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Design and Synthesis of Cu@CuS Yolk-Shell Structures with Enhanced Photocatalytic Activity.

ABSTRACT: Non-spherical Cu@CuS yolk-shell structures are successfully obtained using Cu₂O cube templates in a process combining rapid surface sulfidation followed by disproportionation of the Cu₂O core upon treatment with a hydrochloric acid solution. By employing the above method, Cu@CuS yolk-shell structures with different morphologies, including octahedral, truncated octahedral, and cuboctahedral shapes, can be synthesized. The void space within the hollow structures provides a unique confined space, where the metallic copper present in the core of a shell can be protected from agglomeration and oxidation. Furthermore, the presence of metal copper in these hollow structures contributes to improvement in the photocatalytic properties of these materials. The application of these Cu@CuS structures indeed shows clearly improved photocatalytic performance.

SUBMITTER: Li Q

PROVIDER: S-EPMC6199031 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Synthesis and Photocatalytic Properties of CuO-CuS Core-Shell Nanowires.

Project description:In this study, an efficient method to synthesize CuO-CuS core-shell nanowires by two-step annealing process was reported. CuO nanowires were prepared on copper foil via thermal oxidation in a three-zone horizontal tube furnace. To obtain larger surface area for photocatalytic applications, we varied four processing parameters, finding that growth at 550 °C for 3 h with 16 °C/min of the ramping rate under air condition led to CuO nanowires of appropriate aspect ratio and number density. The second step, sulfurization process, was conducted to synthesize CuO-CuS core-shell nanowires by annealing with sulfur powder at 250 °C for 30 min under lower pressure. High-resolution transmission electron microscopy studies show that a 10 nm thick CuS shell formed and the growth mechanism of the nanowire heterostructure has been proposed. With BET, the surface area was measured to be 135.24 m²·g-1. The photocatalytic properties were evaluated by the degradation of methylene blue (MB) under visible light irradiation. As we compared CuO-CuS core-shell nanowires with CuO nanowires, the 4-hour degradation rate was enhanced from 67% to 89%. This could be attributed to more effective separation of photoinduced electron and hole pairs in the CuO-CuS heterostructure. The results demonstrated CuO-CuS core-shell nanowires as a promising photocatalyst for dye degradation in polluted water.

| S-EPMC6479540 | biostudies-literature

One-pot hydrothermal synthesis of CdS decorated CuS microflower-like structures for enhanced photocatalytic properties.

Project description:CdS decorated CuS structures have been controllably synthesized through a one-pot hydrothermal method. The morphologies and compositions of the as-prepared samples could be concurrently well controlled by simply tuning the amount of CdCl2 and thiourea. Using this strategy, the morphology of the products experienced from messy to flower-like morphologies with multiple porous densities, together with the phase evolution from pure CuS to the CdS/CuS composites. Serving as a photocatalyst, the samples synthesized with the addition of 1 mmol cadmium chloride and 3 mmol thiourea during synthetic process, showed the best photocatalytic activity, which could reach a maximum photocatalytic efficiency of 93% for methyl orange (MO) photodegradation after 150 min. The possible mechanism for the high photocatalytic efficiency of the sample was proposed by investigating the composition, surface area, structure, and morphology before and after photocatalytic reaction.

| S-EPMC5478623 | biostudies-literature

Rational construction of ZnO/CuS heterostructures-modified PVDF nanofiber photocatalysts with enhanced photocatalytic activity.

Project description:PVDF/ZnO/CuS photocatalysts with ZnO/CuS heterojunctions were synthesized via electrospinning, hydrothermal, and ion-exchange techniques. As matrix materials, electrospun PVDF nanofibers are easy to be recycled and reused. ZnO nanorods anchored on PVDF nanofiber with high specific surface area provide abundant active reaction sites for photocatalysis. While the loaded CuS nanoparticles as a photosensitizer compensate the low quantum efficiency of ZnO and improve the visible-light photocatalytic efficiency. As a result, the PVDF/ZnO/CuS composited photocatalyst exhibits outstanding photocatalytic performance in exposure to UV and visible light owing to the suppressed recombination of electron-hole pairs and widened visible light absorption range. The kinetic constants of PVDF/ZnO/CuS nanocomposites under UV irradiation (9.01 × 10-3 min-1) and visible light (6.53 × 10-3 min-1) irradiation were 3.66 and 2.53 times higher than that of PVDF/ZnO (2.46 × 10-3 min-1 & 2.58 × 10-3 min-1), respectively. Furthermore, PVDF/ZnO/CuS nanocomposites demonstrate excellent robustness in terms of recycling and reuse, which is advantageous in practical applications.

| S-EPMC9706242 | biostudies-literature

Growth rate controlled synthesis of hierarchical Bi2S3/In2S3 core/shell microspheres with enhanced photocatalytic activity.

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| S-EPMC3916892 | biostudies-other

Synthesis of open-mouthed, yolk-shell Au@AgPd nanoparticles with access to interior surfaces for enhanced electrocatalysis.

Project description:We have successfully produced open-mouthed, yolk-shell (OM-YS) Au@AgPd nanoparticles (NPs) via galvanic replacement reaction at room temperature; each NP has a large opening on its AgPd shells. Owing to the openings on the AgPd shells, the inner surfaces of the AgPd shells of as-prepared OM-YS Au@AgPd NPs become accessible to the surrounding media. These new structural characters make the present OM-YS Au@AgPd NPs excellent catalysts for electrochemical oxidation of ethanol in alkaline media. Their electrochemical active surface area is 87.8 m2 g-1 and the mass activity is 1.25 A mgPd-1. Moreover, the openings on the AgPd shells also make the surfaces of the Au cores in OM-YS Au@AgPd NPs accessible to the reaction media, which significantly facilitates the removal of CO and other carbonaceous intermediate species, thus leading to substantially enhanced durability and stability. This superior electrocatalytic performance cannot be implemented by using conventional YS Au@AgPd NPs or commercially available Pd/C catalysts.

| S-EPMC5707494 | biostudies-literature

Delicate Design of ZnS@In2S3 Core–Shell Structures with Modulated Photocatalytic Performance under Simulated Sunlight Irradiation

Project description:ZnS@In2S3 core–shell structures

| S-EPMC9835534 | biostudies-literature

Single-step coating of mesoporous SiO2 onto nanoparticles: growth of yolk-shell structures from core-shell structures.

Project description:Yolk-shell nanoparticles based on mesoporous SiO2 (mSiO2) coating of Au nanoparticles (Au NPs) hold great promise for many applications in e.g., catalysis, biomedicine, and sensing. Here, we present a single-step coating approach for synthesizing Au NP@mSiO2 yolk-shell particles with tunable size and tunable hollow space between yolk and shell. The Au NP-mSiO2 structure can be manipulated from core-shell to yolk-shell by varying the concentration of cetyltrimethylammonium chloride (CTAC), tetraethyl orthosilicate (TEOS), Au NPs, and NaOH. The growth mechanism of the yolk-shell particles was investigated in detail and consists of a concurrent process of growth, condensation, and internal etching through an outer shell. We also show by means of liquid-cell transmission electron microscopy (LC-TEM) that Au nanotriangle cores (Au NTs) in yolk-shell particles that are stuck on the mSiO2 shell, can be released by mild etching thereby making them mobile and tumbling in a liquid-filled volume. Due to the systematical investigation of the reaction parameters and understanding of the formation mechanism, the method can be scaled-up by at least an order of magnitude. This route can be generally used for the synthesis of yolk-shell structures with different Au nanoparticle shapes, e.g., nanoplatelets, nanorods, nanocubes, for yolk-shell structures with other metals at the core (Ag, Pd, and Pt), and additionally, using ligand exchange with other nanoparticles as cores and for synthesizing hollow mSiO2 spheres as well.

| S-EPMC8686695 | biostudies-literature

Dual-plasmonic Au@Cu7S4 yolk@shell nanocrystals for photocatalytic hydrogen production across visible to near infrared spectral region.

Project description:Near infrared energy remains untapped toward the maneuvering of entire solar spectrum harvesting for fulfilling the nuts and bolts of solar hydrogen production. We report the use of Au@Cu7S4 yolk@shell nanocrystals as dual-plasmonic photocatalysts to achieve remarkable hydrogen production under visible and near infrared illumination. Ultrafast spectroscopic data reveal the prevalence of long-lived charge separation states for Au@Cu7S4 under both visible and near infrared excitation. Combined with the advantageous features of yolk@shell nanostructures, Au@Cu7S4 achieves a peak quantum yield of 9.4% at 500 nm and a record-breaking quantum yield of 7.3% at 2200 nm for hydrogen production in the absence of additional co-catalysts. The design of a sustainable visible- and near infrared-responsive photocatalytic system is expected to inspire further widespread applications in solar fuel generation. In this work, the feasibility of exploiting the localized surface plasmon resonance property of self-doped, nonstoichiometric semiconductor nanocrystals for the realization of wide-spectrum-driven photocatalysis is highlighted.

| S-EPMC10776726 | biostudies-literature

Synthesis of Double-Shell Hollow TiO2@ZIF-8 Nanoparticles With Enhanced Photocatalytic Activities.

Project description:Synthesis of semiconductor-MOF heterostructure photocatalysts has attracted considerable attention for their thermal stability, controllable crystallinity, and enhanced photocatalytic activity. In this work, the hollow nanostructure of anatase TiO2 was prepared by etching SiO2 from core-shell SiO2@TiO2 nanoparticles. ZIF-8, one of the metal-organic frameworks (MOFs), was hybrid synthesized on the surface of hollow TiO2 and formed double-shell hollow nanoparticles. The photocatalytic activity of the double-shell hollow TiO2@ZIF-8 nanoparticles toward methylene blue (MB) under UV light irradiation was processed, and the highest photocatalytic efficiency of 99.1% was shown compared with TiO2 and SiO2@TiO2 nanoparticles. This study suggests a promising approach to achieve an advanced photocatalytic performance toward dye degradation using MOFs for the surface engineering of semiconductors.

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Nanoporous CuS with excellent photocatalytic property.

Project description:We present the rational synthesis of nanoporous CuS for the first time by chemical dealloying method. The morphologies of the CuS catalysts are controlled by the composition of the original amorphous alloys. Nanoporous Cu2S is firstly formed during the chemical dealloying process, and then the Cu2S transforms into CuS. The nanoporous CuS exhibits excellent photocatalytic activity for the degradation of the methylene blue (MB), methyl orange (MO) and rhodamine B (RhB). The excellent photocatalytic activity of the nanoporous CuS is mainly attributed to the large specific surface area, high adsorbing capacity of dyes and low recombination of the photo generated electrons and holes. In the photo degradation process, both chemical and photo generated hydroxyl radicals are generated. The hydroxyl radicals are favor in the oxidation of the dye molecules. The present modified dealloying method may be extended for the preparation of other porous metal sulfide nanostructures.

| S-EPMC4673457 | biostudies-literature

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