Industrial & Engineering Chemistry Research· 2026Q1
Plasma–Microreactor Integration for Green and Continuous Synthesis of Pt/GO Electrocatalysts
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- Q1SCImago
- 2026year
Short summary
A continuous microflow strategy integrating dielectric barrier discharge (DBD) plasma with microreactor technology synthesizes Pt/graphene oxide (Pt/GO) electrocatalysts at ambient conditions, achieving rapid in situ reduction and deposition of Pt nanoparticles (PtNPs) in 26.4s.
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Key points
- A continuous plasma-microreactor system synthesizes Pt/GO electrocatalysts at ambient temperature and pressure.
- The process achieves rapid in situ reduction and deposition of Pt nanoparticles in a residence time of 26.4 seconds.
- The 15 wt% Pt/GO catalyst features well-dispersed 5.01 nm Pt nanoparticles with preserved GO functional groups.
- The synthesized Pt/GO exhibits competitive HER activity (60 mV overpotential at -10 mA·cm–2 in 1 M KOH) and superior MOR performance (346.85 mA·cm–2 peak current density) with enhanced durability.
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract The green and continuous preparation of supported noble metal catalysts is crucial for both fundamental research and industrial applications but remains highly challenging. Herein, a continuous microflow strategy that integrates dielectric barrier discharge (DBD) plasma with microreactor technology is developed for the synthesis of Pt/graphene oxide (Pt/GO) electrocatalysts under ambient temperature and pressure. This method uses the synergistic effects of both techniques to achieve rapid in situ reduction and deposition of Pt nanoparticles (PtNPs) onto GO nanosheets, avoiding the use of toxic chemical reductants or high-temperature annealing. The resulting Pt/GO composites feature well-dispersed, crystalline PtNPs with small particle sizes and tunable Pt loadings (0–15 wt %), while the oxygen-containing functional groups on GO are well preserved during plasma treatment. The residence time of the reagents is estimated to be 26.4 s, with a mean particle size of 5.01 nm for the 15 wt % Pt/GO catalyst. The resulting Pt/GO composites exhibit apparent electrocatalytic performance toward both the hydrogen evolution reaction (HER) and methanol oxidation reaction (MOR) in acidic and alkaline media. Specifically, in 1 M KOH electrolyte, the 15 wt % Pt/GO catalyst delivers a low overpotential of 60 mV at −10 mA·cm–2 and a Tafel slope of 66.37 mV·dec–1 for HER. For MOR, this catalyst achieves a high peak current density of 346.85 mA·cm–2 in alkaline solution, along with reduced charge-transfer resistance. Compared to the batch plasma-prepared sample and commercial 20 wt % Pt/C, our plasma-microreactor-synthesized 15 wt % Pt/GO catalyst shows competitive HER activity under the present testing conditions, better MOR performance, and enhanced durability in both acidic and alkaline environments. This work demonstrates the feasibility of plasma–microreactor integration as a green, continuous, and intensified route for the synthesis of high-performance supported noble metal catalysts.
The authors' abstract, as published at the source. Industrial & Engineering Chemistry Research, 2026 · DOI ↗
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Field: Renewable Energy, Sustainability and the Environment
Renewable Energy, Sustainability and the EnvironmentEnergy