聚电解质
石墨烯
材料科学
膜
水分
质子
化学工程
纳米技术
复合材料
化学
物理
聚合物
核物理学
工程类
生物化学
作者
Li Guo,Yinbo Liu,Yin-Bo Liu,Wenxia Li,Jia-Yan Gong,Wei Zuo,Yulan Liu,Yulan Liu,Ping Fu
标识
DOI:10.1021/acsanm.4c03847
摘要
Polyelectrolyte membranes used in moisture-electric generators (MEGs) typically face the challenge of producing high voltage but low current. In this study, a PSSA/PVA/GDs membrane (PPGM) was developed by incorporating graphene dots (GDs) into the poly(styrene sulfonic acid) (PSSA) and poly(vinyl alcohol) (PVA) composite system. The abundant oxygen-containing groups in GDs enhance hydrogen bonding and increase the cross-linking density, thereby improving the tensile strength of the PPGM to 25.77 MPa. Additionally, GDs endow the polyelectrolyte membrane with excellent hydrophilicity and a notable self-healing capability. The uniform dispersion of GDs, coupled with their excellent electrical properties, facilitates the formation of rapid proton transport channels, which, in turn, enhances the ionic conductivity to 1.41 S/m. Under a relative humidity (RH) of 83%, the membrane (1 cm 2 ) can deliver an open-circuit voltage ( V OC ) of 0.31 V and a high short-circuit current ( I SC ) of 23 μA, and the high electric current (approximately 23 μA) can be sustained for up to 120 min. The current output performance of this membrane exceeds that of the pristine PSSA/PVA membrane, and this work is anticipated to advance the application of a traditional polyelectrolyte membrane in the field of MEGs.
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