Angstrom‐Scale Triangular Pore in Single‐Layer Hexagonal Boron Nitride Membrane for Molecular Sieving

G Guangwei He (Key Laboratory for Green Chemical Technology of Ministry of Education School of Chemical Engineering and Technology, Tianjin University Tianjin 300072 China) Q Qianfeng Pan (Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology Tianjin University Tianjin China) Z Zhe Yuan L Luis Francisco Villalobos J Ji‐Hoon Park (Department of Electrical Engineering and Computer Sciences Massachusetts Institute of Technology Cambridge Massachusetts USA) H Heng‐Yu Chi (Laboratory of Advanced Separations (LAS) École Polytechnique Fédérale de Lausanne (EPFL) Sion Switzerland) M Matthias Kuehne (Department of Chemical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA) Y Yuwen Zeng (State Key Laboratory of Molecule Engineering of Polymers, Department of Macromolecular Science) Y Yu‐Ming Tu (Department of Chemical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA) J Jing Zhao J Jing Kong Z Zhongyi Jiang (Department Joint School of National University of Singapore and Tianjin University) K Kumar Varoon Agrawal (Laboratory of Advanced Separations (LAS)) D Daniel Blankschtein (Department of Chemical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA) M Michael S. Strano

Abstract

AbstractSingle‐layer crystalline films are ideal separation membrane materials because their atomic thickness could yield the highest possible molecular flux once nanopores are generated. However, the development of single‐layer membranes with well‐defined pore structures remains elusive, which makes the realization of efficient molecular sieving and interpretation of molecular transport a difficult task. Herein, we report the fabrication of single‐layer nanoporous hexagonal boron nitride (hBN) membranes that uniquely contain triangular nanopores with a high density (around 1012 pores per cm2). The hBN membranes exhibit a H2 permeance of 5.43 × 10−6 mol m−2 s−1 Pa−1 with a H2/CH4 selectivity of 14.7; they also show a CO2 permeance of 1.37 × 10−6 mol m−2 s−1 Pa−1, with a CO2/N2 selectivity of 12.3. Importantly, we show that straightforward mathematical modeling can predict and describe the gas transport properties of the hBN, providing new insights into the molecular transport across atomically thin nanopores. The results gained from this study could significantly advance our understanding of molecular transport across hBN nanopores and may promote the development of hBN membranes to address critical separation issues.

Article Details

Volume / Issue Vol. 64, Issue 41
Published October 06, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (15)

G

Guangwei He

Key Laboratory for Green Chemical Technology of Ministry of Education School of Chemical Engineering and Technology, Tianjin University Tianjin 300072 China

Q

Qianfeng Pan

Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology Tianjin University Tianjin China

Z

Zhe Yuan

L

Luis Francisco Villalobos

J

Ji‐Hoon Park

Department of Electrical Engineering and Computer Sciences Massachusetts Institute of Technology Cambridge Massachusetts USA

H

Heng‐Yu Chi

Laboratory of Advanced Separations (LAS) École Polytechnique Fédérale de Lausanne (EPFL) Sion Switzerland

M

Matthias Kuehne

Department of Chemical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA

Y

Yuwen Zeng

State Key Laboratory of Molecule Engineering of Polymers, Department of Macromolecular Science

Y

Yu‐Ming Tu

Department of Chemical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA

J

Jing Zhao

J

Jing Kong

Z

Zhongyi Jiang

Department Joint School of National University of Singapore and Tianjin University

K

Kumar Varoon Agrawal

Laboratory of Advanced Separations (LAS)

D

Daniel Blankschtein

Department of Chemical Engineering Massachusetts Institute of Technology Cambridge Massachusetts USA

M

Michael S. Strano