UCL Discovery
UCL home » Library Services » Electronic resources » UCL Discovery

A Z-scheme Heterojunctional Photocatalyst Engineered with Spatially Separated Dual Redox Sites for Selective CO₂ Reduction with Water: Insight by In situ µs-transient Absorption Spectra

Sun, L; Zhang, Z; Bian, J; Bai, F; Su, H; Li, Z; Xie, J; ... Jing, L; + view all (2023) A Z-scheme Heterojunctional Photocatalyst Engineered with Spatially Separated Dual Redox Sites for Selective CO₂ Reduction with Water: Insight by In situ µs-transient Absorption Spectra. Advanced Materials , 35 (21) , Article e2300064. 10.1002/adma.202300064. Green open access

[thumbnail of Tang_A Z-scheme Heterojunctional Photocatalyst Engineered with Spatially Separated Dual Redox Sites for Selective CO2 Reduction with Water_AAM.pdf]
Preview
Text
Tang_A Z-scheme Heterojunctional Photocatalyst Engineered with Spatially Separated Dual Redox Sites for Selective CO2 Reduction with Water_AAM.pdf

Download (4MB) | Preview

Abstract

Solar-driven CO2 reduction by water with a Z-scheme heterojunction affords an avenue to access energy storage and to alleviate greenhouse gas (GHG) emissions, yet the separation of charge carriers and the integrative regulation of water oxidation and CO2 activation sites remain challenging. Here, a BiVO4/g-C3N4 (BVO/CN) Z-scheme heterojunction as such a prototype is constructed by spatially separated dual sites with CoOx clusters and imidazolium ionic liquids (IL) toward CO2 photoreduction. The optimized CoOx-BVO/CN-IL delivers an ≈80-fold CO production rate without H2 evolution compared with urea-C3N4 counterpart, together with nearly stoichiometric O2 gas produced. Experimental results and DFT calculations unveil the cascade Z-scheme charge transfer and subsequently the prominent redox co-catalysis by CoOx and IL for holes-H2O oxidation and electrons-CO2 reduction, respectively. Moreover, in situ µs-transient absorption spectra clearly show the function of each cocatalyst and quantitatively reveal that the resulting CoOx-BVO/CN-IL reaches up to the electron transfer efficiency of 36.4% for CO2 reduction, far beyond those for BVO/CN (4.0%) and urea-CN (0.8%), underlining an exceptional synergy of dual reaction sites engineering. This work provides deep insights and guidelines for the rational design of highly efficient Z-scheme heterojunctions with precise redox catalytic sites toward solar fuel production.

Type: Article
Title: A Z-scheme Heterojunctional Photocatalyst Engineered with Spatially Separated Dual Redox Sites for Selective CO₂ Reduction with Water: Insight by In situ µs-transient Absorption Spectra
Location: Germany
Open access status: An open access version is available from UCL Discovery
DOI: 10.1002/adma.202300064
Publisher version: https://doi.org/10.1002/adma.202300064
Language: English
Additional information: This version is the author accepted manuscript. For information on re-use, please refer to the publisher's terms and conditions.
Keywords: g-C 3N 4 heterojunction, CO 2 conversions, dual redox sites, electron kinetics, Z-schemes
UCL classification: UCL
UCL > Provost and Vice Provost Offices > UCL BEAMS
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science
UCL > Provost and Vice Provost Offices > UCL BEAMS > Faculty of Engineering Science > Dept of Chemical Engineering
URI: https://discovery.ucl.ac.uk/id/eprint/10170486
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item