4.6 Article

Fluorine substituted (Mn,Ir)O2:F high performance solid solution oxygen evolution reaction electro-catalysts for PEM water electrolysis

Journal

RSC ADVANCES
Volume 7, Issue 28, Pages 17311-17324

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra27354h

Keywords

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Funding

  1. National Science Foundation, CBET [0933141, 1511390]
  2. U.S. Department of Energy, Office of Basic Energy Sciences, Division of Materials Sciences and Engineering [DE-SC0001531]
  3. Edward R. Weidlein Chair Professorship funds
  4. National Science Foundation grant [ACI-1053575]
  5. Directorate For Engineering
  6. Div Of Chem, Bioeng, Env, & Transp Sys [1511390] Funding Source: National Science Foundation
  7. Directorate For Engineering
  8. Div Of Chem, Bioeng, Env, & Transp Sys [0933141] Funding Source: National Science Foundation

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Identification and development of high performance with reduced overpotential (i.e. reduced operating electricity cost) oxygen evolution reaction (OER) electrocatalysts for proton exchange membrane (PEM) based water electrolysis with ultra-low noble metal content (i.e. reduced materials cost) is of significant interest for economic hydrogen production, thus increasing the commercialization potential of PEM water electrolysis. Accordingly, a novel electrocatalyst should exhibit low overpotential, excellent electrochemical activity and durability superior to state of the art noble metal based electro-catalysts (e.g. Pt, IrO2, RuO2). Herein, for the very first time to the best of our knowledge, exploiting first-principles theoretical calculations of the total energies and electronic structures, we have identified a reduced noble metal content fluorine doped solid solution of MnO2 and IrO2, denoted as (Mn1-xIrx)O-2: F (x = 0.2, 0.3, 0.4), OER electrocatalyst system exhibiting lower overpotential and higher current density than the state of the art IrO2 and other previously reported systems for PEM water electrolysis. The doped solid solution displays an excellent electrochemical performance with a lowest reported onset potential to date of similar to 1.35 V (vs. RHE), similar to 80 mV lower than that of IrO2 (similar to 1.43 V vs. RHE) and similar to 15 fold (x similar to 0.3 and 0.4) higher electrochemical activity compared to pure IrO2. In addition, the system displays excellent long term electrochemical durability, similar to that of IrO2 in harsh acidic OER operating conditions. Our study therefore demonstrates remarkable, similar to 60-80% reduction in noble metal content along with lower overpotential and excellent electrochemical performance clearly demonstrating the potential of the (Mn1-xIrx) O-2: F system as an OER electro-catalyst for PEM water electrolysis.

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