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Ligand-Exchange-Assisted Layer-by-Layer Assembly of Au-Pt Bimetallic Nanocomposite Films and Their Electrocatalytic Activities for Hydrogen Evolution Reaction

Authors
이수진Song, YongkwonCho, JinhanJang, Youn JeongYeom, 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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