Visible-light-driven CO2 reduction presents a long-term answer to environmental challenges. The limited effective optical carriers generated by the limited response dynamics of the existing photocatalyst have severely hindered the development of high efficiency photocatalysts. Here, we report a method of cobalt atoms intercalation in ultrathin BiOBr nanosheets for boosted photocatalytic CO2 reduction. The experimental results show that there is a strong spatial charge transfer between the intercalated atoms and the two-dimensional material matrix. Cobalt atom intercalation regulates the reaction kinetics of the catalyst, enhances the distribution of photogenerated carriers on the surface of the catalyst, and inhibits the recombination of photogenerated electrons and holes. This atomic intercalation technique increases the catalyst's light absorption efficiency while also improving adsorption and desorption of reactants and gas products. Combined with DFT calculations, it is demonstrated that cobalt atom intercalation introduces additional catalytic active centres, and reduces the free energy of the reaction intermediate COOH*. As a result, under 420nm visible light irradiation in the gas-solid reaction with low water vapor content without any promoters or sacrificial agents, Co-BiOBr achieve a CO formation rate of 36.7 μmol·g-1·h-1, nine times that of the original BiOBr which without cobalt atom intercalation under the same condition.
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http://dx.doi.org/10.1002/cssc.202500128 | DOI Listing |
J Am Chem Soc
March 2025
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, International Center of Future Science, Jilin University, Changchun 130012, P. R. China.
The scientific community has been actively researching artificial photosynthesis to promote ecologically sustainable living and address environmental issues. However, designing photocatalysts with active sites that are effective for both CO reduction and water oxidation remains a significant challenge. Thus, we present the development of a donor-acceptor covalent organic framework (D-A COF), that integrates two distinct metal coordination environments through structure-activity relationships.
View Article and Find Full Text PDFChemSusChem
March 2025
UOW: University of Wollongong, Australian Institute of Innovative Materials, Innovation Campus, University of Wollongong, Squires Way, 2500, North Wollongong, AUSTRALIA.
Visible-light-driven CO2 reduction presents a long-term answer to environmental challenges. The limited effective optical carriers generated by the limited response dynamics of the existing photocatalyst have severely hindered the development of high efficiency photocatalysts. Here, we report a method of cobalt atoms intercalation in ultrathin BiOBr nanosheets for boosted photocatalytic CO2 reduction.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
March 2025
A new cobalt complex, bis-[tris-(amino-thio-urea)cobalt(III)] bis-[2-(carb-oxy-methyl)-2-hy-droxy-butane-dioato]cobalt(II) tetra-nitrate tetra-hydrate, [Co(CHNS)][Co(CHO)](NO)·2HO, designated as [Co(tsc)][Co(cit)](NO)·4HO, was synthesized. Two crystallographically independent cobalt centers are present. In the first, the central metal atom is chelated by three thio-semicarbazide ligands in a bidentate fashion whereas the second, positioned on a crystallographic inversion center, is hexa-coordinated by two citrate anions in a distorted octa-hedral geometry.
View Article and Find Full Text PDFACS Nano
March 2025
Department of Chemical and Biological Engineering, Monash University, Clayton, VIC 3800, Australia.
Compared with acidic environments, promoting the water dissociation process is crucial for speeding up hydrogen evolution reaction (HER) kinetics in alkaline electrolyte. Although the construction of heterostructured electrocatalysts by hybridizing noble metals with metal (hydr)oxides has been reported as a feasible approach to achieve high performance, the high cost, complicated fabrication process, and unsatisfactory mass activity limit their large-scale applications. Herein, we report a single-phase HER electrocatalyst composed of single-atom ruthenium (Ru) incorporated into a cobalt oxide spine structure (denoted as Ru SA/CoO), which possesses exceptional HER performance in alkaline media via unusual atomic-scale Ru-Co pair sites.
View Article and Find Full Text PDFChem Sci
February 2025
State Key Lab of Urban Water Resource and Environment, School of Science, Harbin Institute of Technology (Shenzhen) Shenzhen 518055 China
Dehalogenative deuteration of organic halides is an efficient and straightforward method for incorporating deuterium atoms at specific locations within target molecules. However, utilizing organic halides in photoredox chemistry, particularly unactivated alkyl halides, presents challenges due to their low reduction potentials. In this work, we present a general and effective photoinduced dehalogenative deuteration method for a diverse array of alkyl halides, employing DO as an economical source of deuterium.
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