An anchoring strategy leads to enhanced proton conductivity in a new metal-organic framework

被引:67
|
作者
Lo, Tien H. N. [1 ]
Nguyen, My V. [1 ,2 ]
Tu, Thach N. [1 ,3 ]
机构
[1] VNU HCM, Ctr Innovat Mat & Architectures INOMAR, Ho Chi Minh City 721337, Vietnam
[2] VNU HCM, Univ Sci, Ho Chi Minh City 721337, Vietnam
[3] VNU HCM, Bach Khoa Univ, Ho Chi Minh City 721337, Vietnam
来源
INORGANIC CHEMISTRY FRONTIERS | 2017年 / 4卷 / 09期
关键词
IMIDAZOLE; CHEMISTRY;
D O I
10.1039/c7qi00350a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new Zr(IV)-based metal-organic framework, termed VNU-17 [Zr6O8(H2O)(8)(HSNDC)(4), where HSNDC2- = 4-sulfonaphthalene-2,6-dicarboxylate], was designed to enhance proton conductivity through the incorporation of Bronsted acid functionalities. The resulting VNU-17 framework adopted the bcu topology and the structure was highlighted by densely packed sulfonic acid groups lining 6 angstrom channels. Following this, the internal void space of VNU-17 was engineered to further enhance proton conductivity, in which the proton transfer agent, imidazole (HIm), was anchored within the structure in two different loadings. Remarkably, the material with the highest HIm load, HIm(11)subset of VNU-17, exhibited a 900-fold enhancement in proton conductivity (5.9 x 10(-3) S cm(-1) at 85% RH and 70 degrees C) in comparison with the parent VNU-17 structure and was shown to maintain its performance over at least 40 h. These findings demonstrate the potential for systematically fine-tuning such materials for use as electrolyte materials in proton exchange membrane fuel cells.
引用
收藏
页码:1509 / 1516
页数:8
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