Enhancing durability and activity toward oxygen evolution reaction using single-site Re-doped NiFeOx catalysts at ampere-level

Xiang Lyu, Naduvile Purayil Dileep, Yulia Pushkar, Max Pupucevski, Judith Lattimer, Hector Colon-Mercado, Prabhu Ganesan, Matthew R. Ryder, Jong K. Keum, David A. Cullen, Haoran Yu, Harry M. Meyer, Jun Yang, Alexey Serov

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

NiFeOx materials are known as among the most active catalysts toward oxygen evolution reaction (OER) for hydrogen generation in alkaline media. Nevertheless, the long-term durability of NiFeOx catalysts for OER is still too far to the industrial application. Herein, we prepared a NiFeReOx catalyst with single-site Re dopants and observed that the single-site Re dopants could significantly enhance the durability without compromising the activity. A cell voltage of 1.82 V without iR correction is noted at the current density of 3000 mA cm−2 in anion-exchange membrane water electrolyzer (AEMWE) with NiFeReOx catalyst, and a very small degradation is observed under 2000 and 1000 mA cm−2, which remarkably outperforms the pristine NiFeOx. Additionally, the overpotential of 305 mV at 10 mA cm−2 is achieved with the NiFeReOx catalyst, which is lower than 50 mV compared with the pristine NiFeOx catalyst, together with a smaller Tafel slope of 54.3 mV dec-1. The boosted OER durability and activity of the NiFeReOx catalyst could be attributed to the strong electron-withdrawing property of Re7+ single atoms leading to the electronic structure optimization and stabilization of Ni/Fe active sites. Our insights propose a new path for designing NiFeOx catalysts with high durability and activity toward OER.

Original languageEnglish
Article number160518
JournalChemical Engineering Journal
Volume507
DOIs
StatePublished - Mar 1 2025

Funding

This research is supported by the U.S. Department of Energy (DOE) Hydrogen and Fuel Cell Technologies Office through the Hydrogen from Next-generation Electrolyzers of Water (H2NEW) consortium. This research was supported by NSF, CHE-2155060 (Y.P.). This work is based on research conducted at the Center for High-Energy X-ray Sciences (CHEXS), which is supported by the National Science Foundation (BIO, ENG and MPS Directorates) under award DMR-1829070. We thank Dr. Christopher Pollock at CHESS PIPOXS beamlines for assistance with XAS experiments. This work was produced by Battelle Savannah River Alliance, LLC under Contract No. 89303321CEM000080 with the U.S. Department of Energy. X.L. acknowledges that the research was sponsored by the Laboratory Directed Research and Development Program of Oak Ridge National Laboratory, managed by UT-Battelle, LLC, for the US Department of Energy Publisher acknowledges the U.S. Government license to provide public access under the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan). This research is supported by the U.S. Department of Energy (DOE) Hydrogen and Fuel Cell Technologies Office through the Hydrogen from Next-generation Electrolyzers of Water (H2NEW) consortium. This research was supported by NSF, CHE-2155060 (Y.P.). This work is based on research conducted at the Center for High-Energy X-ray Sciences (CHEXS), which is supported by the National Science Foundation (BIO, ENG and MPS Directorates) under award DMR-1829070 . We thank Dr. Christopher Pollock at CHESS PIPOXS beamlines for assistance with XAS experiments. This work was produced by Battelle Savannah River Alliance , LLC under Contract No. 89303321CEM000080 with the U.S. Department of Energy . Publisher acknowledges the U.S. Government license to provide public access under the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan).

Keywords

  • Green hydrogen
  • NiFeOx catalyst
  • Oxygen evolution reaction
  • Re-doped
  • Single atom

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