Chemically Stable, Highly Anion Conductive Polymers Composed of Quinquephenylene and Pendant Ammonium Groups

被引:51
作者
Akiyama, Ryo [1 ]
Yokota, Naoki [3 ]
Miyatake, Kenji [1 ,2 ]
机构
[1] Univ Yamanashi, Fuel Cell Nanomat Ctr, 4 Takeda, Kofu, Yamanashi 4008510, Japan
[2] Univ Yamanashi, Clean Energy Res Ctr, 4 Takeda, Kofu, Yamanashi 4008510, Japan
[3] Takahata Precis Co Ltd, 390 Maemada, Fuefuki, Yamanashi 4060843, Japan
基金
日本科学技术振兴机构;
关键词
MEMBRANE FUEL-CELLS; AROMATIC COPOLYMERS; EXCHANGE MEMBRANE; POLY(ARYLENE ETHER)S; ALKALINE STABILITY; FLUORENYL GROUPS; POLYELECTROLYTES; MORPHOLOGY;
D O I
10.1021/acs.macromol.8b02199
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
To evaluate the effect of five consecutive phenylene units on the properties of anion conductive polymer membranes, a series of quaternized copolymers (QP-QAF) composed of quinquephenylene and fluorene groups functionalized with pendant hexyltrimethylammonium groups were designed and synthesized. Precursor copolymers, QP-AF, with controllable copolymer compositions were synthesized by Yamamoto coupling reaction as high molecular weights. Quaternization of QP-AF using dimethyl sulfate followed by solution casting provided bendable and tough QP-QAF membranes with the ion exchange capacity (IEC) ranging from 0.80 to 2.78 mequiv g(-1). The QP-QAF membranes contained phase-separated morphology due to the hydrophilic/hydrophobic differences in the components as confirmed by TEM images. High hydroxide ion conductivity (up to 134 mS cm(-1) in water at 80 degrees C) was obtained with the membrane (IEC = 2.25 mequiv g(-1)). The membranes were stable in strongly alkaline conditions (similar to 4 M KOH at 80 degrees C) for 1000 h. An H-2/O-2 alkaline fuel cell using the QP-QAF membrane exhibited 248 mW cm(-2) of the maximum power density at 60 degrees C under fully humidified conditions.
引用
收藏
页码:2131 / 2138
页数:8
相关论文
共 27 条
[1]   Structurally Well-Defined Anion Conductive Aromatic Copolymers: Effect of the Side-Chain Length [J].
Akiyama, Ryo ;
Yokota, Naoki ;
Otsuji, Kanji ;
Miyatake, Kenji .
MACROMOLECULES, 2018, 51 (09) :3394-3404
[2]   Anion Conductive Aromatic Copolymers from Dimethylaminomethylated Monomers: Synthesis, Properties, and Applications in Alkaline Fuel Cells [J].
Akiyama, Ryo ;
Yokota, Naoki ;
Nishino, Eriko ;
Asazawa, Koichiro ;
Miyatake, Kenji .
MACROMOLECULES, 2016, 49 (12) :4480-4489
[3]   Review of cell performance in anion exchange membrane fuel cells [J].
Dekel, Dario R. .
JOURNAL OF POWER SOURCES, 2018, 375 :158-169
[4]   Cationic Polyelectrolytes, Stable in 10 M KOHaq at 100 °C [J].
Fan, Jiantao ;
Wright, Andrew G. ;
Britton, Benjamin ;
Weissbach, Thomas ;
Skalski, Thomas J. G. ;
Ward, Jonathan ;
Peckham, Timothy J. ;
Holdcroft, Steven .
ACS MACRO LETTERS, 2017, 6 (10) :1089-1093
[5]   Anion exchange membrane fuel cells: Current status and remaining challenges [J].
Gottesfeld, Shimshon ;
Dekel, Dario R. ;
Page, Miles ;
Bae, Chulsung ;
Yan, Yushan ;
Zelenay, Piotr ;
Kim, Yu Seung .
JOURNAL OF POWER SOURCES, 2018, 375 :170-184
[6]  
Holewinski A, 2014, NAT CHEM, V6, P828, DOI [10.1038/NCHEM.2032, 10.1038/nchem.2032]
[7]   A practical method for measuring the ion exchange capacity decrease of hydroxide exchange membranes during intrinsic degradation [J].
Kreuer, Klaus-Dieter ;
Jannasch, Patric .
JOURNAL OF POWER SOURCES, 2018, 375 :361-366
[8]   Thermodynamics of Counterion Release Is Critical for Anion Exchange Membrane Conductivity [J].
Kwasny, Michael T. ;
Zhu, Liang ;
Hickner, Michael A. ;
Tew, Gregory N. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2018, 140 (25) :7961-7969
[9]   Poly(terphenylene) Anion Exchange Membranes: The Effect of Backbone Structure on Morphology and Membrane Property [J].
Lee, Woo-Hyung ;
Park, Eun Joo ;
Han, Junyoung ;
Shin, Dong Won ;
Kim, Yu Seung ;
Bae, Chulsung .
ACS MACRO LETTERS, 2017, 6 (05) :566-570
[10]   Fluorene-Based Hydroxide Ion Conducting Polymers for Chemically Stable Anion Exchange Membrane Fuel Cells [J].
Lee, Woo-Hyung ;
Mohanty, Angela D. ;
Bae, Chulsung .
ACS MACRO LETTERS, 2015, 4 (04) :453-457