Issue 48, 2023

Copper hydroxide/basic copper salt derived Cu0 with a clear grain boundary for selective electrocatalytic CO2 reduction to produce multicarbon products

Abstract

Electrocatalytic CO2 reduction (ECR) is one of the most promising ways to mitigate CO2 and fuel production, and multicarbon products (C2+) with high chemical value attract lots of interest. Cu is a unique electrocatalyst that can convert CO2 to multicarbon products, but with limited selectivity and activity. Here, aiming for a clear Cu0 nanoparticle structure with a clear grain boundary, we report a simple and effective method of Cu(OH)2/basic copper sulphate compound material synthesis, which is in situ reduced to Cu0 nanoparticles with a clear grain boundary (GB) during the ECR process. The Cu(OH)2/basic copper sulphate-derived Cu nanoparticles show a high C2+ faradaic efficiency (FE) of 81% at −1.2 V vs. RHE, which surpasses that of state-of-the-art Cu-based catalysts evaluated in an H-type cell. Extending the method to other basic copper salts (BCS), we successfully synthesized three other Cu(OH)2/BCS species (nitrate, carbonate and chloride), which were also converted to Cu0 with a clear grain boundary during ECR. DFT calculation results reveal that the GB sites could effectively decrease the energy barrier of the reactant CO2 adsorption and critical C–C coupling steps, which endows the derived Cu electrocatalyst with high selectivity for C2H4 and C2+ products.

Graphical abstract: Copper hydroxide/basic copper salt derived Cu0 with a clear grain boundary for selective electrocatalytic CO2 reduction to produce multicarbon products

Supplementary files

Article information

Article type
Paper
Submitted
02 ربيع الأول 1445
Accepted
02 جمادى الأولى 1445
First published
02 جمادى الأولى 1445

J. Mater. Chem. A, 2023,11, 26481-26487

Copper hydroxide/basic copper salt derived Cu0 with a clear grain boundary for selective electrocatalytic CO2 reduction to produce multicarbon products

S. Song, H. Wu, B. Tian, Y. Zhang, Y. Kuang and X. Sun, J. Mater. Chem. A, 2023, 11, 26481 DOI: 10.1039/D3TA05628G

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