Electron-rich Ni2+ in Ni3S2 boosting electrocatalytic CO2 reduction to formate and syngas

IF 5.9 4区 化学 Q1 CHEMISTRY, INORGANIC & NUCLEAR
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Abstract

Rationally constructed new catalyst can promote carbon dioxide reduction reaction (CO2RR) to valuable carbonaceous fuels such as formate and CO, providing a promising strategy for low CO2 emissions. Herein, the synthesized Ni3S2@C as a highly efficient electro-catalyst exhibits remarkable selectivity for formate with 73.9% faradaic efficiency (FE) at −0.7 V vs. RHE. At high applied potential, it shows a high syngas evolution with CO/H2 ratios (0.54–3.15) that are suitable for typical downstream thermochemical reactions. The experimental and theoretical analyses demonstrate that the electron-rich Ni2+ in Ni3S2 enhances the adsorption behavior of OCHO intermediate, reduces the energy barrier of the formation of intermediates, and improves the selectivity of the formate product. Attenuated total reflection surface-enhanced infrared absorption spectra conducted in situ show that OCHO intermediate is more likely to be generated and adsorbed on Ni3S2, enhancing the selectivity and activity of the formate product.

Abstract Image

Abstract Image

Ni3S2 中富含电子的 Ni2+ 促进电催化二氧化碳还原为甲酸盐和合成气
合理构建的新型催化剂可促进二氧化碳还原反应(CORR),将其转化为有价值的碳质燃料,如甲酸酯和一氧化碳,为实现二氧化碳的低排放提供了一种前景广阔的策略。在本文中,合成的 NiS@C 作为一种高效电催化剂,在 -0.7 V RHE 条件下对甲酸盐具有显著的选择性,法拉第效率(FE)为 73.9%。在高电势下,它还能产生大量合成气,其 CO/H 比(0.54-3.15)适用于典型的下游热化学反应。实验和理论分析表明,NiS 中富含电子的 Ni 增强了 OCHO 中间体的吸附行为,降低了中间体形成的能障,提高了甲酸盐产物的选择性。衰减全反射表面增强红外吸收光谱显示,OCHO 中间体更容易在 NiS 上生成和吸附,从而提高了甲酸酯产物的选择性和活性。
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来源期刊
结构化学
结构化学 化学-晶体学
CiteScore
4.70
自引率
22.70%
发文量
5334
审稿时长
13 days
期刊介绍: Chinese Journal of Structural Chemistry “JIEGOU HUAXUE ”, an academic journal consisting of reviews, articles, communications and notes, provides a forum for the reporting and discussion of current novel research achievements in the fields of structural chemistry, crystallography, spectroscopy, quantum chemistry, pharmaceutical chemistry, biochemistry, material science, etc. Structural Chemistry has been indexed by SCI, CA, and some other prestigious publications.
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