Surface nitrided CuBi2O4 electrocatalysts with excellent selectivity for CO2 reduction to methanol

[Display omitted] •Surface nitriding strategies were designed.•The degree of surface nitridation of the catalyst was regulated by controlling the calcination time.•The introduction of N atoms altered the electron transfer capacity of the catalyst and facilitated the generation of the key intermediat...

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Veröffentlicht in:Applied surface science 2024-08, Vol.663, p.160215, Article 160215
Hauptverfasser: Ma, Lin, Liu, Huan, Song, Youchao, Yang, Chenghan, Yu, Huijun, Zhou, Yuming, Zhang, Yiwei
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Sprache:eng
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Zusammenfassung:[Display omitted] •Surface nitriding strategies were designed.•The degree of surface nitridation of the catalyst was regulated by controlling the calcination time.•The introduction of N atoms altered the electron transfer capacity of the catalyst and facilitated the generation of the key intermediate *OCH.•N-CuBi2O4 exhibits excellent methanol production performance in CO2RR. Developing a high-performance electrocatalyst for converting CO2 into methanol is of utmost importance. However, poor selectivity, and unavoidable competitive hydrogenolysis reaction (HER) are still challenges to be solved. In this study, a surface nitrided strategy was designed to synthesize a series N-copper-bismuth bimetallic oxide electrocatalysts (NCBO-t, t = 1, 2, 4 h) for CO2RR. The electrocatalyst NCBO-2 demonstrated a selectivity for methanol reaching 86.43 %, along with an impressive long-term stability lasting for 11 h, all achieved at a relatively low potential of −0.9 V. Experimental results and density functional theory (DFT) calculations indicated the introduction of nitrogen facilitates methanol production by optimizing binding of the reaction intermediate *OCH while promotes Faradaic efficiency of methanol products by suppressing the competitive HER, resulting in high Faradaic efficiency, current density, and stability of CO2RR at low overpotentials. This study offers a feasible idea for synthesis of high-performance CO2 methanol by electroreduction.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2024.160215