Huaimin Tian, Chaoya Han, Zekai Xu, Chao Yao, Xiazhang Li
{"title":"Mechanochemical fabrication of a biochar/pyrite nanocomposite for efficient photocatalytic CO2 reduction coupled with biomass valorization","authors":"Huaimin Tian, Chaoya Han, Zekai Xu, Chao Yao, Xiazhang Li","doi":"10.1039/d6gc02845d","DOIUrl":null,"url":null,"abstract":"<div><div>Coupling solar-driven CO<sub>2</sub> reduction with the valorization of waste biomass-derived platform chemicals represents a pivotal strategy toward achieving carbon neutrality and sustainable resource utilization. However, the high dissociation energy of the CO bond in CO<sub>2</sub> and the complex side reactions involved in biomass conversion often result in low conversion efficiency and poor product selectivity. To address these challenges, herein, a biochar/pyrite nanocomposite was fabricated <em>via</em> a facile mechanical ball-milling method using natural pyrite and biochar derived from waste corn stover. During the ball-milling process, intimate interfacial contact is established between the two components, leading to the formation of a high–low heterojunction that effectively promotes the spatial separation and interfacial migration of photogenerated charge carriers. The optimized 30 wt% biochar/pyrite sample exhibits outstanding photocatalytic performance under simulated visible light irradiation, achieving a CO yield of 320.7 μmol g<sup>−1</sup> h<sup>−1</sup> with a selectivity of 90.7%, together with a 5-hydroxymethylfurfural conversion of 86.4% and a high 2,5-diformylfuran selectivity of 93.2%. The incorporation of biochar not only enhances the adsorption capacity for the reactants but also substantially boosts the photocatalytic activity of pyrite through facilitated interfacial charge transfer. This work provides a new strategy for constructing efficient photocatalytic systems based on natural minerals and waste biomass, enabling the synergistic coupling of CO<sub>2</sub> reduction and biomass valorization.</div></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":"28 26","pages":"Pages 11107-11119"},"PeriodicalIF":10.6000,"publicationDate":"2026-07-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926226005819","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/9 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Coupling solar-driven CO2 reduction with the valorization of waste biomass-derived platform chemicals represents a pivotal strategy toward achieving carbon neutrality and sustainable resource utilization. However, the high dissociation energy of the CO bond in CO2 and the complex side reactions involved in biomass conversion often result in low conversion efficiency and poor product selectivity. To address these challenges, herein, a biochar/pyrite nanocomposite was fabricated via a facile mechanical ball-milling method using natural pyrite and biochar derived from waste corn stover. During the ball-milling process, intimate interfacial contact is established between the two components, leading to the formation of a high–low heterojunction that effectively promotes the spatial separation and interfacial migration of photogenerated charge carriers. The optimized 30 wt% biochar/pyrite sample exhibits outstanding photocatalytic performance under simulated visible light irradiation, achieving a CO yield of 320.7 μmol g−1 h−1 with a selectivity of 90.7%, together with a 5-hydroxymethylfurfural conversion of 86.4% and a high 2,5-diformylfuran selectivity of 93.2%. The incorporation of biochar not only enhances the adsorption capacity for the reactants but also substantially boosts the photocatalytic activity of pyrite through facilitated interfacial charge transfer. This work provides a new strategy for constructing efficient photocatalytic systems based on natural minerals and waste biomass, enabling the synergistic coupling of CO2 reduction and biomass valorization.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.