研究目的
To study the influence of the synthesis method on the electrical storage capacity of graphene-related materials, specifically focusing on their electrochemical properties and physico-chemical characteristics for use in supercapacitors.
研究成果
The multi-step reduction method using ascorbic acid produced AMPRGO with the highest specific capacitance (86.05 F g?1) and best capacitive behavior, making it an ideal candidate for supercapacitor applications due to its ordered structure, low functional oxygen groups, and economical, environmentally friendly synthesis. Reduced materials, particularly AMPRGO, show promise for enhancing energy storage in electrochemical devices.
研究不足
The reduction methods did not completely remove all functional oxygen groups, requiring high temperatures (around 1500°C) for full reduction. The study focused on specific synthesis methods and may not generalize to all graphene-based materials. Electrochemical tests were conducted in aqueous KCl, which might not represent all electrolyte conditions.
1:Experimental Design and Method Selection:
The study involved synthesizing graphene-based materials from graphite through oxidation and reduction methods (thermal and multi-step with ascorbic acid), followed by characterization and electrochemical testing to evaluate capacitive behavior.
2:Sample Selection and Data Sources:
Graphite with particle size < 20 μm from Sigma Aldrich was used as the raw material. Samples included graphite oxide (GrO), graphene oxide (GO), thermally reduced graphene oxide (TRGO), and ascorbic acid multi-phase reduced graphene oxide (AMPRGO).
3:List of Experimental Equipment and Materials:
Equipment included SEM with EDX software (Phenom Pro X), TGA/DSC instrument (METTLER TOLEDO), FTIR spectrophotometer (Perkin-Elmer Spectrum TWO), Raman spectrophotometer (Senterra), XRD diffractometer (Philips PW-1711), and potentiostat-galvanostat (Ivium Vertex 5A.DC). Materials included graphite, ascorbic acid, Nafion solution, isopropanol, carbon paper substrates, and KCl electrolyte.
4:5A.DC). Materials included graphite, ascorbic acid, Nafion solution, isopropanol, carbon paper substrates, and KCl electrolyte. Experimental Procedures and Operational Workflow:
4. Experimental Procedures and Operational Workflow: Synthesis involved oxidation via Improved Hummers Method, exfoliation by sonication, reduction by thermal annealing or multi-step with ascorbic acid. Electrodes were prepared by depositing inks on carbon paper. Characterization included elemental analysis, TGA, FTIR, Raman, XRD, and cyclic voltammetry in a three-electrode cell with Ag/AgCl reference and platinum counter electrode.
5:Data Analysis Methods:
Data were analyzed using equations for XRD parameters (e.g., interlayer space, crystal size) and specific capacitance calculation from cyclic voltammetry. Statistical analysis was not explicitly mentioned, but parameters were derived from instrumental measurements.
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FTIR spectrophotometer
SPECTRUM TWO
Perkin-Elmer
Used for Fourier Transform Infrared analysis.
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Graphite
< 20 μm
Sigma Aldrich
Used as the raw material for synthesizing graphene-based nanomaterials.
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Nafion solution
5 wt.%
Sigma Aldrich
Used as a binder in electrode preparation.
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Isopropanol
99.9% for HPLC
Sigma Aldrich
Used as a solvent in electrode ink preparation.
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Carbon paper
Fuel Cell Earth
Used as substrate for electrode deposition.
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SEM system
Phenom Pro X
Used for elemental analysis with EDX software.
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TGA/DSC instrument
METTLER TOLEDO
Used for thermogravimetric analysis.
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Raman spectrophotometer
Senterra
Used for Raman spectroscopy.
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XRD diffractometer
Philips PW-1711
Philips
Used for X-ray diffraction analysis.
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Potentiostat-galvanostat
Vertex 5A.DC
Ivium Technologies
Used for electrochemical measurements including cyclic voltammetry.
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Reference electrode
Ag/AgCl
Used as reference in electrochemical cell.
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Counter electrode
Platinum foil
Used as counter electrode in electrochemical cell.
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