Crystal Phase Transition Creates a Highly Active and Stable RuCX Nanosurface for Hydrogen Evolution Reaction in Alkaline Media

Authors
Kim, JeonghyeonKim, Hee JinRuqia, BibiKim, Mi JiJang, Yeong-JiJo, Tae HwanBaik, HionsuckOh, Hyung-SukChung, Hee-SukBaek, KangkyunNoh, SiwooJung, MoonjungKim, Ki-jeongLim, Hyung-KyuYoun, Young-SangChoi, Sang-Il
Issue Date
2021-12
Publisher
WILEY-V C H VERLAG GMBH
Citation
ADVANCED MATERIALS, v.33, no.48
Abstract
Although metastable crystal structures have received much attention owing to their utilization in various fields, their phase-transition to a thermodynamic structure has attracted comparably little interest. In the case of nanoscale crystals, such an exothermic phase-transition releases high energy within a confined surface area and reconstructs surface atomic arrangement in a short time. Thus, this high-energy nanosurface may create novel crystal structures when some elements are supplied. In this work, the creation of a ruthenium carbide (RuCX, X < 1) phase on the surface of the Ru nanocrystal is discovered during phase-transition from cubic-close-packed to hexagonal-close-packed structure. When the electrocatalytic hydrogen evolution reaction (HER) is tested in alkaline media, the RuCX exhibits a much lower overpotential and good stability relative to the counterpart Ru-based catalysts and the state-of-the-art Pt/C catalyst. Density functional theory calculations predict that the local heterogeneity of the outermost RuCX surface promotes the bifunctional HER mechanism by providing catalytic sites for both H adsorption and facile water dissociation.
Keywords
RUTHENIUM NANOPARTICLES; REDUCTION; NANOSTRUCTURES; CATALYST; OXIDE; PH; OXOPHILICITY; METALS; HEAT; ACID; RUTHENIUM NANOPARTICLES; REDUCTION; NANOSTRUCTURES; CATALYST; OXIDE; PH; OXOPHILICITY; METALS; HEAT; ACID; alkaline media; hydrogen evolution reaction; nanosurfaces; phase transitions; ruthenium carbide
ISSN
0935-9648
URI
https://pubs.kist.re.kr/handle/201004/116009
DOI
10.1002/adma.202105248
Appears in Collections:
KIST Article > 2021
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