Chang Jiuli, Song Fengfeng, Hou Yan, Wu Dapeng, Xu Fang, Jiang Kai, Gao Zhiyong
School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Normal University, Henan Xinxiang 453007, P.R. China.
School of Chemistry and Chemical Engineering, Collaborative Innovation Center of Henan Province for Green Manufacturing of Fine Chemicals, Key Laboratory of Green Chemical Media and Reactions, Ministry of Education, Henan Normal University, Henan Xinxiang 453007, P.R. China.
J Colloid Interface Sci. 2024 Jul;665:152-162. doi: 10.1016/j.jcis.2024.03.119. Epub 2024 Mar 19.
H and formate are important energy carriers in fuel-cells and feedstocks in chemical industry. The hydrogen evolution reaction (HER) coupling with electro-oxidative cleavage of thermodynamically favorable polyols is a promising way to coproduce H and formate via electrochemical means, highly active catalysts for HER and electrooxidative cleavage of polycols are the key to achieve such a goal. Herein, molybdenum (Mo), tungsten (W) doped cobalt phosphides (CoP) deposited onto nickel foam (NF) substrate, denoted as Mo-CoP/NF and W-CoP/NF, respectively, were investigated as catalytic electrodes for HER and electrochemical glycerol oxidation reaction (GOR) to yield H and formate. The W-CoP/NF electrode exhibited low overpotential (η) of 113 mV to attain a current density (J) of -100 mA cm for HER, while the Mo-CoP/NF electrode demonstrated high GOR efficiency for selective production of formate. In situ Raman and infrared spectroscopic characterizations revealed that the evolved CoO from CoP is the genuine catalytic sites for GOR. The asymmetric electrolyzer based on W-CoP/NF cathode and Mo-CoP/NF anode delivered a J = 100 mA cm at 1.8 V voltage for glycerol electrolysis, which led to 18.2 % reduced electricity consumption relative to water electrolysis. This work highlights the potential of heteroelement doped phosphide in catalytic performances for HER and GOR, and opens up new avenue to coproduce more widespread commodity chemicals via gentle and sustainable electrocatalytic means.
氢气和甲酸盐是燃料电池中的重要能量载体以及化学工业中的原料。将析氢反应(HER)与热力学上有利的多元醇的电氧化裂解相耦合,是通过电化学方法联产氢气和甲酸盐的一种很有前景的方式,用于HER和多元醇电氧化裂解的高活性催化剂是实现这一目标的关键。在此,分别沉积在泡沫镍(NF)基底上的钼(Mo)、钨(W)掺杂的磷化钴(CoP),即Mo-CoP/NF和W-CoP/NF,被研究用作HER和电化学甘油氧化反应(GOR)以产生氢气和甲酸盐的催化电极。W-CoP/NF电极在HER中达到-100 mA cm的电流密度(J)时表现出113 mV的低过电位(η),而Mo-CoP/NF电极在选择性生产甲酸盐方面表现出高GOR效率。原位拉曼光谱和红外光谱表征表明,从CoP析出的CoO是GOR的真正催化位点。基于W-CoP/NF阴极和Mo-CoP/NF阳极的不对称电解槽在1.8 V电压下进行甘油电解时的电流密度J = 100 mA cm,这相对于水电解导致电力消耗降低了18.2%。这项工作突出了异质元素掺杂磷化物在HER和GOR催化性能方面的潜力,并开辟了通过温和且可持续的电催化方法联产更广泛商品化学品的新途径。