Vertical-crystalline Fe-doped beta-Ni oxyhydroxides for highly active and stable evolution reaction

Authors
Kim, ByeongyoonKabiraz, Mrinal KantiLee, JaewanChoi, ChanghyeokBaik, HionsuckJung, YousungOh, Hyung-SukChoi, Sang-IlLee, Kwangyeol
Issue Date
2021-11
Publisher
Cell Press
Citation
Matter, v.4, no.11, pp.3585 - 3604
Abstract
The layered transition metal oxyhydroxides have received increasing interest owing to the efficient energy conversion performance and material stability during the oxygen evolution reaction (OER). In particular, Fe-doped NiOOH has shown record-high OER performance in alkaline media among various catalysts. Theoretically, undercoordinated facets including Ni4+, exposed at the edges of NiOOH, were predicted to perform highly active OER. Therefore, here we suggest a rational catalyst design, a vertical-crystalline beta-Fe/NiOOH layer built on faceted Fe/Ni nanocrystals, which exposes Ni4+ sites and could improve the OER performance dramatically. Electrochemical OER tests recorded the overpotential of 210 mV at a current density of 10 mA cm(-2) GEO and stable operation for 5 days. In situ/operando and density functional theory studies revealed that the Ni valence cycle between +2 and +4 assisted by Fe dopant is the key engine that greatly accelerates OER kinetics and that the vertical-crystalline beta-Fe/NiOOH layers on Ni octahedra are stable under harsh OER conditions.
Keywords
MEMBRANE WATER ELECTROLYSIS; OXYGEN-EVOLUTION; ELECTRONIC-STRUCTURE; REACTION DYNAMICS; REDOX STATES; CATALYSTS; ELECTROCATALYSTS; OXIDE; OXIDATION; XANES; Heteroepitaxy; Oxygen evolution reaction; Crystalline Fe/NiOOH; AEMWE; Facet control
ISSN
2590-2393
URI
https://pubs.kist.re.kr/handle/201004/116203
DOI
10.1016/j.matt.2021.09.003
Appears in Collections:
KIST Article > 2021
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