Regulating the Third Metal to Design and Engineer Multilayered NiFeM (M: Co, Mn, and Cu) Nanofoam Anode Catalysts for Anion-Exchange Membrane Water Electrolyzers

  • Xiaoxuan Yang
  • , Jiashun Liang
  • , Qiurong Shi
  • , Michael J. Zachman
  • , Sadia Kabir
  • , Junwu Liang
  • , Jing Zhu
  • , Benjamin Slenker
  • , Max Pupucevski
  • , Natalia Macauley
  • , A. Jeremy Kropf
  • , Hao Zeng
  • , Derek Strasser
  • , Deborah J. Myers
  • , Hui Xu
  • , Zhenhua Zeng
  • , Yushan Yan
  • , Gang Wu

Research output: Contribution to journalArticlepeer-review

27 Scopus citations

Abstract

Alkaline anion-exchange membrane water electrolyzers (AEMWEs) for green hydrogen production have received intensive attention due to their feasibility of using earth-abundant platinum group metal (PGM)-free catalysts. Herein, the third metal is incorporated into NiFe-based catalysts to regulate their electronic structures and morphologies, aiming to achieve sufficient oxygen evolution reaction (OER) activity and performance in AEMWEs. The ternary NiFeM (M: Cu, Co, or Mn) catalysts are featured with multiple layered structures and nanofoam network morphologies, consisting of highly OER-active amorphous Ni-rich oxide shells and electrically conductive metallic alloy cores. The physical and electronic perturbations to the NiFe induced by a third element lead to a fine-tuning of the redox ability of the metal sites at the reaction centers, which breaks the scaling relationship between OH* and O* intermediates at the reaction centers. Thus, the unique structural configuration and electronic regulation simultaneously benefit catalytic activity and performance improvements. These NiFeM nanofoam catalysts demonstrated promising anode performance in actual AEMWEs, comparable to the IrO2 reference, especially at high current densities. Notably, using various electrolytes (e.g., KOH solution or pure water) for AEMWEs exhibited a different performance trend among studied NiFeM catalysts, likely due to dynamic changes of catalysts under various OER environments.

Original languageEnglish
Article number2400029
JournalAdvanced Energy Materials
Volume14
Issue number26
DOIs
StatePublished - Jul 12 2024

Funding

The authors are grateful for the financial support from the U.S. Department of Energy, Hydrogen and Fuel Cell Technologies Office. STEM and EDS research was supported by the Center for Nanophase Materials Sciences (CNMS), which is a U.S. Department of Energy, Office of Science User Facility at Oak Ridge National Laboratory. The X‐ray absorption (MRCAT, 10‐BM, and 10‐ID) experiments were performed at the Advanced Photon Source (APS), a DOE Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE‐AC02‐06CH11357. The operation of MRCAT at the APS is supported by the Department of Energy and the MRCAT member institutions. The submitted manuscript has been created, in part, by employees of UChicago Argonne, LLC, Operator of Argonne National Laboratory under Contract No. DE‐AC02‐06CH11357. The authors also thank Dr. Stavros Karakalos for the XPS analysis.

Keywords

  • PGM-free electrocatalysts
  • alkaline water electrolyzers
  • core–shell structures
  • hydrogen generation
  • oxygen evolution reaction

Fingerprint

Dive into the research topics of 'Regulating the Third Metal to Design and Engineer Multilayered NiFeM (M: Co, Mn, and Cu) Nanofoam Anode Catalysts for Anion-Exchange Membrane Water Electrolyzers'. Together they form a unique fingerprint.

Cite this