Journal of Food Measurement and Characterization
·
2023
·
IF 3.4
Wei Qingyi,Dong Qirong,Pu Hongbin,Sun Da-Wen
Aquaculture fungicide causes threats to the human community and their sensitive detection are thus essential for food safety. Herein, MoS 2 /g-C 3 N 4 @Au heterojunction-based recyclable SERS substrate was developed for fungicide detection. The optimal substrate exhibited good SERS performance with a detection limit as low as 9.908 × 10 −5 mg L −1 for malachite green (MG). Furthermore, an MCN@Au-based photodegradation of crystal violet (CV) under simulated light irradiation was realized, resulting in a degradation rate of 95.6%. With the dual function of the as-synthesized materials, good reusability of the substrates for at least six “detection-degradation” cycles was achieved. In addition, the MG in prawn extract could be sensitively determined with a satisfactory recovery from 91.60 to 124.00%. This work paves an avenue for the fabrication of heterojunction-based recyclable SERS substrates and provides a novel weapon for food safety protection.
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高影响因子
APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Cheng Yang,Xinyue Yang,LiXun Feng,ZiJian Chen,Jia He,HuiTing Sui,Huajun Sun
Piezoelectric photocatalysis is emerging as a promising approach for green environmental protection. Herein, a molybdenum disulfide/graphitic carbon nitride S-scheme heterojunction catalyst achieved a Rhodamine B degradation rate exceeding 99 % within 30 min under the synergistic effects of light and ultrasound, along with a hydrogen (H 2 ) production rate of 16.2 mmol g −1 h −1 . The synergy of ultrasound and light improved catalytic efficiency by approximately 45 % compared with light alone. Experimental characterizations, including Kelvin probe force microscopy, in situ X-ray photoelectron spectroscopy, and density functional theory calculations, confirmed the presence of dual built-in electric fields arising from band alignment and strain-induced polarization. These fields facilitated efficient electron–hole separation, thereby greatly enhancing the overall piezoelectric photocatalytic performance and resulting in efficient use of mechanical and solar energy for H 2 production and pollutant decomposition.
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS
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2022
·Vol. 33
·期 20
·16077-16098
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IF 2.779
Chen Keke,Feng Hange,Li Lingwei,Luo Menghao,Xue Shaolin,Sang Jingxin
The excellent photoresponse of semiconductors enables them as a promising photocatalyst for photocatalytic degradation of organic pollutants and antibiotics, but their practical applications are limited by photogenerated carrier recombination, instability, and fixed energy band positions. Herein, we designed and synthesized a dual Z-scheme flower-like spherical Ag 3 PO 4 /MoS 2 /g-C 3 N 4 (AMN) photocatalyst loaded with different mass of g-C 3 N 4 (3, 5 and 7 mg). Under visible light irradiation, MoS 2 enhanced the light absorption range of AMN composite. The holes concentrated in the valence band of Ag 3 PO 4 provide strong oxidation capacity, and the electrons retained in conduction band of g-C 3 N 4 provide strong reduction ability in the photocatalytic system. It is helpful to improve the separation efficiency of photogenerated carriers and enhance the photocatalytic activity of AMN composite. The AMN photocatalyst loaded with 5 mg g-C 3 N 4 (AMN-5) has the optimal photocatalytic activity. The photocatalytic degradation efficiency of the photocatalyst for methylene blue (MB) within 24 min is 3.98, 1.85, and 1.17 times that of g-C 3 N 4 , Ag 3 PO 4 , and Ag 3 PO 4 /MoS 2 , respectively. After three cycles, the degradation efficiency of AMN-5 for MB decreased from 99.44% to 90%, about 3.79 times of Ag 3 PO 4 (23.77%). In addition, the optimal AMN-5 photocatalyst also has excellent photocatalytic degradation efficiency for Rhodamine B (RhB) and tetracycline (TC). This design and concept provide a promising insight for the photocatalytic degradation of pollutants.
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Environmental Science-Nano
·
2024
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IF 5.8
Sichen Liu,Haotian Wang,Yumeng Xiao,David G. Calatayud,Boyang Mao,Gaoqi Zhang,Chenhui Yang,Lidong Wang,Meng Li
Drinking water contamination and water shortages are seriously exacerbated by industrial wastewater discharge. However, due to the high complexity of wastewater treatment systems, effective high-concentration pollutant removal and simplified wastewater recycling remain major challenges. Inspired by mangrove interconnected purification mechanisms, a novel cascade water treatment system has been developed using MoS2–g–C3N4 (MoG), an amphiphilic material, as the main and single component to directly produce drinking water from wastewater with high efficiency. This cascade system integrates membrane filtration and solar-powered water evaporation processes to produce clean water, while also overcoming the requirement for less polluted source water that is typically required for standalone solar evaporation-based clean water production. The MoG membrane, featuring an amphiphilic platform, exhibits a high removal rate for organic and heavy metal contaminants and achieves a water flow of 966 L m−2 h−1 bar−1 and an 80% efficiency in pollutant removal. The MoG-based aerogel enables nano- and micro-channels and exhibits a clean water production rate of 1.48 kg m−2 h−1 under 1 sun irradiation. The compact cascade system for practical use can produce drinking water that meets WHO standards from heavily polluted wastewater with an average hourly water production rate of 1.39 kg m−2 h−1. Life cycle assessment confirms that the cascade system displays significant environmental profile improvement with reduced CO2 equivalent (CO2e) levels with only 1/25 of that observed in conventional water treatment systems.
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JOURNAL OF NANOPARTICLE RESEARCH
·
2022
·Vol. 24
·期 4
·1-15
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IF 2.533
Wang Zhentao,Hasan Jaafar,Wang Jingjing,Zhang Caiwei,Iqbal Waheed,Chang Ninghui,Qin Chuanguang
The treatment of dye-bearing wastes by adsorption using low-cost synthetic adsorbents is urgently needed and challenging because it offers the dual benefit of water treatment and waste management. Herein, the flower-like MoS 2 /g-C 3 N 4 nanocomposites with a size range of 200–400 nm and a specific surface area of 70.656 m2/g were synthesized as new methylene blue (MB) adsorbent materials. Their adsorption mechanisms and influences of pH, adsorbent dosage, concentration, and temperature on the adsorption properties were investigated by batch sorption experiments. Adsorption isotherm data were fitted with the Langmuir model, and the adsorption kinetic characteristics conform to the quasi second-order kinetic equation. According to thermodynamic data, methylene blue (MB) adsorption was endothermic and spontaneous, exhibiting a maximum adsorption capacity of 278.4 mg/g at 45 °C. Additionally, the impact of MB effluent on the germination of chickpea and wheat was studied contrastively with treatment of the tested materials. The results indicated that adequate adsorption of flower-like MoS 2 /g-C 3 N 4 nanocomposite could potentially treat wastewater from the textile industry to be used for irrigation and solve the problem of textile effluent disposal. Graphical abstract
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Food and Bioprocess Technology
·
2026
·Vol. 19
·期 3
·152
·
IF 5.6
Yang Lingfan,Liu Ruiqi,Shi Yingkun,Li Changhao,Wang Guangxian,Xie Haijiao,Luo Ruiming,Wang Songlei
Xanthine (XA) and hypoxanthine (HA) are key biochemical markers of meat freshness, yet rapid, wide-range, and enzyme-free quantification in complex meat matrices remains challenging. Here we report a density functional theory (DFT)-guided Cu–MoS 2 /g-C 3 N 4 heterostructure electrochemical sensor for broad-range non-enzymatic detection of XA and HA. The heterojunction prepared via a hydrothermal and ultrasonic strategy provides an efficient charge-transport pathway and enriched catalytic interfaces. DFT calculations reveal pronounced interfacial charge redistribution and strong adsorption of XA and HA on the Cu–MoS 2 /g-C 3 N 4 surface, with adsorption energies of − 0.98 eV for XA and − 2.16 eV for HA, explaining the boosted electrooxidation response. The sensor achieves low detection limits of 0.15 μM for XA and 0.28 μM for HA and wide linear ranges from 0.913 to 1643.5 μM and from 0.918 to 1653.1 μM, respectively, and enables simultaneous quantification from 0.5 to 400 μM with excellent linearity. Good stability, reproducibility, and anti-interference capability are obtained. In real meat samples, recoveries from 90.7% to 108.3% for XA and from 91.3% to 111.4% for HA agree well with high-performance liquid chromatography, supporting rapid meat freshness evaluation.
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CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Zhansheng Wu,Xiufang He,Yongtao Xue,Xia Yang,Yunfeng Li,Qubing Li,Bing Yu
The hydrophobicity of MoS 2 /g-C 3 N 4 based photocatalysts remains a major hurdle to their successful application for the remediation of water-soluble contaminants such as herbicides and heavy metals. Herein, we develop new photocatalysts based on the graft of three different cyclodextrins (α-CD, β-CD and γ-CD) on MoS 2 /g-C 3 N 4 composites (CDs/MoS 2 /g-C 3 N 4 ) for the removal of glyphosate and Cr (VI) from simulated agricultural runoff. CDs/MoS 2 /g-C 3 N 4 show remarkably enhanced photocatalytic activities for glyphosate degradation and Cr (VI) reduction compared to pristine MoS 2 /g-C 3 N 4 . In addition, γ-CD/MoS 2 /g-C 3 N 4 exhibits the highest hydrophilicity and photocatalytic activity among these three different cyclodextrins grafted MoS 2 /g-C 3 N 4 . The mechanistic investigation indicates that cyclodextrins can not only increase the accumulation of glyphosate and Cr (VI) onto the surface of CDs/MoS 2 /g-C 3 N 4 but also facilitate the fleet separation of photo-induced electron-hole pairs. In summary, these results collectively imply that the graft of cyclodextrins could be an effective strategy to improve the photocatalytic efficiency of MoS 2 /g-C 3 N 4 composites for the removal of glyphosate and Cr (VI) from simulated agricultural runoff.
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Journal of Water Process Engineering
·
2025
·
IF 6.7
Yang Yu,Lichao Xu,Kaiyuan Xu,Yan Li,Hao Chen,Dongxu Zhang,Yuanzi Chen,Yue Liu,Wenyue Qi
The construction of S-scheme heterojunctions has drawn widespread attention within the photocatalysis field due to their capacity for efficient separation of photogenerated carriers, leading to excellent photo-oxidation-reduction performance. Herein, a novel S-scheme loofah biochar/MoS 2 /g-C 3 N 4 (LB/MS/CN) heterojunction was successfully constructed by ultrasonication in 50 % ethyl alcohol and heat treatment in N 2 atmosphere. Degradation experiments showed that the 5 % LB/MS/CN ternary photocatalyst had optimal photocatalytic efficiency (96.4 %) for the degradation of rhodamine B (RhB), and the reaction rate (k) of this photocatalyst (0.05420 min −1 ) was 5.4 times that of unmodified CN (0.01001 min −1 ). Ultraviolet-visible diffuse reflectance spectra, Mott-Schottky, and free radical trapping experiments suggested that the photogenerated carriers in LB/MS/CN were transferred through the S-scheme structure. Consequently, the co-catalytic action of LB and the synergistic impact of the heterojunction structure between CN and MS led to a reduced photogenerated carrier recombination rate. Furthermore, LB/MS/CN had outstanding stability and the capacity to maintain RhB degradation performance under various environmental conditions (H 2 PO 4 − , NO 3 − , SO 4 2− , HCO 3 − , NaCl, humic acid (HA), and real water), showing good promise for practical applications. Thus, this work provides a possible strategy for purifying wastewater under visible light.
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Catalysts
·
2025
·Vol. 15
·期 9
·808
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IF 4
Shuai Liu,Yipei Chen,Honglei Zhang,Yang Meng,Tao Wu,Guangsuo Yu
Constructing heterojunction photocatalysts with efficient interfacial charge transfer is critical for solar-driven hydrogen evolution. In this study, a highly dispersed MoS2/g-C3N4composite was successfully synthesized via a stirring-assisted hydrothermal in situ growth strategy. The introduction of stirring during synthesis significantly enhanced the uniform dispersion of MoS2nanosheets and exposed abundant edge sites, leading to well-integrated heterojunctions with enhanced interfacial contact. Comprehensive structural and photoelectronic characterizations (XRD, SEM, TEM, EDS mapping, UV–Vis, TRPL, EIS, EPR) confirmed that the composite exhibited improved visible-light absorption, accelerated charge separation, and suppressed recombination. Under simulated solar irradiation with triethanolamine (TEOA) as a sacrificial agent, the optimized 24% MoS2/g-C3N4-S catalyst achieved a high hydrogen evolution rate of 14.33 mmol·g−1·h−1at a catalyst loading of 3.2 mg, significantly outperforming the unstirred and pristine components, and demonstrating excellent cycling stability. Mechanistic studies revealed that the performance enhancement is attributed to the synergistic effects of Type-II heterojunction formation and edge-site-rich MoS2co-catalysis. This work provides a scalable approach for non-noble metal interface engineering and offers insight into the design of efficient and durable photocatalysts for solar hydrogen production.
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APPLIED SURFACE SCIENCE
·
2025
·
IF 6.9
Yan Zhuang,Shuang Meng,Xue Yang,Dongxuan Guo,Dantong Zhang,Tai Peng,Yue Li,Jinlong Li
The formation of amorphous-crystalline heterojunctions has been recognized as an exceptionally effective strategy for enhancing the separation and transfer of photogenerated charge carriers, thereby improving photocatalytic efficiency. In this study, amorphous-crystalline MoS 2 /g-C 3 N 4 /Co 3 O 4 ternary heterojunctions with a unique flower-like structure were synthesized via the integration of g-C 3 N 4 nanosheets and amorphous MoS 2 onto Co 3 O 4 microspheres with a floral structure using a simple solvothermal method followed by acid treatment. Density functional theory (DFT) calculations revealed that the unique floral morphology, combined with the formation of amorphous-crystalline heterojunctions, facilitates the efficient transfer of photogenerated carriers while simultaneously suppressing the recombination of electron-hole pairs. The optimized MoS 2 /g-C 3 N 4 /Co 3 O 4 (3 %) heterojunction exhibited remarkable photocatalytic performance, achieving 82.1 % degradation of Rhodamine B (5 mg L −1 ) under visible-light irradiation within 90 min. Furthermore, the photocatalyst exhibited excellent stability and reusability, as confirmed through cycling experiments, and efficiently decomposed Rhodamine B and its intermediates into small, non-toxic molecules. This work highlights the successful development of a highly active, recyclable amorphous-crystalline ternary heterojunction with a flower-like structure, providing a novel and efficient strategy for the visible-light-driven removal of organic pollutants.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2020
·
IF 3.99
Haiping Liu,Jing Liang,Li shao,Jinge Du,Qiancheng Gao,Shuai Fu,Li Li,Miao Hu,Fengying Zhao,Jianguo Zhou
The dual defect mediated Z-scheme MoS 2 /g-C 3 N 4 photocatalyst was fabricated via a simple ultrasonic dispersion and annealing method. The structural, optical and electronic property was systematically characterized. X-ray photoelectron spectroscopy (XPS) analysis demonstrated that the MoS 2 was anchored on the g-C 3 N 4 through strong interface electrostatic interaction , which led to the formation of built-in electric field at the contact interface. The optimized MoS 2 /g-C 3 N 4 heterojunction achieved a superior photoefficiency towards bisphenol A (BPA) degradation and exhibited the reaction rate normalized to specific surface area of 3.22 × 10 −4 g·min −1 m −2 , approximately 10.0 and 6.7 times larger than these of g-C 3 N 4 and MoS 2 , respectively. The origin of the enhanced photocatalytic activity of MoS 2 /g-C 3 N 4 was attributed to the formation of intimate Z-scheme surface heterostructure between MoS 2 and g-C 3 N 4 , thus improved the light-harvesting ability, facilitated fast charge separation and created more active sites. The impact of anionic towards degradation efficiency was investigated. The degradation activity and degree of BPA were investigated by three-dimensional excitation-emission matrix (3D EEM) fluorescence technique. The Z-scheme charge transfer mechanism and the significant contribution of holes (h + ) and superoxide radicals ( O 2 − ) were demonstrated by electron spinning resonance (EPR), radical scavenger experiment and spectral quantification technology. This work could offer a new protocol for the design of highly efficient heterostructure photocatalysts towards environmental remediation.
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JOURNAL OF MOLECULAR STRUCTURE
·
2023
·
IF 3.8
Xin Yan,Na Zhang,Zhiliang Liu,Chunfang Du
In this paper, 1T/2H mixed-phase MoS 2 /g-C 3 N 4 composites (1T/2H-MG) were successfully synthesized by a simple two-step calcination method and used for Cr(VI) removal from aqueous environment. A series of characterization methods were used to characterize the microstructure and surface morphology of the prepared materials. The experiment results showed that 1T/2H-MG (1:12) composite with good pH and temperature adaptability could completely remove Cr(VI) (100 mg∙L –1 ) within 50 min and showed an excellent adsorption capacity of 342.06 mg∙g –1 . The presence of abundant sulfur defects in 1T/2H-MG composite could provide more adsorption and reduction active sites, which was the main reason for the enhanced removal efficiency of 1T/2H-MG in comparison with pure MoS 2 and g-C 3 N 4 . This work not only contributes an excellent adsorbent for the wastewater treatment, but also provides evidences for the defects engineering.
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