Fabrication of sulphur-doped graphitic carbon nitride anchored Ag@AgCl electrocatalyst for the sensing of chloramphenicol.

We have developed sulphur-doped graphitic carbon nitride (S-GCN) anchored Ag@AgCl electrocatalyst through a green technique for the first time for the electrochemical sensing of chloramphenicol. The Ag@AgCl nanoparticles were synthesized using Rhoeo discolor (Tradescantia spathacea) plant extract without the use of any external halide source. As per our knowledge, this is the first time Rhoeo discolor (Tradescantia spathacea) plant extract was used for the synthesis of Ag@AgCl nanoparticles without the use of any external halide source. Using sonochemical technique, the green synthesized nanoparticle was combined with S-GCN to form Ag@AgCl/S-GCN electrocatalyst. The synthesized materials were characterized by suitable techniques such as UV-visible spectroscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy, transmission electron microscopy and elemental analysis. The electrocatalytic reduction mechanism of chloramphenicol was studied with the help of electrochemical impedance spectroscopy, cyclic voltammetry, and linear sweep voltammetry. The Ag@AgCl/S-GCN modified electrode has shown a linear response in the range of 1 to 650 µM, with a LOD of 420  nM . Further, the practical application of the developed sensor was analyzed using real samples such as milk and honey and satisfactory recovery rates were observed.

Physicochemical properties, biological chemistry and mechanisms of action of caries-arresting diammine-silver(I) fluoride and silver(I)-fluoride solutions for clinical use: a critical review.

This paper serves as a Part II follow-up of our research investigations performed on the molecular structures of silver(I)-fluoride (SF) and diammine-silver(I) fluoride (SDF) complexes in solution-based commercial products for clinical application, their precise chemical compositions, and their nature in aqueous solution, the latter including rapid fluoride-exchange processes at the silver(I) ion centre monitored by 19F NMR analysis (Part I). Part I of this series also explores the mechanisms of action (MoA) of these complexes, and is therefore largely focused on their chemical reactions with constituents of human saliva, which has access to their sites of application. Such reactions were found to slowly promote the generation of potentially physiologically-active Ag/AgCl nanoparticles from primarily-generated discoloured silver(I) chloride (AgCl) precipitates, a process involving salivary electron-donors such as thiocyanate and L-cysteine. Since this research has shed new light on potential MoAs for these products, in this accompanying report (Part II), we have performed a critical review of scientific literature in order to rationalize our results in relation to current views on these mechanisms for SF and SDF products employed for the successful clinical arrest of dental caries. Following an Introduction to the subject matter ( Section 1), this paper comprises a generalized overview of silver coordination chemistry ( Section 2), which is followed by a section focused on the aqueous solution status and equilibria involved in SF chemistry ( Section 3), the latter including results acquired from an original simulation of the electronic absorption spectra of coloured SF complexes in aqueous solution (Section 3.1). Section 4 then investigates detailed rationales for the biologically-relevant ligand-exchange and redox chemistries, disposition and fates of SF, SDF and silver(I)-nitrate when employed for the treatment of dental caries, with emphasis placed on their therapeutic MoAs. This Section is supported by the provision of valuable information centralized on (1) relevant biomolecular chemistry involved in solution- and solid-state matrices ( Section 4.1); (2) SF and perhaps silver(I)-nitrate as more cost-effective alternatives to SDF therapies ( Section 4.2); and (3) the potential therapeutic benefits and effects offered by silver-based nanoparticles and their associated MoAs ( Section 4.3). Recommendations for future investigations in this area are proposed.

Minimization of Parasitic Capacitance between Skin and Ag/AgCl Dry Electrodes.

Conventional dry electrodes often yield unstable results due to the presence of parasitic capacitance between the flat electrode surface and the non-uniform skin interface. To address this issue, a gel is typically placed between the electrodes to minimize parasitic capacitance. However, this approach has the drawbacks of being unsuitable for repeated use, limited lifetime due to gel evaporation, and the possibility of developing skin irritation. This is particularly problematic in underserved areas since, due to the cost of disposable wet electrodes, they often sterilize and reuse dry electrodes. In this study, we propose a method to neutralize the effects of parasitic capacitance by attaching high-value capacitors to the electrodes in parallel, specifically when applied to pulse wave monitoring through bioimpedance. Skin capacitance can also be mitigated due to the serial connection, enabling stable reception of arterial pulse signals through bioimpedance circuits. A high-frequency structure simulator (HFSS) was first used to simulate the capacitance when injection currents flow into the arteries through the bioimpedance circuits. We also used the simulation to investigate the effects of add-on capacitors. Lastly, we conducted preliminary comparative analyses between wet electrodes and dry electrodes in vivo with added capacitance values ranging from 100 pF to 1 µF, altering capacitance magnitudes by factors of 100. As a result, we obtained a signal-to-noise ratio (SNR) that was 8.2 dB higher than that of dry electrodes. Performance was also shown to be comparable to wet electrodes, with a reduction of only 0.4 dB using 1 µF. The comparative results demonstrate that the addition of capacitors to the electrodes has the potential to allow for performance similar to that of wet electrodes for bioimpedance pulse rate monitoring and could potentially be used for other applications of dry electrodes.

Explorations of the chemical constitution and aqueous solution status of caries-arresting silver(I)-diammine fluoride and silver(I)-fluoride products using high-resolution 19F NMR analysis. Spectroscopic and SEM investigations of their interactions with human saliva: evidence for the in vivo salivary-catalysed autoconstruction of Ag/AgCl-based nanoparticles (IV-SCAN)-part I.

Introduction: Silver(I)-diammine fluoride (SDF) and silver(I)-fluoride (SF) complexes have been successfully employed for the arrest of dental caries for many years. However, to date there are very few studies available reporting on the molecular structural compositional and solution status of these agents [typically applied as highly-concentrated 38% (w/v) solutions]. Here, we explored the solution status and chemical constitution of commercially-available SDF and SF products, and secondly investigated the multicomponent interplay of these products with biomolecules present in intact human whole-mouth salivary supernatants (WMSSs) in vitro. Methods: High-resolution 19F NMR analysis was employed to explore SDF and SF product solutions, and to determine WMSS fluoride (F-) concentrations, whereas ammonia (NH3) release form SDF was tracked by 1H NMR spectroscopy. SEM and thin-film FTIR-ATR analyses were employed to explore the atomic and molecular compositions of sequentially-generated AgCl deposits and chromophoric Ag/AgCl nanoparticles (CSNPs); the time-dependent generation of the latter was followed spectrophotometrically. Results: 19F NMR spectra of aqueous SF solutions contained a very broad F- signal (Δv1/2 70 Hz), demonstrating that much of its solvated F- content was rapidly exchanging with Ag(I) on the NMR timescale, but those of SDF had a much sharper resonance, similar to that of "free" F- (4 Hz). Moreover, further NMR results revealed that a popular SDF product contained high molar excesses of both F- and NH3. Treatment of WMSSs with SDF and SF generated an off-white precipitate, which slowly developed into CSNPs at 23°C; SEM demonstrated high contents of both silver and chloride in this material (ca.1:1 atomic content ratio). FTIR-ATR analysis found that the CSNPs formed contained a range of salivary biomolecules, which appear to encapsulate the Ag/AgCl core (significant thiocyanate contents were also found). In conclusion, NMR results acquired demonstrated that SF, but not SDF, product solutions feature rapidly-exchanging F - between its "free" and Ag(I)-bound forms, and that SDF contains large excesses of both F- and its NH3 ligands. Characterised AgCl deposits and CSNPs were sequentially produced from the interactions of these complexes with WMSS biomolecules. Discussion: In view of their well-known microbicidal and cariostatic properties, the observed autobioconstruction of CSNPs involving salivary catalysis is of much therapeutic significance.

Development of super nanoantimicrobials combining AgCl, tetracycline and benzalkonium chloride.

In this work, we demonstrate that a simple argentometric titration is a scalable, fast, green and robust approach for producing AgCl/antibiotic hybrid antimicrobial materials. We titrated AgNO3 into tetracycline hydrochloride (TCH) aqueous solution, thus forming AgCl/TCH in a one-step procedure. Furthermore, we investigated the one-pot synthesis of triply synergistic super-nanoantimicrobials, combining an inorganic source of Ag+ ions (AgCl), a disinfecting agent (benzyl-dimethyl-hexadecyl-ammonium chloride, BAC) and a molecular antibiotic (tetracycline hydrochloride, TCH). Conventional antimicrobial tests, industrial biofilm detection protocols, and in situ IR-ATR microbial biofilm monitoring, have been adapted to understand the performance of the synthesized super-nanoantimicrobial. The resulting hybrid AgCl/BAC/TCH nanoantimicrobials are found to be synergistically active in eradicating Salmonella enterica and Lentilactobacillus parabuchneri bacteria and biofilms. This study paves the way for the development of a new class of super-efficient nanoantimicrobials that combine relatively low amounts of multiple active species into a single (nano)formulation, thus preventing the development of antimicrobial resistance towards a single active principle.

Chemical kinetics of silver diammine fluoride in demineralization and remineralization solutions-an in vitro study.

Introduction: Silver Diammine Fluoride (SDF) is a clinical minimal intervention to manage dentin caries. Its chemistry in demineralization conditions has been investigated widely, but far less in remineralization conditions. The aim was to investigate and compare the chemical reactions when SDF is added to remineralization and demineralization solutions. Methods: 0.01 ml SDF (Riva Star) was added to deionized water (DW); demineralization (DS = pH4) and remineralization (RS = pH7.0) solutions. The time sequence of concentrations of NH4+, F-, and Ag+ were measured using ion selective electrodes (ISEs) every 2 min. The pH was also measured. Precipitates were characterized using x-ray Diffraction (XRD) and, 31P and 19F nuclear magnetic resonance spectroscopy (NMR). Results: The concentrations of NH4+ and Ag+ showed decreasing trends in DW (-0.12 and -0.08 mM/h respectively), and in DS (-1.06 and -0.5 mM/h respectively); with corresponding increase in F- concentration (0.04 and 0.7 mM/h respectively). However, in RS, NH4+ concentration showed little change (0.001 mM/h), and Ag+ and F- concentrations were negligible. XRD results showed that precipitates (in RS only) contained AgCl, and metallic Ag. NMR showed that fluorapatite/carbonated fluorapatite (FAP/CFAP) were formed. The pH increased after SDF addition in all three solutions. Discussion: SDF dissolved to release NH4+, F- and Ag + . In DW and DS, NH4+ combined with Ag+ to form diamminesilver, causing an increase of F- and pH. In RS, F- reacted with Ca2+ and (PO)43- to form FAP/CFAP, and Ag+ reacted with Cl- to form AgCl/Ag. These suggests why SDF is effective in managing dentin caries.

Influence of Double-Pulse Electrodeposition Parameters on the Performance of Ag/AgCl Electrochemical Electrode for Marine Electric Field.

This paper describes a Ag/AgCl electrochemical electrode for marine electric field measurements, which was prepared by depositing silver chloride on a silver foil substrate using double-pulse electrodeposition. The impact of positive direction peak current density and deposition time on electrode performance in the preparation of Ag/AgCl electrodes through double-pulse electrodeposition was investigated. Scanning electron microscopy and voltammetry have been used to study the properties of the prepared electrodes. This work reveals the correlation between the electrochemical behavior of electrodes and the physical properties of their surfaces, especially specific surface area and porosity. The study verified the characteristics of Ag/AgCl marine electric field electrodes obtained with different pulse parameters by analyzing the potential stability and noise level of the electrode in salt water. The study's results have positive significance for improving the accuracy of marine electric field measurements.

Embeddable Chloride Sensor for Monitoring Chloride Penetration into Cement Mortar.

A composite solid chloride sensor consisting of two single sensors, i.e., Ag/AgCl working electrode and Mn/MnO2 reference electrode, was developed. The Ag/AgCl electrode was prepared by the anodic polarization method, while the Mn/MnO2 reference electrode was prepared using the powder compaction technique. Then, the electrochemical performances such as stability, reproducibility, and sensitivity of the composite and single sensors were investigated in a saturated Ca(OH)2 solution and mortar specimen. A current density of 0.5 mA/cm2 and polarization time of 2.5 h were the optimal preparation parameters of the Ag/AgCl selective electrode. The Ag/AgCl selective electrode showed a linear potential response with the logarithm of chloride ion content in solution and had good stability, reproducibility, and anti-polarization performances. In addition, the Mn/MnO2 electrode exhibited potential stability after being activated in an alkaline solution for 60 days. The composite sensor demonstrated exceptional sensitivity to the Cl- content, boasting a slope of approximately 51.1 mV/decade, and showcased excellent stability in both solution and mortar specimens. In every measurement, the time needed for the potential of a composite sensor to become stable was less than 30 s. The sensor enables non-destructive in situ monitoring of the chloride ion content in cement mortar, thus realizing early warning of deterioration of reinforcement and guaranteeing long service life of the structure.

Coaxial Electrospun Porous Core-Shell Nanofibrous Membranes for Photodegradation of Organic Dyes.

In this study, a series of AgCl/ZnO-loaded nanofibrous membranes were prepared using coaxial electrospinning. Their physical and chemical characteristics were evaluated by SEM, TEM, XRD, XPS, IR, PL, and UV-visible spectrometer, and the photocatalytic experiments using methylene blue (MB) as a model pollutant. The formation of AgCl/ZnO heterojunction and the structure of core-shell nanofibers with porous shell layer were confirmed. AgCl/ZnO photocatalysts were also effectively loaded onto the surfaces of the porous core-shell nanofibers. The results of photocatalytic experiments revealed that the AgCl/ZnO (MAgCl:MZnO = 5:5)-loaded nanofibrous membrane achieved a degradation efficiency of 98% in just 70 min and maintained a photocatalytic efficiency exceeding 95% over the first five experimental cycles, which successfully addressed the issues of photocatalytic efficiency loss during the photodegradation of MB with AgCl/ZnO nanoparticles as photocatalyst. The photodegradation mechanism was also researched and proposed.

A scalable route to quaternary ammonium-functionalized AgCl colloidal antimicrobials inhibiting food pathogenic bacteria and biofilms.

This study explores how a simple argentometric titration-like approach could be evolved into a versatile, scalable, fast, and robust strategy for the production of AgCl/quaternary ammonium compounds (QACs) colloidal nanoantimicrobials (NAMs). These systems, which are green, stable, cost-effective, and reproducible are found to be effective against a wide range of food pathogenic bacteria and biofilms. The option of a large-scale production for such colloidal suspensions was explored via the use of a peristaltic pump. The utilization of various types of biosafe QACs and a wide range of solvents including aqueous and organic ones renders this system green and versatile. Nanocolloids (NCs) were characterized using UV-Vis, X-ray photoelectron and Fourier transform infrared (FTIR) spectroscopies. Their morphology and crystalline nature were investigated by transmission electron microscopy (TEM) and selected area diffraction pattern (SAED). Nanoparticle (NP) size distribution and hydrodynamic radius were measured by dynamic light scattering (DLS), while the ζ-potential was found to be highly positive, thus indicating significant colloidal stability and antimicrobial activity. In fact, the higher the NP surface charge, the stronger was their bioactivity. Furthermore, the antibacterial and antibiofilm effects of the as-prepared NCs were tested against Gram-positive bacteria, such as Staphylococcus aureus (ATCC 29213) and Listeria monocytogenes 46, and Gram-negative bacteria, such as Escherichia coli (ATCC 25922) and Pseudomonas aeruginosa (ATCC 27853). The results clearly indicate that AgCl/QACs provide pronounced antibiofilm activity with long-term bacteriostatic effects against foodborne pathogenic bacteria rendering them an ideal choice for active food packaging systems.

Sphere-rod-like Ag/AgCl@Fe2O3 Z-scheme heterojunction as photocatalysts for efficient degradation of tetracycline under visible light irradiation.

Integration of multi-functional components into one is urgent for creating a viable platform to improve photocatalytic efficiency for environmental treatment. Here, MIL-88B-NH2 (Fe) was firstly employed to capture Ag+ cation for the formation of AgCl@MIL-88B-NH2 (Fe), and then turned into the strongly coupled Ag/AgCl@Fe2O3 with sphere-rod-like structure. As prepared Z-scheme Ag/AgCl@Fe2O3 heterojunction exhibited outstanding photocatalytic performance of tetracycline (TC) with a removal efficiency of 94.9% and a reaction kinetics of 0.0272 min-1, superior to single Ag/AgCl or Fe2O3, which attributed to the broad light absorption range and accelerated electron-hole pair separation stemmed from the synergistic effect between surface plasmon resonance effect (SPR) of metal Ag and AgCl/Fe2O3 heterojunction. Meanwhile, Ag/AgCl@Fe2O3 was found to be highly catalytic in the degradation of TC even after consecutive runs. Moreover, active species trapping experiments combined with ESR techniques revealed that superoxide radical, hydroxyl radical, electron, and hole all were involved in photodegradation of TC process. Importantly, the degradation intermediate products of TC were revealed in depth by LC-MS, and a possible degradation pathway was further proposed. This work opens up new insights into the integration of functional composites for the construction of advanced photocatalysts applied in environmental purification.

Biocidal and synergistic effect of three types of biologically synthesised silver/silver chloride nanoparticles.

Three types of silver/silver chloride nanoparticles were obtained by green synthesis from three types of microbial biomass. Their biocidal capacity was tested against six microorganisms. Two filamentous fungi were used that had previously demonstrated the ability to synthesise nanoparticles, Penicillium sp. 8L2 and Botryosphaeria rhodina MAMB-05. Also, the synthesis capacity of a yeast, Rhodotorula mucilaginosa 1S1, was evaluated. The original protocols underwent slight modifications. At the same time, the fractional inhibitory concentration was obtained. The interaction between specific antibiotics and the nanoparticles that showed the greatest biocidal capacity came from Penicillium sp.8L2, and it was studied further. All nanoparticles were characterised by UV-vis spectrophotometry and transmission electron microscopy (TEM). Also, their size distribution was analysed, which was in the range of 4 to 34 nm. The biocidal capacity of the nanoparticles for a group of bacteria and fungi was studied, presenting very low values in the range of 2.5-10 µg/mL for bacteria and 4-256 µg/mL for fungi. The interactions between the nanoparticles synthesised by Penicillium sp. 8L2 and a group of specific antibiotics for the tested microorganisms were also studied, proving that there was a synergistic interaction with vancomycin and ciprofloxacin and Staphylococcus epidermidis CECT 4183 and Escherichia coli CECT 101 bacteria, respectively.

Novel metal peroxide nanoboxes restrain Clostridioides difficile infection beyond the bactericidal and sporicidal activity.

Clostridioides difficile spores are considered as the major source responsible for the development of C. difficile infection (CDI), which is associated with an increased risk of death in patients and has become an important issue in infection control of nosocomial infections. Current treatment against CDI still relies on antibiotics, which also damage normal flora and increase the risk of CDI recurrence. Therefore, alternative therapies that are more effective against C. difficile bacteria and spores are urgently needed. Here, we designed an oxidation process using H2O2 containing PBS solution to generate Cl- and peroxide molecules that further process Ag and Au ions to form nanoboxes with Ag-Au peroxide coat covering Au shell and AgCl core (AgAu-based nanoboxes). The AgAu-based nanoboxes efficiently disrupted the membrane structure of bacteria/spores of C. difficile after 30-45 min exposure to the highly reactive Ag/Au peroxide surface of the nano structures. The Au-enclosed AgCl provided sustained suppression of the growth of 2 × 107 pathogenic Escherichia coli for up to 19 days. In a fecal bench ex vivo test and in vivo CDI murine model, biocompatibility and therapeutic efficacy of the AuAg nanoboxes to attenuate CDI was demonstrated by restoring the gut microbiota and colon mucosal structure. The treatment successfully rescued the CDI mice from death and prevented their recurrence mediated by vancomycin treatment. The significant outcomes indicated that the new peroxide-derived AgAu-based nanoboxes possess great potential for future translation into clinical application as a new alternative therapeutic strategy against CDI.

A flexible and wearable PET-based chemiresistive H2S gas sensor modified with MoS2-AgCl@AgNPs nanocomposite for the dynamic monitoring of egg spoilage.

In this study, a flexible and wearable chemiresistive hydrogen sulfide (H2S) sensor is developed by modifying the MoS2-AgCl@AgNPs (MAAN) nanocomposite on a flexible PET-based Au interdigital electrode (FPAIDE) (MAAN/FPAIDE) to monitor egg spoilage at room temperature inexpensively. A new method is developed for the low-cost batch fabrication of MAAN/FPAIDEs by laser direct writing. The morphology and composition of the synthesized MAAN nanocomposite are investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), and transmission electron microscopy (TEM). Based on the oxygen adsorption model, a new H2S sensing mechanism is discussed, which is related to the formation of p-n junctions between MoS2 and AgCl and the specific adsorption of H2S by AgNPs on the MAAN sensing layer, causing a decrease in resistance. X-ray photoelectron spectroscopy (XPS) is used to characterize the charge transfer between gas molecules and the MAAN sensing layer and sulfide generation during the response process. The concentration of H2S can be detected down to 27 ppb at 25 °C. Finally, the prepared sensor has been successfully utilized in the real-time monitoring of egg spoilage with satisfactory results, indicating its great potential for the application of fresh food quality and safety supervision and the smart packaging of poultry eggs.

Washable and Flexible Screen-Printed Ag/AgCl Electrode on Textiles for ECG Monitoring.

Electrocardiogram (ECG) electrodes are important sensors for detecting heart disease whose performance determines the validity and accuracy of the collected original ECG signals. Due to the large drawbacks (e.g., allergy, shelf life) of traditional commercial gel electrodes, textile electrodes receive widespread attention for their excellent comfortability and breathability. This work demonstrated a dry electrode for ECG monitoring fabricated by screen printing silver/silver chloride (Ag/AgCl) conductive ink on ordinary polyester fabric. The results show that the screen-printed textile electrodes have good and stable electrical and electrochemical properties and excellent ECG signal acquisition performance. Furthermore, the resistance of the screen-printed textile electrode is maintained within 0.5 Ω/cm after 5000 bending cycles or 20 washing and drying cycles, exhibiting excellent flexibility and durability. This research provides favorable support for the design and preparation of flexible and wearable electrophysiological sensing platforms.

Colorimetric sensor based on biogenic nanomaterials for high sensitive detection of hydrogen peroxide and multi-metals.

Hydrogen peroxide (H2O2) and heavy metals, which are among the wastes of the industrial sector, become a threat to living things and the environment above certain concentrations. Therefore, the detection of both H2O2 and heavy metals with simple, low-cost, and fast analytical methods has gained great importance. The use of nanoparticles in colorimetric sensor technology for the detection of these analytes provides great advantages. In recent years, green synthesis of nanomaterials with products that can be considered biowaste is among the popular topics. In this study, silver/silver chloride nanoparticles (Ag@AgCl NPs) were synthesized using the green synthesis method as an eco-friendly and cheap method, the green algae extract was used as a reducing agent. The characterization of Ag@AgCl nanoparticles and green algae extract was carried out with several techniques such as Transmission Electron Microscopy (TEM), UV-Visible spectrometry (UV-Vis), Fourier-transform infrared spectroscopy (FTIR), and X-ray diffraction patterns (XRD) methods were used for characterization. According to TEM analysis, the Ag@AgCl NPs typically spherical in form and range in size from 4 to 10 nm, and UV-vis showed the formation of surface plasmon resonance (SPR) of the Ag@AgCl between 400 and 450 nm. In addition, its activity as a colorimetric sensor for hydrogen peroxide (H2O2) and multi-metal detection was evaluated. Interestingly, Ag/AgCl NPs caused different color formations for 3 metals simultaneously in the sensor study for heavy metal detection, and Fe3+, Cu2+, and Cr6+ ions were detected. The R2 values for H2O2, Fe3+, Cu2+, and Cr6+ were 0.9360, 0.9961, 0.9787, and 0.9625 the limit of detection (LOD) was 43.75, 1.69, 3.18, and 5.05 ppb (ng/mL), respectively. It was determined that Ag@AgCl NPs have the potential to be used as a colorimetric sensor for the detection of H2O2 and heavy metals from wastewater.

Carboxymethyl cellulose gels immobilized Ag/AgCl-ZnO nanoparticles for improving sunlight-catalyzed antibacterial performance.

Antibacterial sodium carboxymethyl cellulose (CMC) gels were prepared via immobilizing ZnO and/or Ag/AgCl in situ to inhibit the aggregation of nano-photocatalyst. Epichlorohydrin was used as a crosslinking agent to prepare CMC gel, simultaneously introducing chlorine-containing branch chains as Cl reservoir to deposit AgCl. The composite gels presented pH responsive swelling properties, with the minimum swelling ratio at pH 8 and pH 4 for CMC gels containing Ag/AgCl and ZnO, respectively. Zn2+ release from the nanocomposite gels was much greater in acidic than in neutral. Photocatalytic degradation constants of methyl orange by the composite gels under sunlight were greater than UV irradiation. Ag/AgCl loaded gel showed a degradation rate of 71.3 % under sunlight for 1 h, with a rate constant approximately 10.2 times higher than ZnO loaded gel. Extract liquids with the gel content below 0.33 mg/mL were noncytotoxicity. The nanocomposite gels presented good bactericidal rate against E. coli and S. aureus under sunlight for 6 h, comparatively to those in dark for 24 h. Bacteriostatic activity of Ag/AgCl loaded gel under sunlight for 6 h was much greater than that in dark for 24 h. The biocompatible nanocomposite gels with sunlight-catalyzed antibacterial activity would broaden the application of CMC gels.

AgCl Addition to Chalcopyrite Compound for Ultra-Low Thermal Conductivity in Realizing High ZT Thermoelectric Materials.

Optimizing the performance of thermoelectric materials by reducing its thermal conductivity is crucial to enhance its thermoelectric efficiency. Novel thermoelectric materials like the CuGaTe2 compound are hindered by high intrinsic thermal conductivity, which negatively impacts its thermoelectric performance. In this paper, we report that the introduction of AgCl by the solid-phase melting method will influence the thermal conductivity of CuGaTe2. The generated multiple scattering mechanisms are expected to reduce the lattice thermal conductivity while maintaining sufficient good electrical properties. The experimental results were supported by first-principles calculations confirming that the doping of the Ag will decrease the elastic constants, bulk modulus, and shear modulus of CuGaTe2, which makes the mean sound velocity and Debye temperature of Ag-doped samples lower than those of CuGaTe2, indicating the lower lattice thermal conductivity. In addition, the Cl elements within the CuGaTe2 matrix escaping during the sintering process will create holes of various sizes within the sample. These combined effects of holes and impurities will induce phonon scattering, which further reduces the lattice thermal conductivity. Based on our findings, we conclude that the introduction of AgCl into CuGaTe2 has shown a lower thermal conductivity without compromising the electrical performance, resulting in an ultra-high ZT value of 1.4 in the (CuGaTe2)0.96(AgCl)0.04 sample at 823 K.

Novel insights into the multistep chlorination of silver nanoparticles in aquatic environments.

Due to the increasing applications, silver nanoparticles (AgNPs) are inevitably released into the environments and are subjected to various transformations. Chloride ion (Cl-) is a common and abundant anion with a wide range of concentration in aquatic environments and exhibits a strong affinity for silver. The results indicate that AgNPs experienced multistep chlorination, which was dependent on the concentration of Cl- in a non-linear manner. The dissolution of AgNPs was accelerated at Cl/Ag ratio of 1 and the intensive etching effect of Cl- contributed to the significant morphology changes of AgNPs. The dissolved Ag+ quickly precipitated with Cl- to form an amorphous and passivating AgCl(s) layer on the surface of AgNPs, thus the dissolution rate of AgNPs decreased at higher Cl/Ag ratios (100 and 1000). As the Cl/Ag ratio further increased to 10,000, the overall transformation rate increased remarkably due to the complexation of Cl- with AgCl(s) to form soluble AgClx(x-1)- species, which was verified by the reaction of AgCl nanoparticles with Cl-. Besides, several environmental factors (electrolytes, surfactants and natural organic matter) affected AgNPs dissolution and the following chlorination. These results will expand the understanding of the environmental fate and potential risks of AgNPs in natural chloride-rich waters.

Facile construction of Z-scheme AgCl/Bi3TaO7 photocatalysts for effective removal of tetracycline under visible-light irradiation.

A string of AgCl/Bi3TaO7 two-component composite was synthesized by hydrothermal and deposition-precipitation process initially. The photocatalytic activities of mixed-phase AgCl/Bi3TaO7 were evaluated toward the decomposition of tetracycline (TC). Among these as-prepared materials, AgCl/Bi3TaO7 nanocomposites when the molar ratio of baked materials between AgCl and Bi3TaO7 was 1:5 presented the optimal photocatalytic quantum efficiency for TC dissociation (86.82%) with visible-light exposure, which was 1.69 and 2.38 folders higher than that of single Bi3TaO7 and AgCl, respectively. What is more, it illustrated that the photo-generated carriers were markedly isolated on account of the formation of heterojunction confirmed by EIS analysis. Meanwhile, radical trapping experiments implied that the photo-induced holes (h+), hydroxyl radical (·OH), and superoxide radical (·O2-) were the major active species. The escalated photocatalytic activity could be ascribed to the unique construction of Z-scheme AgCl/Bi3TaO7 heterojunction, which could expedite charge separation and transmission, cement light absorption capability and retain the strong redox ability of photo-generated electrons and holes. Our finding suggests that AgCl/Bi3TaO7 nanocomposites possess great potential for photocatalytic oxidation of residual TC in the wastewater effluents and the reported strategy can contribute to the development of novel high-performance photocatalyst.