Coordination Chemistry Reviews, Год журнала: 2024, Номер 521, С. 216177 - 216177
Опубликована: Авг. 29, 2024
Язык: Английский
Coordination Chemistry Reviews, Год журнала: 2024, Номер 521, С. 216177 - 216177
Опубликована: Авг. 29, 2024
Язык: Английский
Energy & Environmental Science, Год журнала: 2021, Номер 15(3), С. 880 - 937
Опубликована: Ноя. 16, 2021
Photocatalytic CO 2 conversion is vital technology to realize global carbon neutrality and generate future energy supplies. This review proposes fundamentals, challenges, strategies, prospects for photocatalytic research.
Язык: Английский
Процитировано
553ACS Nano, Год журнала: 2022, Номер 16(9), С. 13370 - 13429
Опубликована: Сен. 12, 2022
Photocatalytic water splitting, CO2 reduction, and pollutant degradation have emerged as promising strategies to remedy the existing environmental energy crises. However, grafting of expensive less abundant noble-metal cocatalysts on photocatalyst materials is a mandatory practice achieve enhanced photocatalytic performance owing ability extract electrons efficiently from enable rapid/enhanced catalytic reaction. Hence, developing highly efficient, inexpensive, noble-metal-free composed earth-abundant elements considered noteworthy step toward considering photocatalysis more economical strategy. Recently, MXenes (two-dimensional (2D) transition-metal carbides, nitrides, carbonitrides) shown huge potential alternatives for cocatalysts. several excellent properties, including atomically thin 2D morphology, metallic electrical conductivity, hydrophilic surface, high specific surface area. In addition, they exhibit Gibbs free intermediate H atom adsorption close zero than that commercial Pt-based cocatalyst, Fermi level position above H2 generation potential, an capture activate molecules. Therefore, there growing interest in MXene-based various events. this review, we focus recent advances synthesis with 0D morphologies, stability MXenes, photocatalysts evolution, degradation. The challenges possible future directions enhance are also discussed.
Язык: Английский
Процитировано
372Nature Reviews Methods Primers, Год журнала: 2023, Номер 3(1)
Опубликована: Авг. 10, 2023
Язык: Английский
Процитировано
343Chemical Society Reviews, Год журнала: 2022, Номер 51(16), С. 6965 - 7045
Опубликована: Янв. 1, 2022
This review summarizes the recent advances in light driven catalytic H 2 evolution and CO reduction systems towards production of solar fuels, utilizing porphyrin or phthalocyanine derivatives.
Язык: Английский
Процитировано
226Joule, Год журнала: 2022, Номер 6(2), С. 294 - 314
Опубликована: Янв. 31, 2022
Carbon recycling will become a dominant trend toward alleviating extreme climate change and coping with the increasing energy demand in coming years. Solar-driven strategies have potential to convert CO2 solar fuels chemicals. In this forward-looking perspective, framework is outlined achieve "net-zero emission" blueprint by sorting out raw sources, products, feasible pathways, practical implementation through photocatalysis, photothermal catalysis, photoelectrochemical catalysis techniques. We comprehensively inspect compare state-of-art works framework, including solar-driven C1 fuel production from CO2, as well direct stepwise C2+ involving conversion. This analysis aspires provide most pathway forward finds that converting renewable H2 into can currently obtain best solar-to-fuel conversion efficiency target products high selectivity. Future visions on scientific, technological, economic issues are put determine what should be focus following decades.
Язык: Английский
Процитировано
216Chemical Society Reviews, Год журнала: 2023, Номер 52(5), С. 1773 - 1946
Опубликована: Янв. 1, 2023
This review summarizes the use of zeolites and ordered mesoporous silica-based catalysts, development new processes technologies to boost conversion CO 2 into chemicals fuels.
Язык: Английский
Процитировано
192Advanced Materials, Год журнала: 2022, Номер 34(14)
Опубликована: Фев. 3, 2022
Plasmonic nanostructures have tremendous potential to be applied in photocatalytic CO2 reduction, since their localized surface plasmon resonance can collect low-energy-photons derive energetic "hot electrons" for reducing the activation-barrier. However, hot electron-driven reduction is usually limited by poor efficiency and low selectivity producing kinetically unfavorable hydrocarbons. Here, a new idea of plasmonic active spot"-confined photocatalysis proposed overcome this drawback. W18 O49 nanowires on outer Au nanoparticles-embedded TiO2 electrospun nanofibers are assembled obtain lots Au/TiO2 /W18 sandwich-like substructures formed heterostructure. The short distance (< 10 nm) between adjacent induce an intense plasmon-coupling form spots" substructures. These capable not only gathering incident light enhance generation migration, but also capturing protons CO through dual-hetero-active-sites (Au-O-Ti W-O-Ti) at interface, as evidenced systematic experiments simulation analyses. Thus, during 43± 2 °C, these enriched well-designed heterostructure synergistically confine hot-electron, proton, intermediates resulting CH4 production-rates ≈35.55 ≈2.57 µmol g-1 h-1 , respectively, -product ≈93.3%.
Язык: Английский
Процитировано
172Coordination Chemistry Reviews, Год журнала: 2022, Номер 474, С. 214846 - 214846
Опубликована: Сен. 27, 2022
Язык: Английский
Процитировано
167Coordination Chemistry Reviews, Год журнала: 2022, Номер 469, С. 214664 - 214664
Опубликована: Июнь 24, 2022
Язык: Английский
Процитировано
156ACS Catalysis, Год журнала: 2022, Номер 12(15), С. 9670 - 9678
Опубликована: Июль 25, 2022
Sluggish charge kinetics and low CO2 affinity seriously limit the photocatalytic reduction reaction. Herein, simultaneous promotion of transfer activation over two-dimensional (2D) WO3 nanosheets is achieved by coupling surface C-doping oxygen vacancy. The surface-doped C atoms reconstruct atomic extracting lattice to generate intimate vacancy (C–OV coordination) as active center, which facilitates adsorption/activation, thus inducing formation *CO2 species. As a delivery channel, an exclusive W–O–C covalent bond formed C–OV coordination could enhance electron transfer. result, as-designed catalyst exhibits 85.8% selectivity for photoreduction CO under gas–solid phase reaction, with yield rate 23.2 μmol g–1 h–1 stable long-term reactivity 24 h. Moreover, in situ DRIFTS DFT results reveal that this specific enables spontaneous proton-coupled guarantee sustained *COOH and, thus, smooth This work develops feasible strategy electronic structure modification photocatalysts doping-induced boost photoreduction.
Язык: Английский
Процитировано
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