{"title":"利用3d打印镀铂电极可持续电化学合成多孔g-C3N4纳米片以增强光催化活性","authors":"Shubham Kumar Patial, Daya Rani, Mayank Garg, Vijay Kumar Meena, Mansi Pahuja, Kaushik Ghosh, Suman Singh","doi":"10.1021/acs.langmuir.5c01475","DOIUrl":null,"url":null,"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.","PeriodicalId":50,"journal":{"name":"Langmuir","volume":"136 1","pages":""},"PeriodicalIF":3.7000,"publicationDate":"2025-05-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sustainable Electrochemical Synthesis of Porous g-C3N4 Nanosheets via 3D-Printed Platinized Electrodes for Enhanced Photocatalytic Activity\",\"authors\":\"Shubham Kumar Patial, Daya Rani, Mayank Garg, Vijay Kumar Meena, Mansi Pahuja, Kaushik Ghosh, Suman Singh\",\"doi\":\"10.1021/acs.langmuir.5c01475\",\"DOIUrl\":null,\"url\":null,\"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%. 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Sustainable Electrochemical Synthesis of Porous g-C3N4 Nanosheets via 3D-Printed Platinized Electrodes for Enhanced Photocatalytic Activity
Graphitic carbon nitride (g-C3N4), a polymeric metal-free catalyst, is extensively used to degrade industrial toxic waste that contaminates the aqueous system. However, commonly synthesized bulk g-C3N4 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-C3N4 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 m2 g–1 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 × 10–2 min–1, which is approximately 1.8 times higher as compared to the recent findings. A plausible mechanistic understanding reveals that photogenerated holes and hydroxyl radicals (•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.
期刊介绍:
Langmuir is an interdisciplinary journal publishing articles in the following subject categories:
Colloids: surfactants and self-assembly, dispersions, emulsions, foams
Interfaces: adsorption, reactions, films, forces
Biological Interfaces: biocolloids, biomolecular and biomimetic materials
Materials: nano- and mesostructured materials, polymers, gels, liquid crystals
Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry
Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals
However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do?
Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*.
This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).