Tensile-Strained RuO 2 Loaded on Antimony-Tin Oxide by Fast Quenching for Proton-Exchange Membrane Water Electrolyzer.
Bing HuangHengyue XuNannan JiangMinghao WangJianren HuangLunhui GuanPublished in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2022)
Future energy demands for green hydrogen have fueled intensive research on proton-exchange membrane water electrolyzers (PEMWE). However, the sluggish oxygen evolution reaction (OER) and highly corrosive environment on the anode side narrow the catalysts to be expensive Ir-based materials. It is very challenging to develop cheap and effective OER catalysts. Herein, Co-hexamethylenetetramine metal-organic framework (Co-HMT) as the precursor and a fast-quenching method is employed to synthesize RuO 2 nanorods loaded on antimony-tin oxide (ATO). Physical characterizations and theoretical calculations indicate that the ATO can increase the electrochemical surface areas of the catalysts, while the tensile strains incorporated by quenching can alter the electronic state of RuO 2 . The optimized catalyst exhibits a small overpotential of 198 mV at 10 mA cm -2 for OER, and keeps almost unchanged after 150 h chronopotentiometry. When applied in a real PEMWE assembly, only 1.51 V is needed for the catalyst to reach a current density of 1 A cm -2 .
Keyphrases
- metal organic framework
- drug delivery
- reduced graphene oxide
- energy transfer
- oxide nanoparticles
- electron transfer
- highly efficient
- gold nanoparticles
- cancer therapy
- wound healing
- escherichia coli
- density functional theory
- mental health
- current status
- molecular dynamics
- molecular dynamics simulations
- perovskite solar cells
- molecularly imprinted
- mass spectrometry
- visible light
- carbon dioxide
- tandem mass spectrometry
- simultaneous determination