{"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}
引用次数: 0
Abstract
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.