Sustainable Electrochemical Synthesis of Porous g-C<sub>3</sub>N<sub>4</sub> Nanosheets via 3D-Printed Platinized Electrodes for Enhanced Photocatalytic Activity

Graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>), a polymeric metal-free catalyst, is extensively used to degrade industrial toxic waste that contaminates the aqueous system. However, commonly synthesized bulk g-C<sub>3</sub>N<sub>4</sub> is prone to agglomeration, leading to low surface area with fewer effective photoactive centers, limiting its potential toward the facile separation of photo-excitons and resulting in low photocatalytic activity. This study introduces an innovative electrochemical synthesis of in situ exfoliated porous g-C<sub>3</sub>N<sub>4</sub> nanosheets (GCN NSs) featuring a large surface area with effective separation of photo-excitons, leading to the facile production of reactive oxygen species (ROS). The GCN NSs are uniformly dispersed in an alkaline solution grown via a newly designed electrochemical process using 3D-printed platinumized titanium mesh as both anode and cathode under rigorous stirring for 40 min. The morphological study, along with surface area determination, reveals that the as-grown carbonaceous matrix is highly exfoliated with an inherent nanoporous architecture, having a high surface area of 163.73 m<sup>2</sup> g<sup>-1</sup> with an average pore diameter of 8.311 nm. The electrochemically synthesized GCN NSs demonstrate excellent charge transfer kinetics with low charge transfer resistance and superior photocatalytic activity of 98% degradation efficiency against various organic dyes (concentration of 10 ppm) under simulated solar irradiation for 120 min with 5 mg of catalyst. Kinetic studies of the photodegradation process indicate that the reaction follows pseudo-first-order kinetics, with the rate constant of 3.59 × 10<sup>-2</sup> min<sup>-1</sup>, which is approximately 1.8 times higher as compared to the recent findings. A plausible mechanistic understanding reveals that photogenerated holes and hydroxyl radicals (<sup>•</sup>OH) are the primary species for the overall photodegradation process. The stability test depicts that the photocatalyst maintains its efficiency over five consecutive runs with a minimum loss of 7%. This research offers valuable insights into the design and synthesis of advanced photocatalysts with optimized architectures for enhanced industrial waste management.

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Publication Details

Journal
Langmuir
Published
2025-05-22
DOI
https://doi.org/10.1021/acs.langmuir.5c01475
Citations
2
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.73

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article

Sustainable Electrochemical Synthesis of Porous g-C3N4 Nanosheets via 3D-Printed Platinized Electrodes for Enhanced Photocatalytic Activity

Daya Rani, Suman Singh, Kaushik Ghosh, Mansi Pahuja et al.
2 citations
Langmuir
Advanced Photocatalysis Techniques
0.73
article

Sustainable Electrochemical Synthesis of Porous g-C3N4 Nanosheets via 3D-Printed Platinized Electrodes for Enhanced Photocatalytic Activity

Daya Rani, Suman Singh, Kaushik Ghosh, Mansi Pahuja, Mayank Garg, Shubham Kumar Patial, Vijay Kumar Meena
article en
2 citations

Abstract

Graphitic carbon nitride (g-C<sub>3</sub>N<sub>4</sub>), a polymeric metal-free catalyst, is extensively used to degrade industrial toxic waste that contaminates the aqueous system. However, commonly synthesized bulk g-C<sub>3</sub>N<sub>4</sub> is prone to agglomeration, leading to low surface area with fewer effective photoactive centers, limiting its potential toward the facile separation of photo-excitons and resulting in low photocatalytic activity. This study introduces an innovative electrochemical synthesis of in situ exfoliated porous g-C<sub>3</sub>N<sub>4</sub> nanosheets (GCN NSs) featuring a large surface area with effective separation of photo-excitons, leading to the facile production of reactive oxygen species (ROS). The GCN NSs are uniformly dispersed in an alkaline solution grown via a newly designed electrochemical process using 3D-printed platinumized titanium mesh as both anode and cathode under rigorous stirring for 40 min. The morphological study, along with surface area determination, reveals that the as-grown carbonaceous matrix is highly exfoliated with an inherent nanoporous architecture, having a high surface area of 163.73 m<sup>2</sup> g<sup>-1</sup> with an average pore diameter of 8.311 nm. The electrochemically synthesized GCN NSs demonstrate excellent charge transfer kinetics with low charge transfer resistance and superior photocatalytic activity of 98% degradation efficiency against various organic dyes (concentration of 10 ppm) under simulated solar irradiation for 120 min with 5 mg of catalyst. Kinetic studies of the photodegradation process indicate that the reaction follows pseudo-first-order kinetics, with the rate constant of 3.59 × 10<sup>-2</sup> min<sup>-1</sup>, which is approximately 1.8 times higher as compared to the recent findings. A plausible mechanistic understanding reveals that photogenerated holes and hydroxyl radicals (<sup>•</sup>OH) are the primary species for the overall photodegradation process. The stability test depicts that the photocatalyst maintains its efficiency over five consecutive runs with a minimum loss of 7%. This research offers valuable insights into the design and synthesis of advanced photocatalysts with optimized architectures for enhanced industrial waste management.

LangmuirVol. 41(21)
Central Scientific Instruments Organisation (IN), MIT University (MK), Quantum Devices (United States) (US), Center for Nano Science and Technology (IT), Institute of Nano Science and Technology, RMIT University (AU), McMaster University (CA), Academy of Scientific and Innovative Research (IN)
Council of Scientific and Industrial Research, India
Responsible consumption and production
Openalex Percentile: Top 31%
Advanced Photocatalysis Techniques
0.73
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