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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

Metal-ion bridged high conductive RGO-M-MoS2 (M = Fe3+, Co2+, Ni2+, Cu2+ and Zn2+) composite electrocatalysts for photo-assisted hydrogen evolution

Riyue Ge,Wenxian Li,Juanjuan Huo,Ting Liao,Ningyan Cheng,Yi Du,Mingyuan Zhu,Ying Li,Jiujun Zhang

Efficient photo-electrocatalysts for hydrogen evolution reaction (HER) are synthesized using a facile one-step hydrothermal method. With metal-ion bridges, highly dispersed molybdenum disulfide (MoS 2 ) nanolayers are vertically grown on the reduced graphene oxide (RGO) to form RGO-M-MoS 2 photocatalysts for HER, where M = Fe 3+ , Co 2+ , Ni 2+ , Cu 2+ and Zn 2+ . The results show that the cross-bridging ions can modulate the MoS 2 growth priority and act as efficient charge transfer channels between RGO and MoS 2 , and combine the advantages of the high conductivity of graphene with the photo-electrochemical activity of MoS 2 . The metal-ion bridged MoS 2 -M-RGO heterostructures demonstrate superior catalytic activity toward hydrogen evolution reaction in acid medium, evidenced by the remarkable higher catalytic current density at low overpotential compared with that of MoS 2 -RGO without metal-ion bridge. This study provides a novel and facile route for establishing efficient composite photo-electrocatalysts for water splitting to generate hydrogen.

CAS / MDL: 12054-85-2 62-56-6
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SENSORS AND ACTUATORS B-CHEMICAL · 2019 · IF 6.393

Direct growth of 3D porous (Ni-Co)3S4 nanosheets arrays on rGO-PEDOT hybrid film for high performance non-enzymatic glucose sensing

Alan Meng,Xiangcheng Yuan,Zhenjiang Li,Kun Zhao,Liying Sheng,Qingdang Li

A binder-free, rapid and low-cost electrodeposition technology for growing 3D porous (Ni-Co) 3 S 4 nanosheets arrays on glassy carbon electrode (GCE) functionalized by reduced graphene oxide-poly (3,4-ethylenedioxythiophene) (rGO-PEDOT) hybrid film is successfully developed to construct a sensor for non-enzymatic glucose sensing. The main experimental variables affected on the electrochemical performance are optimized. Benefiting from the synergistic effect of the new active material system, the unique morphology and the strong combination among (Ni-Co) 3 S 4 , rGO-PEDOT and bare electrode, the sensor constructed under the optimal conditions manifests wide detection range (1–5000 μM), highly sensitivity (938.4 μA mM −1  cm −2 ), rapid response (<1.5 s) and low detection limit (0.503 μM). Additionally, the sensor exhibits outstanding selectivity, stability and reproducibility. Significantly, the detection results of the sensor for glucose in human blood serum are well consistent with that in hospital. This research work opens an attractive strategy to construct nanocomposites, and provide a new insight into the development of the non-enzymatic glucose biosensor with high performance.

CAS / MDL: 126213-50-1 56570-89-9
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ACS Applied Materials & Interfaces · 2017 · IF 7.504

Nanosheet Array-Like Palladium-Catalysts Pdx/rGO@CoAl-LDH via Lattice Atomic-Confined in Situ Reduction for Highly Efficient Heck Coupling Reaction

Yanna Wang,Liguang Dou,Hui Zhang

A series of novel nanosheet array-like catalysts Pdx/rGO@CoAl-LDH (x = 0.0098–1.9, refers to Pd loading in wt % on ICP, rGO: reduced graphene oxide, LDH: layered double hydroxide) were first prepared via a simple and green lattice atomic-confined in situ reduction of oxidative Pd precursors by the evenly atomic-dispersed reductive Co2+ sites on LDH layers of a nanohybrid rGO@CoAl-LDH with hexagonal LDH nanoplates (∼73 × 7 nm) interdigitated vertical to the surfaces of rGO layer in both sides, fabricated through a simple citric acid-assisted aqueous-phase coprecipitation method. The as-obtained Pd catalysts possess clean Pd nanoclusters (NCs) with tunable sizes in 1.3–1.8 nm on varied Pd loadings. All the Pdx/rGO@CoAl-LDH catalysts show excellent activities for the Heck reaction, and the Pd0.0098/rGO@CoAl-LDH with the ultrafine Pd NCs of 1.3 ± 0.2 nm yields a maximum turnover frequency of 160 000 h–1 over a heterogeneous catalyst so far. The excellent activities can be attributed to the ultrasmall Pd NCs with high dispersion and clean Pd surfaces, increased electron transfer capacity and surface area, and remarkable Pd–CoAl-LDH—rGO three-phase synergistic effect of the present unique nanosheet array-like Pd NCs catalysts. Moreover, the catalyst Pd0.33/rGO@CoAl-LDH shows a broad range of substrate applicability and can be reused more than five runs without obvious loss of activity, giving the present catalysts long-term stability. These findings make the rGO@CoAl-LDH hybrid prepared by a facile and scalable synthesis route a universal green platform to support other noble or nonprecious metal NCs via lattice atomic-confined in situ reduction strategy to construct more desired heterogeneous catalysts.

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PLoS One · 2016 ·Vol. 11 ·期 10 ·e0164657 · IF 3.057

Fabrication of (Co,Mn)3O4/rGO Composite for Lithium Ion Battery Anode by a One-Step Hydrothermal Process with H2O2 as Additive

Zuohua Li,Yanhui Cui,Jun Chen,Lianlin Deng,Junwei Wu

Binary transition metal oxides have been regarded as one of the most promising candidates for high-performance electrodes in energy storage devices, since they can offer high electrochemical activity and high capacity. Rational designing nanosized metal oxide/carbon composite architectures has been proven to be an effective way to improve the electrochemical performance. In this work, the (Co,Mn) 3 O 4 spinel was synthesized and anchored on reduced graphene oxide (rGO) nanosheets using a facile and single hydrothermal step with H 2 O 2 as additive, no further additional calcination required. Analysis showed that this method gives a mixed spinel, i.e. (Co,Mn) 3 O 4 , having 2 + and 3 + Co and Mn ions in both the octahedral and tetrahedral sites of the spinel structure, with a nanocubic morphology roughly 20 nm in size. The nanocubes are bound onto the rGO nanosheet uniformly in a single hydrothermal process, then the as-prepared (Co,Mn) 3 O 4 /rGO composite was characterized as the anode materials for Li-ion battery (LIB). It can deliver 1130.6 mAh g -1 at current density of 100 mA g -1 with 98% of coulombic efficiency after 140 cycles. At 1000 mA g -1 , the capacity can still maintain 750 mAh g -1 , demonstrating excellent rate capabilities. Therefore, the one-step process is a facile and promising method to fabricate metal oxide/rGO composite materials for energy storage applications.

CAS / MDL: 872-36-6
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Advanced Science · 2025 · IF 14.1

“Antenna Effect”-Enhanced AuNPs@rGO Photothermal Coating Promotes 3D Printing of Osteogenic Active Scaffolds to Repair Bone Defects after Malignant Tumor Surgery

Xinyu Xu,Hao Wang,Xiaohan Mei,Dapeng Zeng,Zehao Yu,Shibo Liu,Ruiyan Li,Yanguo Qin

Malignant bone tumor defects are difficult to treat because of the simultaneous need for tumor treatment and bone-repair promotion. This study presents a bioactive composite scaffold (T-rGO@Au) for personalized bone defect repair and bone tumor treatment. The T-rGO@Au scaffold has a porous structure, and its mechanical properties are close to those of human cancellous bone. The T-rGO@Au scaffold can induce upregulation of osteopontin (OPN), RUNX-2, and osteocalcin (OCN) gene expression. In vivo experiments showed that the bone volume/total volume (BV/TV) ratio with the T-rGO@Au scaffold was the highest. The new bone was tightly integrated with the implant, demonstrating effective osseointegration. The T-rGO@Au scaffold locally generated high temperatures and reactive oxygen species under near-infrared excitation, and AuNPs enhanced the photothermal performance of rGO through the “antenna effect.” Furthermore, in vitro experiments showed that the tumor cell nuclei were destroyed, late-stage apoptotic cells increased, and cell morphology was severely damaged. Additionally, RNA-seq revealed that tumor cell destruction was mediated through signaling pathways, such as the MAPK pathway. In vivo antitumor experiments also demonstrated that the T-rGO@Au scaffold significantly inhibited the growth of tumor cells within 2 weeks. Thus, the T-rGO@Au scaffold provides a new treatment strategy for the development of implantable scaffolds for bone tumor defects.

✓ 已验证 产品关联 DOI PubMed 高影响因子
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ADVANCED FUNCTIONAL MATERIALS · 2024 · IF 18.5

Tuning the Multilevel Hierarchical Microarchitecture of MXene/rGO-Based Aerogels Through a Magnetic Field-Guided Strategy Toward Stepwise Enhanced Electromagnetic Wave Dissipation

Yang Yang,Zheng Xiu,Fei Pan,Hongsheng Liang,Haojie Jiang,Hongtao Guo,Xiao Wang,Lixin Li,Bin Yuan,Wei Lu

Hierarchical microarchitecture engineering is a state-of-the-art approach to designing aerogel electromagnetic (EM) wave absorbers, offering huge potential in improving EM energy dissipation. However, the intrinsic feedback mechanism regarding the specific influence of each microarchitecture parameter on EM properties is not comprehensively revealed, making it challenging to fully utilize the potential of aerogels to achieve superior EM wave absorption performance. Herein, a range of MXene/rGO-based aerogels with multilevel hierarchical configurations are fabricated by a magnetic field-guided strategy. Leveraging growth thermodynamics effects under a magnetic field and bridging effect between adjacent rGO units, three hierarchical microarchitecture models (lamellae ordering, interlayer spacing, and layer thickness) are constructed in aerogels. Remarkably, three models progressively improve reflection loss ( RL ), effective absorption bandwidth (EAB), and matching thickness by enhancing dielectric loss, decoupling attenuation-impedance matching, and adjusting power loss density, respectively. Consequently, the MXene/rGO-based aerogels exhibit stepwise enhancement in EM wave performance, achieving a superior RL of −64.6 dB and a broad EAB of 7.0 GHz at 1.8 mm thickness, surpassing alternative aerogels with other configurations. This work elucidates the effect of multilevel hierarchical microarchitecture on the synergistic multi-effect dissipation mechanism of EM waves in aerogels, providing insights for designing advanced EM absorbers through diverse strategies.

CAS / MDL: 7789-24-4
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2021 · IF 19.503

Non-covalent self-assembly synthesis of AQ2S@rGO nanocomposite for the degradation of sulfadiazine under solar irradiation: The indispensable effect of chloride

Cheng-Xin Chen,Shan-Shan Yang,Jie Ding,Guang-Yuan Wang,Le Zhong,Shuang-Yang Zhao,Ya-Ni Zang,Jun-Qiu Jiang,Lan Ding,Yan Zhao,Lu-Ming Liu,Nan-Qi Ren

In this study, the effect of chloride ion (Cl − ) on the degradation of sulfadiazine (SDZ) was evaluated using reduced graphene oxide (rGO) modified with sodium anthraquinone-2-sulfonate (AQ2S) photocatalyst ( [email protected] ), which was prepared in a one-pot hydrothermal synthesis. AQ2S molecules are small organic photoactive components, that are intercalated and immobilized on the rGO surface through noncovalent π-π stacking. Under solar light, SDZ effectively underwent 99 % photodegradation within 150 min in a Cl − -rich solution (0.5 mol/L). The [email protected] system exhibited an excellent photocatalytic removal ability for some typical contaminants. SDZ degradation was driven by 3 AQ2S*. Superoxide radicals ( O 2 − ) and dichlorine radicals (Cl 2 − ) were found to be the dominant reactive species, whereas OH and 1 O 2 have minor roles. Density functional theory (DFT) calculations confirmed the interactions between AQ2S and rGO, and the electronic structural characteristics between Cl − and [email protected] The [email protected] composite has great potential for use in treating micropollutants under saline water conditions under solar irradiation.

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OPTICAL MATERIALS · 2019 · IF 2.687

Study of the photocatalytic performance and carrier migration of reduced graphene oxide-modified infrared-responsive photocatalyst β-NaYF4:Yb3+, Er3+@BiOCl-rGO

Yujie Luo,Shiyu Zhou,Yaofang Sun,Deqiang Zhao,Xiaosong Gu,Qiutong Yan,Fangying Ji,Xuan Xu

To further enhance the photocatalytic performance of BiOCl, a facile hydrothermal reduction reaction was used to synthesize the reduced graphene oxide- (rGO-) modified ternary compound photocatalyst β-NaYF 4 :Yb 3+ , Er 3+ @BiOCl-rGO (NYF–Bi-rGO). rGO prepared using a hydrothermal method showed good conductivity . Furthermore, the specific surface area of NYF-Bi-rGO was 20-fold larger than that of NYF, which is a quality that could prove highly advantageous for use in pollutant adsorption. In addition, the ternary photocatalytic system produced by rGO increased the absorption intensity of NYF-Bi in the visible light region, and caused a red-shift of the entire absorption cross-section. In particular, analysis of carrier migration showed the introduction of rGO promoted the separation of the photoelectron-hole pairs of BiOCl, inhibited its recombination and improved the photocatalytic efficiency of the ternary photocatalyst NYF-Bi-rGO.

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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Sodium acetate trihydrate/melamine foam composite PCM encapsulated by CuS/rGO modified epoxy resin and endowed with light-to-heat conversion properties

Henghua Zhang,Qianbin Dong,Yaping Tang,Jialing Wu,Wenjian Bi,Yue Gao,Jiabang Wang,Hui Yang

In this work, we proposed a novel strategy for the conversion and storage of photothermal energy. This strategy combined hydrothermally prepared CuS/rGO with commercial epoxy resin adhesives. The light-capturing capability of CuS and fast electron transfer rate of rGO was harnessed to endow the modified resin with photothermal conversion capability. Using an inorganic PCM as the energy-storage medium and melamine foam as its support carrier, a form-stabilized composite phase-change material with a latent heat of phase change of 233.7 J/g and a phase-change temperature of 48.7 °C was obtained. In addition, the pre-prepared MER was coated onto the surface of the CPCM . Its purpose was to utilize the photothermal conversion and waterproof properties of modified resins to store solar energy in the internal phase-change materials, while alleviating the leakage problem during the phase-change process of inorganic salt hydrate phase-change materials in the past. The leakage tests showed that the 1.0 mm thick MER provided excellent protection against leakage, significantly reducing leakage of the liquid phase and moisture escape. The composite phase-change material CPCM/MER demonstrated satisfactory results in photothermal conversion experiments. 2% CuS/rGO addition to CPCM/MER can complete the phase change. The samples also showed good stability in the cycling tests. After 100 cycles of testing, the latent heat of the CPCM only decreased by 5.13%. According to the FT-IR results, the CPCM also possessed chemical stability. In this study, a CPCM/MER was successfully prepared, extending the practical application of traditional inorganic phase-change materials in the field of solar energy storage.

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POLYMER COMPOSITES · 2025 · IF 4.7

Construction of S-Scheme Heterojunction by TiO2/rGO Assembled With g-C3N4 for Efficient Visible-Light-Driven Antibacterial Activity of Bone Scaffold

Jiye Jia,Shijie Chen,Haifeng Tian,Dong Wang,Feng Yang,Pei Feng,Cijun Shuai

The low photogenerated charge carriers and quick complex annihilation of titanium dioxide (TiO 2 )/rGO composite leading to an unsatisfactory photocatalysis antibacterial effect limit its application in the bone scaffold. Herein, graphitic carbon nitride (g-C 3 N 4 ) was assembled with TiO 2 /rGO via a solvothermal method for enhancing the photocatalysis antibacterial properties of poly (lactic acid) (PLLA) bone scaffold prepared via selective laser sintering. The results revealed that g-C 3 N 4 expanded the light absorption range of TiO 2 /rGO from blue-violet light to visible light, resulting in the composites having a narrower band gap and producing more photoinduced charge carriers. More importantly, an S-scheme heterojunction was formed between g-C 3 N 4 and TiO 2 , which promoted the recombination of the electrons in the conduction band of TiO 2 and the holes in the valence band of g-C 3 N 4 . Meanwhile, rGO with excellent electrical conductivity reduced the interfacial charge transfer resistance and enhanced charge transfer efficiency, thus further avoiding the recombination rate of electrons and holes, whether TiO 2 or g-C 3 N 4 , and enhancing the photocatalytic properties. Consequently, the holes in the valence band of TiO 2 and the electrons in the conduction band of g-C 3 N 4 possessed high oxidation and reduction capacity, which oxidized H 2 O and reduced O 2 in the microenvironment, respectively, and generated lots of reactive oxygen species. In vitro antibacterial experiments indicated that the PLLA/TiO 2 /g-C 3 N 4 /rGO scaffold showed a better antibacterial effect, with the bacteriostasis rates of E. coli and S. aureus being 99.1% and 98.9%, respectively. In addition, cell adhesion and fluorescence results indicated that the scaffold had good biocompatibility and could provide a suitable microenvironment for the growth and proliferation of cells.

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Journal of Biomedical Nanotechnology · 2022 ·Vol. 18 ·期 11 ·2484-2497 · IF 3.641

Novel Colorimetric Aptasensor for the Detection of Golgi Protein 73 by Exploiting the Peroxidase-Like Activity of the H-rGO-Mn3O4 Nanozyme

Li Guiyin,Chen Min,Li Haimei,Li Xinhao,Yao Xiaoqing,Li Liuxun

Golgi protein 73 (GP73) is a novel biomarker for the detection of hepatocellular carcinoma. We prepare a colorimetric aptasensor for GP73 detection based on the catalytic performance of the H-rGO-Mn3O4 nanozyme. The H-rGO-Mn3O4 nanozyme serves as a peroxidase mimetic which can enhance the reaction with the substrate (3, 3,’ 5, 5′-tetramethylbenzidine, TMB) and H2O2. The peroxidase-like activity of H-rGO-Mn3O4 features a 1.78-fold higher binding affinity value (Km ) for TMB compared with that of horseradish peroxidase. The H-rGO-Mn3O4 nanozyme not only exhibits admirable peroxidase-like activities due to the synergistic effect of Mn3O4 NPs, rGO and hemin, but also has a large specific surface area to endow the GP73 aptamer with specific recognition capabilities. A sandwich colorimetric aptasensor is formed to realize the visual detection of GP73 through catalyzing the H2O2-mediated oxidation peroxidase substrate TMB to oxidized TMB accompanied by a color change from colorless to blue. Under optimal conditions, the logarithm of the GP73 concentration (0.05–50.0 ng/mL) shows a good linear relationship with the absorbance. The calibration equation is Y =−0.0383 lgC+0.4835, with R2 of 0.9964, and the lowest limit of detection is 36.94 pg/mL. Additionally, the content of GP73 in human serum samples is directly detected, and the relative standard deviation is 0.49–4.91%. Compared with the enzyme-linked immunosorbent assay method, the relative error is 0.23–3.61%. All in all, colorimetric aptasensor is demonstrated to exhibit excellent specificity, stability, and reproducibility.

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JOURNAL OF PHYSICAL CHEMISTRY A · 2020 · IF 2.6

Catalytic Effects of rGO–MFe2O4 (M = Ni, Co, and Zn) Nanocomposites on the Thermal Decomposition Performance and Mechanism of Energetic FOX-7

Ming Zhang,Fengqi Zhao,Ting An,Yanjing Yang,Hui Li,Qing Pan,Xiaohong Wang,Zhoufeng Jiang

Thermal decomposition performance of the insensitive energetic compound 1,1-diamino-2,2-dintroethene (FOX-7) is essential for its application in the field of solid propellants. This study seeks to reveal the catalytic effects of reduced graphene oxide–bimetallic oxide nanocomposites (rGO–MFe2O4, M = Ni, Co, and Zn) on the thermal decomposition, kinetic parameters, and pyrolysis mechanism of energetic FOX-7. The results showed that the catalytic activities of the bimetallic iron oxide (NiFe2O4, CoFe2O4, and ZnFe2O4) increased obviously after anchoring on the surface of graphene. Particularly, the rGO–NiFe2O4 nanocomposite possessed the best catalytic activity for FOX-7 thermal decomposition. The high thermal decomposition peak temperature (THDP) and the apparent activation energy (Ea) of FOX-7 were decreased by 57.4 °C and 54.27 kJ mol–1 after mixing with the rGO–NiFe2O4 nanocomposite. The excellent catalytic activity of rGO–NiFe2O4 can be attributed to the synergistic interaction between rGO and NiFe2O4, which is beneficial for the reduction of activation energy and a high thermal decomposition peak temperature of FOX-7. This study is helpful for the rational design of a solid propellant containing FOX-7 and to understand the thermal decomposition kinetics and mechanism of FOX-7.

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