Deposition time-driven growth of gold nanoparticles for enhanced performance in ethanol electrooxidation

Open

Setia Budi, Annisa Auliya, Hilman Syafei

2025 Materials Advances Vol. 6 Issue 23 Article Cited by 0 SDG 17SDG 12 Quartile

Abstract

Gold nanoparticles (AuNPs) exhibit unique catalytic, electronic, and optical properties, making them highly suitable for various applications, particularly in catalysis. This study explores the synthesis of AuNPs on fluorine-doped tin oxide substrates using a square-wave pulse deposition technique, with deposition time as the primary variable influencing nanoparticles growth. The synthesized AuNPs were systematically characterized using field emission scanning electron microscopy, energy dispersive X-ray spectroscopy, and X-ray diffraction techniques. The electrocatalytic performance of the synthesized AuNPs was evaluated through electrochemical impedance spectroscopy and cyclic voltammetry in an alkaline medium. The results revealed that longer deposition duration led to nanoparticle increased coverage, improved charge transfer kinetics, and enhanced catalytic activity. Notably, AuNPs50 deposited for 50 minutes exhibited the the lowest charge transfer resistance and the highest electrochemical surface area, resulting in the highest current density during ethanol electrooxidation. These findings demonstrate the enhanced catalytic performance of the electrodeposited AuNPs for ethanol oxidation, achieved without the use of surfactants or additives. © 2025 The Royal Society of Chemistry

Affiliations

Department of Chemistry, Faculty of Mathematics and Natural Sciences, Universitas Negeri Jakarta, Jl. Rawamangun Muka, Jakarta, 13220, Indonesia; The Center for Science Innovation, Arva Building, Jl. RP. Soeroso, Jakarta Pusat, 10350, Indonesia

Research at a Glance

Premium content — register to unlock

Research at a Glance

Register to unlock

Topics & SDG Alignment

Premium content — register to unlock

Topics & SDG Alignment

Register to unlock

Collaboration

Premium content — register to unlock

Collaboration

Register to unlock

Author Profile (Selected)

Premium content — register to unlock

Author Profile (Selected)

Register to unlock

References Overview

Premium content — register to unlock

References Overview

Register to unlock

Journal & Source

Premium content — register to unlock

Journal & Source

Register to unlock

Metadata & Integrity

Premium content — register to unlock

Metadata & Integrity

Register to unlock