Efficient Electrochemical Reduction of CO2 to CO by Ag-Decorated B-Doped g-C3N4: A Combined Theoretical and Experimental Study

法拉第效率 电催化剂 材料科学 电化学 石墨氮化碳 催化作用 纳米复合材料 掺杂剂 可逆氢电极 兴奋剂 化学工程 电极 纳米技术 无机化学 化学 物理化学 工作电极 光催化 光电子学 生物化学 工程类
作者
Song Lu,Yang Zhang,Mohamed F. Mady,Wakshum Mekonnen Tucho,Fengliu Lou,Zhixin Yu
出处
期刊:Industrial & Engineering Chemistry Research [American Chemical Society]
卷期号:61 (29): 10400-10408 被引量:23
标识
DOI:10.1021/acs.iecr.2c00152
摘要

Electrochemical CO2 reduction (ECR) has received great attention in energy conversion and CO2 mitigation. In recent years, graphitic carbon nitride (g-C3N4) has been regarded as a very promising support for metal nanoparticles (NPs) for many catalytic reactions. In this work, we reported the silver- (Ag) loaded boron-doped g-C3N4 nanocomposite (Ag-B-g-C3N4) for efficient ECR to CO by a joint first-principles study and experimental work. Theoretical simulation demonstrated that the B dopant and Ag NPs could be easily incorporated into g-C3N4. The introduction of Ag NPs and the B atom could greatly decrease the adsorption free energy for the *COOH intermediate generation. Meanwhile, an electron-rich region at the Ag-B-g-C3N4 interface was observed, contributing to improved electrical conductivity and electron transport. B-g-C3N4 could not exhibit the obvious enhancement of ECR performance, while the Ag-B-g-C3N4 catalyst with an average Ag diameter of 4.95 nm exhibited a total current density of 2.08 mA cm–2 and a CO Faradaic efficiency (FECO) of 93.2% under the potential of −0.8 V vs the reversible hydrogen electrode (RHE), indicating that Ag is the only active center. Ag-B-g-C3N4 also displayed excellent stability without any deactivation in a 12-h electrocatalysis. This work revealed the mechanism of electrocatalytic CO2 reduction over metal- (Ag) and nonmetal- (B) modified g-C3N4, which paves the way for broader application of the g-C3N4 nanocomposite in electrocatalytic reactions.
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