Abstract

To alleviate the energy-crisis and achieve sustainable development, developing efficient energy production strategies is urgent. Here, a novel hierarchical photoanode based on metal-organic framework derived N-doped-carbon TiO2/CsPbBr3/TiO2 (MOF-derived TiO2(N-C)/CPB/TiO2) nanorod is constructed as photoanode for high-performance photoelectrochemical (PEC) glycerol oxidation with simultaneous hydrogen production, to demonstrate a high reactant efficiency during water splitting. With the modification of MOF derivatives assisted CPB, the optical-response and carrier separation are greatly enhanced. The chemical bonding between CPB and MOF-derived N-C can anchor the CPB nanoparticles on the MOF-derived framework, ensuring system stability. By optimizing the electrolyte composition with glycerol adding to the acid Na2SO4 electrolyte, the electrode/electrolyte interfacial carrier injection efficiency is greatly enhanced, leading to improved photocurrent density. Simultaneously, this electrolyte composition adjustment produces value-added chemical materials (1,3-dihydroxyacetone and glyaldehyde), thereby improving the overall photo-induced carrier utilization. With the above synergy optimization, the TiO2(N-C)/CPB/TiO2 photoanode achieves enhanced photocurrent density of 4.50 mA cm−2 at the bias of 1.2 V vs. RHE (in acid Na2SO4/glycerol electrolyte). This work provides novel ideas to construct high-efficient PEC systems with improved carrier utilization efficiency for both high-value chemical and clean energy production.

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.