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Zn-induced electron-rich Sn catalysts enable highly efficient CO(2) electroreduction to formate
Renewable-energy-driven CO(2) electroreduction provides a promising way to address the growing greenhouse effect issue and produce value-added chemicals. As one of the bulk chemicals, formic acid/formate has the highest revenue per mole of electrons among various products. However, the scaling up of...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10395268/ https://www.ncbi.nlm.nih.gov/pubmed/37538823 http://dx.doi.org/10.1039/d3sc02790b |
Sumario: | Renewable-energy-driven CO(2) electroreduction provides a promising way to address the growing greenhouse effect issue and produce value-added chemicals. As one of the bulk chemicals, formic acid/formate has the highest revenue per mole of electrons among various products. However, the scaling up of CO(2)-to-formate for practical applications with high faradaic efficiency (FE) and current density is constrained by the difficulty of precisely reconciling the competing intermediates (*COOH and HCOO*). Herein, a Zn-induced electron-rich Sn electrocatalyst was reported for CO(2)-to-formate with high efficiency. The faradaic efficiency of formate (FE(formate)) could reach 96.6%, and FE(formate) > 90% was maintained at formate partial current density up to 625.4 mA cm(−1). Detailed study indicated that catalyst reconstruction occurred during electrolysis. With appropriate electron accumulation, the electron-rich Sn catalyst could facilitate the adsorption and activation of CO(2) molecules to form a [Image: see text] intermediate and then promoted the carbon protonation of [Image: see text] to yield a HCOO* intermediate. Afterwards, the HCOO* → HCOOH* proceeded via another proton-coupled electron transfer process, leading to high activity and selectivity for formate production. |
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