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Activating catalytic behavior of binary transition metal sulfide-shelled carbon nanotubes by iridium incorporation toward efficient overall water splitting

  • Xinfeng Zhu
  • , Dinh Chuong Nguyen
  • , Sampath Prabhakaran
  • , Do Hwan Kim
  • , Nam Hoon Kim*
  • , Joong Hee Lee*
  • *Corresponding author for this work
  • Jeonbuk National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

To meet the future demand for green energy, the development of catalysts for water splitting has become an essential task for scientists worldwide. In this context, a novel catalyst that relies on Ir-doped CoNi2S4 nanosheets assembled on carbon nanotubes, supported on three-dimensional carbon framework has been developed. The outstanding advantages of core-shell heterostructure and heteroatom doping are that they induce high abundance of exposed active sites and excellent ability for mass/charge transport of the catalyst. Thus, the catalyst provides excellent activity for hydrogen evolution reaction, which surpasses that of the noble-metal-free electrocatalysts reported in the literature. The catalyst also shows superior catalytic behavior for oxygen evolution reaction, which is even better than that of the commercial RuO2 catalyst. Impressively, the electrolyzer using the proposed catalyst requires small cell voltages of only 1.60 V and 1.94 V at response current density of 10 mA/cm2 and 50 mA/cm2, respectively. More importantly, this electrolyzer manifests much better stability and durability than those of the electrolyzer using commercial Pt/C and RuO2 catalysts.

Original languageEnglish
Article number100296
JournalMaterials Today Nano
Volume21
DOIs
StatePublished - 2023.03

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

  • CNTs@CoNiS
  • Core-shell structure
  • Electrocatalyst
  • Ir doping
  • Water splitting

Quacquarelli Symonds(QS) Subject Topics

  • Materials Science
  • Physics & Astronomy

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