The photocatalytic reduction of carbon dioxide (CO) has emerged as a compelling strategy for the conversion of renewable energy. However, the expeditious recombination of photogenerated charge carriers and the inadequate light absorption capabilities are currently predominant challenges. Herein, we developed a facile hydrothermal approach to synthesize a sulfur doped BiOCO nanosheet with a tunable energy band structure designed to enhance visible light absorption. Our findings indicate that the incorporation of sulfur into the catalytic sites induces an electron sink effect, significantly improving the separation efficiency of photogenerated charge carriers. Consequently, this sulfur-doped BiOCO catalyst exhibits a remarkable carbon monoxide (CO) yield of 16.64 μmol g h with nearly 100 % selectivity under illumination ranging from 420 to 780 nm. Through in-situ characterization techniques and theoretical calculations, it was revealed that sulfur-coordinated bismuth sites greatly enhance CO adsorption and decrease the energy barrier for critical intermediates formation (*COOH), thus selectively driving the reaction towards CO production. This work not only advances our understanding of mechanisms underlying photocatalytic reduction of CO on sulfur-doped bismuth-based catalysts but also sets a precedent for developing sophisticated photocatalytic systems for enhanced photoreduction reactions.
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http://dx.doi.org/10.1002/cssc.202401054 | DOI Listing |
Chem Sci
January 2025
Department of Chemical Sciences, Indian Institute of Science Education and Research Mohanpur 741246 Kolkata India
Developing a self-sensitized catalyst from earth-abundant elements, capable of efficient light harvesting and electron transfer, is crucial for enhancing the efficacy of CO transformation, a critical step in environmental cleanup and advancing clean energy prospects. Traditional approaches relying on external photosensitizers, comprising 4d/5d metal complexes, involve intermolecular electron transfer, and attachment of photosensitizing arms to the catalyst necessitates intramolecular electron transfer, underscoring the need for a more integrated solution. We report a new Cu(ii) complex, K[CuNDPA] (1[K(18-crown-6)]), bearing a dipyrrin amide-based trianionic tetradentate ligand, NDPA (HL), which is capable of harnessing light energy, despite having a paramagnetic Cu(ii) centre, without any external photosensitizer and photocatalytically reducing CO to CO in acetonitrile : water (19 : 1 v/v) with a TON as high as 1132, a TOF of 566 h and a selectivity of 99%.
View Article and Find Full Text PDFSmall
January 2025
State Key Laboratory of Electromechanical Integrated Manufacturing of High-Performance Electronic Equipments, School of Mechano-Electronic Engineering, Xidian University, Xi'an, 710071, China.
Heterojunctions are sustainable solutions for the photocatalytic CO reduction reaction (CORR) by regulating charge separation behavior at the interface. However, their efficiency and product selectivity are severely hindered by the inflexible and weak built-in electric field and the electronic structure of the two phases. Herein, ferroelectric-based heterojunctions between polarized bismuth ferrite (BFO(P)) and CdS are constructed to enhance the interfacial interactions and catalytic activity.
View Article and Find Full Text PDFChem Asian J
January 2025
CSIR-National Chemical Laboratory: CSIR National Chemical Laboratory, Catalysis and Inorganic Chemistry Division, Dr. Homi Bhabha Road, 411 008, Pune, INDIA.
Present work describes a sol-gel assisted one-pot synthesis of mesoporous Fe₂O₃-TiO₂ nanocomposites (TiFe) with different Ti:Fe ratios, and fabrication of Ag-integrated with TiFe nanocomposites (TiFeAg) by a chemical reduction method and demonstrated for high solar H2 generation activity in direct sunlight. Enhanced solar H2 production is attributed to the light absorption from entire UV+Visible region of solar spectrum combined with Schottky (Ag-semiconductor) and heterojunctions (TiO2-Fe2O3), as evidenced from HRTEM and various characterization studies. TiFeAg-2 thin film (1 wt% Ag-loaded TiFe-4) displayed the highest activity with a solar H2 yield of 7.
View Article and Find Full Text PDFJ Colloid Interface Sci
January 2025
State Key Laboratory Base for Eco-chemical Engineering, Key Laboratory of Multiphase Flow Reaction and Separation Engineering of Shandong Province, College of Chemical Engineering, Qingdao University of Science and Technology, Qingdao 266042, China. Electronic address:
Modifying CdZnS with precious metal at the atomic scale is a promising approach for maximizing its photocatalytic performance. Herein, Rh single atoms (Rh) were successfully anchored on hollow microflower MoS/sulfur-vacancy-rich CdZnS (CZS-SVs) to boost H generation. The optimal catalyst Rh@MoS/CZS-SVs reaches a H productivity of 39,827 μmol h g, representing 5.
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
State Key Laboratory of Catalysis, Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, PR China.
A prevalent challenge in particulate photocatalytic water splitting lies in the fact that while numerous photocatalysts exhibit outstanding hydrogen evolution reaction (HER) activity in organic sacrificial reagents, their performance diminishes markedly in a Z-scheme water splitting system using electronic mediators. This underlying reason remains undefined, posing a long-standing issue in photocatalytic water splitting. Herein, we unveiled that the primary reason for the decreased HER activity in electronic mediators is due to the strong adsorption of shuttle ions on cocatalyst surfaces, which inhibits the initial proton reduction and results in a severe backward reaction of the oxidized shuttle ions.
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