Skip to content
DraconiticResearch
Search Sources API
203,203 studies31 sourcesUpdated just now
Peer-reviewedCC BY-NC-ND 4.0Nature Communications

Universal hydrogen-free synthesis and elemental doping of two-dimensional transition metal selenides

Abstract

Two-dimensional transition metal selenides (TMSs) feature notable bandgap flexibility, versatile doping characteristics, and practical manufacturability, positioning them as promising candidates for next-generation electronics. However, their synthesis remains a critical bottleneck, as conventional chemical vapor deposition (CVD) routes require H2 assistance for selenization, raising safety, cost, and quality concerns and constraining elemental doping. Here we show a universal, H2-free CVD method that overcomes these limitations. Our approach produces a broad spectrum of 2D TMSs, including monolayer binaries, bilayer polytypes, alloys, and heterostructures, and is compatible with diverse substrates. Incorporating common metals (Al, Zn, Fe, Ni, Cu) into the precursor enhances growth kinetics and enables precise doping. Al-doped WSe2 exhibits markedly lower resistance, with centimeter-scale films attaining a hole mobility of 28.36 cm2 V−1 s−1 and an on/off ratio of 3.56×106, comparable to exfoliated and H2-assisted monolayers. This work establishes a safe, scalable, and tunable synthesis strategy for high-performance 2D electronics.

Related

  1. Fine-tuning universal machine learning potentials for transition state search in surface catalysis
    Raffaele Cheula, Mie Andersen, John R. Kitchin
    npj Computational MaterialsPeer-reviewedCC BY-NC-NDFull text7 citedMaterials & polymersOpenAlex
  2. Can Universal Machine-Learning Interatomic Potentials Capture Small Polarons? A Geometry-Based Benchmark in Transition-Metal Oxides
    Vladislav Korostelev, Pjotrs Žguns, Konstantin Klyukin
    arXivPreprintarXiv licenceFull textPhysical chemistryComputational physicsarXiv
  3. Hydrogenolysis triggered formation of zero-valent metals and metal selenides at room temperature from divalent metal aminoxide complexes facilitated by metal-ligand cooperativity
    Lina M Zarnitsa, Oliver E Garcia, Martin-Louis Y Riu +5
    Chemical sciencePeer-reviewedCC BYFull textOrganic chemistryEurope PMCEurope PMCPMC
  4. Covalent Functionalization of Dawson-Type Polyoxometalates to Achieve a Zero to Three-Dimensional Transition for Enhanced Proton Conductivity
    Yun‐Zuo Cui, Qianqian Liu, Yuehua Chen +5
    Journal of the American Chemical SocietyPeer-reviewedLicence not statedFull text7 citedMaterials & polymersOpenAlex
  5. Automated transition state generation for mechanistic exploration in organic synthesis
    Li‐Cheng Xu, Junyi An, Weiqi Liu +4
    Nature CommunicationsPeer-reviewedCC BYFull text7 citedMedicinal chemistry & drug discoveryOpenAlex
BibTeX
@article{man2026universal,
  title = {{Universal hydrogen-free synthesis and elemental doping of two-dimensional transition metal selenides}},
  author = {Ping Man and Lok Wing Wong and Ka Ho Leung and Zhiqiang Guan and Tianren Chen and Honglin Chen and Jiangbo Peng and Mingjie Li and Chun-Sing Lee and Qingming Deng and Jiong Zhao and Thuc Hue Ly},
  journal = {Nature Communications},
  year = {2026},
  month = oct,
  doi = {10.1038/s41467-026-78372-5},
  url = {https://www.nature.com/articles/s41467-026-78372-5},
  note = {CC BY-NC-ND 4.0},
}
RIS
TY  - JOUR
TI  - Universal hydrogen-free synthesis and elemental doping of two-dimensional transition metal selenides
AU  - Ping Man
AU  - Lok Wing Wong
AU  - Ka Ho Leung
AU  - Zhiqiang Guan
AU  - Tianren Chen
AU  - Honglin Chen
AU  - Jiangbo Peng
AU  - Mingjie Li
AU  - Chun-Sing Lee
AU  - Qingming Deng
AU  - Jiong Zhao
AU  - Thuc Hue Ly
PY  - 2026
DA  - 2026/10/08
JO  - Nature Communications
DO  - 10.1038/s41467-026-78372-5
UR  - https://www.nature.com/articles/s41467-026-78372-5
AB  - Two-dimensional transition metal selenides (TMSs) feature notable bandgap flexibility, versatile doping characteristics, and practical manufacturability, positioning them as promising candidates for next-generation electronics. However, their synthesis remains a critical bottleneck, as conventional chemical vapor deposition (CVD) routes require H2 assistance for selenization, raising safety, cost, and quality concerns and constraining elemental doping. Here we show a universal, H2-free CVD method that overcomes these limitations. Our approach produces a broad spectrum of 2D TMSs, including monolayer binaries, bilayer polytypes, alloys, and heterostructures, and is compatible with diverse substrates. Incorporating common metals (Al, Zn, Fe, Ni, Cu) into the precursor enhances growth kinetics and enables precise doping. Al-doped WSe2 exhibits markedly lower resistance, with centimeter-scale films attaining a hole mobility of 28.36 cm2 V−1 s−1 and an on/off ratio of 3.56×106, comparable to exfoliated and H2-assisted monolayers. This work establishes a safe, scalable, and tunable synthesis strategy for high-performance 2D electronics.
SN  - 2041-1723
ER  -