Selective Ethylene Glycol Oxidation to Formate on Nickel Selenide with Simultaneous Evolution of Hydrogen

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Abstract
There is an urgent need for cost‐effective strategies to produce hydrogen from renewable net‐zero carbon sources using renewable energies. In this context, the electrochemical hydrogen evolution reaction can be boosted by replacing the oxygen evolution reaction with the oxidation of small organic molecules, such as ethylene glycol (EG). EG is a particularly interesting organic liquid with two hydroxyl groups that can be transformed into a variety of C1 and C2 chemicals, depending on the catalyst and reaction conditions. Here, a catalyst is demonstrated for the selective EG oxidation reaction (EGOR) to formate on nickel selenide. The catalyst nanoparticle (NP) morphology and crystallographic phase are tuned to maximize its performance. The optimized NiS electrocatalyst requires just 1.395 V to drive a current density of 50 mA cm−2 in 1 m potassium hydroxide (KOH) and 1 m EG. A combination of in situ electrochemical infrared absorption spectroscopy (IRAS) to monitor the electrocatalytic process and ex situ analysis of the electrolyte composition shows the main EGOR product is formate, with a Faradaic efficiency above 80%. Additionally, C2 chemicals such as glycolate and oxalate are detected and quantified as minor products. Density functional theory (DFT) calculations of the reaction process show the glycol‐to‐oxalate pathway to be favored via the glycolate formation, where the CC bond is broken and further electro‐oxidized to formate.
Funding Information
  • Chengdu University
  • Ministerio de Ciencia e Innovación (PID2019‐105490RB‐C32)
  • National Natural Science Foundation of China (22172121)
  • Fundamental Research Funds for the Central Universities
  • Southwest Minzu University (xiao2021102)
  • Generalitat de Catalunya (2021SGR00457)
  • European Commission (PRTR‐C17.I1)
  • Natural Science Foundation of Sichuan Province (23NSFSC6266)

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