Tensile-Strained RuO Loaded on Antimony-Tin Oxide by Fast Quenching for Proton-Exchange Membrane Water Electrolyzer.

Adv Sci (Weinh)

CAS Key Laboratory of Design and Assembly of Functional Nanostructures, Fujian Key Laboratory of Nanomaterials, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences, Fuzhou, 350000, China.

Published: August 2022

AI Article Synopsis

  • Future energy needs for green hydrogen are driving research on proton-exchange membrane water electrolyzers (PEMWE), but effective and affordable oxygen evolution reaction (OER) catalysts are scarce due to the need for expensive materials like Ir.
  • A novel approach using Co-hexamethylenetetramine metal-organic frameworks to create RuO nanorods on antimony-tin oxide has shown promise, enhancing the catalytic performance.
  • The resulting catalyst demonstrates impressive stability and efficiency with a low overpotential and performs well in real PEMWE applications, requiring only 1.51 V to achieve significant current density.

Article Abstract

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 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 . The optimized catalyst exhibits a small overpotential of 198 mV at 10 mA cm 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 .

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9376819PMC
http://dx.doi.org/10.1002/advs.202201654DOI Listing

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