Advantageous of Hybrid Fuel Cell Operation under Self-Humidification for Energy Efficient Bipolar Membrane

被引:33
|
作者
Manohar, Murli [1 ]
Kim, Dukjoon [1 ]
机构
[1] Sungkyunkwan Univ, Sch Chem Engn, Suwon 16419, Kyunggi, South Korea
来源
关键词
Bipolar membrane; Interface; Layer-by-layer; Self-humidification; Bipolar membrane fuel cell; ANION-EXCHANGE MEMBRANES; WATER DISSOCIATION CATALYST; INTERFACIAL LAYER; GRAPHENE OXIDE; POLY(PHENYL ACRYLATE); POLY(STYRENE-CO-ACRYLONITRILE); ELECTRODIALYSIS; DEGRADATION; MISCIBILITY; BLENDS;
D O I
10.1021/acssuschemeng.9b03735
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Because of a unique sandwiched structure of proton and anion exchange membranes, the bipolar membrane (BPM) enables self-humidification at their junction in fuel cell operation. In this work, a novel BPM was prepared from the sulfonated poly(ether ether sulfone) (SPEES) acidic and the quaternized polysulfone (QPS) alkaline membranes via layer-by-layer process. A variety of advantageous membrane and electrochemical properties associated with its self-humidification were investigated under the membrane electrode assembly operation at steady-state with generation of water molecules at the interface even at low humidity. The proton and hydroxide ion conductivity of the membranes used in this BPM were quite high-0.053 S cm(-1) for SPEES and 0.014 S cm(-1) for QPS, respectively. The H-2/O-2 single fuel cell test with this BPM showed the power density up to 75 mW cm(-2) at 100% relative humidity (RH) and 67 mW cm(-2) at 0% RH, while that with the corresponding proton exchange membrane prepared from single SPEES showed lower power density at 0% RH with the collapse of the membrane by burning.
引用
收藏
页码:16493 / 16500
页数:15
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