4.8 Article

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

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 13, 期 25, 页码 29926-29935

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.1c06243

关键词

nanoporous graphene membranes; nanoporous atomically thin membranes (NATMs); protein-selective membranes; plasma etching; nanopore engineering

资金

  1. National Natural Science Foundation of China (NSFC) [62004004]
  2. Peking University Health Science-Information Science Cross-Research Seed Foundation
  3. Boya postdoctoral fellowship
  4. Beijing Municipal Science & Technology Commission, China [Z191100000819008]

向作者/读者索取更多资源

Traditional polymeric membranes face a trade-off between permeance and selectivity, whereas nanoporous atomically thin membranes show potential to break this trade-off and achieve outstanding selectivity and permeance. Through plasma treatments, graphene membranes can be tuned to increase selectivity and achieve high separation performance for various processes.
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.

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