Abstract

Gluconic acid, one of the valuable products of oxidized glucose projected to soon hit a market value of US$1.9 billion is currently produced using relatively expensive electrochemical, environmentally unsafe chemical or thermal selective oxidation methods to meet market demand. Dye-sensitized photoelectrochemical cells (DSPECs) which has effectively been utilized for selective biomass conversion into other valuable products (alongside hydrogen evolution) is a cheaper, greener and safer alternative unexplored in this field. Herein, we explore this green technology for selective oxidation of glucose into gluconic acid in an aqueous system, employing metal-free organic dye (E)-3-(5-(4-(bis(2',4'-dibutoxy-[1,1'-biphenyl]-4-yl) amino) phenyl) thiophen-2-yl)-2-cyanoacrylic acid (D35) with organic catalyst (4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl) ACT at 0 V vs NHE. Photophysical details revealed the occurrence of intermolecular electron transfer between D35 and ACT under 1 sun illumination (100 mW/cm²). Enhanced generation of the strongly oxidizing reactive oxoammonium species, ACT+, by the photoanode drives the conversion of glucose into gluconic acid. The photoanode assembly employed exhibited remarkable stability, sustaining a continuous operation for 3 days and 88% selectivity for gluconic acid at pH 7. The aqueous phase stability, selectivity, neutral environment and ambient operation of the setup indicates it potential for biomass conversion and hydrogen production towards commercialization purposes.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.