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  • Chen, Wenbin  (2)
  • 1
    In: Journal of Materials Chemistry A, Royal Society of Chemistry (RSC), Vol. 10, No. 39 ( 2022), p. 20934-20945
    Abstract: Exploring highly efficient heterostructured photocatalysts for converting CO 2 to value-added chemicals has long been pursued, which is mainly limited by inefficient visible/near-infrared (NIR) photon capture, undesirable electron–hole recombination, and insufficient accessible active sites. Herein, we report a robust heterojunction photocatalyst, consisting of mesh-like Bi 2 S 3 nanoarrays epitaxially grown on BiOBr nanoplates via a facet-selective topotactic transformation process, for synchronically overcoming the aforementioned obstacles and markedly advancing the CO 2 conversion efficiency: (i) vertically aligned Bi 2 S 3 nanowalls harness solar photons from the visible to NIR region beyond 1000 nm and minimize the light shielding effect on BiOBr substrates, while multiple light reflection in the mesh pores enclosed by Bi 2 S 3 walls and BiOBr supports accounts for improved light utilization efficiency; (ii) intimate coupling of BiOBr and Bi 2 S 3 endows the heterojunction with enhanced charge separation efficiency through the interfacial Bi–S/Br–Bi bonds between them; (iii) etched pores and oxygen vacancies on the surface of BiOBr strengthen the adsorption and activation of CO 2 , and decrease the barrier of the rate-determining step in CO 2 -to-CO reduction. By virtue of these distinguished features, the optimized BiOBr/Bi 2 S 3 heterojunction delivers an outstanding CO evolution rate of 103.5 μmol g cat −1 h −1 and selectivity of 90.1% under broadband light irradiation. This work sets up a significant milestone in simultaneously manipulating the three critical steps in photocatalysis during the construction of novel hybrid architectures for solar energy conversion applications.
    Type of Medium: Online Resource
    ISSN: 2050-7488 , 2050-7496
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2022
    detail.hit.zdb_id: 2702232-8
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  • 2
    In: Small, Wiley, Vol. 19, No. 17 ( 2023-04)
    Abstract: Coupling hollow semiconductor with metal–organic frameworks (MOFs) holds great promise for constructing high‐efficient CO 2 photoreduction systems. However, energy band mismatch between them makes it difficult to exert their advantages to maximize the overall photocatalytic efficiency, since that the blockage of desirable interfacial charge transfer gives rise to the enrichment of photoelectrons and CO 2 molecules on the different locations. Herein, an interfacial engineering is presented to overcome this impediment, based on the insertion of plasmonic metal into the heterointerfaces between them, forming a stacked semiconductor/metal@MOF photocatalyst. Experimental observations and theoretical simulations validate the critical roles of embedded Au in maneuvering the charge separation/transfer and surface reaction: (i) bridges the photoelectron transfer from hollow CdS (H‐CdS) to ZIF‐8; (ii) produces hot electrons and shifts them to ZIF‐8; (iii) induces the formation of ZIF‐8 defects in promoting the CO 2 adsorption/activation and transformation to CO with low energy barriers. Consequently, the as‐prepared H‐CdS/Au@ZIF‐8 with optimal ZIF‐8 thickness exhibits distinctly boosted activity and superb selectivity in CO production as compared with H‐CdS@ZIF‐8 and other counterparts. This work provides protocols to take full advantages of components involved for enhanced solar‐to‐chemical energy conversion efficiency of hybrid artificial photosynthetic systems through rationally harnessing the charge transfer between them.
    Type of Medium: Online Resource
    ISSN: 1613-6810 , 1613-6829
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2023
    detail.hit.zdb_id: 2168935-0
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