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Self-supported bimetallic selenide heterostructure catalyst with enhanced electronic interaction for industrial-level seawater electrolysis

  • Yingwei Qi
  • , Jiafu Chen
  • , Di Liu
  • , Xiaotian Wei
  • , Lihang Qu
  • , Cheng Huang
  • , Kai Liu
  • , Yaohai Cai
  • , Dong Liu*
  • , Zhenbo Wang
  • *Corresponding author for this work
  • Shenzhen University
  • University of Macau

Research output: Contribution to journalArticlepeer-review

Abstract

The successful implementation of direct seawater electrolysis for sustainable hydrogen production and seawater desalination hinges on the development of high-efficiency and durable catalysts. In this study, we report the fabrication of a self-supported bimetallic selenide heterostructure catalyst (NiSe2-RuSe2/NF), which achieves an ultralow overpotential of 26 mV at 10 mA cm−2 in natural seawater (unpurified, with 1 M KOH added), outperforming commercial Pt/C. Furthermore, it exhibits exceptional long-term stability, maintaining performance over 250 h at an industrial current density of 500 mA cm−2. Combined density functional theory (DFT) calculations and experimental analyses reveal that the heterostructure modulates the electronic structure, optimizing H* adsorption and enhancing HER catalytic activity. This work provides a straightforward yet effective strategy for designing highly active and efficient HER electrocatalysts for practical seawater electrolysis applications.

Original languageEnglish
Article number162567
JournalChemical Engineering Journal
Volume512
DOIs
StatePublished - 15 May 2025
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

Keywords

  • Bimetallic Selenides
  • Electronic Interaction
  • Heterostructure
  • Hydrogen Evolution Reaction
  • Seawater Electrolysis

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