Photocatalytic conversion of cellulose into C5 oligosaccharides
Nathan Skillen,
Aakash Welgamage,
Guan Zhang,
Peter K J Robertson,
John T S Irvine,
Linda A Lawton
Affiliations
Nathan Skillen
School of Chemistry and Chemical Engineering, Queen’s University Belfast , David Keir Building, Stranmillis Road, Belfast BT9 5AG, United Kingdom
Aakash Welgamage
School of Pharmacy and Life Sciences, Sir Ian Wood Building, Robert Gordon University , Garthdee Road, Aberdeen AB10 7GJ, United Kingdom
Guan Zhang
University of St. Andrews, School of Chemistry , Purdie Building, North Haugh, St Andrews KY16 9ST, United Kingdom; School of Civil and Environmental Engineering, Harbin Institute of Technology , Shenzhen (HITSZ), Shenzhen 518055, People’s Republic of China
Cellulose is made up of linear polymers of glucose monomers that could be a crucial source for valuable chemicals and sustainable liquid fuels. Cellulose is however, very stable and its conversion to a useful fuel or platform chemical products remains a significant challenge (Kimura et al 2015 Sci. Rep. 5 16266; Xia et al 2016 Nat. Commun. 7 11162). Photocatalysis is a versatile technology which has demonstrated potential for solar driven processes such as water splitting or solar fuels production and has also been applied to the degradation of pollutants in air and water and for the production of useful products from biomass. Here, we focus on the products that are produced from cellulose (a glucose (C6) based polymer) photocatalysis that compliment hydrogen production. Probing the initial steps via UV-TiO _2 photocatalysis, we remarkably find that an array of oligosaccharides containing only five (C5) carbon units is initially produced. As the process continues, C6 oligo oligosaccharides grow to dominate. The photocatalytic process is generally not viewed as a controllable synthetic process; however, these findings show, on the contrary that photocatalysis at semiconductor surfaces can achieve novel reaction pathways yielding new products.