Soluble polybenzimidazoles incorporating Troger's base for high-temperature proton exchange membrane fuel cells

被引:48
作者
Dai, Junming [1 ,2 ]
Zhang, Yu [1 ,2 ]
Gong, Chunli [3 ]
Wan, Yinhua [1 ,2 ]
Zhuang, Yongbing [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Proc Engn, State Key Lab Biochem Engn, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Engn, Beijing 100190, Peoples R China
[3] Hubei Engn Univ, Sch Chem & Mat Sci, Xiaogan 432000, Peoples R China
基金
中国国家自然科学基金;
关键词
Troger's base; Polybenzimidazoles; High-temperature proton exchange membrane; Fuel cells; COMPOSITE MEMBRANES; ACID; ELECTROLYTES; POLYIMIDES; EFFICIENT; PROGRESS; PBI;
D O I
10.1016/j.cej.2023.143151
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this work, a novel dicarboxylic acid (TB-COOH) containing Tro center dot ger's base (TB) was synthesized, and newly TB -based polybenzimidazole (PBI) membranes were prepared as electrolytes for high-temperature proton exchange membrane (HT-PEM) fuel cells. The TB-based PBIs, upon treatment with triethylammonium salts, showed good processability. The as-prepared TB-based PBI membranes exhibit superior tensile strength above 126.6 MPa and high decomposition temperatures at 5% weight loss ranging from 374 degrees C to 411 degrees C. The residual weights of the TB-based PBI membranes remained at above 80% in Fenton's reagent at 80 degrees C for 48 h. Notably, with extra nitrogen atoms in the TB-based PBIs, their phosphoric acid uptakes show obvious improvement over the cor-responding sulfonated polybenzimidazole (sPBI) without TB units, achieving the highest proton conductivity (93.2 mS cm-1) at 160 degrees C, 2.3 times that of 41.2 mS cm-1 from the sulfonated PBI (sPBI) membrane. The highest peak power density of the H2/air fuel cell reached 225.5 mW cm-2 under non-humidity conditions at 160 degrees C, much higher than the value of the sPBI membrane. Based on their excellent comprehensive performance, incorporating TB into chain backbones optimized the PBI electrolytes for HT-PEM applications.
引用
收藏
页数:10
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