石墨烯
膜
位阻效应
氧化物
水运
纳米片
材料科学
分子动力学
分子
密度泛函理论
功能群
化学工程
化学物理
水流
纳米技术
化学
计算化学
复合材料
立体化学
有机化学
环境工程
工程类
冶金
聚合物
生物化学
作者
Ruosang Qiu,Yuan Shi,Jie Xiao,Xiao Dong Chen,Cordelia Selomulya,Xiwang Zhang,Meng Wai Woo
标识
DOI:10.1021/acsami.9b00492
摘要
Graphene oxide (GO) membranes assembled by GO nanosheets exhibit high water flux because of the unique water channels formed by their functionalized layer-by-layer structure. Although water transport in the GO membrane is in principle influenced by the functional groups at the edges of GO nanosheets, this is yet to be fully understood. To fill this knowledge gap, molecular dynamics simulation was employed in this work to gain insights into the influences of three typical edge functional groups of GO nanosheets: carboxyl (COOH), hydroxyl (OH), and hydrogen (H). A well-controlled numerical analysis with complete isolation of the functional groups at the edges was undertaken. The results reveal that the COOH group has a negative impact on water transport because of its relatively large steric geometric structure, which resists water flow. By contrast, the OH group promotes water transport by uniquely "pulling" water molecules across the nanosheet layer because of its relatively stronger interaction with water. The H atom promotes water transport as well, mainly because of its low-resistance steric structure. Moreover, the size of the inter-edge hub has an apparent impact on the influence of these functional groups on water transport. The results suggest that in the design of high water flux GO membranes, it would be strategic to remove COOH edge functional groups while maintaining a mixture of OH and H edge functional groups.
科研通智能强力驱动
Strongly Powered by AbleSci AI