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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Bio-photoelectrochemcial system constructed with BiVO4/RGO photocathode for 2,4-dichlorophenol degradation: BiVO4/RGO optimization, degradation performance and mechanism

Lingli Tu,Yanping Hou,Guiyun Yuan,Zebin Yu,Shanming Qin,Yimin Yan,Hongxiang Zhu,Hongfei Lin,Yongli Chen,Shuangfei Wang

A single-chamber bio-photoelectrochemical system (BPES) constructed with BiVO 4 /reduced graphene oxide (RGO) photocathode was proposed for 2,4-dichlorophenol (2,4-DCP) degradation under simulated solar irradiation. The BiVO 4 /RGO (B/G) composites were synthesized, optimized and characterized by various techniques to analyze their physico-chemical and photocatalytic properties. Results showed that B/G (5 wt% - 9 h - 150 °C) exhibited the best photocatalytic activity for 2,4-DCP degradation, which was 1.5 times of that of BiVO 4 , due to its better light absorption, faster electrons transfer, and more efficient photo-generated e − - h + separation. Reactive species trapping experiments revealed that ·OH was the main radical leading to 2,4-DCP degradation, and h + also influenced 2,4-DCP removal. The 2,4-DCP (20 mg/L) removal rate and current output from the illuminated BPES were much higher than those of the unilluminated reactor (68.5 % vs. 41.8 %, 60.31 A/m 3 vs. 40.07 A/m 3 ) in 24 h, and the cathode potential was more negative, indicating that photocathode catalytic process was favorable to pollutants degradation and energy generation. Intermediates of 2,4-DCP degradation in the BPES were identified, and accordingly, possible degradation pathway and mechanism were proposed. This research advanced the development of efficient photocathode and mechanism of recalcitrant wastewater treatment in the BPES.

研究领域: 环境科学 · 材料科学 · 化学工程
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APPLIED SURFACE SCIENCE · 2015 · IF 2.711

Fabrication of ITO-rGO/Ag NPs nanocomposite by two-step chronoamperometry electrodeposition and its characterization as SERS substrate

Rong Wang,Yi Xu,Chunyan Wang,Huazhou Zhao,Renjie Wang,Xin Liao,Li Chen,Gang Chen

A novel composite structure of reduced graphene oxide (rGO)–Ag nanoparticles (Ag NPs) nanocomposite, which was integrated on the indium tin oxide (ITO) glass by a facile and rapid two-step chronoamperometry electrodeposition route, was proposed and developed in this paper. SERS-activity of the rGO/Ag NPs nanocomposite was mainly affected by the structure and size of the fabricated rGO/Ag NPs nanocomposite. In the experiments, the operational conditions of electrodeposition process were studied in details. The electrodeposited time was the important controllable factor, which decided the particle size and surface coverage of the deposited Ag NPs on ITO glass. Under the optimized conditions, the detection limit for rhodamine6G (R6G) was as low as 10 −11   M and the Raman enhancement factor was as large as 5.9   ×   10 8 , which was 24 times higher than that for the ITO–Ag NPs substrate. Apart from this higher enhancement effect, it was also illustrated that extremely good uniformity and reproducibility with low standard deviation could be obtained by the prepared ITO-rGO/Ag NPs nanocomposite for SRES detection.

CAS / MDL: 7782-42-5 7761-88-8
研究领域: 材料科学 · 分析化学
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JOURNAL OF MATERIALS RESEARCH · 2019 ·Vol. 34 ·期 18 ·3186-3194 · IF 1.982

In situ hydrothermal synthesis of rGO-wrapped Fe1−xS particles for lithium storage

Meng-Han Wang,Huai-Guo Xue,Sheng-Ping Guo

Iron sulfides have attracted much interests for their potential as anode materials in energy storage devices in view of their low costs, and environmentally benign and high theoretical capacities. Among them, Fe1−xS is relatively rarely investigated. In this work, Fe1−xS@rGO has been synthesized using a facile in situ hydrothermal method. After wrapped by rGO, the morphology of Fe1−xS particles changes from hexagonal flakes to irregular particles with much smaller sizes. As the anode material for lithium ion batteries, Fe1−xS@rGO exhibits excellent lithium storage ability. It can deliver an initial discharge capacity of 1575.5 mA h/g in the potential window of 0.005–3 V, and a reversible capacity of 907.8 mA h/g can be maintained after 200 cycles at 100 mA/g. Its improved electrochemical performance can be attributed to the effect of enhanced contact area and shortened Li+ ion transport distance because of rGO’s contribution.

研究领域: 材料科学 · 能源存储
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2018 · IF 11.698

Synergy removal of Cr (VI) and organic pollutants over RP-MoS2/rGO photocatalyst

Xue Bai,Yanyan Du,Xiaoyun Hu,Yudong He,Chunliang He,Enzhou Liu,Jun Fan

A novel RP-MoS 2 /rGO nanocomposite as low-cost, environmental sustanable, stability and high-performance photocatalyst was successfully fabricated for the first time through a facile two-step hydrothermal method. Even without a noble-metal cocatalyst, the introduction of MoS 2 /rGO hybrid made RP exhibit excellent photocatalytic performance, including photoreduction of Cr (VI) and photooxidation of different organic pollutants, owing to the increased number of excited electrons/holes and enhanced separation efficiency of charge carriers. Importantly, the synergy of photocatalytic reduction and oxidation, as well as photocatalysis and adsorption played an important role in enhancing photocatalytic activity and reaching a high efficiency. Besides, the chemical structure of the RP-MoS 2 /rGO with P–S and P O bands ensure the stability of the nanocomposite materials. Overall, the photocatalytic elimination of the Cr (VI)-Organic molecule coexistence system in this work shows promising application to treatment the reality wastewater.

CAS / MDL: 7723-14-0
研究领域: 环境科学 · 材料科学
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SENSORS AND ACTUATORS B-CHEMICAL · 2018 · IF 5.667

Effective hydrogen gas sensor based on NiO@rGO nanocomposite

Haibo Ren,Cuiping Gu,Sang Woo Joo,Jingjuan Zhao,Yufeng Sun,Jiarui Huang

A NiO@rGO nanocomposite is prepared by a freeze-drying method combined with heat treatment. The morphology and structure are analyzed through X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Raman spectra, and X-ray photoelectron spectroscopy. The results clearly show that NiO nanoparticles are uniformly anchored on the surface of the rGO nanosheet. The gas-sensing performance of the nanocomposite is also investigated to detect hydrogen. The NiO@rGO sensor exhibits good gas-sensing performance with high sensitivity, fast response, good reversibility, and selectivity toward hydrogen. The relative response of the sensor to 1% hydrogen is 0.64, the response time is 28 s, and the recovery time is 142 s. The improved sensing performance is due to the effective electron transfer between the NiO nanoparticles and rGO nanosheet.

CAS / MDL: 1313-99-1
研究领域: 材料科学 · 传感器技术
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CHEMOSPHERE · 2022 · IF 8.943

Efficient removal of TBBPA with a Z-scheme BiVO4-(rGO-Cu2O) photocatalyst under sunlight irradiation

Yaoyi Li,Kexin Chen,Xi Wang,Zijun Xiao,Gaozu Liao,Jing Wang,Xukai Li,Yiming Tang,Chun He,Laisheng Li

In this study, reduced graphene oxide (rGO) was used to fabricate a Z-scheme BiVO 4 -(rGO-Cu 2 O) photocatalyst for the degradation of Tetrabromobisphenol A (TBBPA) under sunlight irradiation. The photocatalyst was synthesized using a three-step method BiVO 4 -(rGO-Cu 2 O) photocatalyst with an rGO loading of 1% and (rGO-Cu 2 O) to BiVO 4 ratio of 50% achieved the best degradation effect for TBBPA removal. Electron paramagnetic resonance spectroscopy (EPR) confirmed that the charge transfer path of BiVO 4 -(rGO-Cu 2 O) follows that of Z-scheme photocatalysts. Moreover, the addition of rGO increases the charge transfer efficiency. High performance liquid chromatography-mass spectrometry (HPLC-MS) was used to detect and analyze intermediate products, allowing the proposal of the main degradation pathway of TBBPA. Photogenerated electrons of BiVO 4 -(rGO-Cu 2 O) were then transferred into the conduction band of Cu 2 O. Cu 2 O is located in the surface layer, which has the most effective contact area with pollutants, and therefore has a good outcome for the photocatalytic reduction of TBBPA. Photogenerated electrons (e − ) and hydroxyl radicals (∙OH) are the main factors affecting TBBPA degradation. The degradation process of TBBPA includes electron reduction debromination , hydroxylation , and β-cleavage. In our work, BiVO 4 -(rGO-Cu 2 O) was successfully synthesized to degrade TBBPA; this study brings forth a novel approach for the degradation of halogenated organic pollutants using a Z-scheme photocatalytic composite.

研究领域: 环境科学 · 材料科学
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2020 · IF 3.306

Highly efficient visible-light driven photocatalytic hydrogen production over (MoSe2-RGO)/(Er3+:Y3Al5O12/ZnS)/RuO2 photocatalyst

Shuguang Li,Zhiyu Liu,Chunxiao Lu,Zhihui Qu,Congcong Piao,Jianhe Tang,Dawei Fang,Jun Wang

The use of co-catalysts can observably enhance photocatalytic hydrogen production activity. In this work, a novel visible-light driven photocatalyst, (MoSe 2 -RGO)/(Er 3+ :Y 3 Al 5 O 12 /ZnS)/RuO 2 nanocomposite, is prepared for the first time by loading Er 3+ :Y 3 Al 5 O 12 , MoSe 2 -RGO and RuO 2 on the surface of ZnS nanoparticles. Er 3+ :Y 3 Al 5 O 12 as an effective visible-to-ultraviolet up-conversion luminescence agent can provide the ultraviolet-light to activate wide band-gap ZnS. MoSe 2 -RGO and RuO 2 , acting as conduction band co-catalyst and valence band co-catalyst, respectively, can effectively separate the photo-generated carriers and supply more reactive sites. The activities of the photocatalysts were assessed via photocatalytic hydrogen production in Na 2 S and Na 2 SO 3 aqueous solution under 300 W xenon lamp irradiation. In addition, the visible-light irradiation time and used times of the prepared samples as influence factors on the photocatalytic hydrogen production were also investigated. It was easily found that the prepared (MoSe 2 -RGO)/(Er 3+ :Y 3 Al 5 O 12 /ZnS)/RuO 2 nanocomposite shows fairly high activity in photocatalytic hydrogen production, compared with single ZnS photocatalyst. It was mainly attributed to the excellent up-conversion luminescence property of Er 3+ :Y 3 Al 5 O 12 and the efficient separation of photo-generated electrons and holes caused by MoSe 2 -RGO and RuO 2 . This research may pave an effective way for photocatalytic hydrogen production utilizing solar light.

CAS / MDL: 1313-84-4
研究领域: 材料科学 · 能源化学 · 纳米技术
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MICROCHIMICA ACTA · 2020 ·Vol. 187 ·期 8 ·1-10 · IF 6.232

Photoelectrochemical aptasensor for thrombin based on Au-rGO-CuS as signal amplification elements

Zou Lina,Yang Lingxi,Zhan Yi,Huang Di,Ye Baoxian

A photoelectrochemical platform for thrombin determination was developed based on Au-rGO-CuS as multiple signal amplification elements. CuInS 2 QDs was used to sensitize burr-shape TiO 2 (b-TiO 2 ) to obtain a strong photocurrent. Under the specific recognition between aptamer and thrombin, a sandwichlike structure was formed and the Au-rGO-CuS-labeled aptamer (S2@Au-rGO-CuS) was immobilized on the electrode surface. This induced a sharp decrease in photocurrent. The phenomenon is mainly due to the fact that CuS NPs can competitively consume the light energy and electron donor with CuInS 2 /b-TiO 2 . The rGO can increase the amount of CuS NPs and the Au NPs can accelerate charge transferring which depress the recombination of photogenerated electrons and holes in CuS to further enhance the competitive capacity of CuS. The sandwichlike structure has a steric hindrance effect. Therefore, the S2@Au-rGO-CuS has a multiple signal amplification function for thrombin determination. Under optimal conditions, the PEC aptasensor exhibited a wide linear concentration range from 0.1 pM to 10 nM with a low detection limit of 30 fM (S/ N  = 3) for thrombin. Besides, the designed aptasensor performed well in the assay of human serum sample, indicating good potential for the determination of thrombin in real samples. Graphical abstract

研究领域: 生物化学 · 分析化学 · 医学检测
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CERAMICS INTERNATIONAL · 2018 · IF 3.057

V2O3/rGO composite as a potential anode material for lithium ion batteries

Bin Xiao,Bao Zhang,Lin-bo Tang,Chang-sheng An,Zhen-jiang He,Hui Tong,Wan-jing Yu,Jun-chao Zheng

V 2 O 3 is a promising anode material and has attracted the interests of researchers because of its high theoretical capacity of 1070 mAh g −1 , low discharge potential, inexpensiveness, abundant sources, and environmental friendliness. However, the development and application of V 2 O 3 have been hindered by the low conductivity and drastic volume change of V 2 O 3 composites. In this work, V 2 O 3 /reduced graphene oxide (rGO) nanocomposites are successfully prepared through a facile solvothermal method and annealing process. In this synthesis protocol, V 2 O 3 nanoparticles (NPs) are encapsulated by rGO. This unique structure enables rGO to inhibit volume changes and improve the ion and electronic conductivity of V 2 O 3 . In addition, V 2 O 3 NPs, which exhibit sizes of 5–40 nm, are uniformly dispersed on rGO sheets without aggregation. The Li + storage behavior of V 2 O 3 /rGO is systematically investigated in the potential range 0.01–3.0 V. The V 2 O 3 /rGO nanocomposite can achieve a high reversible specific capacity of 823.4 mAh g −1 under the current density of 0.1 A g −1 , and 407.3 mAh g −1 under the high current density of 4.0 A g −1 . The results of this study provide insight into the fabrication of rGO-based functional materials with extensive applications.

CAS / MDL: 107-21-1
研究领域: 材料科学 · 能源存储
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Heliyon · 2024 · IF 3.4

Fabrication of rGO/BiOI photocathode and its catalytic performance in the degradation of 4-Fluoroaniline

Chenhan Lv,Haixiang Cheng,Rui Fan,Jingyu Sun,Xinghai Liu,Yinghui Ji

Organic fluorine compounds are acute carcinogenic and mutagenic to humans. Photoelectrocatalysis (PEC) treatment is an innovative technology in the field of the removal of fluorine compounds, and thus current research focused on improving stability and catalytic ability of photoanode. In this study, it has been synthesized a rGO/BiOI photocathode for the efficient degradation of 4-Fluoroaniline (4-FA). The physical characterization and photoelectrochemical properties of the photocathode was determined. The results indicate that the PEC treatment with the rGO/BiOI photocathode was more efficient compared with individual processes. During the optimization experiments, the PEC treatment achieved 99.58 % and 72.12 % of 4-FA degradation and defluorination within 1 h. Cyclic stability experiments show that rGO/BiOI photocathode was efficient and stable, which reached 96.91 % and 67.64 % of 4-FA degradation and defluorination after five cycles. Mechanism analysis indicates that the PEC process was based on an electrochemical reaction and photo-induced processes. The degradation product of 4-FA was mainly 2,4-di-t-butylphenol, and trapping experiments indicates that h + is the primary oxidizing species. Therefore, PEC treatment with rGO/BiOI photocathode is a competitive green approach to remove fluorine compounds pollutants and brings new insights into development of PEC treatment.

研究领域: 环境科学 · 材料科学
✓ 已验证 DOI PubMed 高影响因子
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ChemistrySelect · 2024 ·Vol. 9 ·期 9 ·e202302529 · IF 1.9

Preparation of nZVI/MCM-41/rGO for Adsorption of Nickel Ions from Water

Mingyue Piao,Xue Peng,Hao Liu,Wei Zhang,Honghui Teng

Graphical nZVI/MCM-41/rGO is designed for improving the properties of nZVI, and the results show that it has an apparent Fe(0) crystallinity and modest rGO crystallinity, as well as a rough and porous structure. There are many oxygen-containing groups found on the surface of nZVI/MCM-41/rGO, such as −OH, −COOH, and Si−O. The pore diameter is concentrated at 23.82 nm, and the specific surface area is 15.94 cm 2 /g. The best performance is occurred at pH 6, C 0 =80 mg/L with a 2 g/L adsorbent dosage, and after 180 min, a maximum adsorption capacity of 41.82 mg/g is reached at 333 K. The Dubinin-Radushkevich isotherm and second order kinetic models fit the Ni(II) adsorption process well. It is determined through analysis of the thermodynamic parameters that the adsorption progress is endothermic (ΔH 0 >0) and spontaneous (ΔG 0 <0). nZVI/MCM-41/rGO has proven to be an effective and alternative material for the removal of Ni(II) ions from aqueous media due to its excellent removal ability, availability, and low cost. Emissions of nickel (Ni) are harmful to the environment and people‘s health. Although nano zero-valent iron (nZVI) has a lot of potential for treating water pollution, its instability and tendency for aggregation have limited its application. In order to improve its properties, composite adsorbent MCM-41/rGO supported nZVI (nZVI/MCM-41/rGO) is designed for improving the properties of nZVI, and it is characterized by SEM, XRD, FTIR and BET. The results show that it has an apparent Fe (0) crystallinity and modest rGO crystallinity, as well as a rough and porous structure. There are many oxygen-containing groups found on the surface of nZVI/MCM-41/rGO, such as −OH, −COOH, and Si−O. The pore diameter is concentrated at 23.82 nm, and the specific surface area is 15.94 cm 2 /g. The consequences of several parameters such as contact time, initial metal ion concentration, adsorbent dosage, and pH for adsorption efficiency were investigated. The best performance is occurred at pH 6, C 0 =80 mg/L with a 2 g/L adsorbent dosage, and after 180 min, a maximum adsorption capacity of 41.82 mg/g is reached at 333 K. The Dubinin-Radushkevich isotherm and second order kinetic models fit the Ni(II) adsorption process well. It is determined through analysis of the thermodynamic parameters that the adsorption progress is endothermic ( ΔH 0 >0) and spontaneous ( ΔG 0 <0). nZVI/MCM-41/rGO has proven to be an effective and alternative material for the removal of Ni(II) ions from aqueous media due to its excellent removal ability, availability, and low cost.

研究领域: 环境科学 · 材料科学
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JOURNAL OF APPLIED POLYMER SCIENCE · 2019 ·Vol. 137 ·期 15 ·48564 · IF 2.188

Fe3O4@rGO hybrids intercalated nanocellulose-based aerogels for enhanced ferromagnetic and mechanical properties

Yunyun Yu,Yanlai Wang,Penghu Deng,Tonghua Zhang

This work presented a new method for preparing cellulose nanofibril (CNF)/Fe 3 O 4 @rGO composite aerogels with enhanced magnetic and mechanical properties. The composite aerogels were obtained through compounding, gelling, washing, tert -butanol replacing, and freeze-drying. The structural characteristics of composite aerogels were investigated via scanning electron microscopy, Fourier transform infrared, and X-ray diffraction. Results showed that the composite aerogels had interconnected three-dimensional porous network microstructures, and the Fe 3 O 4 @rGO hybrids were uniformly dispersed in the aerogels. Moreover, the aerogels' magnetization and compression characteristics were also studied. Magnetic measurements indicated that composite aerogels had good magnetization characteristics with the saturation magnetization value of 6.75 emu/g. The uniaxial compression tests showed that the compression strength and Young's modulus of the composite aerogels were significantly improved by 32.33 and 118.56%, respectively, relative to those of CNF aerogels. The perfect combination of structure and performance may render the composite aerogels useful for commercial applications in the fields of environmental engineering, biomedical engineering, electronics, and energy. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137 , 48564.

CAS / MDL: 7681-52-9 2564-83-2
研究领域: 材料科学 · 环境工程 · 生物医学工程
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