Sieving Hydrogen Isotopes via Machine Learning Assisted Chemical Vapor Deposition (CVD) of High‐Quality Monolayer Hexagonal Boron Nitride (h‐BN) on Iron Foils

P Pavan Chaturvedi (Chemical and Biomolecular Engineering Department Vanderbilt University Nashville TN 37212 USA) A Andrew E. Naclerio (Chemical and Biomolecular Engineering Department Vanderbilt University Nashville TN 37212 USA) S Saban M. Hus (Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA) I Ivan V. Vlassiouk N Nickolay Lavrik (Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA) M Marti Checa L Liam Collins A An‐Ping Li (Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA) P Piran R. Kidambi (Mechanical and Aerospace Engineering Department University of Florida Gainesville FL 32611 USA)

Abstract

Abstract Atomically thin two‐dimensional (2D) ceramics, such as monolayer hexagonal boron nitride (h‐BN), present potential for disruptive advances in separations. However, sub‐atomic scale separation of hydrogen isotopes (H + /D + ) require near pristine 2D material membranes, and scalable synthesis of such high‐quality h‐BN comparable to mechanically exfoliated crystals remains a significant challenge. Here, we report a scalable Fe‐catalyzed chemical vapor deposition (CVD) process for bottom‐up synthesis of large‐area, high‐quality monolayer h‐BN films, overcoming key limitations of conventional ammonia‐based routes. By leveraging mechanistic insights and higher CVD temperatures, we suppress multilayer formation and achieve uniform monolayer h‐BN coverage on commercially available Fe foils. Machine learning enables systematic exploration of the complex, multi‐dimensional CVD parameter space (growth time, temperature, precursor temperature, multilayer faction, coverage), providing data‐driven approaches to visualize and identify process regimes facilitating predominantly monolayer h‐BN growth with minimal secondary nuclei/ad‐layers. The optimized Fe‐catalyzed CVD h ‐BN membranes show high‐quality as observed by proton/deuteron (H + /D + ) selectivity ≈8.45, approaching the highest quality benchmark of mechanically exfoliated h‐BN (H + /D + selectivity ≈10) as well as significantly outperforming Cu‐catalyzed CVD h ‐BN membranes (H + /D + selectivity ≈3.62, control selectivity ≈1.7). Our work provides a scalable cost‐effective route for high‐quality monolayer h‐BN synthesis for sub‐atomic scale separations (H + /D + ) and demonstrates the broader potential of machine learning‐guided optimization of CVD for advancing synthesis of 2D materials.

Article Details

Volume / Issue Vol. 38, Issue 7
Published February 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (9)

P

Pavan Chaturvedi

Chemical and Biomolecular Engineering Department Vanderbilt University Nashville TN 37212 USA

A

Andrew E. Naclerio

Chemical and Biomolecular Engineering Department Vanderbilt University Nashville TN 37212 USA

S

Saban M. Hus

Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA

I

Ivan V. Vlassiouk

N

Nickolay Lavrik

Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA

M

Marti Checa

L

Liam Collins

A

An‐Ping Li

Center for Nanophase Materials Sciences Oak Ridge National Laboratory Oak Ridge TN 37831 USA

P

Piran R. Kidambi

Mechanical and Aerospace Engineering Department University of Florida Gainesville FL 32611 USA