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Magnetic Field Manipulation of Tetrahedral Units in Spinel Oxides for Boosting Water Oxidation.

Xiao LyuYanan ZhangZhengwei DuHao ChenSicheng LiAlexandre I RykovChen ChengWeina ZhangLing ChangWang KaiJunhu WangLiang ZhangQiang WangChengxi HuangErjun Kan
Published in: Small (Weinheim an der Bergstrasse, Germany) (2022)
Magnetic field enhanced electrocatalysis has recently emerged as a promising strategy for the development of a viable and sustainable hydrogen economy via water oxidation. Generally, the effects of magnetic field enhanced electrocatalysis are complex including magnetothermal, magnetohydrodynamic and spin selectivity effects. However, the exploration of magnetic field effect on the structure regulation of electrocatalyst is still unclear whereas is also essential for underpinning the mechanism of magnetic enhancement on the electrocatalytic oxygen evolution reaction (OER) process. Here, it is identified that in a mixed NiFe 2 O 4 (NFO), a large magnetic field can force the Ni 2+ cations to migrate from the octahedral (O h ) sites to tetrahedral (T d ) sites. As a result, the magnetized NFO electrocatalyst (NFO-M) shows a two-fold higher current density than that of the pristine NFO in alkaline electrolytes. The OER enhancement of NFO is also observed at 1 T (NFO@1T) under an operando magnetic field. Our first-principles calculations further confirm the mechanism of magnetic field driven structure regulation and resultant OER enhancement. These findings provide a strategy of manipulating tetrahedral units of spinel oxides by a magnetic field on boosting OER performance.
Keyphrases
  • metal organic framework
  • hydrogen peroxide
  • density functional theory
  • single molecule
  • molecular dynamics
  • molecular dynamics simulations
  • room temperature
  • mass spectrometry