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MoS2
LANGMUIR · 2025 · IF 3.9

Preparation of ZnIn2S4/MoS2–SA Photocatalyst Gel for Wastewater Treatment: Photocatalytic Performance and Solar Interfacial Evaporation

Yuxuan Liu,Qianzhi Chen,Xiaoying Feng,JiYan Li,Hanxue Sun,Weidong Liang

With the rapid advancement of industrialization, wastewater pollution has become an increasingly severe environmental issue. The integration of photocatalysis with solar interfacial evaporation technology, which leverages the abundant and clean energy of solar power, has drawn growing attention as effective solutions to this problem. In this study, MoS2 nanosheets with low-dimensional and controllable morphology were successfully grown on layered ZnIn2S4 using a simple template method, resulting in a novel nanoflower heterojunction photocatalyst. This photocatalyst was then combined with sodium alginate, and aerogels were fabricated through directional freezing technology. The ZnIn2S4/MoS2 photocatalytic aerogel demonstrated excellent photocatalytic performance under visible light, efficiently degrading various pollutants such as rhodamine B(RhB)(30 min, 99%), methyl orange(MO)(30 min, 99%), tetracycline(TC)(1h, 88%), and other antibiotics and dyes. Notably, the degradation efficiency for tetracycline remained at 88% even after five cycles of use, highlighting the aerogel’s strong reusability and stability across different pollutants. Additionally, the current aerogel composite exhibits an evaporation rate of up to 1.984 kg m–2 h–1 and a photothermal conversion efficiency of 95.5%. These results demonstrate that the ZnIn2S4/MoS2 photocatalytic aerogel is a promising candidate for sustainable water treatment, with broad applicability and stable photocatalytic degradation efficiency and interfacial evaporation efficiency under different polluted environments.

CAS / MDL: 1313-84-4
研究领域: 环境科学 · 材料科学
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Nanoscale · 2019 ·Vol. 12 ·期 3 ·1958-1966 · IF 6.97

Remarkable quality improvement of as-grown monolayer MoS2 by sulfur vapor pretreatment of SiO2/Si substrates

Peng Yang,Yabing Shan,Jing Chen,Garel Ekoya,Jinkun Han,Zhi-Jun Qiu,Junjie Sun,Fei Chen,Haomin Wang,Wenzhong Bao,Laigui Hu,Rong-Jun Zhang,Ran Liu,Chunxiao Cong

Monolayer MoS2 is a direct bandgap semiconductor which is believed to be one of the most promising candidates for optoelectronic devices. Chemical vapor deposition (CVD) is the most popular method to synthesize monolayer MoS2 with a large area. However, many defects are always found in monolayer MoS2 grown by CVD, such as sulfur vacancies, which severely degrade the performance of devices. This work demonstrates a concise and effective method for direct growth of high quality monolayer MoS2 by using SiO2/Si substrates pretreated with sulfur vapor. The MoS2 monolayer obtained using this method shows about 20 times PL intensity enhancement and a much narrower PL peak width than that grown on untreated substrates. Detailed characterization studies reveal that MoS2 grown on sulfur vapor pretreated SiO2/Si substrates has a much lower density of sulfur vacancies. The synthesis of monolayer MoS2 with high optical quality and low defect concentration is critical for both fundamental physics studies and potential practical device applications in the atomically thin limit.

研究领域: 材料科学 · 光学 · 半导体物理
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Synergistic removal of chromium(VI) and tetracycline by porous carbon sponges embedded with MoS2: Performance and radical mechanism of piezoelectric catalysis

Hongwei Xu,Xiaxia Chen,Chao Liu,Mingyang Xu,Chenxi Guo,Yinglong Wang,Zhaoyou Zhu,Fanqing Meng

The presence of hexavalent chromium(Ⅵ) Cr(Ⅵ) and antibiotics in the environment can lead to the formation of combined pollutants that are harmful to ecosystems. To address this problem, we synthesized MoS 2 embedded in the porous super-hydrophilic polyurethane (PU) sponge and used weak water flow to drive the piezoelectric catalytic synergistic degradation of Cr(Ⅵ) and tetracycline (TC). In this study, the piezoelectric properties of MoS 2 /PU were confirmed via piezoresponse force microscopy (PFM) and COMSOL multiphysics calculations. Additionally, dynamics experiments, quenching experiments, electron paramagnetic resonance (EPR) spectroscopy, three-dimensional fluorescence excitation-emission matrix (3D-EEM) spectroscopy, and free radical generation rate analysis were conducted to explore the removal performance and mechanisms of MoS 2 /PU on the TC-Cr(VI) system. The results indicated that the coexistence of the two pollutants promotes the transfer of charge in MoS 2 /PU, further combined with O 2 to produce H 2 O 2 and continued to produce OH. The removal rates of TC and Cr(VI) in the TC-Cr (VI) mixed system at 30 min were 97 % and 94 %, respectively, which were 1.45 and 1.46 times those of the single TC and single Cr(VI) systems, respectively. Finally, potentially vulnerable sites of TC were calculated and analyzed according to density functional theory (DFT). Our results provide a new strategy for improving the degradation efficiency of antibiotics and Cr(VI) metals.

研究领域: 环境科学 · 材料科学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2024 · IF 3.8

Controllable Synthesis of Porous 1T-MoS2 with Large Surface Area via Continuous Hydrothermal System

Zhiyuan Yu,Tianyi Huang,Shafqat Ullah,Yujun Wang,Guangsheng Luo

1T-phase MoS2, a versatile two-dimensional transition-metal dichalcogenide, is typically synthesized using a one-pot hydrothermal method. However, inadequate control of the sulfurization, reduction, and crystallization processes in the autoclave leads to multilayer 1T-MoS2 with high crystallinity, a small surface area, and few defects. Considering the aforementioned issues, a two-stage microreactor continuous hydrothermal flow synthesis (CHFS) system coupled with accurate control and rapid processing is used to prepare 1T-MoS2 with abundant voids and a large surface area under 250 °C and 4.0–4.5 MPa. And density functional theory calculations reveal that nitrogenous species, acting as reductants and electron donors, lower the energy of 1T-MoS2 by intercalation and surface adsorption, facilitating its swift synthesis within the presulfurization stage for 10 min and reduction stage for 24 min. The precisely controlled synthesis of porous 1T-MoS2, originating from prenucleation clusters, results in a large surface area of 201.5 m2/g, concentrated mesopores of 2–5 nm, and a pore volume of 0.58 cm3/g. Moreover, a significant transformation from the 1T to the 2H phase is prevented by rapid cooling downstream of the CHFS system.

研究领域: 材料科学 · 化学工程
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APPLIED ORGANOMETALLIC CHEMISTRY · 2019 ·Vol. 33 ·期 9 ·e5060 · IF 3.259

Enhanced Thermal Decomposition Properties and Catalytic Mechanism of Ammonium Perchlorate over CuO/MoS2 Composite

Yinghui Hu,Yulin Yang,Ruiqing Fan,Kaifeng Lin,Dongyu Hao,Debin Xia,Ping Wang

In this report, CuO/MoS 2 composites were successfully prepared by the hydrothermal method where nano-sized CuO was uniformly distributed on the surface of hierarchical MoS 2 substrates (CuO/MoS 2 composites). Their physicochemical properties and catalytic performance in ammonium perchlorate (AP) decomposition were investigated and characterized by XRD, SEM, TEM, BET, XPS, TG/DSC and combustion measurement. The results showed that it could decrease AP decomposition temperature at high decomposition stage from 416.5 °C to 323.5 °C and increase the heat release from 378 J/g (pure AP) to 1340 J/g (AP with catalysts), which was better than pure CuO nanoparticles (345.5 °C and 1046 J/g). Meanwhile, it showed excellent performance in combustion reaction either in N 2 or air atmosphere. The results obtained by photocurrent spectra, photoluminescence spectra and time-resolved fluorescence emission spectra indicated that loading CuO mediated the generation rate and combination rate of electrons and holes, thus tuning the catalytic performance on AP decomposition. This study proved that employing the supports that can synergistically interact with CuO is an efficient strategy to enhance the catalytic performance of CuO.

研究领域: 材料科学 · 催化化学
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NEW JOURNAL OF CHEMISTRY · 2024 ·Vol. 48 ·期 16 ·7439-7448 · IF 2.7

Modification of a MoS2 composite membrane using nano-silica for high-efficiency dye separation

Xiaoyu Yang,Hongdan Wu,Zhihui Zhou,Yehao Zhao,Yuedong Li

Two-dimensional (2D) layered MoS2 membrane has a unique pore structure, adjustable interlayer spacing and excellent transmission performance, which has wide-ranging and excellent application prospects for water treatment. However, the MoS2 membrane exhibits a narrow interlayer height, which can only accommodate one layer of water molecules, causing low water permeation and flux. In this work, a MoS2/SiO2 composite membrane with regular transport channels was prepared by the vacuum-assisted self-assembly (VASA) process using the intercalation of nano-silica (SiO2) nanoparticles. The resulting membrane showed an increase in interlayer widths from 0.61 nm to 0.69 nm. The MoS2/SiO2 composite membrane featured a high-efficiency dye separation performance and aqueous stability as the mass ratio of MoS2/SiO2 was 2.5, and the water permeance flux could reach 979 L m−2 h−1 bar−1, with a rejection of 100% for Evans blue (EB), methyl blue (MB) and neutral red (NR) and a rejection of over 98% for rhodamine B (RhB). MoS2 membranes decorated by SiO2 nanosheet nanoparticles could effectively achieve precision regulation of interlayer spacings and hold the channel order of MoS2 laminates. In addition, the rejection rate of the composite membrane remained 100% after remaining immersed in strong oxidizing acid for up to 60 days, which showed their stability toward strong acid and oxidative environments. This work suggests that an interlayer manipulation strategy in 2D laminar membranes could improve membrane performance for wastewater treatment and other separations.

CAS / MDL: 553-24-2
研究领域: 材料科学 · 环境工程 · 化学工程
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Thermo-responsive and biodegradable MoS2-based nanoplatform for tumor therapy and postoperative wound management

Yichen Yin,Nan Wang,Bin Hu,Jiaxuan Guo,Qian Chen,Zheng Chen,Mohammad-Ali Shahbazi,Lissette Agüero,Shige Wang,Cheng Li

Inorganic nanoparticles serve as versatile nanoplatforms for efficient cancer diagnosis and therapy. However, their limited in vivo degradability and excretion rates may lead to various adverse effects. Furthermore, the cascade-controlled release of drugs remains a challenge. In this study, we developed a free-radical triggered degradable MoS 2 -AIPH@LA nanoplatform for tumor photothermal and oxygen-independent thermodynamic therapy. This was achieved by loading the free radical initiator (2,2′-azobis[2-(2-imidazolin-2-yl) propane] dihydrochloride (AIPH)) onto MoS 2 nanoparticles and encapsulating them with thermo-responsive lauric acid (LA). Upon laser irradiation, the hyperthermia generated by MoS 2 induces cancer cell death and releases AIPH, an oxygen-independent and thermal-responsive radical initiator capable of producing toxic alkyl free radicals for tumor therapy and inhibiting bacterial growth. Importantly, these free radicals promote the degradation rate of MoS 2 -AIPH@LA, further facilitating a rapid AIPH release and improving the biocompatibility of the MoS 2 -AIPH@LA nanoplatform. In particular, the thermo-responsive nature of LA in this formulation effectively regulates the release of AIPH, thus reducing potential AIPH leakage into the bloodstream and minimizing safety risks. With its free-radical-triggered degradation and cascade-controlled release capabilities, MoS 2 -AIPH@LA shows significant promise for inhibiting tumor proliferation and managing postoperative bacterial infection.

研究领域: 肿瘤学 · 纳米医学 · 材料科学
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ADVANCED MATERIALS · 2024 ·Vol. 36 ·期 48 ·2412844 · IF 27.4

Fully Printed and Sweat-Activated Micro-Batteries with Lattice-Match Zn/MoS2 Anode for Long-Duration Wearables

Xinyi Zhang,Linyu Hu,Kemeng Zhou,Linqing Zhang,Xiaolong Zeng,Yuqing Shi,Weizheng Cai,Jiazhen Wu,Yuanjing Lin

Aqueous zinc-ion batteries with superior operational safety have great promise to serve as wearable energy storage devices. However, the poor cycling stability and low output voltage limited their practical applications. Here, fully printable Zn/MoS 2 -MnO 2 micro-batteries are developed and demonstrated significantly enhanced cycling stability with sweat activation. 2D MoS 2 is utilized to enable lattice-matching with Zn powders to realize printed Zn anodes with desirable stability and promote electron/ion transfer. Interestingly, the mild acid epidermal sweat also contributed to eliminating the MnO 2 cathode by-products and compensating for the hydrogel electrolytes' water loss. The Zn/MoS 2 -MnO 2 micro-batteries achieve a high specific capacity of 318.9 µAh cm −2 at the current density of 0.16 mA cm −2 , and an energy density of 424.6 µWh cm −2 , with remarkable cycle stability of ≈90% after 250 cycles. In-battery electrochromic display of capacity level and feasible electronics charging are demonstrated. The as-printed micro-batteries with innovative sweat activation would inspire the advances of sustainable power supply for wearables.

CAS / MDL: 1317-33-5 7440-66-6
研究领域: 材料科学 · 能源技术
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Molecular Catalysis · 2024 · IF 3.9

MoS2 decorated CdS composite catalyst for photoredox-mediated C–N coupling of amines to imines and hydrogen production

Xin-Ni Shao,Yin-Feng Wang,Ming-Yu Qi,Zi-Rong Tang

Simultaneous utilization of photogenerated electrons and holes within a photoredox system enables effective hydrogen (H 2 ) production and organic synthesis, aligning with eco-friendly chemistry principles and current energy challenges. Here, we report the preparation and application of cocatalyst MoS 2 decorated CdS (MoS 2 CdS) composites for the photoredox-mediated C–N coupling of amines to imines and H 2 generation under visible light illumination. The H 2 and N-benzylidenebenzylamine yields for the optimal MoS 2 CdS are 28.9 and 15.0 times higher than those of bare CdS, respectively. Mechanism studies reveal that the enhanced photocatalytic activity results from the MoS 2 acting as an electron sink, which accelerates the separation and migration of photogenerated charge carriers. Additionally, the pH(•CH)NH 2 intermediates are found to play a pivotal role in the dehydrogenative coupling of benzylamine. Furthermore, the MoS 2 CdS composites exhibit universal applicability in the conversion of various aromatic amines into corresponding imines integrated with H 2 evolution.

CAS / MDL: 10022-68-1 780-25-6
研究领域: 化学 · 材料科学 · 能源科学
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CHEMISTRY LETTERS · 2020 ·Vol. 50 ·期 3 ·452-455 · IF 1.361

A Study of All-solid-state Planar Micro-supercapacitors Using Printable MoS2 Inks

Han Zhao,Xia Tong,Xu Shiwei,Li Gang,Zhang Liying,Hu Nantao,Yu Jian,Li Bin,Yang Zhi,Zhang Yafei

Wearable energy storage electronics with high safety and long life have been promising candidates in recent years. Herein, all-solid-state planar micro-supercapacitors (MSCs) were demonstrated by inkjet printing of molybdenum disulfide (MoS2) electrodes. The preprinted PEDOT: PSS film on PI (Polyimide) substrate prepared with a simple and low-cost desktop inkjet printer can greatly improve the electrode conductivity. Additionally, the obtained planar MSCs show good electrochemical performance with high areal capacitance of 323 µF cm−2 and areal energy density of 0.016 µWh cm−2. More importantly, the MSCs exhibit outstanding flexibility with almost no degradation under various bending angles. The capacitance retention can still be maintained at 88.5% even after 8000 cycles, indicating good cycle stability of MSCs. The in-plane flexible MSCs hold great application potential for wearable and integrated energy storage electronics.

研究领域: 材料科学 · 能源存储技术
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JOURNAL OF ALLOYS AND COMPOUNDS · 2018 · IF 3.779

One-step hydrothermal synthesis of a CoS2@MoS2 nanocomposite for high-performance supercapacitors

Feng Huang,Rongde Meng,Yanwei Sui,Fuxiang Wei,Jiqiu Qi,Qingkun Meng,Yezeng He

A MoS 2 -coated CoS 2 composite has been prepared successfully via a one-step hydrothermal method . This CoS 2 @MoS 2 hybrid material has a distinct morphology with few-layer MoS 2 wrapping the CoS 2 nanoparticles . Serving as a supercapacitor electrode, the obtained CoS 2 @MoS 2 hybrid material exhibits a remarkable specific capacitance of 1038 F/g, a high rate capability of 71.7%, and excellent cycling stability of 84.76% retention after 10000 cycles. The superior electrochemical properties of the CoS 2 @MoS 2 nanocomposite are attributed to the synergistic effects between the layered MoS 2 and conductive CoS 2 .

研究领域: 材料科学 · 能源存储与转换
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JOURNAL OF MAGNETISM AND MAGNETIC MATERIALS · 2019 · IF 2.683

Controlled assembly of MnFe2O4 nanoparticles on MoS2 nanosheets by a facile sonochemical method

Guangshuo Wang,Fei Zhou,Tianxiang Du,Ziwei Lu,Yingying Ma,Jingbo Mu,Yanming Wang,Zhixiao Zhang,Hongwei Che,Xiaoliang Zhang,Ruitao Yu

This study established a facile one-step strategy to anchor MnFe 2 O 4 nanoparticles on the surface of MoS 2 nanosheets in a controlled manner. The as-prepared MnFe 2 O 4 /MoS 2 nanocomposites were investigated by TEM, XRD, XPS, Raman, BET and VSM in detail. The MnFe 2 O 4 nanoparticles with an average particle size of 26 nm were densely and uniformly decorated on MoS 2 nanosheets, and consequently, both the aggregation of MnFe 2 O 4 nanoparticles and restacking of MoS 2 nanosheets were effectively prevented. More importantly, the MnFe 2 O 4 /MoS 2 nanocomposites exhibited high specific surface area, typical superparamagnetic behavior and excellent solution dispersion, showing a great potential for biomedical applications in the fields of magnetic resonance imaging, targeted drug delivery and tumor hyperthermia.

CAS / MDL: 1317-33-5
研究领域: 材料科学 · 纳米技术 · 生物医学工程
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