Yu Chen-Chiang, Kim Sanwi, Baek Jong Dae, Li Yong, Su Pei-Chen, Kim Taek-Soo
§Energy Research Institute @ NTU, Interdisciplinary Graduate School, Nanyang Technological University, 50 Nanyang Avenue 639798, Singapore.
⊥Department of Mechanical Engineering, Korea Advanced Institute of Science and Technology, 291 Daehak-ro Yuseong-gu, Daejeon 305-701, South Korea.
ACS Appl Mater Interfaces. 2015 Mar 25;7(11):6036-40. doi: 10.1021/acsami.5b00134. Epub 2015 Mar 12.
Nanoporous platinum electrode thin films were delaminated from yttria-stabilized zirconia (YSZ) substrates via double cantilever beam delamination to reveal the structure located at the interface between electrode and electrolyte. The thermally driven morphological evolution between the electrode top surface and the substrate contact interface of agglomerated nanoporous platinum thin films were compared. We found the temperature required for significant agglomeration to occur was approximately 100 °C higher at the electrolyte contact interface side than at the top surface side. Judging the reaction active site from the electrode top surface could be inaccurate because higher resistance of thermal agglomeration at the interface could retain the reaction active site during fuel cell operation.
通过双悬臂梁分层法将纳米多孔铂电极薄膜从氧化钇稳定的氧化锆(YSZ)衬底上分层,以揭示位于电极和电解质之间界面处的结构。比较了团聚纳米多孔铂薄膜电极顶面与衬底接触界面之间的热驱动形态演变。我们发现,在电解质接触界面一侧发生显著团聚所需的温度比顶面一侧大约高100℃。从电极顶面判断反应活性位点可能不准确,因为界面处较高的热团聚电阻在燃料电池运行期间可能会保留反应活性位点。