Indexed by:
期刊论文
First Author:
Yan, Xiaoming
Correspondence Author:
He, GH (reprint author), Dalian Univ Technol, Sch Petr & Chem Engn, State Key Lab Fine Chem, 2 Dagong Rd, Panjin 124221, LN, Peoples R China.
Co-author:
Deng, Runlian,Pan, Yu,Xu, Xiaowei,El Hamouti, Issam,Ruan, Xuehua,Wu, Xuemei,Hao, Ce,He, Gaohong
Date of Publication:
2017-07-01
Journal:
JOURNAL OF MEMBRANE SCIENCE
Included Journals:
SCIE、EI
Document Type:
J
Volume:
533
Page Number:
121-129
ISSN No.:
0376-7388
Key Words:
Anion exchange membrane; Alkaline stability; Fuel cell; Imidazolium;
Morpholinium
Abstract:
Hydroxide exchange membrane fuel cells (HEMFCs) are attracting growing interest owing to their advantages such as low cost and high power density. However, their applications are hindered due to the poor stability of the membrane. Here, we proposed a novel strategy to improve the alkaline stability of hydroxide exchange membranes (HEMs) using the interactions between strongly polar nitrile groups and side-chain functional cations. A poly(ether nitrile) (PEN) was synthesized by the polycondensation of bisphenol A and 2,6-difluorobenzonitrile, and then imidazolium and morpholinium functional groups were integrated by the typical chloromethylation-functionalization method. The existence of the interactions between nitrile groups and cation groups i.e. imidazolium and morpholinium, was proved by the density functional theory calculations. The interactions have two positive effects that contribute to the improvement of the alkaline stability of the PEN based membranes. On the one hand, they increase the LUMO energies of the functional groups; and on the other hand they reduce the free volume around hydrated cationic groups. As a result, PEN based membranes showed much better alkaline stabilities compared to the membrane based on commercial polysulfone that has a similar chemical structure. In addition, given similar swelling ratios, PEN based membranes exhibited higher hydroxide conductivities than simple polysulfone based ones.
Translation or Not:
no
