High-activity electrodeposited NiW catalysts for hydrogen evolution in alkaline water electrolysis

Authors
Hong, Sung HoonAhn, Sang HyunChoi, JihuiKim, Jin YeongKim, Ho YoungKim, Hyoung-JuhnJang, Jong HyunKim, HaekyoungKim, Soo-Kil
Issue Date
2015-09
Publisher
ELSEVIER
Citation
APPLIED SURFACE SCIENCE, v.349, pp.629 - 635
Abstract
NiW alloy catalysts were prepared on a Cu foil substrate by using a co-electrodeposition method for use in the hydrogen evolution (HER) in alkaline water electrolysis. The compositions of the alloy catalysts were controlled over a wide range by varying the molar ratio [W6+]/[Ni2+] in the electrolyte. At high W contents (similar to 41 at.%) in the deposited catalyst, the morphologies of the NiW alloys showed drastic changes compared with those of electrodeposited Ni, in particular a significant decrease in surface coverage and aggregates' sizes. All of NiW alloys deposited in a citrate-containing bath demonstrated an amorphous structure, regardless of W content. Electrochemical measurements employing repeated cyclic voltammetry (CV) showed enhanced HER activities for the NiW alloy catalysts compared with the pure Ni catalyst. The maximum HER activity was obtained with a W content of 41 at.%; the alloying effects, including morphological changes, and the high affinity for hydrogen absorption shown by this alloy's amorphous structure are dominant factors in the enhanced HER activity. The results presented herein provide advanced information of significant relationship between material properties and HER activity of NiW alloys. (C) 2015 Elsevier B.V. All rights reserved.
Keywords
NICKEL; ALLOYS; ELECTROCATALYSTS; TUNGSTEN; FABRICATION; BEHAVIOR; ENERGY; LAYER; FILMS; Alkaline water electrolysis; Hydrogen evolution reaction; Alloy deposition; Amorphous nickel tungsten alloy catalyst
ISSN
0169-4332
URI
https://pubs.kist.re.kr/handle/201004/125037
DOI
10.1016/j.apsusc.2015.05.040
Appears in Collections:
KIST Article > 2015
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE