{"title":"负载钴的氮化碳证明了从木质纤维素生物质组分中增强光催化生产H2。","authors":"Mitchell Beckedorf, Jenna Holland, Robert Godin","doi":"10.1021/aps.4c00007","DOIUrl":null,"url":null,"abstract":"<p><p>Photocatalytic production of hydrogen (H<sub>2</sub>) from biomass is a promising avenue for advancing sustainable energy generation. We prepared carbon nitride (CN <sub><i>x</i></sub> ) with cobalt (Co) as an oxidation cocatalyst (denoted CN <sub><i>x</i></sub> /Co) to improve photocatalytic H<sub>2</sub> production through photoreforming components of lignocellulosic biomass under visual light irradiation. CN <sub><i>x</i></sub> /Co was synthesized by loading Co onto preformed CN <sub><i>x</i></sub> through a straightforward thermal deposition. The thermal loading of Co at 450 °C led to the formation of a mixed valence CoO <sub><i>x</i></sub> , which shifted Co<sup>2+</sup> character to Co<sup>3+</sup> over the course of the hydrogen evolution reaction (HER). Compared to CN <sub><i>x</i></sub> without Co, our materials with 0.3 and 0.6 wt % Co demonstrate twice the apparent quantum yield (AQY) for H<sub>2</sub> production under irradiation at 405 nm using glucose as a sacrificial electron donor (3.0% and 2.8%, respectively, vs 1.4%). Time-resolved spectroscopic investigations indicate that the Co extracts charges in the subnanosecond time scale and promotes the formation of beneficial long-lived charges. Impressively, some photocatalytic activity is observed when using the robust polymers of cellulose and lignin as the oxidation substrates (0.2 and 0.1% AQY, respectively). The ability to oxidize abundant biomass without extensive prepreparation is promising for waste upcycling applications.</p>","PeriodicalId":520501,"journal":{"name":"Artificial photosynthesis (Washington, D.C.)","volume":"1 1","pages":"50-62"},"PeriodicalIF":0.0000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11783807/pdf/","citationCount":"0","resultStr":"{\"title\":\"Cobalt-Loaded Carbon Nitride Demonstrates Enhanced Photocatalytic Production of H<sub>2</sub> from Lignocellulosic Biomass Components.\",\"authors\":\"Mitchell Beckedorf, Jenna Holland, Robert Godin\",\"doi\":\"10.1021/aps.4c00007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Photocatalytic production of hydrogen (H<sub>2</sub>) from biomass is a promising avenue for advancing sustainable energy generation. We prepared carbon nitride (CN <sub><i>x</i></sub> ) with cobalt (Co) as an oxidation cocatalyst (denoted CN <sub><i>x</i></sub> /Co) to improve photocatalytic H<sub>2</sub> production through photoreforming components of lignocellulosic biomass under visual light irradiation. CN <sub><i>x</i></sub> /Co was synthesized by loading Co onto preformed CN <sub><i>x</i></sub> through a straightforward thermal deposition. The thermal loading of Co at 450 °C led to the formation of a mixed valence CoO <sub><i>x</i></sub> , which shifted Co<sup>2+</sup> character to Co<sup>3+</sup> over the course of the hydrogen evolution reaction (HER). Compared to CN <sub><i>x</i></sub> without Co, our materials with 0.3 and 0.6 wt % Co demonstrate twice the apparent quantum yield (AQY) for H<sub>2</sub> production under irradiation at 405 nm using glucose as a sacrificial electron donor (3.0% and 2.8%, respectively, vs 1.4%). Time-resolved spectroscopic investigations indicate that the Co extracts charges in the subnanosecond time scale and promotes the formation of beneficial long-lived charges. Impressively, some photocatalytic activity is observed when using the robust polymers of cellulose and lignin as the oxidation substrates (0.2 and 0.1% AQY, respectively). The ability to oxidize abundant biomass without extensive prepreparation is promising for waste upcycling applications.</p>\",\"PeriodicalId\":520501,\"journal\":{\"name\":\"Artificial photosynthesis (Washington, D.C.)\",\"volume\":\"1 1\",\"pages\":\"50-62\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11783807/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Artificial photosynthesis (Washington, D.C.)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1021/aps.4c00007\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/23 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Artificial photosynthesis (Washington, D.C.)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1021/aps.4c00007","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/23 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
从生物质中光催化生产氢(H2)是推进可持续能源生产的一个有前途的途径。我们用钴(Co)作为氧化助催化剂(表示为CN x /Co)制备了氮化碳(CN x),通过在可见光照射下光重整木质纤维素生物质的组分来提高光催化H2的产量。通过直接热沉积将Co加载到预成型的CN x上,合成了CN x /Co。450°C时Co的热负荷导致混合价CoO x的形成,在析氢反应(HER)过程中将Co2+的性质转变为Co3+。与不含Co的CN x相比,我们的材料中Co含量分别为0.3 wt %和0.6 wt %,在405nm辐照下,葡萄糖作为牺牲电子供体,H2生产的表观量子产率(AQY)分别为3.0%和2.8%,而不是1.4%。时间分辨光谱研究表明,Co在亚纳秒时间尺度上提取电荷,促进有益的长寿命电荷的形成。令人印象深刻的是,当使用坚固的纤维素和木质素聚合物作为氧化底物(分别为0.2和0.1% AQY)时,观察到一些光催化活性。氧化丰富的生物质而无需广泛的预处理的能力是有希望的废物升级回收应用。
Cobalt-Loaded Carbon Nitride Demonstrates Enhanced Photocatalytic Production of H2 from Lignocellulosic Biomass Components.
Photocatalytic production of hydrogen (H2) from biomass is a promising avenue for advancing sustainable energy generation. We prepared carbon nitride (CN x ) with cobalt (Co) as an oxidation cocatalyst (denoted CN x /Co) to improve photocatalytic H2 production through photoreforming components of lignocellulosic biomass under visual light irradiation. CN x /Co was synthesized by loading Co onto preformed CN x through a straightforward thermal deposition. The thermal loading of Co at 450 °C led to the formation of a mixed valence CoO x , which shifted Co2+ character to Co3+ over the course of the hydrogen evolution reaction (HER). Compared to CN x without Co, our materials with 0.3 and 0.6 wt % Co demonstrate twice the apparent quantum yield (AQY) for H2 production under irradiation at 405 nm using glucose as a sacrificial electron donor (3.0% and 2.8%, respectively, vs 1.4%). Time-resolved spectroscopic investigations indicate that the Co extracts charges in the subnanosecond time scale and promotes the formation of beneficial long-lived charges. Impressively, some photocatalytic activity is observed when using the robust polymers of cellulose and lignin as the oxidation substrates (0.2 and 0.1% AQY, respectively). The ability to oxidize abundant biomass without extensive prepreparation is promising for waste upcycling applications.