Integrating 3D porous morphology with efficient plasmonic Au nanoparticles in photo-responsive g-C3N4/Au hybrid photocatalyst for the enhancement of CO2 reduction

光催化 材料科学 表面等离子共振 纳米颗粒 等离子体子 吸附 可见光谱 多孔性 吸收(声学) 化学工程 纳米技术 石墨氮化碳 辐照 光化学 催化作用 光电子学 复合材料 化学 有机化学 工程类 物理 核物理学
作者
Zixi Fang,Qingtong Wang,Xinkun Zhao,Yao Li,Wang Zhang,Di Zhang
出处
期刊:Journal of environmental chemical engineering [Elsevier]
卷期号:11 (2): 109478-109478 被引量:11
标识
DOI:10.1016/j.jece.2023.109478
摘要

Various modification methods for graphitic carbon nitride (g-C3N4) have been widely used to improve the photocatalytic carbon dioxide reduction reaction (CO2RR) efficiency. Herein, we demonstrate a composite strategy combining three-dimensional (3D) morphology construction and plasmonic Au nanoparticle anchoring to prepare a porous g-C3N4/Au composite catalyst with effective photoresponse. In the presence of gaseous CO2 and liquid H2O without any sacrificial agent, compared with pure g-C3N4, the photocatalytic efficiency of the optimized PCN-18A was significantly improved: under the UV-Visible light irradiation of 320–780 nm, the yields of CO, CH4, and C2H4 were increased by ∼27.1, ∼17.9, and ∼19.3 times, respectively; under visible light irradiation from 420 to 780 nm, the yield of CO increased ∼48.6 times. Detailed characterization analysis and finite-difference time-domain (FDTD) simulations demonstrate that the significant increase can be mainly attributed to two reasons related to photoresponse. First, the construction of 3D porous enhanced the light absorption, and partially ordered porous regions formed inverse opal structures, causing the slow photon effect. Besides, the anchoring of Au nanoparticles facilitated electron transfer and introduced the localized surface plasmon resonance (LSPR) effect to inject hot electrons into g-C3N4. In addition, the increase of reactive sites and the enhancement of CO2 adsorption also contributed to the improvement of photocatalytic efficiency. Our work provides a new reference for the further design and optimization of photo-responsive g-C3N4-based photocatalysts.
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