合成气
材料科学
纳米孔
电催化剂
催化作用
化学工程
电化学
多孔性
微型多孔材料
纳米技术
电极
有机化学
复合材料
化学
物理化学
工程类
作者
Wen-Yuan Yan,Cheng Zhang,Cheng Zhang
标识
DOI:10.1021/acsami.1c10564
摘要
Electrochemical CO2 reduction reaction (CO2RR) coupled with hydrogen evolution reaction (HER) is a renewable route to produce syngas (CO + H2), an essential feedstock for liquid fuel production. However, the development of high-performance electrocatalyst with tunable H2/CO ratio, high-rate syngas production, and long-term electrochemical stability remains challenging. Here, a metal three-dimensional (3D) printing technique followed by dealloying was utilized to develop three-dimensional hierarchical porous (termed as 3D hp) CuAg catalysts for the concurrent generation of CO and H2. By purposely designing the precursor compositions, the resultant 3D hp CuAg catalysts with a high density of phase-segregated Ag and Cu nanodomains exhibit a tunable H2/CO ratio from 3:1 to 1:2. Through further porosity engineering, the 3D hp CuAg catalysts show significantly enhanced syngas production rate of 140 μmol/h/cm2 and electrochemical stability up to 140 h (which is the highest value reported so far). The remarkable electrochemical stability of the 3D hp CuAg arises from three-level hierarchical porous configurations, wherein the macroporous structure benefits gas bubble growth and detachment, the microporous structure stabilizes the active nanoporous layer, while the nanoporous structure provides a large active surface area and enables efficient mass transfer. The results of this study offer a new vision for the development of hierarchically porous catalysts for CO2 reduction.
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