纳米复合材料
石墨烯
三聚氰胺
氧化物
膜
材料科学
化学工程
质子交换膜燃料电池
原位聚合
剥脱关节
纳米技术
聚合
化学
聚合物
复合材料
工程类
冶金
生物化学
作者
Zhiwei Ling,Bei Wang,Qingting Liu,Xudong Fu,Rong Zhang,Xiao Li,Feng Zhao,Xujin Bao,Shengfei Hu,Jun Yang
标识
DOI:10.1016/j.jcis.2024.09.007
摘要
The traditional preparation of nanocomposite proton exchange membranes (PEM) is hindered by poor organic-inorganic interface compatibility, insufficient proton-conducting sites, easy aggregation of nanoparticles, and difficulty in leveraging nanoscale advantages. In this study, a novel method involving electrochemical anodic oxidation exfoliation was employed to prepare melamine-coated graphene oxide (Me@GO), which was subsequently subjected to in-situ polymerization with poly(2,5-benzimidazole) (ABPBI) to prepare a Me@GO/ABPBI composite proton exchange membrane. Benefiting from the strong hydrogen bonding and large π stacking interactions, melamine (Me) tightly bound to graphene oxide (GO), effectively preventing the secondary aggregation of GO after exfoliation. Moreover, the abundant alkaline functional groups of melamine enhanced the enhancement of phosphoric acid (PA) retention in the Me@GO/ABPBI membranes, thereby increasing the number of proton-conducting sites. The experimental results indicated that the introduction of Me@GO enhanced membrane properties. For Me@GO at a concentration of 1 wt%, the tensile strength of the 1Me@GO/ABPBI composite membrane reached 207 MPa, nearly 2.52 times that of the pure membrane. The proton conductivity of the 1Me@GO/ABPBI composite membrane reached 0.01 S cm
科研通智能强力驱动
Strongly Powered by AbleSci AI