钒
流动电池
导线
质子
石墨氮化碳
氧化还原
氮化钒
材料科学
碳纤维
电池(电)
质子导体
膜
氮化物
质子输运
化学工程
质子交换膜燃料电池
无机化学
化学
纳米技术
复合材料
电极
冶金
物理化学
电解质
催化作用
有机化学
物理
复合数
工程类
光催化
量子力学
生物化学
功率(物理)
图层(电子)
作者
Penghua Qian,Cheng Chen,Ying Chen,Liang Zhang,Ming Song,Nong Zhang
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2025-06-13
卷期号:39 (25): 12197-12208
被引量:5
标识
DOI:10.1021/acs.energyfuels.5c00789
摘要
To balance the contradiction between proton conductivity and vanadium ion permeability of sulfonated aromatic polymer proton exchange membranes (PEMs), sulfonated poly(ether ether ketone) (SPEEK)-based hybrid membranes (S/SGN) were prepared, incorporating amphoteric graphitic carbon nitride nanosheets (SGN) with triangular nanopores. The SGN nanosheets were prepared by grafting 1,4-butane sultone onto graphitic carbon nitride (g-C3N4) sheets. Structural characterization revealed that the triangular nanopore architecture, along with amino, imino, and sulfonic acid functional groups, as well as the acid–base interactions formed at the interface with the hybrid membrane, provide the S/SGN hybrid membrane with excellent physicochemical properties and battery performance. Notably, the S/SGN-1 membrane containing 1 wt% SGN loading demonstrated optimal electrochemical performance, achieving a proton conductivity of 27.9 mS cm–1 and an ion selectivity of 21.3 × 103 S min cm–3. In vanadium redox flow battery (VRFB) evaluations, the S/SGN-1 demonstrated significantly higher energy efficiency (86.2–71.5%) at a current density of 60–200 mA cm–2 compared to Nafion 212 (82.2–64.0%) and longer self-discharge time (91.2 h vs 23.2 h of Nafion 212). This indicates that a balanced proton conductivity and vanadium-ion resistance enhances membrane performance. Additionally, the S/SGN-1 hybrid membrane has a charge capacity retention of 71.0% after 50 cycles at a current density of 150 mA cm–2, and the energy efficiency stabilizes at 76.0 ± 1.0% after 500 charge–discharge cycles. These results suggest that the combination of physical barriers and acid–base interactions of SGN nanofillers synergistically improve the battery efficiency of the S/SGN hybrid membrane. The above results validate that developing two-dimensional nanomaterials with self-nanopores and surface functional groups to construct high-performance proton exchange membranes is a simple and feasible method.
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