矿(结构)
光催化
化学
催化作用
溴
制氢
氢
无机化学
溴化物
分解
光化学
化学工程
过氧化氢
光电解
卤化氢
反应机理
煅烧
乙醇
材料科学
有机合成
激进的
作者
Yueying Wu,Guoyang Wang,Yaqiang Wu,Qianqian Zhang,Zeyan Wang,Yuanyuan Liu,Zhaoke Zheng,Hefeng Cheng,Buwei Huang,Peng Wang
摘要
ABSTRACT Perovskite‐based photocatalytic hydrogen bromide (HBr) splitting offers a promising route for solar‐driven hydrogen production. However, the accumulation of the oxidation product bromine often impedes reaction kinetics due to its sluggish oxidation, which faces a substantial energy barrier of 1.09 V versus NHE. This study introduces acetaldehyde as a stable and highly reductive agent in a perovskite‐saturated HBr system, enabling simultaneous high‐performance H 2 evolution and oxidative upgrading of acetaldehyde to valuable acetic acid. Using a Pt single‐atom‐modified FAPbBr 3 perovskite with exposed (100) and (111) facets, which is different from the traditional morphology of perovskites and provides efficient charge separation, the system achieves remarkable production rates of 1033.13 µmol h −1 for H 2 and 1017.20 µmol h −1 for acetic acid. High apparent quantum efficiencies of 30.62% at 450 nm and 31.78% at 520 nm are attained, with acetaldehyde conversion exceeding 90%. The process demonstrates stability over 15 h, recovering 0.8 mL of acetic acid at an 85% extraction efficiency. This strategy effectively utilizes both electrons and holes to simultaneously produce clean energy hydrogen and high‐value organic products.
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