Coupling Electrochemical Sulfion Oxidation with CO2 Reduction over Highly Dispersed p‐Bi Nanosheets and CO2‐Assisted Sulfur Extraction

Author:

Teng Xue12,Shi Kai12,Chen Lisong123,Shi Jianlin4ORCID

Affiliation:

1. Shanghai Key Laboratory of Green Chemistry and Chemical Processes School of Chemistry and Molecular Engineering East China Normal University 200062 Shanghai China

2. State Key Laboratory of Petroleum Molecular and Process engineering SKLPMPE East China Normal University 200062 Shanghai China

3. Institute of Eco-Chongming 202162 Shanghai China

4. Shanghai Institute of Ceramics Chinese Academy of Sciences 200050 Shanghai P. R. China

Abstract

AbstractWe report herein an electrocatalytic CO2 reduction‐coupled sulfion oxidation system for the co‐productions of valuable formate and sulfur at much enhanced atom utilization. Specifically, an organic ligand‐assisted two‐step reconstruction approach has been developed to fabricate the highly dispersed p‐Bi nanosheets (p‐Bi NSs) for cathodic CO2 reduction reaction (CO2RR), and meanwhile porous Co−S nanosheets (Co−S NSs) was applied for anodic sulfion oxidation reaction (SOR). Significantly high Faradaic Efficiencies of about 90 % for formate production by CO2RR in a wide potential range from −0.6 V to −1.1 V, and excellent SOR performances including an ultra‐low onset potential of about 0.2 V and recycle capacity of S2− in the 0.1 M and 0.5 M S2− solutions, have been simultaneously achieved. In the meantime, both the structure transformation of the catalysts and the reaction pathways are explored and discussed in detail. A two‐electrode CO2RR||SOR electrolyzer equipped with above electrocatalysts has been established, which features as low as about 1.5 V to run the electrolyzer at 100 mA cm−2, manifesting extremely lowered electricity consumption in comparison to conventional CO2RR system. Moreover, a sulfur separation approach has been proposed by using CO2, which is efficient, environmentally friendly and cost effective with value‐added NaHCO3 be obtained as the byproduct.

Funder

National Key Research and Development Program of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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