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Electrodeposition of Tin-Based Electrocatalysts with Different Surface Tin Species Distributions for Electrochemical Reduction of CO2 to HCOOH

机译:用不同表面锡物种的锡基电催化剂电化沉积用于电化学减少CO2至HCOOH的分布

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摘要

Tin-based electrocatalysts with different tin species distributions were deposited on the carbon paper substrate by three electrodeposition methods and applied to the selective electroreduction of carbon dioxide to formic acid. Among them, the electrocatalysts prepared using unipolar pulse electrodeposition (UPED) method exhibited the maximum HCOOH faradaic efficiency of 89% at -1.7 V (vs Ag/AgCl) with a current density of 6.0 mA cm(-2) and long-term stability in the 0.1 M CO2- saturated KHCO3 solution. Moreover, the effects of surface oxides species on the performance of tin-based electrocatalysts were systematically investigated via density functional theory (DFT) calculations. The calculation results indicated that both metal tin and tin oxides had excellent catalytic ability for the electrochemical reduction of CO, to HCOOH. Specifically, the tetravalent tin (Sn4+) and divalent tin (Sn2+) species can reduce the overpotential and improve the HCOOH selectivity, respectively. In addition, we found that the tin oxides/metal tin interface can suppress the evolution of H-2, but we observed no obvious effect on the formations of HCOOH and CO. Thus, the actual CO, catalytic electroreduction process should be synergistically controlled by the complex surface oxide species on the tin-based electrocatalysts.
机译:用不同的锡物物种分布的锡基电催化剂通过三种电沉积方法沉积在碳纸基材上,并施加到二氧化碳中的选择性电荷。其中,使用单极脉冲电沉积(Umed)方法制备的电催化剂在-1.7V(Vs Ag / AgCl)的最大HCOOH Farada效率,电流密度为6.0 mA cm(-2)和长期稳定性在0.1M CO 2饱和KHCO 3溶液中。此外,通过密度泛函理论(DFT)计算,系统地研究了表面氧化物物种对锡基电催化剂性能的影响。计算结果表明,金属锡和锡氧化物均具有优异的催化能力,用于将CO的电化学还原到HCOOH。具体地,四价锡(SN4 +)和二价锡(SN2 +)物质可以分别减少过电位并改善HCOOH选择性。此外,我们发现锡氧化锡/金属锡界面可以抑制H-2的演变,但我们观察到对HCOOH和CO的形成无明显影响。因此,实际的CO,催化电荷工艺应协同控制锡基电催化剂上的复杂表面氧化物物种。

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