An overview on the recent developments of Ag-based electrodes in the electrochemical reduction of CO2 to CO

Author(s): Samah A. Mahyoub ¹ ^, ² ^, ³ ^, ⁴ ^, ⁵ , Fahim A. Qaraah ⁶ ^, ³ ^, ⁴ ^, ⁵ , Chengzhen Chen ¹ ^, ² ^, ³ ^, ⁴ ^, ⁵ , Fanghua Zhang ¹ ^, ² ^, ³ ^, ⁴ ^, ⁵ , Shenglin Yan ¹ ^, ² ^, ³ ^, ⁴ ^, ⁵ , Zhenmin Cheng ¹ ^, ² ^, ³ ^, ⁴ ^, ⁵

Publication date (Electronic): 2020

Journal: Sustainable Energy & Fuels

Publisher: Royal Society of Chemistry (RSC)

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Abstract

A diagram illustrating the electrochemical reduction of CO ₂ to CO on Ag-based electrode nanostructures.

Abstract

Conversion of aqueous CO ₂ into CO through the electrochemical reduction reaction (ERR) suffers from poor selectivity and low current density with the classic Ag-based catalysts due to the inert nature of CO ₂ and the low activity of the active sites. Recently, it has been reported that nanostructured catalysts can display very distinctive behavior compared to their bulk counterparts. To explore the reasons behind this, the latest developments in Ag-based nanostructured materials in the CO ₂ ERR are summarized into six aspects in this review: (1) the size effect, (2) the morphology effect, (3) the porous effect, (4) the alloying effect, (5) the support effect, and (6) the surface modification effect. In particular, Ag-based alloy catalysts could exhibit a superior catalytic activity and long-term stability owing to the synergistic effect. Besides, the morphology of Ag-based alloy catalysts could also be controlled through adjusting their compositions. From the current literature survey we find that the maximum FE for CO obtained from Ag-based nanocatalysts reaches as high as 99.3%, which is a breakthrough over that from the traditional Ag foil. This review aims to offer a comprehensive understanding of Ag-based nanostructured catalysts in the CO ₂ ERR and consequently improve the catalyst design for active and selective electro-reduction of CO ₂ to CO.