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Nanointerface Coupling Activates Earth-Abundant Elements for Enhanced Oxygen Evolution Electrode Process

delete2025-12-01
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PRE
AI
M
M. Wang
W
Wenqin Peng
A
Andrey Lyalin
N
Nattamon Suwannaharn
T
T. Tsuji
D
Daiju Matsumura
T
Tetsuro Morooka
T
Tomoaki Kumeda
T
Tetsuya Taketsugu
T
Tadakatsu Ohkubo
T
Takuya Masuda
T
Taisuke Sasaki
K
Ken Sakaushi *
DOI:10.1021/acs.jpcc.5c06544delete
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Abstract

Abstract

En 中文
Understanding how compositional complexity influences electrocatalytic kinetics remains a major challenge in the design of multicomponent materials. The multifaceted interactions between constituent elements are able to obscure the factors governing kinetics of electrode processes. Here, we introduce a small compositional change to modulate the rate-determining step of the oxygen evolution reaction (OER) by tuning the binding energies of key intermediates. We combine advanced characterization, including in situ electrochemical X-ray absorption spectroscopy, with first-principles calculations to demonstrate that the drastic enhancement in OER activity of MnFeNi-based materials is driven by synergistic interactions among the constituent elements. This enhancement stems from targeted modulation of intrinsic reaction pathways, shifting the rate-determining step via controlled stabilization of key intermediates. Our findings introduce a clear viewpoint for understanding how compositional tuning governs kinetics in complex electrocatalytic systems, offering new design principles for next-generation electrochemical materials.
Keywords:
IMPEDANCE SPECTRA
OXIDE
WATER
ATOM
DECONVOLUTION
MECHANISMS
REDUCTION
CATALYSIS
OXIDATION
CO

Journal

Journal of Physical Chemistry C cover
Journal of Physical Chemistry C
IF:
3.2
Papers:
5.6W
Citations:
15.0W

Organization

N
national institute for materials science
Scholars:
9.5K
Papers: 1.3W
Citations: 28
J
Japan Atomic Energy Agency
Scholars:
3.9K
Papers: 3.8K
Citations: 2.8K
H
hokkaido university
Scholars:
4.9K
Papers: 1.7K
Citations: 0
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