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High-Performance Detectors Based on the Novel Electronic and Optoelectronic Properties of Crystalline 2D van der Waals Solids

In this work, we study the properties and device applications of MoS2, black phosphorus, MoOx, and NbSe2. We first start with the design, fabrication, and characterization of ultra-high responsivity photodetectors based on mesoscopic multilayer MoS2. The device architecture is comprised of a metal-semiconductor-metal (MSM) photodetector, where Mo was used as the contact metal to suspended MoS2 membranes. The dominant photocurrent mechanism was determined to be the photoconductive effect, while a contribution from the photogating effect was also noted from trap-states that yielded a wide spectral photoresponse from UV-to-IR with an external quantum efficiency (EQE) ~ 104. From time-resolved photocurrent measurements, a fast decay time and response time were obtained with a stream of incoming ON/OFF white light pulses. Another interesting semiconductor 2D material that has attracted special attention due to its small bandgap and ultra-high hole mobility is the black phosphorus. An analysis of the optoelectronic properties and photocurrent generation mechanisms in two-dimensional (2D) multilayer crystallites of black phosphorus (BP) was conducted from 350 K down to cryogenic temperatures using a broad-band white light source. The Mo-BP interface yielded a low Schottky barrier "φ" _"SB" ~ -28.3 meV and a high photoresponsivity R of ~ 2.43 x 105 A/W at a source-drain bias voltage of ~ 0.5 V (300 K, and incident optical power ~ 3.16 μW/cm2). Our report is the first to highlight the empirical use of Mo as a contact metal with BP. From the analysis conducted on the BP devices, the thermally driven photocurrent generation mechanism arising from the photobolometric effect (PBE) dominated the carrier dynamics for T > 181 K since the photocurrent Iph and the bolometric coefficient β undergo a transition in polarity from positive to negative. Our results show the promise of BP to potentially advance thermoelectric and optoelectronic devices stemming from this mono-elemental, direct bandgap 2D van der Waals solid. Another intriguing metallic 2D material is superconducting 2H-NbSe2. Here we present the temperature-dependent Raman spectroscopy and electronic transport on bulk NbSe2, carried out to investigate the scattering mechanisms. We report on the photoresponse of direct probed mesoscopic 2H-NbSe2 as a function of laser energy for lasers at 405 nm, 660 nm, and 1060 nm wavelengths used to irradiate the device, where the modulation from the superconducting-to-normal-state is detected through photomodulation. Additionally, the various oxidation levels of molybdenum oxide have interesting optical and electrical properties as a function of the oxygen vacancy and stoichiometry. The substoichiometric MoOx (2 < x < 3) behaves as a high work function conductor due to its metallic defect band. As a result, one of the potential applications of MoOx is for electrical contacts providing high hole injection or extraction. In this work, we have synthesized MoOx nanosheets via chemical vapor deposition and a four-terminal device was fabricated via e-beam lithography and electronic transport was measured as a function of temperature. Outstanding properties were obtained from our MoOx nanosheets, including a high conductivity of ~ 6,680.3 S cm-1, a superior temperature coefficient of resistance ~ -0.10%, and a high sensitivity based on the bolometric coefficient β of ~ 0.152 mS K-1. In summary, this work pushes the state-of-the-art in enabling 2D van der Waals materials for next-generation high-performance detectors.

Identiferoai:union.ndltd.org:unt.edu/info:ark/67531/metadc1703294
Date05 1900
CreatorsSaenz Saenz, Gustavo Alberto
ContributorsKaul, Anupama B, Mahbub, Ifana, Varanasi, Murali, Choi, Wonbong, Jimenez, Jose
PublisherUniversity of North Texas
Source SetsUniversity of North Texas
LanguageEnglish
Detected LanguageEnglish
TypeThesis or Dissertation
Formatxvii, 189 pages, Text
RightsPublic, Saenz Saenz, Gustavo Alberto, Copyright, Copyright is held by the author, unless otherwise noted. All rights Reserved.

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