Catalytic reduction of carbon dioxide over two-dimensional boron monolayer

材料科学 催化作用 二氧化碳 还原(数学) 单层 二氧化碳电化学还原 化学工程 无机化学 碳纤维 纳米技术 化学 复合材料 一氧化碳 有机化学 复合数 工程类 数学 几何学
作者
Chuangwei Liu,Tianyi Wang,Derek Hao,Qinye Li,Song Li,Chenghua Sun
出处
期刊:Journal of Materials Science & Technology [Elsevier]
卷期号:110: 96-102 被引量:11
标识
DOI:10.1016/j.jmst.2021.08.082
摘要

• This work studies the electrochemical reduction of CO 2 on boron nanosheets, metal-free catalyst, under the scheme of density functional theory (DFT) and microkinetic modeling. • The strain can turn metallic two-dimensional boron nanosheet to semiconductor, not only making boron sheets possess photo(electro)catalytic activity (1.4 eV), but also improving energy efficiency and selectivity performance against hydrogen evolution reaction. • Thermodynamic and microkinetic models are applied to demonstrate the favorable products, critical steps and hydrogenation mechanisms. • By introducing the aqueous electrolytes, the hydrated alkali cations not only effect on the CO 2 concentration, but also produce a bigger surface charge density and stronger interfacial electric filed. Carbon dioxide reduction (CRR) is an attractive strategy for alleviating global warming and producing valuable fuels. In this work, we study the catalytic conversion of CO 2 to C 1 -C 3 products on boron nanosheet in the presence of compressive strain by using density functional theory. Thermodynamic and microkinetic models are applied to demonstrate the favorable products, critical steps, and hydrogenation mechanisms. As demonstrated, the strain can turn metallic two-dimensional boron nanosheet to semiconductor, not only making boron sheets possess photo(electro)catalytic activity, but also improving energy efficiency and selectivity performance against hydrogen evolution reaction. By introducing the aqueous electrolytes, the hydrated alkali cations not only effect on the CO 2 concentration, but also produce a bigger surface charge density and stronger interfacial electric filed. Especially, the selectivity of C 2+ products is enhanced with the increase of alkali cations size by decreasing the kinetic barrier for CO dimerization and stabilizing the intermediates. The results highlight the significance of metal-free catalysts for CRR by the photoelectrochemical method and provide novel avenues for the development of new solar-energy utilization catalysts.

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