材料科学
石墨烯
格式化
铋
气凝胶
法拉第效率
氧化物
化学工程
电化学
催化作用
吸附
氧化还原
无机化学
可逆氢电极
纳米技术
电极
工作电极
物理化学
有机化学
化学
工程类
冶金
作者
Xiaoting Jing,Zhejiaji Zhu,Li‐Wei Chen,Di Liu,Hui‐Zi Huang,Wenjing Tian,Anxiang Yin
标识
DOI:10.1021/acsami.3c02578
摘要
Electrochemical CO2 reduction reaction (CO2RR), which uses renewable electricity to produce high-value-added chemicals, offers an alternative clean path to the carbon cycle. However, bismuth-based catalysts show great potential for the conversion of CO2 and water to formate, but their overall efficiency is still hampered by the weak CO2 adsorption, low electrical conductivity, and slow mass transfer of CO2 molecules. Herein, we report that a rationally modulated nitrogen-doped graphene aerogel matrix (NGA) can significantly enhance the CO2RR performance of bismuth nanoplates (BiNPs) by both modulating the electronic structure of bismuth and regulating the interface for chemical reaction and mass transfer environments. In particular, the NGA prepared by reducing graphene oxide (GO) with hydrazine hydrate (denoted as NGAhdrz) exhibits significantly enhanced strong metal-support interaction (SMSI), increased specific surface area, strengthened CO2 adsorption, and modulated wettability. As a result, the Bi/NGAhdrz exhibits significantly boosted CO2RR properties, with a Faradaic efficiency (FE) of 96.4% at a current density of 51.4 mA cm-2 for formate evolution at a potential of -1.0 V versus reversible hydrogen electrode (vs RHE) in aqueous solution under ambient conditions.
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