Graphene oxide is a derivate of graphene obtained by oxidation of graphite and other carbonaceous materials. The more accepted structure consists in carbonyl and carboxyl groups located at the edge of the graphene network and hydroxyl and epoxy groups attached to the basal plane. The percentage of O-groups depends on the synthesis route and the material used as carbon source. In addition, highly oxidized fragments, called oxidative debris, OD, are produced during the oxidation process. These fragments are adsorbed onto the graphene oxide network and can be removed by alkaline washing. The purified material has lower O/C ratio than graphene oxide and its properties are also quite different. Due to its structure, graphene oxide can be adsorbed at the air-water interface of the aqueous solution by diffusion, Gibbs monolayers, or by spreading on a clean water subphase resulting in a Langmuir film. This review is intended to provide information on the importance of controlling the chemical composition, structure, size, and oxidative debris, on the manufacture of graphene oxide films. To this end the review shows the influence of the synthesis route and the starting material on the structure of graphene oxide and analyzes several examples of the behavior and properties of films prepared with different types of graphene oxides. The great variability of behaviors of graphene oxide films caused by the different structure of this material provides a great opportunity to fine-tune the properties of films according to the needs of different applications.
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http://dx.doi.org/10.1016/j.cis.2020.102312 | DOI Listing |
RSC Adv
January 2025
College of Food Science and Technology, Jiangsu Agri-animal Husbandry Vocational College Taizhou 225300 China
Bacterial infections are a major global health challenge, posing severe risks to human well-being. Although numerous strategies have been developed to combat bacterial pathogens, their practical application is often hindered by operational constraints. Photocatalytic materials have emerged as promising candidates for bacterial disinfection and food preservation due to their efficiency and sustainability.
View Article and Find Full Text PDFNanoscale Horiz
January 2025
Laboratory of Advanced Materials, Shanghai Key Lab of Molecular Catalysis and Innovative Materials, Academy for Engineering & Technology, Advanced Coatings Research Center of Ministry of Education of China, Fudan University, Shanghai 200438, P. R. China.
A porous hedgehog-like CoO/NiO/graphene oxide (denoted as PHCNO/GO) microsphere was prepared by a facile solvothermal method, followed by an annealing treatment under argon atmosphere. Benefiting from the thin CoO/NiO nanosheets with a large specific surface area, abundant pores distributed between the CoO/NiO nanosheets, and GO firmly wrapped around the surface of PHCNO microspheres, the PHCNO/GO microspheres showed excellent lithium storage performance. The CoO/NiO nanosheets provided numerous active sites, achieving a high reversible specific capacity.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Peking University Shenzhen Graduate School, Shool of Chemical Biology and Biotechnology, Lishui Road, Nanshan District, -, Shenzhen, CHINA.
Regulating the coordination environment of active sites has proved powerful for tapping into their catalytic activity and selectivity in homogeneous catalysis, yet the heterogeneous nature of copper single-atom catalysts (SACs) makes it challenging. This work reports a bottom-up approach to construct a SAC (rGO@Cu-N(Hx)-C) by inlaying preformed amine coordinated Cu2+ units into reduced graphene oxide (rGO), permitting molecular level revelation on how the proximal N-site functional groups (N-H or N-CH3) impact on the carbon dioxide reduction reaction (CO2RR). It is demonstrated that the N-H moiety of rGO@Cu-NHx-C can serve as an in-situ protonation agent to accelerate the CO2-to-methane reduction kinetics, delivering a methane current density (163 mA/cm2) 2.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Mechanical Engineering, Hebei University of Technology, Tianjin 300401, P. R. China.
Wirelessly driven flexible actuators are crucial to the development of flexible robotic crawling. However, great challenges still remain for the crawling of flexible actuators in complex environments. Herein, we reported a wireless flexible actuator synergistically driven by wireless power transmission (WPT) technology and near-infrared (NIR) light, which consists of a poly(dimethylsiloxane)-graphene oxide (PDMS-GO) composite layer, eutectic gallium-indium alloy (EGaIn), a PDMS layer, and a polyimide (PI) layer.
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