Chen Xiaobo, Zhang Shengping, Hou Dandan, Duan Hongwei, Deng Bing, Zeng Zhiyang, Liu Bingyao, Sun Luzhao, Song Ruiyang, Du Jinlong, Gao Peng, Peng Hailin, Liu Zhongfan, Wang Luda
Institute of Microelectronics, School of Electronics Engineering and Computer Science, Peking University, Beijing 100871, China.
Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China.
ACS Appl Mater Interfaces. 2021 Jun 16. doi: 10.1021/acsami.1c06243.
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 graphene NATMs with sub-nanometer pores can separate KCl and Allura Red with a selectivity of 104 and a permeance of 1.1 × 10 m s. 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 CO and N. 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.
膜是化学提纯、生物分离和海水淡化中的关键组件。传统聚合物膜在渗透率和选择性之间普遍存在权衡,这严重阻碍了分离性能。纳米多孔原子级薄膜(NATM),如石墨烯NATM,有潜力打破这种权衡。由于其二维结构的独特性和潜在的纳米孔结构可控性,NATM有望通过分子筛作用实现出色的选择性,同时达到极限渗透率。然而,石墨烯膜在概念验证演示和可扩展分离应用之间存在巨大的选择性差异。在本文中,我们提供了一种可能的解决方案,通过两次连续的等离子体处理分别调节孔径密度和孔径来缩小这种差异。我们证明,通过缩小孔径分布,石墨烯膜的选择性可以大大提高。首先施加低能氩等离子体在石墨烯中形成高密度缺陷。然后利用可控氧等离子体将缺陷选择性地扩大为所需尺寸的纳米孔。这种方法具有可扩展性,制备的具有亚纳米孔的1厘米石墨烯NATM可以以104的选择性和1.1×10米/秒的渗透率分离氯化钾和诱惑红。NATM中的孔可以进一步从气体选择性亚纳米孔调节到几纳米大小。制备的NATM在一氧化碳和氮气之间的选择性为35。延长扩大时间,溶菌酶和牛血清白蛋白之间的选择性也可以达到21.2,渗透率比商业透析膜高约四倍。这项研究提供了一种解决方案,以实现具有窄孔径分布的可调孔径NATM,用于从气体分离或海水淡化中的亚纳米到透析中的几纳米的不同分离过程。