Colocalization of light harvesting and catalytic units in a 'soft' coordination polymer hydrogel toward visible-light driven photocatalytic hydrogen production. Issue 23 (1st June 2021)

• Record Type: Journal Article
• Authors: Verma, Parul; Singh, Ashish; Rahimi, Faruk Ahamed; Maji, Tapas Kumar
• Is Part Of: Journal of materials chemistry. Volume 9:Issue 23(2021)
• Page Start: 13608
• Page End: 13614
• Publication Date: 2021-06-01
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/d1ta02425f
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : An anthracene based coordination polymer gel (CPG) material has been prepared which acted as a stable visible light driven photocatalyst without adding any co-catalyst for hydrogen evolution from water with the maximum rate of 0.97 mmol g −1 h −1 . Abstract : Colocalization of essential molecular components in a solvated soft supramolecular assembly towards realizing visible-light-driven hydrogen evolution would be an exciting approach for sustainable energy by generating clean solar fuel. In this study, we report the preparation and characterization of a coordination polymer gel (Zn-TPY-ANT CPG) formed by the self-assembly of Zn 2+ and an anthracene–terpyridine based low molecular weight gelator (TPY-ANT LMWG). The 1D nanofibrous CPG in the hydrogel state shows the potential to perform visible-light-driven (400–750 nm) photocatalytic water reduction and produce a considerable amount of hydrogen (12.02 mmol g −1 in 22 h). Furthermore, H2 evolution can be enhanced significantly (18.03 mmol g −1 in 22 h) upon illumination with the full-range of light (290–750 nm). In this supramolecular assembly, the ANT unit acts as a light-harvesting moiety whereas the [Zn(TPY)2 ] 2+ center acts as a catalytic site. We believe that such a design of soft hybrid materials would have a positive impact on developing a non-precious, stable, and recyclable photocatalyst material for H2 production.