Search Results (6)

N-butanol (C₄H₉OH) is a volatile organic compound (VOC) that is susceptible to industrial explosions. It has become imperative to develop n-butanol sensors with high selectivity and fast response and recovery kinetics. CdS/Ag₂S composite nanomaterials were designed and prepared by the solvothermal method. The incorporation of Ag₂S engendered a notable augmentation in specific surface area and a consequential narrow band gap. The CdS/Ag₂S-based sensor with 3% molar ratio of Ag₂S, operating at 200 °C, demonstrated a remarkably elevated response (S = R_a/R_g = 24.5) when exposed to 100 ppm n-butanol, surpassing the pristine CdS by a factor of approximately four. Furthermore, this sensor exhibited notably shortened response and recovery times, at a mere 4 s and 1 s, respectively. These improvements were ascribed to the one-dimensional single-crystal nanorod structure of CdS, which provided an effective path for expedited electron transport along its axial dimension. Additionally, the electron and chemical sensitization effects resulting from the modification with precious metal sulfides Ag₂S were the primary reasons for enhancing the sensor response. This work can contribute to mitigating the safety risks associated with the use of n-butanol in industrial processes. Full article

The construction of semiconductor heterojunction photocatalysts that improve the separation and transfer of photoinduced charge carriers is an effective and widely employed strategy to boost photocatalytic performance. Herein, we have successfully constructed a CdS/Ag/Bi₂WO₆ Z-scheme heterojunction with an Ag-bridge as an effective charge transfer channel by a facile process. The heterostructure consists of both CdS and Ag nanoparticles anchored on the surface of Bi₂WO₆ nanosheets. The photocatalytic efficiency of the CdS/Ag/Bi₂WO₆ system was studied by the decontamination of tetracycline (TC) and Rhodamine B (RhB) under visible light irradiation (λ ≥ 420). The results exhibited that CdS/Ag/Bi₂WO₆ shows markedly higher photocatalytic performance than that of CdS, Bi₂WO₆, Ag/Bi₂WO₆, and CdS/Bi₂WO₆. The trapping experiment results verified that the ^•O₂⁻ and h⁺ radicals are the key active species. The results of photoluminescence spectral analysis and photocurrent responses indicated that the CdS/Ag/Bi₂WO₆ heterojunctions exhibit exceptional efficiency in separating and transferring photoinduced electron−hole pairs. Based on a series of characterization results, the boosted photocatalytic activity of the CdS/Ag/Bi₂WO₆ system is mostly due to the successful formation of the Ag-bridged Z-scheme heterojunction; these can not only inhibit the recombination rate of photoinduced charge carriers but also possess a splendid redox capacity. The work provides a way for designing a Z-scheme photocatalytic system based on Ag-bridged for boosting photocatalytic performance. Full article

The construction of a heterojunction by coupling two semiconductor photocatalysts with appropriate band positions can effectively reduce the recombination of photogenerated charge carriers, thus improving their catalytic efficiency. Recently, ZnO photocatalysts have been highly sought after in the synthesis of semiconductor heterostructures due to their wide band gap and low conduction band position. Particularly, transition metal-doped ZnO nanoparticles are attractive due to the additional charge separation caused by temporary electron trapping by the dopant ions as well as the improved absorption of visible light. In this paper, we compare the effect of doping ZnO nanoparticles with 3d (Co and Mn) and 4d (Ag) transition metals on the structural and optical properties of ZnO/CdZnS heterostructures and their photocatalytic performance. With the help of scanning electron microscopy, the successful anchoring of doped and undoped ZnO nanoparticles onto CdZnS nanostructures was confirmed. Among the different heterostructures, Ag-doped ZnO/CdZnS exhibited the best visible-light-driven degradation of rhodamine B at a rate of 1.0 × 10⁻² min⁻¹. The photocurrent density analysis showed that AgZnO/CdZnS has the highest amount of photogenerated charges, leading to the highest photocatalytic performance. The reduction in the photocatalytic performance in the presence of hole scavengers and hydroxyl radical scavengers confirmed that the availability of photogenerated electrons and holes plays a pivotal role in the degradation of rhodamine B. Full article

We have demonstrated a two-step wet chemical approach for synthesizing ternary Ag/Ag₂S/CdS heterostructures for efficient photocatalytic hydrogen evolution. The CdS precursor concentrations and reaction temperatures are crucial in determining the efficiency of photocatalytic water splitting under visible light excitation. In addition, the effect of operational parameters (such as the pH value, sacrificial reagents, reusability, water bases, and light sources) on the photocatalytic hydrogen production of Ag/Ag₂S/CdS heterostructures was investigated. As a result, Ag/Ag₂S/CdS heterostructures exhibited a 3.1-fold enhancement in photocatalytic activities compared to bare CdS nanoparticles. Furthermore, the combination of Ag, Ag₂S, and CdS can significantly enhance light absorption and facilitate the separation and transport of photogenerated carriers through the surface plasma resonance (SPR) effect. Furthermore, the Ag/Ag₂S/CdS heterostructures in seawater exhibited a pH value approximately 2.09 times higher than in de-ionized water without an adjusted pH value under visible light excitation. The ternary Ag/Ag₂S/CdS heterostructures provide new potential for designing efficient and stable photocatalysts for photocatalytic hydrogen evolution. Full article

The development of new-generation photovoltaic devices through more sustainable production techniques and materials is driven by the need to contain the threats to the biosphere while guaranteeing the safety of the supply, accounting for the limited availability of fossil fuels. This study investigates the crystal structure of thin films of chalcogenides, particularly a junction with a p-type (Cu₂S) and an n-type (CdS) layer deposited one on top of the other on a Ag(111) substrate, starting from an aqueous solution and by means of electrochemical atomic layer deposition (E-ALD) (the system is denoted by (Cu₂S)₆₀/(CdS)₆₀/Ag(111)). The experiment highlights the profound epitaxial relationship existing between the films and the bulk, consequent to the homogenization of the metrics of the CdS and the Cu₂S structures to values commensurate to the surface periodicity of the substrate. Cadmium sulfide develops an elementary cell with crystallographic axes parallel to those of the Ag(111) and parameters |a|, |b| and |c| not found in any of the known mineral phases. The comparison with the wurtzite-type structure of greenockite shows a compensation mechanism related to the strain imposed by the film growth on the crystallographic Ag(111) surface. The positions in the reciprocal space of the Cu₂S reflection is compatible with a pseudo-hexagonal pattern rotated by 30° with respect to the Ag, as already noticed in relation to a Cu₂S/Ag(111) E-ALD deposit (Giaccherini et al., 2017). The Cu₂S c axis results parallel to the direction [111] of the Ag substrate and its structure is characterized by the strong occurrence of the 3.963 Å periodicity, which corresponds to the interatomic distance S-S in the triangular CuS₃ groups, the basis of all the mineral Cu_2-xS group structures. These data suggest a pseudo-hexagonal chalcocite-like structure with a planarization of S layers (Giaccherini et al., 2017) as a result of the strong epitaxial relationship existing with the CdS below. This study confirms E-ALD as an energy efficient method for the growth of semiconducting heterostructures with tailored properties. Full article

In this study, we introduce a biological method for the production of ternary Quantum Dots (QDs): complex nanostructures with tunable optical and structural properties that utilizes post-synthesis modifications through cation exchange. This versatile in-situ cation exchange method being reported for the first time shows great potential for extending the scope of microbial synthesis. By using this bacterial-based method, we easily synthesize and purify CdS, CdSAg, and Ag₂S nanocrystals of a size below 15 nm and with variable morphologies that exhibit fluorescence emissions covering a broad spectral range (from 400 to 800 nm). Energy-dispersive X-ray spectroscopy (EDS) results indicate the partial replacement of Cd²⁺ by Ag⁺ when AgNO₃ concentration is increased. This replacement produces CdSAg ternary QDs hetero-structures with high stability, fluorescence in the NIR-I (700 - 800 nm), and 36.13% quantum yield. Furthermore, this reaction can be extended for the production of soluble Ag₂S nanoparticles (NPs) without any traces of Cd. QDs biosynthesized through this cation exchange process display very low toxicity when tested in bacterial or human cell lines. Biosynthesized ternary hetero-structures were used as red fluorescent dyes to label HeLa cells in confocal microscopy studies, which validates its use in bioimaging applications in the near infrared region. In addition, the application of biologically-produced cadmium NPs in solar cells is reported for the first time. The three biosynthesized QDs were successfully used as photosensitizers, where the CdSAg QDs show the best photovoltaic parameters. Altogether, obtained results validate the use of bacterial cells for the controlled production of nanomaterials with properties that allow their application in diverse technologies. We developed a simple biological process for obtaining tunable Quantum Dots (QDs) with different metal compositions through a cation exchange process. Nanoparticles (NPs) are produced in the extracellular space of bacterial cells exposed to cysteine and CdCl₂ in a reaction that depends on S²⁻ generation mediated by cysteine desulfhydrase enzymes and uses cellular biomolecules to stabilize the nanoparticle. Using this extracellular approach, water-soluble fluorescent CdS, CdSAg, and Ag₂S Quantum Dots with a tunable emission ranging from 400 to 800 nm were generated. This is the first study reporting the use of microorganisms to produce tunable ternary QDs and the first time that a cation exchange process mediated by cells is described. Obtained results validate the use of biological synthesis to produce NPs with new characteristics and opens a completely new research field related to the use of microorganisms to synthesize complex NPs that are difficult to obtain with regular chemical methods. Full article