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Bimetallic Nickel/Ruthenium Catalysts Synthesized by Atomic Layer Deposition for Low-Temperature Direct Methanol Solid Oxide Fuel Cells

Authors
Jeong, HeonjaeKim, Jun WooPark, JoonsukAn, JihwanLee, TonghunPrinz, Fritz B.Shim, Joon Hyung
Issue Date
9-11월-2016
Publisher
AMER CHEMICAL SOC
Keywords
atomic layer deposition; heterogeneous catalysts; direct methanol solid oxide fuel cell; nickel; ruthenium
Citation
ACS APPLIED MATERIALS & INTERFACES, v.8, no.44, pp.30090 - 30098
Indexed
SCIE
SCOPUS
Journal Title
ACS APPLIED MATERIALS & INTERFACES
Volume
8
Number
44
Start Page
30090
End Page
30098
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/86847
DOI
10.1021/acsami.6b08972
ISSN
1944-8244
Abstract
Nickel and ruthenium bimetallic catalysts were heterogeneously synthesized via atomic layer deposition (ALD) for use as the anode of direct methanol solid oxide fuel cells (DMSOFCs) operating in a low-temperature range. The presence of highly dispersed ALD Ru islands over a porous Ni mesh was confirmed, and the Ni/ALD Ru anode microstructure was observed. Fuel cell tests were conducted using Ni-only and Ni/ALD Ru anodes with approximately 350 mu m thick gadolinium-doped ceria electrolytes and platinum cathodes. ThC performance of fuel cells was assessed using pure methanol at operating temperatures of 300-400 degrees C. Micromorphological changes of the anode after cell operation were investigated, and the content of adsorbed carbon on the anode side of the operated samples was measured. The difference in the maximum power density between samples utilizing Ni/ALD Ru and Pt/ALD Ru, the latter being the best catalyst for direct methanol fuel cells, was observed to be less than 7% at 300 degrees C and 30% at 350 degrees C. The improved electrochemical activity of the Ni/ALD Ru anode compared to that of the Ni-only anode, along with the reduction of the number of catalytically active sites due to agglomeration of Ni and carbon formation on the Ni surface as compared to Pt, explains this decent performance.
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