Related Experiment Video
Updated: Sep 24, 2025

Scalable Syntheses of Graphene Oxide and Reduced Graphene Oxide using Cascade Design Oxidation and Highly Basic Reduction Reactions
Published on: July 3, 2025
Enhanced oxygen evolution reaction on amine functionalized graphene oxide in alkaline medium
Vijay S Sapner1, Balaji B Mulik1, Renuka V Digraskar1
1Department of Chemistry, Dr. Babasaheb Ambedkar Marathwada University Aurangabad 431004 Maharashtra India bhaskarsathe@gmail.com.
A new metal-free tyramine functionalized graphene oxide (T-GO) electrocatalyst efficiently drives the oxygen evolution reaction (OER) in alkaline solutions. This T-GO material shows superior performance for clean fuel generation and water splitting applications.
Area of Science:
- Materials Science
- Electrochemistry
- Catalysis
Background:
- Efficient oxygen evolution reaction (OER) electrocatalysts are crucial for cost-effective clean fuel production.
- Developing metal-free catalysts addresses cost and environmental concerns associated with traditional catalysts.
Purpose of the Study:
- To develop and characterize a novel metal-free tyramine functionalized graphene oxide (T-GO) electrocatalyst for enhanced OER performance.
- To evaluate the electrocatalytic activity and stability of T-GO in alkaline electrolytes for water splitting applications.
Main Methods:
- Synthesis of tyramine functionalized graphene oxide (T-GO).
- Characterization using SEM, XRD, FTIR, XPS, and Raman spectroscopy.
- Electrochemical evaluation of OER activity, including onset potential, Tafel slope, and stability using techniques like RRDE.
Main Results:
- T-GO demonstrated a low OER onset potential of ~1.39 V and a small Tafel slope of 69 mV dec⁻¹, outperforming bare graphene oxide (GO).
- GO exhibited an OER onset potential of 1.51 V and a Tafel slope of 92 mV dec⁻¹.
- T-GO showed outstanding current stability and diffusion-controlled response, indicating its efficiency and durability.
Conclusions:
- Metal-free T-GO is an efficient electrocatalyst for the oxygen evolution reaction in alkaline media.
- T-GO shows significant promise for applications in water splitting and clean fuel generation.
Related Concept Videos
Aldehydes and Ketones with Amines: Enamine Formation Mechanism
Aldehydes and Ketones with Amines: Imine Formation Mechanism
Imines are formed under mildly acidic conditions. A pH of 4.5 is ideal for the reaction.
If the pH is low or the solution is too acidic, the reaction slows down in the...
Aldehydes and Ketones with Amines: Imine and Enamine Formation Overview
Preparation of Amines: Reduction of Oximes and Nitro Compounds
Though catalytic hydrogenation can reduce nitrobenzenes, the reduction is nonselective in the presence of other functional groups. For instance, if nitrobenzene contains an aldehyde group,...
Amides to Amines: LiAlH4 Reduction
Amide reduction requires two equivalents of the reducing agent, acting as a source of hydride ions. As shown in the figure, the reaction is initiated with a nucleophilic attack by the hydride ion at the carbonyl carbon to form a tetrahedral intermediate.
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.

