Enhancing the durability of hydrocarbon-membrane-based polymer electrolyte water electrolysis using a radical scavenger-embedded interlocking interfacial layer

被引:32
作者
Choi, Sungyu [1 ]
Shin, Sang-Hun [2 ]
Lee, Dong-Hyun [1 ]
Doo, Gisu [1 ]
Lee, Dong Wook [1 ]
Hyun, Jonghyun [1 ]
Lee, Jang Yong [2 ]
Kim, Hee-Tak [1 ,3 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem & Biomol Engn, 291 Daehak Ro, Daejeon 34141, South Korea
[2] Korea Res Inst Chem Technol, Ctr Membranes, 141 Gajeong Ro, Daejeon 34114, South Korea
[3] Korea Adv Inst Sci & Technol, KAIST Inst NanoCentury, Adv Battery Ctr, 291 Daehak Ro, Daejeon 34141, South Korea
关键词
PROTON-EXCHANGE MEMBRANE; BONDING LAYER; COPOLYMERS; STABILITY; TRANSPORT; HYDROGEN; CERIUM; CELLS;
D O I
10.1039/d1ta08222a
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrocarbon membranes are an attractive alternative to Nafion membranes for use in proton exchange membrane water electrolysis (PEMWE) due to their low gas permeability and high proton conductivity. However, hydrocarbon membranes and Nafion-based catalyst layers are prone to delamination, not allowing long-term operation of hydrocarbon-membrane-based PEMWE. In the present study, we propose a radical-scavenger-embedded interlocking interfacial layer (IIL) that addresses this interfacial delamination issue. The ball-socket joint structure of the IIL leads to mechanical interlocking at the interface, and the presence of cerium oxide as a radical scavenger prevents the hydrothermal degradation of the IIL. Cerium oxide-containing IIL-based PEMWE subsequently operates for more than 500 h with lower polarization at a voltage increase rate of 48 mu V h(-1), which is much lower than that of state-of-the-art hydrocarbon-based PEMWE and is even lower than that of Nafion-based PEMWE (53 mu V h(-1)). The long-term durability of a hydrocarbon-membrane-based PEMWE system, reported for the first time in the present study, represents an important milestone for the development of cost-effective PEMWE systems.
引用
收藏
页码:789 / 798
页数:10
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