Electrosynthesized Metal/Polymer Hybrid: Unlocking Selective Formate Production via CO2 Electroreduction

Evin Jacob,  and , Anitha Varghese*, 
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Abstract

Carbon dioxide reduction via electrochemical means offers a sustainable pathway to mitigate CO2 emissions and synthesize value-added chemicals. Here, we report the synthesis and performance of a metal/polymer-carbon paper (CuxOy/PoPD/CFP) electrode prepared via a simple two-step in situ electrodeposition method for the electrochemical CO2 reduction reaction (CO2ER). Unlike most reported catalysts that yield multiple liquid products and complicate downstream separation processes, CuxOy/PoPD/CFP selectively produces formate as the sole liquid product across all of the test potentials. The amine-rich and porous PoPD matrix synergistically enhanced CO2 capture, provided a conductive scaffold for efficient electron transfer, and facilitated intimate interfacial contact with copper oxides, enabling improved catalytic performance. The catalyst demonstrated an onset potential of ∼−0.27 V (vs RHE) and achieved a faradaic efficiency of 72.6% for formate with a current density of 6.70 mA/cm2 at −0.80 V (vs RHE). Studies showcased an electrochemically active surface area (ECSA) of 16.625 cm2 and a roughness factor of 8.31. The long-duration electrolysis experiment demonstrated stable performance for an extended period, maintaining continuous electrolysis for up to 9.5 h without significant fluctuations or degradation in activity.

Abstract Image

电合成金属/聚合物混合物:通过CO2电还原解锁选择性甲酸生产
通过电化学手段减少二氧化碳为减少二氧化碳排放和合成增值化学品提供了一条可持续的途径。本文报道了一种用于电化学CO2还原反应(CO2ER)的金属/聚合物-碳纸(CuxOy/PoPD/CFP)电极的合成和性能,该电极采用简单的两步原位电沉积法制备。与大多数催化剂产生多种液体产物和复杂的下游分离过程不同,CuxOy/PoPD/CFP在所有测试电位中选择性地产生甲酸盐作为唯一的液体产物。富含胺的多孔PoPD基质协同增强了CO2捕获,为有效的电子转移提供了导电支架,并促进了与铜氧化物的密切界面接触,从而提高了催化性能。该催化剂的起始电位为- 0.27 V(相对于RHE),在- 0.80 V(相对于RHE)电流密度为6.70 mA/cm2时,甲酸酯的法拉第效率为72.6%。研究表明,电化学活性表面积(ECSA)为16.625 cm2,粗糙度系数为8.31。长时间电解实验证明了长时间的稳定性能,保持连续电解长达9.5小时,活性没有明显波动或下降。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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