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Homogeneous Metastable Hexagonal Phase Iridium Enhances Hydrogen Evolution Catalysis.

Shize GengYujin JiJiaqi SuZhiwei HuMiaomiao FangDan WangShangheng LiuLing LiYouyong LiJin-Ming ChenJyh-Fu LeeXiaoqing HuangQi Shao
Published in: Advanced science (Weinheim, Baden-Wurttemberg, Germany) (2023)
Catalytic reactions are surface-sensitive processes. Fabrication of homogeneous metastable metals can be used to promote phase-dependent catalytic performance; however, this has been a challenging task. Herein, homogeneous metastable hexagonal close-packed (hcp) Ir is epitaxially grown onto metastable phase hcp Ni, as demonstrated using spherical aberration electron microscopy. The as-fabricated metastable hcp Ir exhibits high intrinsic activity for the alkaline hydrogen evolution reaction (HER). In particular, metastable hcp Ir delivers a low overpotential of 17 mV at 10 mA cm -2 and presents a high specific activity of 8.55 mA cm -2 and a high turnover frequency of 38.26 s -1 at -0.07 V versus the reversible hydrogen electrode. Owing to its epitaxially grown structure, metastable hcp Ir is highly stable. Theoretical calculations reveal that metastable hcp Ir promotes H 2 O adsorption and fast H 2 O dissociation, which contributes to its remarkable HER activity. Findings can elucidate the crystal phase-controlled synthesis of advanced noble metal nanomaterials for the fundamental catalytic applications.
Keyphrases
  • climate change
  • crystal structure
  • molecular dynamics simulations
  • drinking water
  • transition metal