Chung Jaehoon, Won Da Hye, Koh Jaekang, Kim Eun-Hee, Woo Seong Ihl
Department of Chemical and Biomolecular Engineering, Korea Advanced Institute of Science and Technology, Daejeon (34141), Republic of Korea.
Graduate School of EEWS, Korea Advanced Institute of Science and Technology, Daejeon (34141), Republic of Korea.
Phys Chem Chem Phys. 2016 Feb 17;18(8):6252-8. doi: 10.1039/c5cp07964k.
To achieve high performance of electrochemical CO2 reduction, a series of Cu pillar electrodes (Cu-2.5 h, Cu-5 h) were fabricated by using an electrodeposition method, and then their catalytic activities and reaction mechanisms were investigated. The series of Cu pillar electrodes exhibited improved electrocatalytic activities toward CO2 reduction to formic acid (HCOOH) as Cu pillars on electrodes developed. The Cu-5 h electrode performed well with a 28% Faradaic efficiency for formic acid at -0.5 V (vs. RHE). X-ray diffraction (XRD) analysis indicated that the enhanced catalytic activities were primarily attributable to the increased (111) facet, which is energetically favourable for the production of HCOOH. Also, ultraviolet photoelectron spectroscopy (UPS) and in situ electrochemical impedance spectroscopy (EIS) results suggested that the series of Cu pillar structure electrodes improved the electron transfer to adsorbed CO2 due to the decreased work function of the Cu pillar structure.
为实现高效的电化学二氧化碳还原,采用电沉积法制备了一系列铜柱电极(Cu-2.5 h、Cu-5 h),并对其催化活性和反应机理进行了研究。随着电极上铜柱的形成,该系列铜柱电极对二氧化碳还原生成甲酸(HCOOH)表现出更高的电催化活性。Cu-5 h电极表现出色,在-0.5 V(相对于可逆氢电极)下对甲酸的法拉第效率为28%。X射线衍射(XRD)分析表明,催化活性增强主要归因于(111)晶面的增加,这在能量上有利于甲酸的生成。此外,紫外光电子能谱(UPS)和原位电化学阻抗谱(EIS)结果表明,由于铜柱结构的功函数降低,该系列铜柱结构电极改善了向吸附二氧化碳的电子转移。