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Modulating Built-In Electric Field Strength in Ru/RuO2 Interfaces through Ni Doping to Enhance Hydrogen Conversion at

Tao Liu1, Lianqin Wang1, Bin Chen1

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Developing efficient alkaline hydrogen evolution reaction (HER) catalysts is key for anion exchange membrane water electrolyzers (AEMWEs). Ni-RuO2 demonstrates superior performance due to a built-in electric field (BIEF) enhancing electron transfer and HER kinetics.

Keywords:
AEMWEampere-levelbuilt-in electric fieldhydrogen evolution reaction

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Area of Science:

  • Electrochemistry
  • Materials Science
  • Computational Chemistry

Background:

  • Efficient hydrogen evolution reaction (HER) is crucial for anion exchange membrane water electrolyzers (AEMWEs) operating at industrial current densities.
  • Developing cost-effective and high-performance electrocatalysts is essential for advancing AEMWE technology.

Purpose of the Study:

  • To identify optimal 3d transition metal-doped RuO2 catalysts for alkaline HER.
  • To investigate the mechanism behind enhanced catalytic activity using computational methods.

Main Methods:

  • Density functional theory (DFT) calculations were employed to screen various M-RuO2 (M = Sc, Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zn) catalysts.
  • Analysis of electronic structure and interface properties to understand catalytic mechanisms.

Main Results:

  • Ni-RuO2 was identified as the leading candidate, showing a significant built-in electric field (BIEF) at the Ni-Ru/RuO2 interface.
  • The BIEF facilitates electron transfer, lowers energy barriers, and accelerates HER kinetics.
  • Ni-RuO2 achieved an overpotential of 134 mV at 1 A/cm², a Tafel slope of 20.85 mV/dec, with low Ru loading (0.03 mg/cm²).
  • A Ni-RuO2 based AEMWE demonstrated stable operation at 1 A/cm² for 1000 hours, requiring only 1.71 V.

Conclusions:

  • The Ni-RuO2 catalyst exhibits exceptional performance for alkaline HER, driven by the BIEF effect.
  • This finding offers a promising pathway for developing highly efficient and stable AEMWEs for industrial applications.