van der Waals Nanoreactors
Abstract
Advancing the chemical synthesis of crystals is important for both fundamental research and practical applications of quantum materials. While established bulk-phase and thin-film growth methods have enabled enormous progress, synthesizing single crystals suitable for quantum electronic discoveries remains challenging for many emerging materials. Here, we introduce van der Waals (vdW) stacks as nanochemical reactors for single-crystal synthesis and demonstrate their broad applicability in growing both elemental and compound crystals at the micrometer scale. By encapsulating atomically thin reactants that are stacked compactly with inert vdW layers such as hexagonal boron nitride (hBN), we achieve nanoconfined synthesis with the resulting crystals remaining encapsulated. As proof of concept, we synthesized isolated single crystals of elemental tellurium and distinct types of Pd-Te compounds. Structural characterization, including atomic-resolution scanning transmission electron microscopy, confirms the high crystalline quality of the products. We confirm the intrinsic semiconducting gap of tellurium and observe that non-stoichiometric PdTe1-x with a significantly reduced Te content (x ~ 0.18, a regime not previously achieved) retains uniform crystallinity and exhibits superconductivity below a critical temperature of 3.8 K. This nanochemical synthesis is broadly generalizable, chip-integrable, well-suited to a wide range of processing conditions, and compatible with nanofabrication routines for constructing devices. The concept of vdW nanoreactors offers a powerful and versatile pathway to expand the accessible landscape of quantum materials.
Cite
@article{arxiv.2512.11991,
title = {van der Waals Nanoreactors},
author = {Zhaoyi Joy Zheng and Haosen Guan and Danrui Ni and Guangming Cheng and Yanyu Jia and Ipsita Das and Yue Tang and Ayelet July Uzan-Narovlansky and Lihan Shi and Kenji Watanabe and Takashi Taniguchi and Nan Yao and Robert J Cava and Sanfeng Wu},
journal= {arXiv preprint arXiv:2512.11991},
year = {2026}
}