正电子湮没谱学
辐照
介电谱
膜
化学
电子束处理
材料科学
化学物理
化学工程
多孔性
分析化学(期刊)
正电子
电子
复合材料
电化学
物理化学
电极
有机化学
正电子湮没
核物理学
工程类
物理
量子力学
生物化学
作者
Zhe Liu,Wanqi Liu,Fengyao Wang,Shunli Qiu,Yonghong Hu,Chunqing He,Libing Qian,Zhe Chen,Zhiyuan Chen
出处
期刊:Langmuir
[American Chemical Society]
日期:2025-07-24
卷期号:41 (30): 20207-20214
标识
DOI:10.1021/acs.langmuir.5c02487
摘要
Polymer membrane modification via electron beam irradiation has emerged as a powerful technique for tailoring filtration and separation performance. However, the fundamental role of environmental conditions during irradiation, particularly hydration state, remains poorly understood despite its potential to dramatically alter energy deposition pathways and subsequent structural evolution. This study systematically investigates hydration-state-dependent modification of polysulfone membranes through electron beam irradiation. By comparing atmospheric versus aqueous environment irradiation across graded doses, we demonstrate distinct pore structure evolution mechanisms. Electrochemical impedance spectroscopy analyses consistently revealed superior charge transfer resistance in dry-state membranes relative to their hydrated counterparts under equivalent irradiation conditions. Complementary positron annihilation characterization disclosed a critical hydration effect: irradiated hydrated membranes exhibited prolonged positron lifetimes, suggesting pore expansion, whereas dry-processed samples showed enhanced annihilation intensity indicative of increased porosity. These antiparallel trends in pore dimension versus density modulation establish that the hydration state fundamentally governs electron beam energy deposition pathways. The revealed environment-dependent structural control mechanism provides a new paradigm for precisely tailoring membrane architectures through irradiation parameter-space engineering.
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