Tunable Pore Size from Sub-Nanometer to a Few Nanometers in Large-Area Graphene Nanoporous Atomically Thin Membranes

被引:22
|
作者
Chen, Xiaobo [1 ]
Zhang, Shengping [1 ,2 ,3 ,4 ]
Hou, Dandan [1 ,3 ]
Duan, Hongwei [1 ,2 ]
Deng, Bing [5 ]
Zeng, Zhiyang [1 ]
Liu, Bingyao [2 ,3 ,4 ,6 ]
Sun, Luzhao [5 ]
Song, Ruiyang [1 ]
Du, Jinlong [6 ]
Gao, Peng [2 ,3 ,6 ,7 ,8 ]
Peng, Hailin [3 ,5 ]
Liu, Zhongfan [3 ,5 ]
Wang, Luda [1 ,2 ,3 ,4 ]
机构
[1] Peking Univ, Sch Elect Engn & Comp Sci, Inst Microelect, Beijing 100871, Peoples R China
[2] Peking Univ, Acad Adv Interdisciplinary Studies, Beijing 100871, Peoples R China
[3] Beijing Graphene Inst, Beijing 100095, Peoples R China
[4] Peking Univ, Coll Chem & Mol Engn, Ctr Nanochem, Beijing Sci & Engn Ctr Nanocarbons, Beijing 100871, Peoples R China
[5] Peking Univ, Coll Chem & Mol Engn, Ctr Nanochem, Beijing Sci & Engn Ctr Nanocarbons,Beijing Natl L, Beijing 100871, Peoples R China
[6] Peking Univ, Sch Phys, Electron Microscopy Lab, Beijing 100871, Peoples R China
[7] Peking Univ, Int Ctr Quantum Mat, Sch Phys, Beijing 100871, Peoples R China
[8] Collaborat Innovat Ctr Quantum Matter, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
nanoporous graphene membranes; nanoporous atomically thin membranes (NATMs); protein-selective membranes; plasma etching; nanopore engineering; SINGLE-CRYSTAL GRAPHENE; RAMAN-SPECTROSCOPY; BLOCK-COPOLYMER; LAYER GRAPHENE; IONIC TRANSPORT; DEFECTS; MONODISPERSE; SEPARATION; PROTEINS; NUMBER;
D O I
10.1021/acsami.1c06243
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Membranes are key components in chemical purification, biological separation, and water desalination. Traditional polymeric membranes are subjected to a ubiquitous trade-off between permeance and selectivity, which significantly hinders the separation performance. Nanoporous atomically thin membranes (NATMs), such as graphene NATMs, have the potential to break this trade-off. Owing to their uniqueness of two-dimensional structure and potential nanopore structure controllability, NATMs are expected to have outstanding selectivity through molecular sieving while achieving ultimate permeance at the same time. However, a drastic selectivity discrepancy exists between the proof-of-concept demonstrations and scalable separation applications in graphene membranes. In this paper, we offer a possible solution to narrow this discrepancy by tuning the pore density and pore size separately with two successive plasma treatments. We demonstrate that by narrowing the pore size distribution, the selectivity of graphene membranes can be greatly increased. Low-energy argon plasma is first applied to nucleate high density of defects in graphene. Controlled oxygen plasma is then utilized to selectively enlarge the defects into nanopores with desired sizes. This method is scalable, and the fabricated 1 cm(2) graphene NATMs with sub-nanometer pores can separate KCl and Allura Red with a selectivity of 10(4) and a permeance of 1.1 x 10(-6) m s(-1). The pores in NATMs can be further tuned from gas-selective sub-nanometer pores to a few nanometer size. The fabricated NATMs show a selectivity of 35 between CO2 and N-2. With longer enlargement time, a selectivity of 21.2 between a lysozyme and bovine serum albumin can also be achieved with roughly four times higher permeance than that of a commercial dialysis membrane. This research offers a solution to realize NATMs of tunable pore size with a narrow pore size distribution for different separation processes from sub-nanometer in gas separation or desalination to a few nanometers in dialysis.
引用
收藏
页码:29926 / 29935
页数:10
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