摘要
The selective and effective conversion of CO2into available chemicals by electrochemical methods was applied as a promising way to mitigate the environment and energy crisis. Metal silver is regarded as an efficient electrocatalyst that can selectively convert CO2into CO at room temperature. In this paper, a series of coral-like porous Ag (CD-Ag) catalysts were fabricated by calcining silver-carbonaceous microsphere (Ag/CM) precursors with different Ag content and the formation mechanism of CD-Ag catalysts was proposed involving the Ag precursor reduction and CM oxidation. In the selective electrocatalytic reduction of CO2to CO, the catalyst 15 CD-Ag showed a stable current density at −6.3 mA/cm2with a Faraday efficiency (FE) of ca. 90% for CO production over 5 h in −0.95 V vs. RHE. The excellent performance of the 15 CD-Ag catalysts is ascribed to the special surface chemical state and the particular nano-coral porous structure with uniformly distributed Ag particles and pore structure, which can enhance the electrochemical active surface areas (ECSA) and provide more active sites and porosity compared with other CD-Ag catalysts and even Ag foil.Keywords:carbon dioxide reduction;silver;carbonaceous microsphere;carbon monoxide;electrochemical
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