• 文献标题:   Enhancing Iridium Nanoparticles' Oxygen Evolution Reaction Activity and Stability by Adjusting the Coverage of Titanium Oxynitride Flakes on Reduced Graphene Oxide Nanoribbons' Support
  • 文献类型:   Article
  • 作  者:   MORIAU L, PODBORSEK GK, SURCA AK, PARPARI SS, SALA M, PETEK U, BELE M, JOVANOVIC P, GENORIO B, HODNIK N
  • 作者关键词:   carbonceramics composite, electrocatalyst, iridium nanoparticle, oxygen evolution reaction, reduced graphene oxide nanoribbon, titanium oxynitride
  • 出版物名称:   ADVANCED MATERIALS INTERFACES
  • ISSN:   2196-7350
  • 通讯作者地址:  
  • 被引频次:   7
  • DOI:   10.1002/admi.202100900 EA AUG 2021
  • 出版年:   2021

▎ 摘  要

Hydrogen production from solar energy is currently considered the best alternative to fossil fuels. Thus, materials enabling efficient and sustainable energy conversion and storage need to be developed. Iridium is still the only material used in proton exchange membrane electrolyzers that efficiently catalyze hydrogen evolution counter-reaction, namely, the oxygen evolution reaction (OER) for electrochemical water splitting in acidic media. With no practical alternatives that can sustain the harsh reaction conditions, new approaches need to be developed to increase the utilization of this scarce metal. Hereby, a carbon-ceramic nanocomposite material is investigated, where Ir nanoparticles and nanoflakes of titanium oxynitride (TiONx) are deposited on the surface of reduced graphene oxide nanoribbons (rGONRs). OER performance is shown to be dependent on the mutual distribution of the Ir-TiONx-rGONR phases and in the best case leads up to 30 times higher activity relative to the commercial IrO2 benchmark. Adjusting the domains of different chemical nature within the same hybrid nanocomposite material through the formation of heterojunctions is shown to boost OER performance. This work demonstrates how fine-tuning of morphology, composition, and particle distribution of the carbon-ceramic catalytic material can introduce a strong synergistic effect on OER activity and stability of iridium.