光催化
硫黄
氢氧化物
铟
兴奋剂
材料科学
金属
催化作用
金属氢氧化物
还原(数学)
化学
无机化学
环境化学
矿物学
化学工程
有机化学
工程类
冶金
几何学
光电子学
数学
作者
Qinhui Guan,Weiguang Ran,Dapeng Zhang,Wenjuan Li,Na Li,Baibiao Huang,Tingjiang Yan
出处
期刊:Advanced Science
[Wiley]
日期:2024-06-13
卷期号:11 (30): e2401990-e2401990
被引量:40
标识
DOI:10.1002/advs.202401990
摘要
Abstract Photocatalytic CO 2 reduction is considered as a promising strategy for CO 2 utilization and producing renewable energy, however, it remains challenge in the improvement of photocatalytic performance for wide‐band‐gap photocatalyst with controllable product selectivity. Herein, the sulfur‐doped In(OH) 3 (In(OH) x S y ‐z) nanocubes are developed for selective photocatalytic reduction of CO 2 to CH 4 under simulated light irradiation. The CH 4 yield of the optimal In(OH) x S y ‐1.0 can be enhanced up to 39 times and the CH 4 selectivity can be regulated as high as 80.75% compared to that of pristine In(OH) 3 . The substitution of sulfur atoms for hydroxyl groups in In(OH) 3 enhances the visible light absorption capability, and further improves the hydrophilicity behavior, which promotes the H 2 O dissociation into protons (H * ) and accelerates the dynamic proton‐feeding CO 2 hydrogenation. In situ DRIFTs and DFT calculation confirm that the non‐metal sulfur sites significantly weaken the over‐potential of the H 2 O oxidation and prevent the formation of ·OH radicals, enabling the stabilization of * CHO intermediates and thus facilitating CH 4 production. This work highlights the promotion effect of the non‐metal doping engineering on wide‐band‐gap photocatalysts for tailoring the product selectivity in photocatalytic CO 2 reduction.
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