Fan Linfeng, Ji Yaxin, Wang Genxiang, Chen Junxiang, Chen Kai, Liu Xi, Wen Zhenhai
CAS Key Laboratory of Design and Assembly of Functional Nanostructures, and Fujian Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, Fujian 350002, China.
University of Chinese Academy of Science, Beijing 100049, P. R. China.
J Am Chem Soc. 2022 Apr 27;144(16):7224-7235. doi: 10.1021/jacs.1c13740. Epub 2022 Apr 11.
Electrochemical glycerol oxidation reaction (GOR) is an attractive alternative anodic reaction to oxygen evolution reaction for a variety of electrolytic synthesis, thanks to the possibility of mass production of glycerol from biomass and the relative low thermodynamic potential of GOR. The development of high-activity cheap electrocatalysts toward GOR yet faces a daunting challenge. Herein, we experimentally prepare a new range of high entropy alloy (HEA) self-supported electrodes with uniform HEA nanoparticles grown on carbon cloth. The systematic electrochemical studies verify that the HEA-CoNiCuMnMo electrode exhibits attractive performance for GOR electrocatalysis with low overpotential and high selectivity toward formate products. The surface atomic configurations of HEA-CoNiCuMnMo are studied by a self-developed machine learning-based Monte Carlo simulation, which points out the catalytic active center to be Mo sites coordinated by Mn, Mo, and Ni. We further develop a hybrid alkali/acid flow electrolytic cell by pairing alkaline GOR with acidic hydrogen evolution reaction using the HEA-CoNiCuMnMo and the commercial RhIr/Ti as the anode and the cathode, respectively, which only requires an applied voltage of 0.55 V to reach an electrolytic current density of 10 mA cm and maintains long-term electrolysis stability over 12 days continuous running at 50 mA cm with Faraday efficiencies of over 99% for H in the cathode and 92% for formate production in the anode.
电化学甘油氧化反应(GOR)对于各种电解合成而言,是一种有吸引力的替代析氧反应的阳极反应,这得益于从生物质大量生产甘油的可能性以及GOR相对较低的热力学电位。然而,开发用于GOR的高活性廉价电催化剂仍面临巨大挑战。在此,我们通过实验制备了一系列新的高熵合金(HEA)自支撑电极,在碳布上生长有均匀的HEA纳米颗粒。系统的电化学研究证实,HEA-CoNiCuMnMo电极在GOR电催化方面表现出具有吸引力的性能,具有低过电位和对甲酸盐产物的高选择性。通过自行开发的基于机器学习的蒙特卡罗模拟研究了HEA-CoNiCuMnMo的表面原子构型,指出催化活性中心为与Mn、Mo和Ni配位的Mo位点。我们进一步开发了一种混合碱/酸流动电解槽,分别使用HEA-CoNiCuMnMo和商业RhIr/Ti作为阳极和阴极,将碱性GOR与酸性析氢反应配对,该电解槽仅需施加0.55 V的电压即可达到10 mA cm的电解电流密度,并在50 mA cm下连续运行12天以上保持长期电解稳定性,阴极中H的法拉第效率超过99%,阳极中甲酸盐生成的法拉第效率为92%。