首页 | 本学科首页   官方微博 | 高级检索  
     


Anode-supported solid oxide fuel cell with yttria-stabilized zirconia/gadolinia-doped ceria bilalyer electrolyte prepared by wet ceramic co-sintering process
Affiliation:1. Department of Chemistry, Harbin Institute of Technology, Harbin, 150001, PR China;2. State Key Laboratory of Urban Water Resource and Environment, School of Municipal and Environmental Engineering, Harbin Institute of Technology, Harbin, 150090, PR China;3. Academy of Fundamental and Interdisciplinary Sciences, Harbin Institute of Technology, Harbin, 150001, PR China;1. School of Computer Science and Information Engineering, Hubei University, Wuhan, Hubei 43062, PR China;2. Center for Innovative Fuel Cell and Battery Technologies, School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332, USA
Abstract:To protect the ceria electrolyte from reduction at the anode side, a thin film of yttria-stabilized zirconia (YSZ) is introduced as an electronic blocking layer to anode-supported gadolinia-doped ceria (GDC) electrolyte solid oxide fuel cells (SOFCs). Thin films of YSZ/GDC bilayer electrolyte are deposited onto anode substrates using a simple and cost-effective wet ceramic co-sintering process. A single cell, consisting of a YSZ (~3 μm)/GDC (~7 μm) bilayer electrolyte, a La0.8Sr0.2Co0.2Fe0.8O3–GDC composite cathode and a Ni–YSZ cermet anode is tested in humidified hydrogen and air. The cell exhibited an open-circuit voltage (OCV) of 1.05 V at 800 °C, compared with 0.59 V for a single cell with a 10-μm GDC film but without a YSZ film. This indicates that the electronic conduction through the GDC electrolyte is successfully blocked by the deposited YSZ film. In spite of the desirable OCVs, the present YSZ/GDC bilayer electrolyte cell achieved a relatively low peak power density of 678 mW cm?2 at 800 °C. This is attributed to severe mass transport limitations in the thick and low-porosity anode substrate at high current densities.
Keywords:
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号