Asmita Dileep Gaonkar, Shraddha Paniya, Srinivasu Kancharlapalli and Kiran Vankayala
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P-doping into g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> was achieved using an eco-friendly P source. P doping induced changes in the light-harvesting capacity of g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>, and its consequence on the dual-functional photocatalytic activity of P-doped g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> was systematically investigated using various characterization techniques. P-doped g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> exhibited an ≈3-fold increase in photocatalytic activity in the production of H<small><sub>2</sub></small> and benzaldehyde as compared to that of pristine g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>. Density functional theory (DFT) studies reveal that the P-dopant preferentially replaces the corner C-site as compared to the N site of the tri-<em>s</em>-triazine ring of g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>, which results in the creation of mid-gap states that enable the enhanced visible light absorption of P-doped g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>. Mechanistic investigation studies suggest that photogenerated holes drive the selective oxidation of benzyl alcohol to benzaldehyde while photogenerated electrons drive H<small><sub>2</sub></small> evolution, leading to concomitant production of H<small><sub>2</sub></small> and benzaldehyde by P-doped g-C<small><sub>3</sub></small>N<small><sub>4</sub></small>. The selective conversion of benzyl alcohol proceeds through a carbon-centred radical mechanism, according to experimental and DFT studies. This work elucidates the importance of P-doping in g-C<small><sub>3</sub></small>N<small><sub>4</sub></small> for the simultaneous production of solar fuels (such as H<small><sub>2</sub></small>) and high-value chemicals (such as benzaldehyde).</p>","PeriodicalId":104,"journal":{"name":"Sustainable Energy & Fuels","volume":" 21","pages":" 4914-4926"},"PeriodicalIF":5.0000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/se/d4se00826j?page=search","citationCount":"0","resultStr":"{\"title\":\"Boosted photoredox capability of visible light-active P-doped C3N4 with efficient harvesting of electron–hole pairs†\",\"authors\":\"Asmita Dileep Gaonkar, Shraddha Paniya, Srinivasu Kancharlapalli and Kiran Vankayala\",\"doi\":\"10.1039/D4SE00826J\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Photocatalytic production of solar fuels and high-value chemicals by photogenerated carriers has been at the forefront as one of the promising sustainable approaches. 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引用次数: 0
摘要
利用光生载体进行光催化生产太阳能燃料和高价值化学品一直是最前沿的可持续发展方法之一。然而,大多数研究都只关注其中一个半反应,即光还原或光氧化反应,导致电子-空穴对的收集效率低下,无法充分利用光催化的潜力。在此,我们采用掺磷石墨氮化碳(掺磷 g-C3N4)作为可见光活性光催化剂,证明了光生电子-空穴对的高效利用,这种催化剂能够同时从苯甲醇中产生氢气和苯甲醛。g-C3N4 中的 P 掺杂是利用环保型 P 源实现的。利用各种表征技术系统地研究了掺杂 P 引起的 g-C3N4 光收集能力的变化及其对掺杂 P 的 g-C3N4 双功能光催化活性的影响。与原始 g-C3N4 相比,掺杂 P 的 g-C3N4 在产生 H2 和苯甲醛方面的光催化活性提高了≈3 倍。密度泛函理论(DFT)研究表明,与 g-C3N4 的三-s-三嗪环的 N 位相比,P-掺杂剂优先取代了角 C 位,从而产生了中隙态,增强了 P 掺杂 g-C3N4 对可见光的吸收。机理调查研究表明,光生空穴驱动苯甲醇选择性氧化为苯甲醛,而光生电子驱动 H2 演化,导致掺杂 P 的 g-C3N4 同时产生 H2 和苯甲醛。根据实验和 DFT 研究,苯甲醇的选择性转化是通过以碳为中心的自由基机制进行的。这项工作阐明了在 g-C3N4 中掺杂 P 对于同时生产太阳能燃料(如 H2)和高价值化学品(如苯甲醛)的重要性。
Boosted photoredox capability of visible light-active P-doped C3N4 with efficient harvesting of electron–hole pairs†
Photocatalytic production of solar fuels and high-value chemicals by photogenerated carriers has been at the forefront as one of the promising sustainable approaches. However, most of the studies focus only on one of the half reactions, either photoreduction or photooxidation, leading to underutilization of the potentiality of photocatalysis due to inefficient harvesting of electron–hole pairs. Herein, the efficient utilization of photogenerated electron–hole pairs was demonstrated by employing phosphorous-doped graphitic carbon nitride (P-doped g-C3N4) as a visible light-active photocatalyst that is capable of simultaneously producing hydrogen and benzaldehyde from benzyl alcohol. P-doping into g-C3N4 was achieved using an eco-friendly P source. P doping induced changes in the light-harvesting capacity of g-C3N4, and its consequence on the dual-functional photocatalytic activity of P-doped g-C3N4 was systematically investigated using various characterization techniques. P-doped g-C3N4 exhibited an ≈3-fold increase in photocatalytic activity in the production of H2 and benzaldehyde as compared to that of pristine g-C3N4. Density functional theory (DFT) studies reveal that the P-dopant preferentially replaces the corner C-site as compared to the N site of the tri-s-triazine ring of g-C3N4, which results in the creation of mid-gap states that enable the enhanced visible light absorption of P-doped g-C3N4. Mechanistic investigation studies suggest that photogenerated holes drive the selective oxidation of benzyl alcohol to benzaldehyde while photogenerated electrons drive H2 evolution, leading to concomitant production of H2 and benzaldehyde by P-doped g-C3N4. The selective conversion of benzyl alcohol proceeds through a carbon-centred radical mechanism, according to experimental and DFT studies. This work elucidates the importance of P-doping in g-C3N4 for the simultaneous production of solar fuels (such as H2) and high-value chemicals (such as benzaldehyde).
期刊介绍:
Sustainable Energy & Fuels will publish research that contributes to the development of sustainable energy technologies with a particular emphasis on new and next-generation technologies.