Abstract
A number of van der Waals materials can be gradually tuned from electron to hole conductance with an increasing or decreasing thickness, which offers a novel route to modulate nanoscale charge-carrier distribution and thus functionality in devices.
The past decade has seen an explosion of research interest in atomically thin materials, typically those bonded via Van-der-Waals forces, due to their intriguing physical properties, such as topology1, superconductance2,3, valley spin4, moiré excitons5, ferromagnetic and antiferromagnetic states6, bulk-7 and flexo-8 photovoltaic response. This class of materials also have unique advantages in logic computing9, memory storing10, polarization11, and multicolor photodetection12, which promises the solution of (opto-) electronics devices at the ultimate thickness limit.
However, to put those intriguing functionalities into industry-use/reality, one critical issue has to be addressed — a general approach to dope two-dimensional (2D) semiconductors to enable homogeneous junction applications13.
Laser14, chemical15 and surface-transfer16 doping techniques where laser illumination is used to produce donor- or acceptor-like defects, chemical dopants (metal atoms, like Cu and Co) are intercalated into the vdWs gap, oxidant and reductant species are used to capture or inject electrons by a surface reaction, respectively have been demonstrated in the past. But, as is well documented in literature, these techniques are mostly customed designed for some specific layered materials, that cannot extend to the whole van der Waals materials family14,15,16.
Recently, writing in this issue of Light: Science & Applications, Hui Xia and colleagues at the Shanghai Institute of Technical Physics, Nantong University and Shanghai-Tech University in China report that a variety of van der Waals semiconductor materials (MoS2, WSe2, MoTe2, black-phosphorus) don’t need artificial, external doping and are capable of doping themselves from electron (n) to hole (p) type doping conductance with increasing or decreasing thickness17. As schematically shown in Fig. 1, monolayer MoS2 is typically n-doped, while multilayer counterpart turns to p-doped. Considering that the self-doping materials span from elemental-layered-semiconductors such as black phosphorus to transition-metal sulfides, selenides, and tellurides, the observed and reported phenomenon might apply to many other layered materials significant expanding their applicability and scope in device design.
In such a framework, every monolayer-step change in thickness can ideally serve as a finely tunable knob to spatially modulate the charge-carrier polarity and doping concentration. Further, the geometric boundary serves as a sharp barrier for carrier concentration change. This doping framework therefore offers an opportunity to fabricate atomically abrupt conduction channels and junction. Note that such devices can be very difficult to fabricate by conventional approaches due to uncontrolled dopant interdiffusion process18.
The self-doping behavior could benefit the semiconductor manufacturing process of 2D devices, since one only needs to focus on the geometrical morphology, while the van der Waals materials depending on their thickness will address distributing the electrons and holes as required. In the present work the authors have developed and demonstrated a variety of devices based on this concept such as diodes, solar cell and avalanche photodetector.
In the future, more efforts are needed to attain a fundamental understanding of the doping mechanism. What are the factors that drive few- and multilayer- layers to an opposite polarity of doping? Similarly, what is impact of contact fabrication scheme and source material in determining doping type and concentration as a function of thickness? These are outstanding questions they need further investigations. Likewise, for practical realization, attempts for large scale device fabrication with controlled doping as a function of thickness are equally important that will ultimately determine how far can this new doping concept can go.
References
Otrokov, M. M. et al. Prediction and observation of an antiferromagnetic topological insulator. Nature 576, 416–422 (2019).
Cao, Y. et al. Unconventional superconductivity in magic-angle graphene superlattices. Nature 556, 43–50 (2018).
Kezilebieke, S. et al. Topological superconductivity in a van der Waals heterostructure. Nature 588, 424–428 (2020).
Li, L. F. et al. Room-temperature valleytronic transistor. Nat. Nanotechnol. 15, 743–749 (2020).
Tran, K. et al. Evidence for moiré excitons in van der Waals heterostructures. Nature 567, 71–75 (2019).
Xu, Y. et al. Coexisting ferromagnetic–antiferromagnetic state in twisted bilayer CrI3. Nat. Nanotechnol. 17, 143–147 (2022).
Akamatsu, T. et al. A van der Waals interface that creates in-plane polarization and a spontaneous photovoltaic effect. Science 372, 68–72 (2021).
Jiang, J. et al. Flexo-photovoltaic effect in MoS2. Nat. Nanotechnol. 16, 894–901 (2021).
Chen, H. W. et al. Logic gates based on neuristors made from two-dimensional materials. Nat. Electron. 4, 399–404 (2021).
Tong, L. et al. 2D materials–based homogeneous transistor-memory architecture for neuromorphic hardware. Science 373, 1353–1358 (2021).
Bullock, J. et al. Polarization-resolved black phosphorus/molybdenum disulfide mid-wave infrared photodiodes with high detectivity at room temperature. Nat. Photonics 12, 601–607 (2018).
Wu, P. S. et al. Van der Waals two-color infrared photodetector. Light.: Sci. Appl. 11, 6 (2022).
Gong, Y. J. et al. Spatially controlled doping of two-dimensional SnS2 through intercalation for electronics. Nat. Nanotechnol. 13, 294–299 (2018).
Seo, S. Y. et al. Reconfigurable photo-induced doping of two-dimensional van der Waals semiconductors using different photon energies. Nat. Electron. 4, 38–44 (2021).
Acerce, M., Voiry, D. & Chhowalla, M. Metallic 1T phase MoS2 nanosheets as supercapacitor electrode materials. Nat. Nanotechnol. 10, 313–318 (2015).
Lei, S. D. et al. Surface functionalization of two-dimensional metal chalcogenides by Lewis acid-base chemistry. Nat. Nanotechnol. 11, 465–471 (2016).
Xia, H. et al. Pristine PN junction toward atomic layer devices. Light Sci. Appl. 11, 170 (2022).
Colinge, J. P. et al. Nanowire transistors without junctions. Nat. Nanotechnol. 5, 225–229 (2010).
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
About this article
Cite this article
Jariwala, D. Functionalizing Van der Waals materials by shaping them. Light Sci Appl 11, 206 (2022). https://doi.org/10.1038/s41377-022-00900-x
Published:
DOI: https://doi.org/10.1038/s41377-022-00900-x