Adhra Sury, Kiruthika Samuthirapandi, Soham Ghosh, Subhajit Kar, Dr. Sunandan Sarkar, Dr. Bramhaiah Kommula, Dr. Santanu Bhattacharyya
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Based on the fundamental investigations, all these different types of nanostructures have been utilized as photocatalysts for solar hydrogen production without using any cocatalysts, and it was found that the spherical nanostructure exhibits significantly higher H<sub>2</sub> production rates of ∼1682 μ mole/g, which is a few folds higher than other 1D and 2D nanostructured materials. The experimental findings were further supported by the TD-DFT study. Furthermore, the detailed computational studies suggest that the spherical aggregates exhibited a more vital interaction between the ZnTPP molecules, causing significant electronic coupling between bright local excited and charge transfer states, which supports our experimental findings. Finally, we have selectively utilized the oxidative half-reaction for the simultaneous transformation of glycerol to valuable chemicals along with photocatalytic H<sub>2</sub> production through reductive half-reaction.</p>","PeriodicalId":10108,"journal":{"name":"ChemPhotoChem","volume":"8 10","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2024-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Controlled Self-Assembly of Zn-Tetraphenylporphyrins for Efficient Photocatalytic Solar H2 Production and Simultaneous Organic Transformation to Valuable Chemicals\",\"authors\":\"Adhra Sury, Kiruthika Samuthirapandi, Soham Ghosh, Subhajit Kar, Dr. Sunandan Sarkar, Dr. Bramhaiah Kommula, Dr. Santanu Bhattacharyya\",\"doi\":\"10.1002/cptc.202400105\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Herein, we have designed aqueous dispersed self-assembled nanostructures with diverse morphologies from the zinc tetraphenyl porphyrin (ZnTPP) monomer employing simple solution-based coprecipitation methods. 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引用次数: 0
摘要
在此,我们采用简单的溶液共沉淀方法,从四苯基卟啉锌(ZnTPP)单体中设计出了形态各异的水分散自组装纳米结构。通过各种电子显微镜技术进行了详细的形态学研究。最后,利用稳态和时间分辨光谱法将结构特征与基础光物理过程联系起来。详细研究表明,控制形态和高度确定的分子间相互作用会影响整个光诱导电荷转移过程。在基础研究的基础上,所有这些不同类型的纳米结构都被用作光催化剂,在不使用任何共催化剂的情况下进行太阳能制氢,结果发现,球形纳米结构的 H2 产率明显更高,达到约 1682 m 摩尔/克,比其他一维和二维纳米结构材料高出几倍。TD-DFT 研究进一步支持了实验结果。此外,详细的计算研究表明,球形聚合体的 ZnTPP 分子之间表现出了更重要的相互作用,在明亮的局部激发态和电荷转移态之间产生了显著的电子耦合,这也支持了我们的实验结果。最后,我们选择性地利用氧化半反应将甘油转化为有价值的化学物质,并通过还原半反应光催化产生 H2。
Controlled Self-Assembly of Zn-Tetraphenylporphyrins for Efficient Photocatalytic Solar H2 Production and Simultaneous Organic Transformation to Valuable Chemicals
Herein, we have designed aqueous dispersed self-assembled nanostructures with diverse morphologies from the zinc tetraphenyl porphyrin (ZnTPP) monomer employing simple solution-based coprecipitation methods. Detailed morphological studies have been carried out by various electron microscopy techniques. Finally, the structural features were correlated with the underpinning photophysical processes using steady-state and time-resolved spectroscopy. Detailed studies suggest that controlled morphology and highly defined intermolecular interactions affect the overall photoinduced charge transfer process. Based on the fundamental investigations, all these different types of nanostructures have been utilized as photocatalysts for solar hydrogen production without using any cocatalysts, and it was found that the spherical nanostructure exhibits significantly higher H2 production rates of ∼1682 μ mole/g, which is a few folds higher than other 1D and 2D nanostructured materials. The experimental findings were further supported by the TD-DFT study. Furthermore, the detailed computational studies suggest that the spherical aggregates exhibited a more vital interaction between the ZnTPP molecules, causing significant electronic coupling between bright local excited and charge transfer states, which supports our experimental findings. Finally, we have selectively utilized the oxidative half-reaction for the simultaneous transformation of glycerol to valuable chemicals along with photocatalytic H2 production through reductive half-reaction.