光催化
材料科学
咪唑
贵金属
吸附
催化作用
氧化还原
吉布斯自由能
光化学
化学
金属
化学工程
纳米技术
无机化学
物理化学
立体化学
有机化学
热力学
物理
工程类
冶金
作者
Fangxu Dai,Mingming Zhang,Qian Chen,Mingzhong Mi,Zhenjiang Li,Jishu Han,Jun Xing,Shouhua Feng,Lei Wang
标识
DOI:10.1016/j.apcatb.2023.122934
摘要
Developing highly efficient and low-cost photocatalysts for CO2 reduction is of critical importance for the conversion of CO2 to value-added chemicals. Here we report a Co-based zeolitic imidazole framework (ZIF-67) based photocatalyst with exceptional photocatalytic activity and durability for CO2 reduction. ZIF-67 is doped with dicyandiamide (DCD), the intermediate link with the trace Ru cocatalyst (0.0127 wt. %). The underlying reduction mechanism was unraveled by the joint experiment-theory study. The strong orbital coupling of ZIF-67-DCD-Ru series structure leads to strong CO2 adsorption, electron enrichment on cocatalyst, and minimum Gibbs free energy barrier of CO generation. The synthesized ZIF-67/DCD/Ru sample exhibits excellent CO2 photoreduction performance with a CO generation rate of 1495 mmol gRu−1 h−1 and achieves a record turnover frequency (TOF) of 151 h−1, representing top-level photocatalytic activity among all reported ZIFs-based photocatalysts. For the first time, our work points out a novel way to achieve high activity of ultralow noble metal loading photocatalyst and provides an in-depth understanding of the advances of the series structure.
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