石墨烯
材料科学
氚
Nafion公司
氢
膜
氘
电解质
化学工程
单层
水运
电化学
纳米技术
化学
有机化学
物理化学
电极
原子物理学
核物理学
工程类
物理
环境工程
水流
生物化学
作者
Hyojoo Kim,Hongdoo Kim,Bhupendra Kumar Singh,Jonghoon Park,Juhwan Ahn,Hyung Gyu Park,Wooyong Um
标识
DOI:10.1021/acsami.5c08414
摘要
The separation and enrichment of tritium from radioactive wastewater remain critical challenges in the nuclear power and fusion industries. While hydrogen isotope separation from H2/D2 gas mixtures has been demonstrated using electrochemical pumping systems with Nafion|graphene composite membranes, their application in liquid water remains limited, despite tritium and deuterium predominantly existing as water molecules. This limitation primarily arises from the swelling behavior of Nafion, which absorbs water and induces defects in the graphene layer. In this study, we propose a modified Nafion|graphene composite membrane structure, where graphene is transferred onto polytetrafluoroethylene-reinforced Nafion, to enable efficient hydrogen isotope (1H, 2H, and 3H) separation in liquid water. The monolayer graphene exhibited six-fold higher conductivity for H+ over D+ under electrically driven conditions, while diffusion-driven transport showed lower isotope selectivity due to the contribution of the vehicular mechanism. Notably, graphene imposed a 1.7-fold higher diffusion energy barrier for tritium than for deuterium, indicating that the separation is governed by zero-point energy differences in O-H(D, T)···O bonding. These results highlight the role of transport mechanism and graphene integrity in isotope separation performance and suggest a practical pathway toward implementing graphene-based membranes in polymer electrolyte membrane water electrolysis systems for tritium concentration and removal.
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