选择性
光催化
催化作用
吸附
钴
光化学
化学
生物量(生态学)
材料科学
化学工程
纳米技术
无机化学
物理化学
有机化学
海洋学
工程类
地质学
作者
Xinying Tan,Shenghe Si,Difei Xiao,Xiaolei Bao,Kepeng Song,Zeyan Wang,Yuanyuan Liu,Zhaoke Zheng,Peng Wang,Ying Dai,Baibiao Huang,Hefeng Cheng
标识
DOI:10.1021/acscatal.3c03332
摘要
Photocatalytic selective biomass aerobic oxidation to high-value products is promising for meeting carbon-neutral demand; however, great challenges remain in the lack of appropriate active sites for molecular O2 activation and understanding their role at the atomic scale to reveal the underlying mechanism. Herein, we report that a rational decoration of ultralow-amount (0.08 wt %) Co single atoms on ZnIn2S4 nanosheets (Co1/ZIS) enables both high activity and selectivity for photocatalytic 5-hydroxymethylfurfural (HMF) oxidation to the high-value 2,5-dicarbonylfuran (DFF) product. Under visible light irradiation in an air atmosphere, Co1/ZIS exhibits 98.6% conversion of HMF that outperforms pristine ZIS by two times, along with 92.4% selectivity of DFF. Uncovered by combined experimental results and computational calculations, the introduction of Co single atoms not only facilitates the transfer of photogenerated carriers but also provides active sites to promote the adsorption/activation of O2 to generate reactive oxygen species of •O2– and 1O2, thereby leading to its superior photocatalytic performance to the pristine ZIS counterpart.
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