ABSTRACT
Ultraviolet photodetectors (UV PDs) have attracted significant attention due to their wide range of applications, such as underwater communication, biological analysis, and early fire warning systems. Indium oxide (In2O3) is a candidate for developing high-performance photoelectrochemical (PEC)-type UV PDs owing to its high UV absorption and good stability. However, the self-powered photoresponse of the previously reported In2O3-based PEC UV PDs is unsatisfactory. In this work, high-performance self-powered PEC UV PDs were constructed by using an In2O3 nanocube film (NCF) as a photoanode. In2O3 NCF photoanodes were synthesized on FTO by using hydrothermal methods with a calcining process. The influence of the electrolyte concentration, bias potential, and irradiation light on the photoresponse properties was systematically studied. In2O3 NCF PEC UV PDs exhibit outstanding self-powered photoresponses to 365 nm UV light with a high responsivity of 44.43 mA/W and fast response speed (20/30 ms) under zero bias potential, these results are superior to those of previously reported In2O3-based PEC UV PDs. The improved self-powered photoresponse is attributed to the higher photogenerated carrier separation efficiency and faster charge transport of the in-situ grown In2O3 NCF. In addition, these PDs exhibit excellent multicycle stability, maintaining the photocurrent at 98.69% of the initial value after 700 optical switching cycles. Therefore, our results prove the great promise of In2O3 in self-powered PEC UV PDs.
ABSTRACT
The exploration and development of self-powered visible-blind ultraviolet photodetectors (VBUV PDs) with high responsivity and wavelength selectivity have far-reaching significance for versatile applications. Although In2O3 shows potential for UV detection due to good UV absorption and electrical transport properties, the poor wavelength selectivity impedes further application in VBUV PDs. Here, a self-powered photoelectrochemical-type (PEC) VBUV PD is demonstrated by using gallium-indium oxide alloys (Ga-In OAs). The self-powered Ga-In OAs-based PEC VBUV PDs exhibit good VBUV photodetection performance, including a high responsivity of 50.04 mA/W and a high detectivity of 6.03 × 1010 Jones under 254 nm light irradiation, a good wavelength selectivity (UV/visible light rejection ratio of 262.45), and a fast response time (0.45/0.38 s). The good self-powered VBUV detection performance of Ga-In OAs is attributed to the larger band gap and smaller charge-transfer resistance induced by alloy engineering, which not only suppresses the absorption of visible light but also accelerates interfacial charge transfer. Moreover, an underwater optical communication system is demonstrated by using the self-powered Ga-In OAs PEC VBUV PDs. This study demonstrates that alloy engineering is a powerful tool to improve the performance of In2O3-based PEC PDs, and Ga-In OAs have great application potential for underwater optoelectronic devices.
ABSTRACT
Ga2O3is a good candidate for deep ultraviolet photodetectors due to its wide-bandgap, good chemical, and thermal stability. Ga2O3-based photoelectrochemical (PEC) photodetectors attract increasing attention due to the simple fabrication and self-powered capability, but the corresponding photoresponse is still inferior. In this paper, the oxygen vacancy (Vo) engineering towardsα-Ga2O3was proposed to obtain high-performance PEC photodetectors. Theα-Ga2O3nanorods were synthesized by a simple hydrothermal method with an annealing process. The final samples were named as Ga2O3-400, Ga2O3-500, and Ga2O3-600 for annealing at 400 â, 500 â, and 600 â, respectively. Different annealing temperatures lead to different Voconcentrations in theα-Ga2O3nanorods. The responsivity is 101.5 mA W-1for Ga2O3-400 nanorod film-based PEC photodetectors under 254 nm illumination, which is 1.4 and 4.0 times higher than those of Ga2O3-500 and Ga2O3-600 nanorod film-based PEC photodetectors, respectively. The photoresponse ofα-Ga2O3nanorod film-based PEC photodetectors strongly depends on the Voconcentration and high Voconcentration accelerates the interfacial carrier transfer of Ga2O3-400, enhancing the photoresponse of Ga2O3-400 nanorod film-based PEC photodetectors. Furthermore, theα-Ga2O3nanorod film-based PEC photodetectors have good multicycle, long-term stability, and repeatability. Our result shows thatα-Ga2O3nanorods have promising applications in deep UV photodetectors.
ABSTRACT
The lithium sulfur (Li-S) battery is an active research area in the field of energy storage systems, but the shuttle effect is a serious obstacle hindering its application. Herein, a CoSe2/CoO Mott-Schottky catalyst is blended with carbon nanotubes (CNTs) and subsequently coated onto a commercial separator as a modifier, whereby the synergy between the high electrocatalytic activity of the CoSe2/CoO heterostructure and high conductivity of the CNTs selectively mediate the conversion of sulfur species. As a result, a cell with a CoSe2/CoO-CNTs modified separator displays a high initial discharge capacity of 1573 and 910 mAh/g at 0.1 and 2C, respectively. Furthermore, a low decay rate of 0.070% per cycle can be obtained over 500 cycles at 2C. The results of this study suggest that the as-prepared CoSe2/CoO-CNTs is an effective modifier that can improve the performance of Li-S batteries for use in next-generation energy storage systems. This study provides fundamental insights into the rational design of Mott-Schottky catalysts for practical high-performance Li-S batteries.
ABSTRACT
Ultraviolet photodetectors (UV PDs) have attracted extensive attention owing to their wide applications, such as optical communication, missile tracking, and fire warning. Wide-bandgap metal-oxide semiconductor materials have become the focus of high-performance UV PD development owing to their unique photoelectric properties and good stability. Compared with other wide-bandgap materials, studies on indium oxide (In2O3)-based photoelectrochemical (PEC) UV PDs are rare. In this work, we explore the photoresponse of In2O3-based PEC UV PDs for the first time. In2O3 microrods (MRs) were synthesized by a hydrothermal method with subsequent annealing. In2O3 MR PEC PDs have good UV photoresponse, showing a high responsivity of 21.19 mA/W and high specific detectivity of 2.03 × 1010 Jones, which surpass most aqueous-type PEC UV PDs. Moreover, In2O3 MR PEC PDs have good multicycle and long-term stability irradiated by 365 nm. Our results prove that In2O3 holds great promise in high-performance PEC UV PDs.
ABSTRACT
Cobalt diselenide (CoSe2) is considered to be a promising economical and efficient electrocatalyst for the hydrogen evolution reaction (HER). Here carbon nanotubes (CNTs) were employed as a conductive skeleton to optimize the electrocatalytic performance of CoSe2 through a simple one-step hydrothermal method. Beyond the expected, the introduction of CNTs not only accelerates electron transportation and ion diffusion, but also improves the reaction kinetics for HER by forming a CoSe2/CNT heterointerface. Consequently, the CoSe2/CNTs composite exhibits an optimal overpotential of 153 mV with a weight ratio of 10 : 1, and sustains a long period of 48 hours with an negligible overpotential deterioration. In addition, a Faraday efficiency of 97.67% is achieved with a H2/O2 molar ratio of 2 : 1. Therefore, these results open up further opportunities for yielding efficient and durable hydrogen evolving electrocatalysts from low-cost transition metal compounds.
ABSTRACT
Robust and economical catalysts are imperative to realize the versatile applications of hydrogen. Herein, a 1T-MoS2/N-doped NiSe2 composite was rationally synthesized via a solvothermal method, in which the MoS2 nanosheets have a stable 1T phase structure, and the NiSe2 nanoparticles serve as a cocatalytic support for MoS2. The nonnegligible electronic couplings between NiSe2 and MoS2 could facilitate the optimization of their electronic structure and then improve the hydrogen adsorption. What is more, the nitrogen dopants in the NiSe2 nanoparticles could intensify the intercalation of ammonium ions in the 1T-MoS2 nanosheets, and further enlarge their interlayer spacing, thus the electrolyte could infiltrate into the catalyst more easily and sufficiently. This work provides a new route for rationally designing highly active and low cost hydrogen evolution reaction (HER) catalysts, and enriches the study of transition metal chalcogenides toward HER.
