In-situ electrochemical restructuring of Cu2BiSx solid solution into Bi/CuxSy heterointerfaces enabling stabilization intermediates for high-performance CO2 electroreduction to formate

Bismuth-based materials are prevalent catalysts for CO2 electroreduction to formate, enduring high hydrogen evolution reactions and inadequate activity and stability. Herein, we reveal that in-situ electrochemical transformation of Cu2BiSx solid solution into Bi/CuxSy heterointerfaces, which can stabilize the intermediates and achieve highly selective and consistent CO2 electroreduction. It shows over 85% Faraday efficiency (FE) of formate with a potential window of -0.8 to -1.2 V-RHE (RHE: reversible hydrogen electrode) and a stability above 90% over 27 h in H-type cell at -0.9 V-RHE. It maintains more than 85% of FEformate at the current density of -25 to -200 mA & BULL;cm(-2), and has stability of about 80% of FEformate at least 10 h at -150 mA & BULL;cm(-2) in flow cell. In-situ Fourier transform infrared (FT-IR) spectroscopy measurement confirms that the preferred route of catalytic reaction is to generate *CO2- and *OCHO intermediates. The density functional theory (DFT) calculations illustrate that heterointerfaces facilitate the prior process of CO2 to HCOOH through *OCHO by additional Bi hybrid orbitals. This study is expected to open up a new idea for the design of CO2 electroreduction catalyst.