Zn-induced electron-rich Sn catalysts enable highly efficient CO2 electroreduction to formate

Renewable-energy-driven CO2 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 C...

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Veröffentlicht in:Chemical science (Cambridge) 2023-08, Vol.14 (30), p.8214-8221
Hauptverfasser: Tan, Xingxing, Jia, Shunhan, Song, Xinning, Ma, Xiaodong, Feng, Jiaqi, Zhang, Libing, Wu, Limin, Du, Juan, Chen, Aibing, Zhu, Qinggong, Sun, Xiaofu, Han, Buxing
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Sprache:eng
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Zusammenfassung:Renewable-energy-driven CO2 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 CO2-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 CO2-to-formate with high efficiency. The faradaic efficiency of formate (FEformate) could reach 96.6%, and FEformate > 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 CO2 molecules to form a [Formula Omitted] intermediate and then promoted the carbon protonation of [Formula Omitted] 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.
ISSN:2041-6520
2041-6539
DOI:10.1039/d3sc02790b