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基于含有咪唑鎓官能化侧链的聚合物网络的高导电阴离子交换膜。

Highly conductive anion exchange membranes based on polymer networks containing imidazolium functionalised side chains.

作者信息

Abouzari-Lotf Ebrahim, Jacob Mohan V, Ghassemi Hossein, Zakeri Masoumeh, Nasef Mohamed Mahmoud, Abdolahi Yadollah, Abbasi Ali, Ahmad Arshad

机构信息

Advanced Materials Research Group, Center of Hydrogen Energy, Institute of Future Energy, Universiti Teknologi Malaysia, 54100, Kuala Lumpur, Malaysia.

Helmholtz Institute Ulm (HIU) Electrochemical Energy Storage, Helmholtzstraße 11, 89081, Ulm, Germany.

出版信息

Sci Rep. 2021 Feb 12;11(1):3764. doi: 10.1038/s41598-021-83161-9.

Abstract

Two novel types of anion exchange membranes (AEMs) having imidazolium-type functionalised nanofibrous substrates were prepared using the facile and potentially scalable method. The membranes' precursors were prepared by graft copolymerization of vinylbenzyl chloride (VBC) onto syndiotactic polypropylene (syn-PP) and polyamide-66 (PA-66) nanofibrous networks followed by crosslinking with 1,8-octanediamine, thermal treatment and subsequent functionalisation of imidazolium groups. The obtained membranes displayed an ion exchange capacity (IEC) close to 1.9 mmol g and ionic (OH) conductivity as high as 130 mS cm at 80 °C. This was coupled with a reasonable alkaline stability representing more than 70% of their original conductivity under accelerated degradation test in 1 M KOH at 80 °C for 360 h. The effect of ionomer binder on the performance of the membrane electrode assembly (MEA) in AEM fuel cell was evaluated with the optimum membrane. The MEA showed a power density of as high as 440 mW cm at a current density is 910 mA cm with diamine crosslinked quaternized polysulfone (DAPSF) binder at 80 °C with 90% humidified H and O gases. Such performance was 2.3 folds higher than the corresponding MEA performance with quaternary ammonium polysulfone (QAPS) binder at the same operating conditions. Overall, the newly developed membrane was found to possess not only an excellent combination of physico-chemical properties and a reasonable stability but also to have a facile preparation procedure and cheap ingredients making it a promising candidate for application in AEM fuel cell.

摘要

采用简便且具有潜在可扩展性的方法制备了两种新型的具有咪唑鎓型功能化纳米纤维基底的阴离子交换膜(AEM)。通过将乙烯基苄基氯(VBC)接枝共聚到间规聚丙烯(syn-PP)和聚酰胺-66(PA-66)纳米纤维网络上,随后与1,8-辛二胺交联、进行热处理以及对咪唑鎓基团进行后续功能化,制备了膜的前驱体。所获得的膜在80℃时显示出接近1.9 mmol g的离子交换容量(IEC)和高达130 mS cm的离子(OH)电导率。这还伴随着合理的碱性稳定性,即在80℃下于1 M KOH中进行360小时的加速降解测试后,仍保留其原始电导率的70%以上。使用最佳膜评估了离聚物粘合剂对AEM燃料电池中膜电极组件(MEA)性能的影响。在80℃、90%湿度的H₂和O₂气体条件下,使用二胺交联季铵化聚砜(DAPSF)粘合剂的MEA在电流密度为910 mA cm时显示出高达440 mW cm的功率密度。在相同操作条件下,这种性能比使用季铵化聚砜(QAPS)粘合剂的相应MEA性能高2.3倍。总体而言,新开发的膜不仅具有优异的物理化学性质组合和合理稳定性,而且制备过程简便且成分便宜,使其成为AEM燃料电池应用的有前途的候选材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/139b/7881124/634c31d8a1c7/41598_2021_83161_Fig1_HTML.jpg

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