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Advanced Catalytic and Electrocatalytic Performances of Polydopamine-Functionalized Reduced Graphene Oxide-Palladium Nanocomposites

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posted on 2024-07-11, 08:01 authored by Li Fu, Guosong Lai, Deming Zhu, Baohua Jia, Francois MalherbeFrancois Malherbe, Aimin YuAimin Yu
A polydopamine-functionalized reduced graphene oxide (PDA-RGO)/Pd nanocomposite was synthesized by a simple wet chemical approach at room temperature. Graphene oxide (GO) was first modified with PDA by the self-polymerization of dopamine (DA) followed by the deposition of Pd nanoparticles. UV/Vis and FTIR spectroscopies confirmed the reduction of GO to RGO during the self-polymerization of DA. SEM images revealed that Pd nanoclusters were formed on both sides of the PDA-RGO sheets. The as-prepared PDA-RGO/Pd nanocomposites exhibited excellent catalytic activity in the chemical degradation of methylene blue with a reaction rate constant of 0.6028 min−1, which was 2.5-fold faster than that of the PDA/Pd catalyst without RGO. Moreover, the PDA-RGO/Pd nanocomposite also showed an outstanding electrocatalytic activity towards the electro-oxidation of paracetamol. The current response had a linear relationship to the concentration of paracetamol in the range of 0.28–100 μm with a low detection limit of 0.087 μm (S/N=3). In addition, the sensor also exhibited good selectivity for the detection of paracetamol.

Funding

ARC | DP150102972

Study on Electrochemical Properties and High Sensitive Detection Methods of Antibacterial Drugs : National Natural Science Foundation of China | 21475033

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ISSN

1867-3899

Journal title

ChemCatChem

Volume

8

Issue

18

Pagination

2975-2980

Publisher

Wiley

Copyright statement

Copyright © 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at https://doi.org/10.1002/cctc.201600532 . This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.

Language

eng

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