Abstract The field of photovoltaics is revolutionized in recent years by the development of two–dimensional (2D) type‐II heterostructures. These heterostructures are made up of two different materials with different electronic properties, which allows for the capture of a broader spectrum of solar energy than traditional photovoltaic devices. In this study, the potential of vanadium (V)‐doped WS2is investigated, hereafter labeled V‐WS2, in combination with air‐stable Bi2O2Se for use in high‐performance photovoltaic devices. Various techniques are used to confirm the charge transfer of these heterostructures, including photoluminescence (PL) and Raman spectroscopy, along with Kelvin probe force microscopy (KPFM). The results show that the PL is quenched by 40%, 95%, and 97% for WS2/Bi2O2Se, 0.4 at.% V‐WS2/Bi2O2Se, and 2 at.% V‐WS2/Bi2O2Se, respectively, indicating a superior charge transfer in V‐WS2/Bi2O2Se compared to pristine WS2/Bi2O2Se. The exciton binding energies for WS2/Bi2O2Se, 0.4 at.% V‐WS2/Bi2O2Se and 2 at.% V‐WS2/Bi2O2Se heterostructures are estimated to be ≈130, 100, and 80 meV, respectively, which is much lower than that for monolayer WS2. These findings confirm that by incorporating V‐doped WS2, charge transfer in WS2/Bi2O2Se heterostructures can be tuned, providing a novel light‐harvesting technique for the development of the next generation of photovoltaic devices based on V‐doped transition metal dichalcogenides (TMDCs)/Bi2O2Se.
more »
« less
Ultrathin Bi 2 O 2 S nanosheet near-infrared photodetectors
Recently, a zipper two-dimensional (2D) material Bi 2 O 2 Se belonging to the layered bismuth oxychalcogenide (Bi 2 O 2 X: X = S, Se, Te) family, has emerged as an alternate candidate to van der Waals 2D materials for high-performance electronic and optoelectronic applications. This hints towards exploring the other members of the Bi 2 O 2 X family for their true potential and bismuth oxysulfide (Bi 2 O 2 S) could be the next member for such applications. Here, we demonstrate for the first time, the scalable room-temperature chemical synthesis and near-infrared (NIR) photodetection of ultrathin Bi 2 O 2 S nanosheets. The thickness of the freestanding nanosheets was around 2–3 nm with a lateral dimension of ∼80–100 nm. A solution-processed NIR photodetector was fabricated from ultrathin Bi 2 O 2 S nanosheets. The photodetector showed high performance, under 785 nm laser illumination, with a photoresponsivity of 4 A W −1 , an external quantum efficiency of 630%, and a normalized photocurrent-to-dark-current ratio of 1.3 × 10 10 per watt with a fast response time of 100 ms. Taken together, the findings suggest that Bi 2 O 2 S nanosheets could be a promising alternative 2D material for next-generation large-area flexible electronic and optoelectronic devices.
more »
« less
- Award ID(s):
- 1831133
- PAR ID:
- 10176277
- Date Published:
- Journal Name:
- Nanoscale
- ISSN:
- 2040-3364
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
null (Ed.)Bismuth oxide is an important bismuth compound having applications in electronics, photo-catalysis and medicine. At the nanoscale, bismuth oxide experiences a variety of new physico-chemical properties because of its increased surface to volume ratio leading to potentially new applications. In this manuscript, we report for the very first time the synthesis of bismuth oxide (Bi 2 O 3 ) nano-flakes by pulsed laser ablation in liquids without any external assistance (no acoustic, electric field, or magnetic field). The synthesis was performed by irradiating, pure bismuth needles immerged in de-ionized water, at very high fluence ∼160 J cm −2 in order to be highly selective and only promote the growth of two-dimensional structures. The x - and y -dimensions of the flakes were around 1 μm in size while their thickness was 47.0 ± 12.7 nm as confirmed by AFM analysis. The flakes were confirmed to be α- and γ-Bi 2 O 3 by SAED and Raman spectroscopy. By using this mixture of flakes, we demonstrated that the nanostructures can be used as antimicrobial agents, achieving a complete inhibition of Gram positive (MSRA) and Gram negative bacteria (MDR-EC) at low concentration, ∼50 ppm.more » « less
-
Low temperature synthesis of high quality two-dimensional (2D) materials directly on flexible substrates remains a fundamental limitation towards scalable realization of robust flexible electronics possessing the unique physical properties of atomically thin structures. Herein, we describe room temperature sputtering of uniform, stoichiometric amorphous MoS 2 and subsequent large area (>6.25 cm 2 ) photonic crystallization of 5 nm 2H-MoS 2 films in air to enable direct, scalable fabrication of ultrathin 2D photodetectors on stretchable polydimethylsiloxane (PDMS) substrates. The lateral photodetector devices demonstrate an average responsivity of 2.52 μW A −1 and a minimum response time of 120 ms under 515.6 nm illumination. Additionally, the surface wrinkled, or buckled, PDMS substrate with conformal MoS 2 retained the photoconductive behavior at tensile strains as high as 5.72% and over 1000 stretching cycles. The results indicate that the photonic crystallization method provides a significant advancement in incorporating high quality semiconducting 2D materials applied directly on polymer substrates for wearable and flexible electronic systems.more » « less
-
Lithium–sulfur (Li–S) batteries are regarded as one of the most promising next-generation electrochemical cells. However, shuttling of lithium polysulfide intermediates and sluggish kinetics in random deposition of lithium sulfide (Li 2 S) have significantly degraded their capacity, rate and cycling performance. Herein, few-layered MoS 2 nanosheets enriched with sulfur vacancies are anchored inside hollow mesoporous carbon (MoS 2−x /HMC) via S–C bonding and proposed as a novel functional mediator for Li–S batteries. Ultrathin MoS 2 sheets with abundant sulfur vacancies have strong chemical affinity to polysulfides and in the meantime catalyze their fast redox conversion with enhanced reaction kinetics as proved by experimental observations and first-principles density functional theory (DFT) calculations. At a current density of 1C, the MoS 2−x /HMC-S composite cathode exhibits a high initial capacity of 945 mA h g −1 with a high retained capacity of 526 mA h g −1 and a coulombic efficiency of nearly 100% after 500 cycles. The present work sheds light on the design of novel functional electrodes for next-generation electrochemical cells based on a simple yet effective vacancy engineering strategy.more » « less
An official website of the United States government

