Ligand-Exchange-Assisted Layer-by-Layer Assembly of Au-Pt Bimetallic Nanocomposite Films and Their Electrocatalytic Activities for Hydrogen Evolution Reaction
- Authors
- 이수진; Song, Yongkwon; Cho, Jinhan; Jang, Youn Jeong; Yeom, Bongjun
- Issue Date
- Nov-2023
- Publisher
- AMER CHEMICAL SOC
- Keywords
- water splitting; hydrogen evolution reaction; layer-by-layer assembly; Au-Pt bimetallic film; electrocatalyst
- Citation
- ACS APPLIED ENERGY MATERIALS, v.6, no.21, pp 10961 - 10969
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACS APPLIED ENERGY MATERIALS
- Volume
- 6
- Number
- 21
- Start Page
- 10961
- End Page
- 10969
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/196310
- DOI
- 10.1021/acsaem.3c01739
- ISSN
- 2574-0962
2574-0962
- Abstract
- Platinum (Pt) is a popular electrocatalyst for the hydrogen evolution reaction (HER) for water splitting. However, a facile synthesis route with improved activity and stability remains to be established. In this study, Au-Pt bimetallic nanocomposite electrodes for the HER are prepared by ligand-exchange-assisted layer-by-layer (LbL) self-assembly methods. Pt and Au nanoparticles (NPs) are alternately deposited onto Ti electrodes paired with short alkyl amines. This process is accompanied by the removal of the preattached bulky surface ligands. The resulting Pt and Au NP LbL nanocomposite films are characterized by uniform thin-film depositions with high electrical conductivity (8.7 x 10(4) S cm(-1)). With the increase in the number of depositions, the overpotentials of the Au-Pt LbL samples gradually decrease and reach 66 mV at a current density of 10 mA cm(-2) under an acidic condition of 0.5 M H2SO4, which is accomplished with a significantly small Pt loading (0.73 wt %). Furthermore, the overpotentials of the Au-Pt bimetallic LbL films are one-third of the Pt NP LbL films. The enhanced activity can be attributed to the synergistic effect of the d-band shift from the bimetallic heterostructure, high electrical conductivity, rapid charge transfer, and increased electrochemical surface area.
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