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Enhancing Charge Transfer Kinetics by Nanoscale Catalytic Cermet Interlayer

Authors
An, JihwanKim, Young-BeomGuer, Turgut M.Prinz, Fritz B.
Issue Date
Dec-2012
Publisher
AMER CHEMICAL SOC
Keywords
solid oxide fuel cell; atomic layer deposition; interlayer; cermet; nanoparticle
Citation
ACS APPLIED MATERIALS & INTERFACES, v.4, no.12, pp.6789 - 6794
Indexed
SCIE
SCOPUS
Journal Title
ACS APPLIED MATERIALS & INTERFACES
Volume
4
Number
12
Start Page
6789
End Page
6794
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/164047
DOI
10.1021/am3019788
ISSN
1944-8244
Abstract
Enhancing the density of catalytic sites is crucial for improving the performance of energy conversion devices. This work demonstrates the kinetic role of 2 nm thin YSZ/Pt cermet layers on enhancing the oxygen reduction kinetics for low temperature solid oxide fuel cells. Cermet layers were deposited between the porous Pt cathode and the dense YSZ electrolyte wafer using atomic layer deposition (ALD). Not only the catalytic role of the cermet layer itself but the mixing effect in the cermet was explored. For cells with unmixed and fully mixed cermet interlayers, the maximum power density was enhanced by a factor of 1.5 and 1.8 at 400 degrees C, and by 2.3 and 2.7 at 450 degrees C, respectively, when compared to control cells with no cermet interlayer. The observed enhancement in cell performance is believed to be due to the increased triple phase boundary (TPB) density in the cermet interlayer. We also believe that the sustained kinetics for the fully mixed cermet layer sample stems from better thermal stability of Pt islands separated by the ALD YSZ matrix, which helped to maintain the high-density TPBs even at elevated temperature.
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