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February 22, 2026The Journal of Physical Chemistry Letters0 citations

Low-Temperature, Rapid Synthesis of Plasma-Exsolved FeNi/NiFe 2 O 4 Composites for Enhanced Oxygen Evolution Reaction

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XHXihang HuLWLinfeng WanWCWei Cheng

Key Points

  • The aim is to enhance the oxygen evolution reaction efficiency through low-temperature, rapid synthesis of plasma-exsolved catalysts.
  • Developed a hydrogen plasma treatment for rapid exsolution under low temperatures (∼200 °C)
  • Synthesis of FeNi/NiFe2O4 composite structures modified with active nanoparticles
  • Measured electrocatalytic activity through overpotential and Tafel slope analysis
  • Achieved an overpotential of 290 mV at 10 mA cm-2, outperforming pristine NiFe2O4
  • Demonstrated a Tafel slope of 68.18 mV dec-1, lower than that of NiFe2O4
  • Showed stability by maintaining initial current density for over 240 h

Abstract

Exsolution of active nanoparticles (NPs) on substrate surfaces is a promising route to enhance the oxygen evolution reaction (OER) efficiently. However, conventional exsolution methods often suffer from protracted long processing times (4-10 h), substantial energy consumption, and high-temperature (500-1000 °C) reduction under H2/Ar atmospheres. To address these limitations, this work introduces a hydrogen plasma treatment that facilitates rapid exsolution of NPs in a few minutes at low temperatures (∼200 °C), resulting in NPs-modified spinel structures. The resulting FeNi/NiFe2O4 composite structure exhibits remarkable OER activity, demonstrating an overpotential of 290 mV at 10 mA cm-2 and a Tafel slope of 68.18 mV dec-1, superior to pristine NiFe2O4 (315 and 98.97 mV dec-1, respectively). The catalyst also presents robust stability, maintaining its initial current density for over 240 h. This work offers valuable insights into plasma-induced exsolution for enhancing the electrocatalytic activity of spinel structures.

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Cite This Study

Hu et al. (2026) studied this question.

synapsesocial.com/papers/699a9d7a482488d673cd36c6https://doi.org/10.1021/acs.jpclett.5c03958
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