Journal
JOURNAL OF ENERGY CHEMISTRY
Volume 72, Issue -, Pages 432-441Publisher
ELSEVIER
DOI: 10.1016/j.jechem.2022.04.040
Keywords
Transition metal nitrides; Heterostructures; Hydrogen evolution reaction; Glycerol and ethylene glycol oxidation; Formic acid
Funding
- National Natural Science Foundation of China [22072107, 21872105]
- Science & Technology Commission of Shanghai Municipality [19DZ2271500]
- Fundamental Research Funds for the Central Universities
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This study demonstrates the preparation of free-standing heterostructured Ni3N-Ni0.2Mo0.8N nanowire arrays on carbon cloth electrodes, which effectively promote glycerol oxidation reaction (GOR) to produce high-purity formate and achieve efficient hydrogen evolution reaction (HER) at a lower voltage. Moreover, the same electrode catalyzes the conversion of ethylene glycol from PET plastic hydrolysate into formate, providing a new strategy for improving energy utilization efficiency.
Electrocatalytic water splitting provides a potentially sustainable approach for hydrogen production, but is typically restrained by kinetically slow anodic oxygen evolution reaction (OER) which is of lesser value. Here, free-standing, hetero-structured Ni3N-Ni0.2Mo0.8N nanowire arrays are prepared on carbon cloth (CC) electrodes for hydrogen evolution reaction (HER) and glycerol oxidation reaction (GOR) to formate with a remarkably high Faradaic efficiency of 96%. A two-electrode electrolyzer for GOR-assisted hydrogen production operates with a current density of 10 mA cm(-2) at an applied cell voltage of 1.40 V, 220 mV lower than for alkaline water splitting. In-situ Raman measurements identify Ni (III) as the active form of the catalyst for GOR rather than Ni (IV) and in-situ Fourier transform infrared (FTIR) spectroscopy measurements reveal pathways for GOR to formate. From density functional theory (DFT) calculations, the Ni3N-Ni0.2Mo0.8N heterostructure is beneficial for optimizing adsorption energies of reagents and intermediates and for promoting HER and GOR activities by charge redistribution across the heterointerface. The same electrode also catalyzes conversion of ethylene glycol from polyethylene terephthalate (PET) plastic hydrolysate into formate. The combined results show that electrolytic H-2 and formate production from alkaline glycerol and ethylene glycol solutions provide a promising strategy as a cost-effective energy supply. (C) 2022 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by ELSEVIER B.V. and Science Press. All rights reserved.
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