材料科学
石墨烯
调制(音乐)
基质(水族馆)
化学物理
电子
分离(统计)
纳米技术
化学工程
物理
海洋学
量子力学
机器学习
地质学
计算机科学
声学
工程类
作者
Kuang‐Jung Hsu,Heng‐Yu Chi,Yueqing Shen,Shiqi Huang,Ranadip Goswami,Kumar Varoon Agrawal
标识
DOI:10.1002/adfm.202503121
摘要
Abstract Tuning the reactivity of graphene enables molecular‐level engineering of the lattice, achieving desired chemical and structural properties through functionalization, doping, and etching. Atom‐thin graphene film hosting Å‐scale pores, with capability to differentiate molecules with sub‐Å resolution, is ideal to advance performance for challenging molecular separation. Control over pore formation is needed to improve pore size distribution (PSD), in particular, to increase the percentage of molecular selective pores. An attractive approach is to modulate the energy barriers involved in the pore formation to control PSD. In this study, it is shown that electron‐hole puddles induced in graphene by the underlying Cu substrate increase its reactivity toward O 3 . These puddles promote electron transfer during O 3 chemisorption and reduce the energy barrier for lattice gasification. This strategy is implemented to increase the density of molecular‐selective pores by expanding small non‐permeable pores. The resulting porous graphene membranes demonstrate highly promising separation performance for the CO 2 /N 2 gas pair. This approach provides a new pathway to finely control pore formation for advanced applications in molecular separation and beyond.
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