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The widespread distribution of antibiotics in natural waters is a great threat to human health. Photocatalytic degradation is an environmentally friendly technology to remediate antibiotic-polluted waters, driven by endless solar energy. Herein, a Z-scheme Ag 2 S-Ag-In 2 O 3 heterostructure photocatalyst is prepared to remove antibiotics under environmental conditions. Under natural sunlight (light intensity: ∼78 mW/cm 2 ) irradiation, the optimal Ag 2 S-Ag-In 2 O 3 (10-ASAIO) exhibits considerable performance for decomposing diverse antibiotics, including norfloxacin (NOR), tetracycline hydrochloride, sulfisoxazole, ciprofloxacin, chlortetracycline hydrochloride, and ofloxacin. The NOR photodegradation rate constant of 10-ASAIO reaches 0.025 min -1 , which is 12.50, 5.00, and 6.25 times higher than that of In 2 O 3 (0.002 min -1 ), Ag-In 2 O 3 (0.005 min -1 ), and Ag 2 S-In 2 O 3 (0.004 min -1 ), respectively. This performance of the 10-ASAIO photocatalyst for decomposing NOR under natural sunlight exceeds most of the previously reported photocatalysts under a xenon lamp. Particularly, due to the intermittency of natural sunlight, a light-emitting diode (LED) lamp (light intensity: 5.1 mW/cm 2 ) is also used as a light source, and 72.20% of NOR can be degraded with irradiation for 12 h. The effects of many water characteristics (water bodies, coexisting inorganic anions, pH, and humic acid) on the degradation performance of 10-ASAIO have been investigated, which exhibits stable degradation efficiency in variable aquatic environments. A 10-ASAIO catalyst-coated frosted glass sheet is fabricated to settle the problem of recovery of powder photocatalysts, and the immobilized catalyst shows outstanding activity and stability to decompose NOR. The photocatalytic mechanism and pathway of degrading NOR over 10-ASAIO have also been systemically investigated and proposed. The ecotoxicity (phytotoxicity and biotoxicity) of the 10-ASAIO photocatalyst and treated NOR solution have been tested by their toxic effects on cabbage seeds and Staphylococcus aureus ( S. aureus ). This work provides a feasible photocatalytic system for environmental pollutant remediation under natural sunlight or an LED lamp.

Light-driven endogenous water oxidation has been considered as an attractive and desirable way to obtain O 2 and reactive oxygen species (ROS) in the hypoxic tumor microenvironment. However, the use of a second near-infrared (NIR-II) light to achieve endogenous H 2 O oxidation to alleviate tumor hypoxia and realize deep hypoxic tumor phototherapy is still a challenge. Herein, novel plasmonic Ag-AgCl@Au core-shell nanomushrooms (NMs) were synthesized by the selective photodeposition of plasmonic Au at the bulge sites of the Ag-AgCl nanocubes (NCs) under visible light irradiation. Upon NIR-II light irradiation, the resulting Ag-AgCl@Au NMs could oxidize endogenous H 2 O to produce O 2 to alleviate tumor hypoxia. Almost synchronously, O 2 could react with electrons on the conduction band of the AgCl core to generate superoxide radicals (O 2 •- )for photodynamic therapy. Moreover, Ag-AgCl@Au NMs with an excellent photothermal performance could further promote the phototherapy effect. In vitro and in vivo experimental results show that the resulting Ag-AgCl@Au NMs could significantly improve tumor hypoxia and enhance phototherapy against a hypoxic tumor. The present study provides a new strategy to design H 2 O-activatable, O 2 - and ROS-evolving NIR II light-response nanoagents for the highly efficient and synergistic treatment of deep O 2 -deprived tumor tissue.

The serious problem of pharmaceutical and personal care product pollution places great pressure on aquatic environments and human health. Herein, a novel coating photocatalyst was synthesized by adhering Ag-AgCl/WO 3 /g-C 3 N 4 (AWC) nanoparticles on a polydopamine (PDA)-modified melamine sponge (MS) through a facile layer-by-layer assembly method to degrade trimethoprim (TMP). The formed PDA coating was used for the anchoring of nanoparticles, photothermal conversion, and hydrophilic modification. TMP (99.9%; 4 mg/L) was removed in 90 min by the photocatalyst coating (AWC/PDA/MS) under visible light via a synergistic photocatalytic-photothermal performance route. The stability and reusability of the AWC/PDA/MS have been proved by cyclic experiments, in which the removal efficiency of TMP was still more than 90% after five consecutive cycles with a very little mass loss. Quantitative structure-activity relationship analysis revealed that the ecotoxicities of the generated intermediates were lower than those of TMP. Furthermore, the solution matrix effects on the photocatalytic removal efficiency were investigated, and the results revealed that the AWC/PDA/MS still maintained excellent photocatalytic degradation efficiency in several actual water and simulated water matrices. This work develops recyclable photocatalysts for the potential application in the field of water remediation.

The immunosuppressive tumor microenvironment has caused great obstacles to tumor immunotherapy, especially where less tumor-associated antigens are released from tumor sites. Herein, a Ag2S QD/DOX/Bestatin@PC10ARGD genetically engineered polypeptide hydrogel PC10ARGD as a sustained-release material was developed for mammary carcinoma treatment. A near-infrared silver sulfide (Ag2S) QD as a photosensitizer was encapsulated into the hydrophobic cavity formed by the self-assembly of the polypeptide nanogel (PC10ARGD) for photothermal therapy. The water-soluble drug DOX and Bestatin were integrated into the PC10ARGD hydrogel. The photothermal effect could trigger the sustained release of the DOX, which could be applied to initiate in situ vaccination. Bestatin as an immune-adjuvant drug could amplify the body's immune function. The results of in vivo therapy tests exhibited that the Ag2S QD/DOX/Bestatin@PC10ARGD hydrogel with laser irradiation could activate anti-tumor immune effects that inhibit the growth of primary tumors and distal lung metastatic nodules. Meanwhile, a safer lower-temperature with multiple laser irradiation treatment strategy exhibited more effective tumor-killing performance (84.4% tumor inhibition rate) and promoted the penetration of immune cells into the tumor tissue. The CD8+ and CD4+ cytotoxic T cells ratio was increased by 5.3 and 10 times, respectively, thus exhibiting a good prognostic signal. The multifunctional polypeptide hydrogel as a green manufacturing and engineering material is promising to serve as a cancer vaccine for anticancer applications.

An intramolecular photoelectrochemical (PEC) system is designed from the novel electron donor YYYHWRGWV (Y3-H) peptide ligand for the first time. The bifunctional nonapeptide cannot only rely on the HWRGWV sequence as a site-oriented immobilizer to recognize the crystallizable fragment (Fc) domains of the antibody but also acts as electron donors for PEC generation via three tyrosine (Y) of the N-terminal. The Bi 2 WO 6 /AgInS 2 heterojunction with a significant visible-light absorption is utilized as a photoelectric generator, and the motivation is ascribed to a proven proposition, namely, that short-wavelength illuminant radiates proteins, causing a decline in bioactivity of immune protein. An innovative biosensor is fabricated using the above strategies for the detection of CYFRA21-1, a biomarker of squamous cell lung carcinoma. This sort of PEC-based sensing platform shows convincing experimental data and could be an effective candidate for clinical application in the future due to their extremely skillful conception.

We report here sensitive photoelectrochemical immunosensing of Staphylococcus aureus (S. aureus) using ZnS-Ag 2 S/polydopamine (PDA) as a novel photoelectric material and Cu 2 O as the peroxidase mimic tag. ZnS-Ag 2 S heterojunctions were prepared on indium tin oxide (ITO) via electrodeposition of ZnS nanoparticles, followed by silver ion exchange. To prepare a PDA/ZnS-Ag 2 S/ITO, the ZnS-Ag 2 S/ITO electrode was coated with PDA by self-polymerization of dopamine. The photocurrent of the PDA/ZnS-Ag 2 S/ITO is 1.55 times that of the ZnS-Ag 2 S/ITO and 7.87 times that of the ZnS/ITO, indicating a high-performance photoelectric material. A sandwiched-type photoelectrochemical immunosensor was constructed by using PDA/ZnS-Ag 2 S/ITO as the photoelectrode and Cu 2 O nanocubes as the labels. Cu 2 O nanocubes can serve as peroxidase mimic to generate catalytic precipitates on the immunoelectrodes, and both the Cu 2 O nanocubes and the generated precipitates can decrease the photocurrents of the immunoelectrodes, so a photoelectrochemical immunosensor for detecting S. aureus was constructed, showing a linear range between 10 and 10 7  CFU mL -1 and a low detection limit of 2 CFU mL -1 . Owing to the signal amplification of Cu 2 O labeling, the sensitivity of the Cu 2 O-labeled immunosensor is 4 times that of a label-free immunosensor for detecting S. aureus, and the detection limit (2 CFU mL -1 ) is lower than that of a label-free immunosensor (10 CFU mL -1 ). This work not only provides a new and efficient photoelectric material but also demonstrated an efficient signal-amplification strategy for photoelectrochemical biosensing., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Silver iodide/graphitic carbon nitride nanocomposites have been successfully fabricated through sonication-assisted deposition-precipitation route at room temperature and hydrothermal method. Varied mass ratios and preparation processes can modify the structure, purity, shape, and scale of specimens. The purity of the product was confirmed by Energy Dispersive X-Ray Spectroscopy (EDS) and X-ray crystallography. The morphology and size of specimens could be observed with transmission electron microscopy (TEM) and field emission scanning electron microscopy (FESEM). The bandgap was evaluated around 2.82 eV for pure g-C 3 N 4 . The bandgap has reduced to 2.70 eV by increasing the quantity of silver iodide in the nanocomposites. The photocatalytic activity of AgI/C 3 N 4 has been studied over the destruction of rhodamine B (RhB) and methyl orange (MO) through visible radiation due to their suitable bandgap. The as-prepared AgI/C 3 N 4 nanocomposites photocatalyst revealed better photocatalytic behavior than the genuine AgI and C 3 N 4 which ascribed to synergic impacts at the interconnection of C 3 N 4 and AgI. Furthermore, these nanocomposites have great potential for being a great antibacterial agent., Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2020 Elsevier B.V. All rights reserved.)

Photocatalytic catalysis is widely used for pollutant degradation. Since some pollutants with oxidative nature are readily reduced rather than oxidized and reductive reaction caused by photogenerated electrons is limited in the presence of oxygen, photocatalytic reduction process is more applicable for the degradation of pollutants with oxidative nature than oxidation. In this work, a novel bio-photoelectric reductive degradation system (BPRDS), composed of an electrochemically active bacterium Shewanella oneidensis MR-1 and a visible-light photocatalyst Ag 3 PO 4 , was established under anaerobic conditions and its photodegradation performance was evaluated through degrading rhodamine B (RhB), a typical organic pollutant. The as-synthesized Ag 3 PO 4 nanoparticles exhibited absorption in the entire visible spectral range of 400-800 nm. RhB could be degraded in BPRDS with visible light irradiation under anaerobic conditions, but not be decomposed in the absence of Shewanella cells. Block of Mtr respiratory pathway, a transmembrane electron transport chain, resulted in a reduction in degradation rate of RHB in BPRDS. Dose of riboflavin also substantially decreased the RhB degradation. These results suggest that the electrons released by Shewanella were involved in the RhB photodegradation, which was achieved via a stepwise N-deethylation process. In BPRDS, RhB was degraded by photoreduction, rather than photooxidation. This work is useful to develop integrated physico-chemical-microbial systems for pollutant degradation, facilitate better understanding about the biophotoelectric reductive degradation mechanisms and beneficial to their applications for environmental remediation., (Copyright © 2019. Published by Elsevier Ltd.)

CeO 2 /Ag 2 CrO 4 composite photocatalyst was successfully fabricated using electrospinning and calcination and chemical precipitation method based on CeO 2 ribbon-like fibers and characterized by field-emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX), X-ray diffraction (XRD), UV-Vis diffuse reflectance spectroscopy (DRS) and Fourier-transform infrared spectroscopy (FT-IR). The as-obtained CeO 2 /Ag 2 CrO 4 composite used photocatalytic performance in the sonophotodegradation of rhodamine B in aqueous solution under visible-light (LED) irradiation. DRS analysis illustrates that CeO 2 /Ag 2 CrO 4 composite exhibited enhanced absorption in the visible region-attributed CeO 2 nanofibers . The effect of four effective parameters including initial concentration of rhodamine B (RhB), photocatalyst dosage, pH, and irradiation time was studied and optimized using central composite design. The kinetic studies confirmed ability of pseudo first-order reaction based on the Langmuir-Hinshelwood model for fitting empirical data, while its rate constant (k obs ), L-H rate constants (k r ), and L-H adsorption constants (K A ) were 0.0449 min -1 , 11.66 mg L -1  min -1 and 1.09E-3 mg L -1 , respectively. The enhanced photocatalytic activity could be ascribed to the ultrasound field and formation of a heterojunction system among CeO 2 and Ag 2 CrO 4 , which lead to a better mass transfer and higher efficiency of charge electron-hole separation, respectively.

To promote the utilization of collagen fiber, silver salts/collagen fiber hybrid composites with photocatalytic and antibacterial activities were successfully prepared in this study via the in-situ organic-inorganic process. The surface morphology, chemical composition and structure were discussed. Scanning electron microscopy (SEM) observation showed that the silver salts/collagen fiber hybrid composites were successfully prepared with silver salt particles (300-500 nm) distributing evenly on the surface of collagen fiber. X-ray diffraction (XRD) patterns and Fourier transform infrared spectroscopy (FTIR) analysis provided strong evidence for the successful coating of silver salts on the surface of collagen fiber and the hybrid mechanism was subsequently discussed. The photocatalytic activity was evaluated by degrading methyl orange (MO) under ultraviolet (UV) light and visible light, respectively. The results indicated that AgCl/Collagen Fiber showed the most efficient photocatalytic activity under UV and visible light irradiation. Furthermore, the introduction of Ag + endowed the photocatalysts with antibacterial performance, which was investigated by measuring the width of the bacteriostatic belts. The results indicated the antibacterial activity of the composites, proving that the photocatalysts were durable and reusable., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Magnetic Fe 3 O 4 @BiOI@AgI (FBA) spheres were synthesized through a multi-step process. The fabricated photocatalysts were characterized by different techniques. To testify the visible light driven photocatalytic activity of FBA, Rhodamine B and Bisphenol A were chosen as model common and emerging organic contaminants, respectively. While, gram-negative strain Escherichia coli was selected as model waterborne bacteria. The results showed that under visible light irradiation, FBA contained strong photocatalytic degradation capacity towards both RhB and BPA. Moreover, FBA was also found to exhibit excellent disinfection activity towards E. coli. The photocatalytic mechanisms for different pollutants by FBA were determined and found to vary for different pollutants. Specifically, scavenger experiments, degradation intermediates determination, as well as theoretical density functional theory (DFT) analysis showed that RhB and BPA were degraded via photosensitization (dominated by e - and ·O 2 - ) and direct photocatalytic oxidation (contributed by h + , e - and ·O 2 - ), respectively. Whereas, E. coli cells yet were found to be inactivated by the generation of e - and ·O 2 - rather than by the released Ag + . Since it contained superparamagnetic property, FBA could be easily separated from the reaction suspension after use. Due to the excellent photo stability, FBA exhibited strong photocatalytic activity in the fourth reused recycle. Therefore, FBA could serve as a promising alternative for water purification., (Copyright © 2018 Elsevier Ltd. All rights reserved.)

Removal of antibiotics from aqueous solutions by photocatalysis is an advanced technology for environmental remediation. Herein, we have fabricated a series of AgX (X = I, Br)/CuBi 2 O 4 composites through an in-situ precipitation method. The photocatalytic activity of the obtained photocatalysts was measured by the degradation of tetracycline (TC) under visible light irradiation (λ > 420 nm). All the AgX (X = I, Br)/CuBi 2 O 4 composites exhibit much higher photocatalytic activity than that of pure CuBi 2 O 4 . The enhanced photocatalytic activity is mainly attributed to the efficient interfacial charge separation and migration in the AgX (X = I, Br)/CuBi 2 O 4 heterojunctions. Meanwhile, AgX (X = I, Br)/CuBi 2 O 4 heterojunctions display excellent photocatalytic stability, and the photocatalytic degradation rates were not obvious decreased even after five successive cycles. Based on the energy band structure, the radicals trapping and electronic spin resonance (ESR) experiments, the Z-scheme mechanism of AgBr/CuBi 2 O 4 and type II mechanism of AgI/CuBi 2 O 4 heterojunction photocatalysts were tentatively discussed, respectively., (Copyright © 2018 Elsevier B.V. All rights reserved.)

Research on the incorporation of cutting-edge nano-antibacterial agent for designing dental materials with potent and long-lasting antibacterial property is demanding and provoking work. In this study, a novel resin-based dental material containing photocurable core-shell AgBr/cationic polymer nanocomposite (AgBr/BHPVP) was designed and developed. The shell of polymerizable cationic polymer not only provided non-releasing antibacterial capability for dental resins, but also had the potential to polymerize with other methacrylate monomers and prevented nanoparticles from aggregating in the resin matrix. As a result, incorporation of AgBr/BHPVP nanocomposites did not adversely affect the flexural strength and modulus but greatly increased the Vicker's hardness of resin disks. By continuing to release Ag + ions without the impact of anaerobic environment, resins containing AgBr/BHPVP nanoparticles are particularly suitable to combat anaerobic cariogenic bacteria. By reason of the combined bactericidal effect of the contact-killing cationic polymers and the releasing-killing Ag + ions, AgBr/BHPVP-containing resin disks had potent bactericidal activity against S. mutans. The long-lasting antibacterial activity was also achieved through the sustained release of Ag + ions due to the core-shell structure of the nanocomposites. The results of macrophage cytotoxicity showed that the cell viability of dental resins loading less than 1.0 wt% AgBr/BHPVP was close to that of neat resins. The AgBr/BHPVP-containing dental resin with dual bactericidal capability and long term antimicrobial effect is a promising material aimed at preventing second caries and prolonging the longevity of resin composite restorations.

AgCl and Ag 2 S prevalently exist in the environment as minerals and/or the chlorination and sulfidation products of ionic silver and elemental silver nanoparticles (AgNPs). In this work, we investigated the chemical transformation of AgCl and Ag 2 S under simulated sunlight (in water) and incineration (in sludge and simulated municipal solid waste, SMSW). In the presence of natural organic matter, AgCl in river water was observed to be transformed into AgNPs under simulated sunlight, while photo-reduction of Ag 2 S could not take place under the same experimental conditions. During the course of incineration, pure Ag 2 S was transformed into elemental silver while AgCl remained stable; however, both Ag 2 S in sludge and AgCl in SMSW can be transformed to elemental silver under incineration, evident by the results of X-ray absorption spectroscopy and scanning electron microscopy measurements. Incineration temperature played an important role in the transformation of Ag 2 S and AgCl into elemental silver. These results suggest that chemical transformations of Ag 2 S and AgCl into elemental silver could be a possible source of naturally occurring or unintentionally produced AgNPs, affecting the fate, transport, bioavailability and toxicity of silver. Therefore, it is necessary to include the contributions of this transformation process when assessing the risk of ionic silver/AgNPs and the utilization and management of incineration residues., (Copyright © 2016 Elsevier Ltd. All rights reserved.)

Visible light-driven photocatalytic inactivation of Escherichia coli was performed using hydroxyapatite-supported Ag3PO4 nanocomposites (Ag3PO4/HA). The antibacterial performance was evaluated by the methods of zone of inhibition plates and minimum inhibitory concentration test. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were employed to investigate the instability and transformation of the nanocomposite by comparing the crystalline, phase, and the morphology before and after exposure to Luria-Bertani culture medium under visible light irradiation. Ag3PO4 nanoparticles on the support were found to be shortly transformed into AgCl due to high chloride concentration of Luria-Bertani culture medium. The AgCl/HA nanocomposite showed both excellent intrinsic antibacterial performance contributed by the released silver ions and visible light-induced photocatalytic disinfection toward E. coli cells. This dual antibacterial function mechanism was validated by trapping the hydroxyl free radical and detecting the silver ions during the photocatalytic antibacterial process. The morphological change of E. coli cells in different reaction intervals was obtained by scanning electron microscopy (SEM) to complementally verify photocatalytic inactivation of E. coli. This work suggests that an essential comparison study is required for the antibacterial materials before and after the photocatalytic inactivation of bacterial cells using Ag3PO4 nanoparticles or Ag3PO4-related nanocomposites in mediums containing high-concentration chloride ions.

As a high-quantum-efficiency photocatalyst, the serious photo-corrosion of silver phosphate (Ag3PO4), limits the practical applications in water purification and challenges us. Herein, Ag3PO4 is found to have a high stability under natural indoor weak light irradiation, suggesting that we can employ it by adopting a new application strategy. In our studies, rhodamine B (RhB, cationic dye), methyl orange (MO, anionic dye) and RhB-MO mixture aqueous solutions are used as the probing reaction for the degradation of organic wastewater. It is found that RhB, MO and RhB-MO can be completely degraded after 28 h under natural indoor weak light irradiation, indicating that multi-component organic contaminants can be efficiently degraded by Ag3PO4 under natural indoor weak light irradiation. The density of natural indoor weak light is measured to be 72cd, which is merely one-thousandth of 300 W xenon lamp (68.2 × 10(3)cd). Most importantly, Ag3PO4 shows a high stability under natural indoor weak light irradiation, demonstrated by the formation of fairly rare Ag. Furthermore, we also investigate the influence of inorganic ions on organic dyes degradation. It shows that the Cl(-) and Cr(6+) ions with high concentrations in wastewater have significantly decreased the degradation rate. From the viewpoint of energy saving and stability, this study shows us that we can utilize the Ag-containing photocatalysts under natural indoor weak light, which could be extended to indoor air cleaning process., (Copyright © 2015 Elsevier Ltd. All rights reserved.)

Since the photocatalytic capability is determined by the separation and transmission efficiency of photoinduced charges, its improvement remains a challenge for development of efficient photocatalysts. Here, we made large improvement on the surface of Ag3PO4 using Co(II)-grafted Ag3PO4 by a hydrothermal method. During the photocatalytic process, Co(II) was oxidized to Co(III) by the photogenerated holes under visible light radiation, which enhanced the separation efficiency of photogenerated charges. Meanwhile, the Co(III) as-formed could oxidize dye molecules, which recovered the Co(II). The synergy of Co(II) and Ag3PO4 greatly promoted the separation and transmission efficiency of the photogenerated charges, and severely improved the photocatalytic activity of Ag3PO4. The surface grafted Co(II) on Ag3PO4 is responsible for the enhancement of photocatalytic activity., (Copyright © 2015 Elsevier B.V. All rights reserved.)

Core-shell Ag@ZIF-8 nanowires, where single Ag nanowires are coated with uniform zeolitic-imidazolate-framework-8 (ZIF-8) shells, successfully realize renewable adsorptive separation of low concentrations of butanol from an aqueous medium under solar light irradiation by taking advantage of the exceptional adsorption capability of the ZIF-8 shells toward butanol and the unique plasmonic photothermal effect of the Ag nanowire cores. Impressively, the high separation efficiency is maintained as almost unchanged, even after 10 adsorption/desorption cycles., (© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.)

The kinetics and mechanism of light-mediated formic acid (HCOO(-)) degradation in the presence of semiconducting silver chloride particles are investigated in this study. Our experimental results show that visible-light irradiation of AgCl(s) results in generation of holes and electrons with the photo-generated holes and its initial oxidation product carbonate radical, oxidizing HCOO(-) to form CO2. The HCOO(-) degradation rate increases with increase in silver concentration due to increase in rate of photo-generation of holes while the increase in chloride concentration decreases the degradation rate of HCOO(-) as a result of the scavenging of holes by Cl(-), thereby resulting in decreased holes and carbonate radical concentration. The results obtained indicate that a variety of other solution conditions including dioxygen concentration, bicarbonate concentration and pH influence the availability of holes and hence the HCOO(-) degradation rate in a manner consistent with our understanding of key processes. Based on our experimental results, we have developed a kinetic model capable of predicting AgCl(s)-mediated HCOO(-) photo-degradation over a wide range of conditions., (Copyright © 2014 Elsevier Inc. All rights reserved.)

A unique Ag-bridged Ag2O nanowire network/TiO2 nanotube array p-n heterojunction (Ag-Ag2O/TiO2 NT) was fabricated by simple electrochemical method. Ag nanoparticles were firstly electrochemically deposited onto the surface of TiO2 NT and then were partly oxidized to Ag2O nanowires while the rest of Ag mother nanoparticles were located at the junctions of Ag2O nanowire network. The Ag-Ag2O/TiO2 NT heterostructure exhibited strong visible-light response, effective separation of photogenerated carriers, and high adsorption capacity. The integration of Ag-Ag2O self-stability structure and p-n heterojunction permitted high and stable photocatalytic activity of Ag-Ag2O/TiO2 NT heterostructure photocatalyst. Under 140-min visible light irradiation, the photocatalytic removal efficiency of both dye acid orange 7 (AO7) and industrial chemical p-nitrophenol (PNP) over Ag-Ag2O/TiO2 NT reached nearly 100% much higher than 17% for AO7 or 13% for PNP over bare TiO2 NT. After 5 successive cycles under 600-min simulated solar light irradiation, Ag-Ag2O/TiO2 NT remained highly stable photocatalytic activity., (Copyright © 2014 Elsevier B.V. All rights reserved.)

The effect of the water matrix components of a secondary effluent of a urban wastewater treatment plant on the photocatalytic activity of Ag/AgCl @ chiral TiO2 nanofibers and the undergoing reaction mechanisms were investigated. These effects were evaluated through the water components-induced changes on the net rate of hydroxyl radical (˙OH) generation and modeled using a relative rate technique. Dissolved organic matter DOM (k=-2.8×10(8) M(-1) s(-1)) scavenged reactive oxygen species, Cl(-) (k=-5.3×10(8) M(-1) s(-1)) accelerated the transformation from Ag to AgCl (which is not photocatalytically active under visible-light irradiation), while Ca(2+) at concentrations higher than 50 mM (k=-1.3×10(9) M(-1) s(-1)) induced aggregation of Ag/AgCl and thus all of them revealed inhibitory effects. In contrast, NO3(-) (k=6.9×10(8) M(-1) s(-1)) and CO3(2-) (k=3.7×10(8) M(-1) s(-1)) improved the photocatalytic activity of Ag/AgCl slightly by improving the rate of HO˙ generation. Other ubiquitous secondary effluent components including SO4(2-) (k=3.9×10(5) M(-1) s(-1)), NH3(+) (k=3.5×10(5) M(-1) s(-1)) and Na(+) (k=2.6×10(4) M(-1) s(-1)) had negligible effects. 90% of 17-α-ethynylestradiol (EE2) spiked in the secondary effluent was removed within 12 min, while the structure and size of Ag/AgCl @ chiral TiO2 nanofibers remained stable. This work may be helpful not only to uncover the photocatalytic mechanism of Ag/AgCl based photocatalyst but also to elucidate the transformation and transportation of Ag and AgCl in natural water., (Copyright © 2014 Elsevier B.V. All rights reserved.)

AgCl/BiOCl heteronanostructures were synthesized by a room-temperature chemical coprecipitation method. The as-obtained products were characterized by energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and UV-Vis diffuse spectra, which show the structures, morphologies, and optical properties. The results revealed that the absorption edge of AgCl/BiOCl shifted towards visible light regions. Meanwhile, the AgCl/BiOCl heteronanostructures showed better photocatalytic properties than the pure BiOCl to degrade rhodamine B and the 5% AgCl/BiOCl showed the best photocatalytic ability, which completely decomposed the target molecules in 17 minites with the visible-light illumination. The formation of heteronanostructures might improve the separation of photogenerated electrons and holes derived from the coupling effect of BiOCl and AgCl heteroarchitectures, which was regarded as the main reason for the high photocatalytic activity.

Ag(3)PO(4)/graphene-oxide (Ag(3)PO(4)/GO) composite has been synthesized by a liquid phase deposition method, and used for the photodegradation of organic dyes in water under visible light. The as-synthesized samples were characterized by X-ray diffraction, scanning electron microscope, N(2) sorption-desorption, and UV-vis diffuse reflectance spectra. The SEM image indicated that Ag(3)PO(4) particles were mainly distributed on the surface of GO sheets uniformly. DRS analysis revealed that the samples had good visible light response. The photocatalytic activity of Ag(3)PO(4)/GO composite was evaluated by decomposing of dyes (such as methyl orange, rhodamine B) in water under visible or UV-vis light irradiation. The degradation results indicated that the photocatalytic performance of Ag(3)PO(4)/GO was greatly enhanced due to the improved adsorption performance and separation efficiency of photo-generated carriers. The Ag(3)PO(4)/GO composite with GO content of 15 wt.% exhibited superior activity under visible light irradiation. After 50 min of reaction, the degradation ratio of MO was about 86.7%, while RhB solution could be completely degraded within 30 min of reaction. Further study proved that the direct oxidation of pollutants by holes has played a major role in the degradation process. The results of this work would provide a new sight for the construction of visible light-responsive photocatalysts with high performance., (Copyright © 2012 Elsevier B.V. All rights reserved.)

In this paper, we report that cube-like Ag/AgCl nanostructures could be facilely fabricated in a one-pot manner through a direct-precipitation protocol under ambient conditions, wherein no additional issues such as external energy (e.g., high temperature or high pressure), surfactants, or reducing agents are required. In terms of using sodium chloride (NaCl) as chlorine source and silver acetate (CH₃COOAg) as silver source, it is disclosed that simply by adding an aqueous solution of NaCl into an aqueous solution of CH₃COOAg, Ag/AgCl nanostructures with a cube-like geometry, could be successfully formulated. We show that thus-formulated cube-like Ag/AgCl nanospecies could be used as high-performance yet durable visible-light-driven or sunlight-driven plasmonic photocatalysts for the photodegradation of methyl orange (MO) and 4-chlorophenol (4-CP) pollutants. Compared with the commercially available P25-TiO₂, and the Ag/AgCl nanospheres previously fabricated via a surfactant-assisted method, our current cube-like Ag/AgCl nanostructures could exhibit much higher photocatalytic performance. Our template free protocol might open up new and varied opportunities for an easy synthesis of cube-like Ag/AgCl-based high-performance sunlight-driven plasmonic photocatalysts for organic pollutant elimination.

Nano-structures of AgBr have been prepared by reaction between AgNO(3) and KBr under ultrasound irradiation. Particle sizes and morphology of nanoparticle are depending on temperature, power of sonicating, reaction time and concentration. The effects of these parameters in growth and morphology of the nano-structures have been studied. Results suggest that an increasing of temperature, sonication power and concentration led to a decreasing of particle size. The samples were characterized with powder X-ray diffraction (XRD) and scanning electron microscopy (SEM)., (Copyright © 2011 Elsevier B.V. All rights reserved.)

Kinetic studies for the non-isothermal decomposition of unirradiated and γ-irradiated silver acetate with 10(3) kGy total γ-ray doses were carried out in air. The results showed that the decomposition proceeds in one major step in the temperature range of (180-270 °C) with the formation of Ag(2)O as solid residue. The non-isothermal data for un-irradiated and γ-irradiated silver acetate were analyzed using Flynn-Wall-Ozawa (FWO) and nonlinear Vyazovkin (VYZ) iso-conversional methods. These free models on the investigated data showed a systematic dependence of Ea on α indicating a simple decomposition process. No significant changes in the thermal decomposition behavior of silver acetate were recorded as a result of γ-irradiation. Calcinations of γ-irradiated silver acetate (CH(3)COOAg) at 200 °C for 2 hours only led to the formation of pure Ag(2)O mono-dispersed nanoparticles. X-ray diffraction, FTIR and SEM techniques were employed for characterization of the synthesized nanoparticles.

A highly active photocatalyst, silver loaded mesoporous WO(3), was successfully synthesized by an ultrasound assisted insertion method. The photodegradation of a common air pollutant acetaldehyde was adopted to evaluate the photocatalytic performance of the as-prepared sample under visible-light irradiation. The photocatalytic activity was about three and six times higher than that of pure mesoporous WO(3) and nitrogen-doped TiO(2), respectively. The photocatalytic mechanism was investigated to understand the much enhanced photocatalytic activity, which was mainly attributed to the largely improved electron-hole separation in the Ag-WO(3) heterojunction., (Copyright 2010 Elsevier B.V. All rights reserved.)

We synthesized silver methacrylate, added it to resin for dental use, and observed color changes in the resin from colorless to red-purple following light irradiation. Therefore, 0.01-0.10 wt% silver methacrylate was added to two types of resin powder, i.e., self-curing resin produced by the polymerization of a barbituric acid derivative, quaternary ammonium, and an organometallic compound (Type I), and BPO-tertiary amine resin (Type II), and samples were produced by polymerization with the attached monomer. Changes with time in the color of samples from 3 hours (new samples) to 16 days (old samples) after polymerization and also color changes of old and new samples after heating were evaluated. Subsequently, changes in color with variations in the light intensity, irradiation time, and wavelength were evaluated in terms of color differences.

Controlled iodization and Sn doping of vacuum-evaporated Ag films has helped understand the initial-stage kinetics of AgI nanoparticle growth under ambient conditions. Use of XRD, optical spectroscopy, and AFM has unravelled systematic correlation between Sn-induced disorder in Ag crystal structure, nanoparticle size, and exciton growth dynamics. Sn doping of Ag leads to three specific effects: removal of UV absorption minimum in Ag, introduction of a plasmon-type absorption in the red region, and a reduction in particle size in thicker (than 10 nm) films (but an increase in particle size in 10 nm films) relative to that in undoped Ag films.

Permanent records of the results of electrophoretic separations of radiolabeled proteins and membrane-bound proteins (and RNA and DNA) can be made using autoradiography, fluorography, and phosphor imaging. These images can subsequently be quantified using densitometry to obtain a relative measure of the amount of radioactivity in a sample. This unit also includes descriptions of image-enhancement techniques and guidelines for selection of appropriate recording media.

X-ray or UV irradiation at room temperature of Rh3+ doped AgCl emulsion powders leads to the production of three paramagnetic Rh2+ related centres, labeled R4, R5 and R6. A combined X and Q band electron paramagnetic resonance (EPR) and electron nuclear double resonance (ENDOR) study allowed the determination of a nearly complete structural model for these centres. In the X band ENDOR spectra of R4 and R5 interactions of the unpaired electron with nearby protons have been identified, indicating that for these centres Cl- ligands have been exchanged by H2O or OH-. The R6 centre, identified as a (RhCl6)4- complex, has been found to be fundamentally different from the dominant centre in large Rh2+ doped AgCl single crystals grown from the melt. The results are compared with recent work by other researchers in the same field.