Unveiling the solar-driven synergistic production of a cyclic fuel-additive and carbon-free solar fuel from biogenic furfural: mediated by a metal-free organic semiconductor†

IF 9.5 2区 材料科学 Q1 CHEMISTRY, PHYSICAL Journal of Materials Chemistry A Pub Date : 2024-11-06 DOI:10.1039/D4TA03730H
Shivali Dhingra, Arpna Jaryal, Deepak Kumar Chauhan and Kamalakannan Kailasam
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Abstract

Photocatalytic biomass upgradation to fine chemicals and fuels offers a promising strategy to address the current energy crisis and presents a prominent step towards carbon neutrality. Despite several reports in recent years, biomass valorization is still facing a lot of challenges including poor selectivity and inefficient conversion. Notably, photooxidation of biomass results in inefficient utilization of charge carriers which hampers the overall efficiency of the photocatalytic process. In the ongoing quest for effective biomass upgradation, here, we present a metal-free urea-derived carbon-nitride for the photocatalytic acetalization of furfural (Ffal) with ethylene glycol (EG) to generate a cyclic acetal i.e. 2-furyl-1,3-dioxolane (FD), a promising bio-fuel additive integrated with H2O2 production under visible light for the first time. Importantly, an 85% cyclic acetal yield is achieved in 6 h with 99% selectivity along with 162 µmol g−1 of H2O2 production. Under natural sunlight, an exceptionally high yield of FD has been achieved, reaching 70% yield, presenting the practicality of the UCN photocatalyst for the large-scale production of cyclic acetals. In situ EPR analysis, photoluminescence spectroscopy, and photo-electrochemical studies along with various control experiments elucidated the charge transfer mechanism involved in the photoredox process. Thus, the current study offers an encouraging approach for harnessing a metal-free photocatalyst to generate solar fuel coupled with biomass upgradation to fuel additives, thereby presenting a viable pathway for the sustainable production of fuels and fine chemicals.

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揭示生物源糠醛在太阳能驱动下协同生产循环燃料添加剂和无碳太阳能燃料的过程:由无金属有机半导体介导
光催化生物质升级为精细化学品和燃料为解决当前的能源危机提供了一个前景广阔的战略,也是实现碳中和的重要一步。尽管近年来有一些报道,但生物质的价值化仍然面临着许多挑战,包括选择性差和转化效率低。值得注意的是,生物质的光氧化会导致电荷载体的低效利用,从而影响光催化过程的整体效率。在不断寻求有效生物质升级的过程中,我们在此提出了一种无金属脲衍生氮化碳,用于糠醛(Ffal)与乙二醇(EG)的光催化缩醛反应,生成环状缩醛,即 2-糠基-1,3-二氧戊环(FD),这是一种很有前景的生物燃料添加剂,首次在可见光下与 H2O2 生成相结合。重要的是,在 6 小时内实现了 85% 的环缩醛产量,选择性高达 99%,同时还产生了 162 µmol g-1 的 H2O2。在自然光下,FD 的产量也特别高,达到了 70%,这表明 UCN 光催化剂在大规模生产环缩醛方面的实用性。原位 EPR 分析、光致发光光谱和光电化学研究以及各种对照实验阐明了光氧化还原过程中的电荷转移机制。因此,目前的研究为利用无金属光催化剂生成太阳能燃料以及将生物质升级为燃料添加剂提供了一种令人鼓舞的方法,从而为燃料和精细化学品的可持续生产提供了一条可行的途径。
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来源期刊
Journal of Materials Chemistry A
Journal of Materials Chemistry A CHEMISTRY, PHYSICAL-ENERGY & FUELS
CiteScore
19.50
自引率
5.00%
发文量
1892
审稿时长
1.5 months
期刊介绍: The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.
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