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ELECTROCHIMICA ACTA · 2020 · IF 6.215

Boron nitride quantum dots as electrochemiluminescence coreactants of rGO@Au@Ru–SiO2 for label-free detection of AFP in human serum

Dongmiao Qin,Xiaohua Jiang,Guichun Mo,Jinsu Feng,Biyang Deng

A label-free electrochemiluminescence (ECL) immunosensor is developed to detect alpha-fetoprotein (AFP). Ru (bpy) 3 2+ -doped silica nanoparticles (Ru–SiO 2 ) and gold nanoparticle-modified reduced graphene oxide (rGO@Au) are integrated to form an rGO@Au@Ru–SiO 2 composite. The composite is employed as a carrier for immobilizing the target antibody, and a label-free ECL immunosensor is constructed via antigen–antibody interaction. Owing to the numerous Ru (bpy) 3 2+ molecules in the Ru–SiO 2 , a high ECL signal is acquired. With excellent conductivity and a large surface area, the rGO@Au composite not only accelerates electron transfer but also improved the ECL signal and captures antibodies, thus enhancing ECL response and sensitivity. Moreover, boron nitride quantum dots (BNQDs) are used as rGO@Au@Ru–SiO 2 coreactants, achieving high ECL intensity. The proposed ECL system exhibits significant potential in bioanalysis , which is attributed to the excellent biocompatibility and good stability of BNQDs. Under optimal experimental conditions, the sensor has a linear range of 0.0001 ng mL −1 to 100 ng mL −1 and a limit of detection equal to 0.03 pg mL −1 (S/N = 3). The proposed technique is successfully applied in the susceptible detection of AFP in human serum. The recovery ranges from 99% to 100%, and the RSD is less than 2.8%. The constructed ECL immunosensor exhibits acceptable performance during actual application.

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JOURNAL OF HAZARDOUS MATERIALS · 2018 · IF 6.434

Enhanced catalytic degradation by using RGO-Ce/WO3 nanosheets modified CF as electro-Fenton cathode: Influence factors, reaction mechanism and pathways

Xueyue Mi,Jingjing Han,Yan Sun,Yi Li,Wenping Hu,Sihui Zhan

Development of an efficient cathode in advanced oxidation process is an important challenge. In this work, we synthesized a low-cost, high-catalytic-active and stable reduced graphene oxide (RGO)-Ce/WO 3 nanosheets (RCW) to modify carbon felt (CF) as cathode to degrade ciprofloxacin (CIP) in electro-Fenton process. Compared to traditional heterogeneous electro-Fenton process, carbon black was substituted by RGO and poly tetra fluoroethylene was avoided to be used as binder. We found that RCW/CF cathode reached about 100% degradation efficiency of CIP after 1 h and 98.55% mineralization degree after 8 h. Meanwhile, it had a very high current density, about 2.5 times that of CF. RCW/CF cathode produced more O 2 − , H 2 O 2 and OH via one-electron reduction process (O 2 → O 2 - →H 2 O 2 ). The modified cathode kept a stable performance for high CIP degradation efficiency during 5 cycles. The introduction of RGO could promote electron transfer, and the adding of Ce into the WO 3 lattice provided superior conditions for the adsorption and activation of oxygen molecules, thus promoting the formation of active oxygen species on the surface of RCW. This novel RCW/CF composite is an efficient and promising electrode for removal of CIP in the wastewater.

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JOURNAL OF MATERIALS SCIENCE · 2018 ·Vol. 53 ·期 16 ·11607-11619 · IF 2.993

Self-assembly and performances of wrinkled rGO@carbon fiber with embedded SnO2 nanoparticles as anode materials for structural lithium-ion battery

Li Huagen,Wang Shubin,Feng Mengjie,Yang Jiping,Zhang Boming

To meet the requirements for the mechanical and electrochemical performance for carbon fiber-based (CF-based) composite electrode materials in the structural lithium-ion batteries application, better CF-based composite is urgently needed. Herein, we report a novel hierarchical structure formed by wrinkled reduced graphene oxide/tin oxide (rGO/SnO 2 ) coating wrapping on the surface of CF for the first time via a facile self-assembly approach and subsequent annealing treatment. Although the mass ratio of rGO/SnO 2 coating in this composite is only about 12.8%, it exhibits excellent tensile strength which is up to 5.01 GPa and cycling stability including a high reversible capacity of 369 mAh g −1 at 100 mA g −1 , which increases 230% than that of the CF. Besides, the morphology of this composite after 100 cycles is firstly observed to further confirm it still maintains a layered and fibrous structure. The excellent properties may benefit from the design of hierarchical hybrid rGO/SnO 2 coating and the synergistic effects of SnO 2 , rGO and CF.

CAS / MDL: 7782-42-5 26062-79-3
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APPLIED ORGANOMETALLIC CHEMISTRY · 2018 ·Vol. 32 ·期 8 ·e4428 · IF 3.581

Amorphizing of Ag Nanoparticles under Bioinspired One-step Assembly of Fe3O4-Ag/rGO Hybrids via Self-redox Process with Enhanced Activity

Songfang Zhao,Haobo Jiang,Jinhui Li,Xiangying Meng,Tianyu Chao,Zhe Zhang,Peng Zhang,Yongju Gao,Duxia Cao

Efficient and reusable nanocatalysts fabricated via a facile assembly are highly desirable for the cost-effective hydrogenation reduction. Inspired by a fishing process with a fishnet, multifunctional nanostructured catalysts are rationally designed to combine interesting features via the self-redox assembly of Fe 3 O 4 -Ag composites on reduced graphene oxide (rGO) (Fe 3 O 4 -Ag/rGO). In detail, Fe 3 O 4 nanoparticles (NPs) endow the ternary hybrids with superparamagnetism (21.42 emu g −1 ), facilitating catalysts to be separated from the reaction system. rGO could provide electron transfer pathways, enhancing catalytic activity. More interestingly, GO and Ag + could behave as oxidants to oxidize Fe 2+ for the in situ assembly of Fe 3 O 4 -Ag/rGO without any addition of reductant/oxidant or organic solvents, and AgNPs endow the ternary hybrids with excellent catalytic behaviour. Meaningfully, the bioinspired process enables the ternary hybrids to possess more abundant micro−/nanopores, larger surface area, and more amorphization. They exhibit exceptional catalytic performance, and could be recycled with excellent activity by means of convenient magnetic separation (at least 7 times). Moreover, the ternary hybrids could degrade methylene blue under UV light due to different valence states of Fe in Fe 3 O 4 . Therefore, the proposed bioinspired assembly and structure design for hierarchical catalysts would pave a promising way to assemble other catalysts.

CAS / MDL: 7782-42-5
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NANO · 2018 · IF 1.1

Wrinkled rGO Sheets-Wrapped Carbon Fibers with High Tensile Strength and Excellent Electrochemical Stability as Anodes for Structural Li-Ion Battery

Huagen Li,Shubin Wang,Mengjie Feng,Jiping Yang,Boming Zhang

Herein, we report a hierarchical structure formed by wrinkled reduced graphene oxide (rGO) sheets-wrapped carbon fiber via a facile and efficient electrostatic self-assembly method and subsequent annealing treatment. For this material, the Weibull scale parameter is 4.77 GPa. After 100 cycles, the rGO@CF retains 91% of its second charge capacity at 50 mA ⋅g −1 , corresponding to a capacity fading of only 0.09% per cycle. Thus, this structural anode material exhibits enhanced capacity, high initial Coulombic efficiency and high tensile strength. Meanwhile, the carbon fiber and interweaved rGO sheets together form the whole conductive networks to provide multichannel highways for charge transfer (lithium-ion diffusion and electron transport) during discharge–charge processes, promising excellent electrochemical performance of this structural anode material.

CAS / MDL: 7782-42-5 26062-79-3
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ACS Applied Materials & Interfaces · 2014 · IF 5.9

Novel and Facile Method, Dynamic Self-Assemble, To Prepare SnO2/rGO Droplet Aerogel with Complex Morphologies and Their Application in Supercapacitors

Mingxi Chen,Huan Wang,Lingzhi Li,Zhe Zhang,Cong Wang,Yu Liu,Wei Wang,Jianping Gao

A facile and novel method to prepare SnO2/reduced graphene oxide (rGO) droplet aerogels with complex morphologies had been developed. This method has been named dynamic self-assemble. Aerogels with both “egg-tart” and “mushroom” shapes were obtained by this method. The changes in the graphene oxide (GO) droplet morphologies during the dynamic process of a GO droplet falling into a SnCl2 target solution were monitored using a high speed camera. The formed SnO2/rGO aerogels were then characterized by Raman spectroscopy, thermogravimetric analysis, X-ray diffraction analysis, and X-ray photoelectron spectroscopy. The microstructures of the SnO2/rGO aerogels were observed with scanning electron microscopy and transmission electron microscopy. Finally, the SnO2/rGO droplet aerogels were used as the electrode material in a symmetrical two-electrode supercapacitor and the electrochemical performance of the supercapacitor was investigated using cyclic voltammetry and galvanostatic charge/discharge methods. The SnO2/rGO electrodes demonstrated excellent electrochemical performance and stability. At a scan rate of 5 mV/s, their highest gravimetric and volumetric specific capacitances were 310 F/g and 180 F/cm3, respectively, and their energy and power densities were as high as 30 Wh·kg–1 and 8.3 kW·kg–1, respectively.

CAS / MDL: 7220-79-3 10025-69-1
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ACS Applied Materials & Interfaces · 2016 · IF 7.145

A Facile Electrophoretic Deposition Route to the Fe3O4/CNTs/rGO Composite Electrode as a Binder-Free Anode for Lithium Ion Battery

Yang Yang,Jiaqi Li,Dingqiong Chen,Jinbao Zhao

Fe3O4 is regarded as an attractive anode material for lithium ion batteries (LIBs) due to its high theoretical capacity, natural abundance, and low cost. However, the poor cyclic performance resulting from the low conductivity and huge volume change during cycling impedes its application. Here we have developed a facile electrophoretic deposition route to fabricate the Fe3O4/CNTs (carbon nanotubes)/rGO (reduced graphene oxide) composite electrode, simultaneously achieving material synthesis and electrode assembling. Even without binders, the adhesion and mechanical firmness of the electrode are strong enough to be used for LIB anode. In this specific structure, Fe3O4 nanoparticles (NPs) interconnected by CNTs are sandwiched by rGO layers to form a robust network with good conductivity. The resulting Fe3O4/CNTs/rGO composite electrode exhibits much improved electrochemical performance (high reversible capacity of 540 mAh g–1 at a very high current density of 10 A g–1, and a remarkable capacity of 1080 mAh g–1 can be maintained after 450 cycles at 1 A g–1) compared with that of commercial Fe3O4 NPs electrode.

CAS / MDL: 74-79-3 7553-56-2
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SENSORS AND ACTUATORS B-CHEMICAL · 2016 · IF 4.758

Flexible paper sensor fabricated via in situ growth of Cu nanoflower on RGO sheets towards amperometrically non-enzymatic detection of glucose

Bin Wang,Yuanya Wu,Yanfen Chen,Bo Weng,Changming Li

A flexible free-standing paper sensor was fabricated for the first time via in situ growth of Cu nanoflower on reduced graphene oxide (RGO) sheets towards amperometrically non-enzymatic detection of glucose. The low cost of copper (Cu) and graphene made the prepared sensor inexpensive in comparison with sensors made from noble metal catalysts . This Cu-RGO paper sensor exhibited high sensitivity and good selectivity when utilised in glucose sensing attributed to the synergistic effects of graphene paper and Cu nanoflowers. The combination of excellent catalytic activity , largely reactive surface area of Cu nanoflower and good conductivity of graphene paper enabled the sensor to perform well in glucose detection. The prepared glucose sensor holds a great promise for inexpensive flexible electrochemical non-enzymatic glucose sensors.

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FOOD CHEMISTRY · 2024 · IF 8.5

Construction of a self–reporting molecularly–imprinted electrochemical sensor based on CuHCF modified by rGNR–rGO for the detection of zearalenone

Binbin Zhou,Hao Xie,Xinyi Li,Yongbo Zhu,Lijun Huang,Ming Zhong,Liang Chen

A self–reporting molecularly–imprinted electrochemical sensor is prepared for the detection of Zearalenone (ZEA). Firstly, the reduced graphene nanoribbons and reduced graphene oxide (rGNR–rGO) were simultaneously modified onto a glassy carbon electrode (GCE) to improve the sensor's sensitivity. After electrodepositing copper nanoparticles onto the rGNR–rGO/GCE, cyclic voltammetry scanning was performed in potassium ferrocyanide solution, and copper hexacyanoferrate (CuHCF) was deposited onto rGNR–rGO/GCE to further improve the sensor's sensitivity while giving it self–reporting capability. Then, molecularly–imprinted polymer films were prepared on the CuHCF/rGNR–rGO/GCE to ensure the selectivity of the sensor. It is found that the linear range of ZEA detection by the constructed sensor is 0.25–500 ng·mL −1 , with a detection limit of 0.09 ng·mL −1 . This sensor shows the merits of good selectivity, high sensitivity and accurate detection, providing a great possibility for the precise detection of low concentration ZEA in food.

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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Composite of CoS1.97 nanoparticles decorated CuS hollow cubes with rGO as thin film electrode for high-performance all solid flexible supercapacitors

Zhihan Yang,Maozhuang Zhang,Yawen Liu,Mingyuan Jiang,Yuesheng Sun,Jianhua Wang,Jiangtao Xu,Jingquan Liu

Stretchable flexible thin-film electrodes are extensively explored for developing new wearable energy storage devices. However, traditional carbon-based materials used in such independent electrodes have limited practical applications owing to their low energy storage capacity and energy density. To address this, a unique structure and remarkable mechanical stability thin-film flexible positive electrode comprising CoS 1.97 nanoparticles decorated hollow CuS cubes and reduced graphene oxide (rGO), hereinafter referred to as CCSrGO, is prepared. Transition metal sulfide CoS 1.97 and CuS shows high energy density owing to the synergistic effects of its active components. The electrode can simultaneously meet the high-energy density and safety requirements of new wearable energy storage devices. The electrode has excellent electrochemical performance (1380 F/g at 1 A/g) and ideal capacitance retention (93.8 % after 10,000 cycles) owing to its unique three-dimensional hollow structure and polymetallic synergies between copper and cobalt elements, which are attributed to their different energy storage mechanisms. Furthermore, a flexible asymmetric supercapacitor (FASC) was constructed using CCSrGO as the positive electrode and rGO as the negative electrode (CCSrGO//rGO), which delivers an energy density of 100 Wh kg −1 and a corresponding power density of 2663 W kg −1 within a voltage window of 0–1.5 V. The resulting FASC can power a light-emitting diode (LED) at different bending and twisting angles, exerting little effect on the capacitance. Therefore, the prepared CCSrGO//rGO FASC devices show great application prospects in energy storage.

CAS / MDL: 1313-82-2
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CHEMICAL ENGINEERING JOURNAL · 2024 · IF 13.3

Construction of wetting resistance surface of highly hydrophobic PVDF-HFP/rGO coated supported PVDF hollow fiber composite membrane for membrane distillation

Mohammed Karama Alsebaeai,Abdul Latif Ahmad,Boon Seng Ooi

In this research, the construction of a highly wetting-resistance membrane surface was achieved through an integrated dip-coating phase inversion process to accelerate water mass transfer of membrane distillation (MD). The synergistic effect of incorporating reduced graphene oxide (rGO) embedded Poly (vinylidene fluoride- co -hexafluoropropylene) (PVDF-HFP) on the surface of a PVDF hollow fiber support membrane using a dilute coating solution was studied. Various loadings of rGO nanosheets were incorporated into the dilute PVDF-HFP coating to systematically investigate its physicochemical characteristics, including surface morphology, hydrophobicity and wetting resistance which could be analyzed using scanning electron microscopy (SEM), atomic force microscopes (AFM), water contact angle (WCA), porosity measurement, pore size, x-ray diffraction (XRD), and liquid entry pressure (LEP) tests. The membrane separation performance for desalination was evaluated using direct contact membrane distillation (DCMD) process. Compared to the PVDF hollow fiber support membrane, the rGO-embedded PVDF-HFP coating layer demonstrates outstanding enhancements. The membrane surface exhibits enhanced hydrophobicity, as evidenced by an increased WCA from 105.37° (for the PVDF support membrane) to 148.37° (for the rGO/PVDF-HFP composite membrane). Additionally, the water permeability significantly improved, achieving a water flux of 25.9 kg m -2 h -1 (compared to 11.55 kg m -2 h -1 for the PVDF support membrane). These enhancements occur without compromising NaCl rejection, which remains consistently above 99.99 % (3.5 wt% NaCl aqueous solution at a feed temperature of 70 °C and a permeate temperature of 18 °C). These findings underscore the potential of rGO/PVDF-HFP in enhancing MD performance. The composite HF membrane demonstrates remarkable stability during continuous MD operation over a 48 h period. Pore wetting is effectively avoided, indicating that the composite membrane has superior resistance to wetting and excellent stability.

CAS / MDL: 112945-52-5
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DIAMOND AND RELATED MATERIALS · 2024 · IF 4.3

Fabrication of β-CD/SiO2@rGO/MXenes composite materials with three-dimensional structures for sensitive detection of baicalin in Chinese medicine

YuXuan Xiong,Dandan Luo,Guowen He,Saiwen Liu,Jin Zhang,Chao Chen

Baicalin is a principal component of traditional Chinese medicine and plays a crucial role in treating conditions such as arthritis, respiratory tract infections, chronic and acute hepatitis, and tumors. Graphene oxide is bonded to silicon dioxide (SiO 2 ) through covalent bonds or hydrogen bonds and then reduced to SiO 2 @rGO through hydrazine hydrate to solve the problem of easy accumulation of SiO 2 and improve the conductivity of the material. Next, β-cyclodextrin (β-CD) self-assembles on SiO 2 @rGO to form a stable inclusion complex. The hydrophobic inner cavity of β-CD can effectively accommodate various guest molecules to form inclusion complexes, enhancing molecular recognition and detection capabilities. Finally, β-CD/SiO 2 @rGO is bridged and surface-loaded between clay-like Ti 3 C 2 T x (MXenes) nanosheets through electrostatic interactions to form a stable three-dimensional composite material. It is precisely because of MXenes, due to their unique layered microstructure, excellent conductivity, and extensive hydrophilic surface area, that they are conducive to self-assembly or embedding nanoparticles in aqueous solution. The composite was characterized via X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy. Under optimized conditions, the electrochemical sensor constructed from this composite exhibited a broad detection range (0.008–10 μM) and a low detection limit (0.191 nM) for baicalin. In comparison to existing methods for detecting baicalin, this approach demonstrates strong anti-interference capabilities and stability. It can efficiently, sensitively, and accurately quantify baicalin in Chinese patent medicine samples, including Scutellaria baicalensis root, Shuanghuanglian oral liquid, and Bear Bile Scutellaria baicalensis eye drops, achieving a satisfactory recovery rate. This study introduces a novel approach for the electrochemical detection of baicalin.

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