Synthesis of Ni–Ag–ZnO solid solution nanoparticles for photoreduction and antimicrobial applications

ZnO is one of the most promising and efficient semiconductor materials for various light-harvesting applications. Herein, we reported the tuning of optical properties of ZnO nanoparticles (NPs) by co-incorporation of Ni and Ag ions in the ZnO lattice. A sonochemical approach was used to synthesize pure ZnO NPs, Ni–ZnO, Ag–ZnO and Ag/Ni–ZnO with different concentrations of Ni and Ag (0.5%, 2%, 4%, 8%, and 15%) and Ni doped Ag–ZnO solid solutions with 0.25%, 0.5%, and 5% Ni ions. The as-synthesized Ni–Ag–ZnO solid solution NPs were characterized by powdered X-ray diffraction (pXRD), FT-IR spectroscopy, scanning electron microscopy (SEM), energy dispersive spectroscopy (EDS), UV-vis (UV) spectroscopy, and photoluminescence (PL) spectroscopy. Ni–Ag co-incorporation into a ZnO lattice reduces charge recombination by inducing charge trap states between the valence and conduction bands of ZnO and interfacial transfer of electrons. The Ni doped Ag–ZnO solid solution NPs have shown superior 4-nitrophenol reduction compared to pure ZnO NPs which do not show this reaction. Furthermore, a methylene blue (MB) clock reaction was also performed. Antibacterial activity against E. coli and S. aureus has inhibited the growth pattern of both strains depending on the concentration of catalysts.

The synergic effect of Ni and Ag in Ni–Ag–ZnO solid solutions has tuned the optoelectronic properties of ZnO for photoreduction reactions.     

Synthesis of Sn/Ag–Sn nanoparticles via room temperature galvanic reaction and diffusion

Tin (Sn) has a low melting temperature, i.e., 231.9 °C for the bulk, and the capability to form compounds with many metals. The galvanic reaction between Sn nanoparticles (NPs) as the core and silver nitrate at room temperature under argon gas in an organic solvent without any reducing power, was employed for the first time to coat an Ag–Sn intermetallic shell, i.e., Ag₃Sn and/or Ag₄Sn, on Sn NPs. For spherical Sn NPs, the NPs retained a spherical shape after coating. Uniform and Janus structures consisting of a β-Sn core with Ag–Sn shell were observed in the resulting NPs and their population related to the input molar ratios of the metal precursors. The observation of the intermetallic shell is general for both spherical and rod-shape Sn NPs. The formation of the intermetallic shell indicated that two reactions occurred sequentially, first reduction of Ag ions to Ag atoms by the Sn core, followed by interdiffusion of Ag and Sn to form the Ag–Sn intermetallic shell.

Coating of Ag–Sn intermetallic compound on Sn nanoparticles at room temperature.     

Generalized nano-thermodynamic model for capturing size-dependent surface segregation in multi-metal alloy nanoparticles

Multi-metal alloy nanoparticles (NPs) offer new avenues for exploration and design of nanoscale-properties, e.g., catalytic, electronic and optical properties, by virtue of their tunable composition. A method that can aid such exploration by accurately predicting the size-, shape- and composition-dependent elemental distribution associated with nanomaterials is crucially missing. A nano-thermodynamic model based on distribution coefficients Δ is introduced to fill this gap. Δ is employed to predict surface segregation in NPs as a function of the NP size and composition. Interestingly, we find Δ to be independent of size for NPs beyond 2 nm. This key finding motivates the construction of thermodynamic tables for distribution coefficients using segregation observed with one or more NP sizes. The tables can enable accurate prediction of phase diagrams for nanomaterials across a wide-range of sizes. Key concepts of this new theory are demonstrated with Au–Pt–Pd, Ag–Au–Pd and Ni–Pt–Pd, which are found to exhibit complex size-dependent segregation behavior for 2–6 nm NPs and relatively weaker size-dependence beyond 6 nm. Numerically well-converged values of Δ are calculated for small NPs using Monte Carlo simulations in the canonical ensemble. Simulations are based on an embedded atom method (EAM) potential for metal alloys.

Nano-thermodynamic model captures thermodynamic preference of metal species for different regions of a nanoparticle while accounting for size effects.     

Enhanced visible-light photodegradation of fluoroquinolone-based antibiotics and E. coli growth inhibition using Ag–TiO2 nanoparticles

Antibiotics in wastewater represent a growing and worrying menace for environmental and human health fostering the spread of antimicrobial resistance. Titanium dioxide (TiO₂) is a well-studied and well-performing photocatalyst for wastewater treatment. However, it presents drawbacks linked with the high energy needed for its activation and the fast electron–hole pair recombination. In this work, TiO₂ nanoparticles were decorated with Ag nanoparticles by a facile photochemical reduction method to obtain an increased photocatalytic response under visible light. Although similar materials have been reported, we advanced this field by performing a study of the photocatalytic mechanism for Ag–TiO₂ nanoparticles (Ag–TiO₂ NPs) under visible light taking in consideration also the rutile phase of the TiO₂ nanoparticles. Moreover, we examined the Ag–TiO₂ NPs photocatalytic performance against two antibiotics from the same family. The obtained Ag–TiO₂ NPs were fully characterised. The results showed that Ag NPs (average size: 23.9 ± 18.3 nm) were homogeneously dispersed on the TiO₂ surface and the photo-response of the Ag–TiO₂ NPs was greatly enhanced in the visible light region when compared to TiO₂ P25. Hence, the obtained Ag–TiO₂ NPs showed excellent photocatalytic degradation efficiency towards the two fluoroquinolone-based antibiotics ciprofloxacin (92%) and norfloxacin (94%) after 240 min of visible light irradiation, demonstrating a possible application of these particles in wastewater treatment. In addition, it was also proved that, after five Ag–TiO₂ NPs re-utilisations in consecutive ciprofloxacin photodegradation reactions, only a photocatalytic efficiency drop of 8% was observed. Scavengers experiments demonstrated that the photocatalytic mechanism of ciprofloxacin degradation in the presence of Ag–TiO₂ NPs is mainly driven by holes and ˙OH radicals, and that the rutile phase in the system plays a crucial role. Finally, Ag–TiO₂ NPs showed also antibacterial activity towards Escherichia coli (E. coli) opening the avenue for a possible use of this material in hospital wastewater treatment.

Ag nanoparticles decorated-TiO₂ P25 are a viable alternative for the degradation, through a rutile-mediated mechanism, of fluoroquinolone-based antibiotics under visible light irradiation and, at the same time, for bacteria inactivation in water.     

Preparation of a novel palladium catalytic hydrogel based on graphene oxide/chitosan NPs and cellulose nanowhiskers

The present paper focuses on the synthesis of a novel hydrogel support by combining polysaccharides (chitosan NPs and dialdehyde cellulose nanowhiskers) and graphene oxide nanosheets to obtain a biocompatible material for catalytic applications. The hydrogel was synthesized via green chemistry processes and used as a support to prepare Pd nanoparticles. Finally, the hydrogel@Pd NPs was employed as the catalyst in the Mizoroki–Heck reaction to generate new C–C bonds. SEM analysis indicated that the hydrogel has macroporous morphology, which is in good correlation with its high crosslinking degree. The as-synthesized nanocomposite hydrogel exhibits beneficial properties such as ease of separation and excellent recyclability for at least six cycles without considerable loss in its activity. The yields of the products range from 81% to 98%. Additionally, this study provides the possibility to perform the Mizoroki–Heck reaction with aryl chloride in the presence of the as-prepared catalyst.

Pd NPs dispersed on a polysaccharide-based hydrogel as a novel catalyst show high catalytic activity and recyclability for coupling reactions.     

Ultrafine Pd nanoparticles loaded benzothiazole-linked covalent organic framework for efficient photocatalytic C–C cross-coupling reactions

We proposed a strategy that a benzothiazole-linked covalent organic framework (TTT-COF) was used as a substrate to prepare metal composite photocatalyst Pd NPs@TTT-COF. Firstly, benzothiazole linked TTT-COF exhibited superior chemical stability and photoresponse. Moreover, a finer particle size (2.01 nm) and more uniform distribution of Pd NPs were observed in Pd NPs@TTT-COF owing to the binding interaction between Pd NPs and S in benzothiazole groups. Pd NPs@TTT-COF exhibited superior efficiency and reusability in photocatalytic C–C cross-coupling reactions. Mechanism study suggested that photogenerated electrons and holes on TTT-COF played important roles in these reactions.

Benzothiazole-linked covalent organic framework with characteristic properties loaded Pd nanoparticles for photocatalytic C–C cross-coupling reactions.     

Peptide-directed Pd-decorated Au and PdAu nanocatalysts for degradation of nitrite in water

In this work, a palladium binding peptide, Pd4, has been used for the synthesis of catalytically active palladium-decorated gold (Pd-on-Au) nanoparticles (NPs) and palladium–gold (Pd_xAu_100−x) alloy NPs exhibiting high nitrite degradation efficiency. Pd-on-Au NPs with 20% to 300% surface coverage (sc%) of Au showed catalytic activity commensurate with sc%. Additionally, the catalytic activity of Pd_xAu_100−x alloy NPs varied based on palladium composition (x = 6–59). The maximum nitrite removal efficiency of Pd-on-Au and Pd_xAu_100−x alloy NPs was obtained at sc 100% and x = 59, respectively. The synthesized peptide-directed Pd-on-Au catalysts showed an increase in nitrite reduction three and a half times better than monometallic Pd and two and a half times better than Pd_xAu_100−x NPs under comparable conditions. Furthermore, peptide-directed NPs showed high activity after five reuse cycles. Pd-on-Au NPs with more available activated palladium atoms showed high selectivity (98%) toward nitrogen gas production over ammonia.

In this work, a palladium binding peptide, Pd4, has been used for the synthesis of catalytically active palladium-decorated gold (Pd-on-Au) nanoparticles (NPs) and palladium–gold (Pd_xAu_100−x) alloy NPs exhibiting high nitrite degradation efficiency.     

Bimetallic Au–Pd alloy nanoparticles supported on MIL-101(Cr) as highly efficient catalysts for selective hydrogenation of 1,3-butadiene

Gold–palladium (Au–Pd) bimetallic nanoparticle (NP) catalysts supported on MIL-101(Cr) with Au : Pd mole ratios ranging from 1 : 3 to 3 : 1 were prepared through coimpregnation and H₂ reduction. Au–Pd NPs were homogeneously distributed on the MIL-101(Cr) with mean particle sizes of 5.6 nm. EDS and XPS analyses showed that bimetallic Au–Pd alloys were formed in the Au(2)Pd(1)/MIL-101(Cr). The catalytic performance of the catalysts was explored in the selective 1,3-butadiene hydrogenation at 30–80 °C on a continuous fixed bed flow quartz reactor. The bimetallic Au–Pd alloy particles stabilized by MIL-101(Cr) presented improved catalytic performance. The as-synthesized bimetallic Au(2)Pd(1)/MIL-101(Cr) with 2 : 1 Au : Pd mole ratio showed the best balance between the activity and butene selectivity in the selective 1,3-butadiene hydrogenation. The Au–Pd bimetallic-supported catalysts can be reused in at least three runs. The work affords a reference on the utilization of a MOF and alloy nanoparticles to develop high-efficiency catalysts.

Bimetallic Au–Pd alloy particles stabilized by MIL-101(Cr) showed high activity and butene selectivity for 1,3-butadiene hydrogenation reaction.     

Synthesis and characterization of a supported Pd complex on volcanic pumice laminates textured by cellulose for facilitating Suzuki–Miyaura cross-coupling reactions

Herein, a novel high-performance heterogeneous catalytic system made of volcanic pumice magnetic particles (VPMP), cellulose (CLS) natural polymeric texture, and palladium nanoparticles (Pd NPs) is presented. The introduced VPMP@CLS-Pd composite has been designed based on the principles of green chemistry, and suitably applied in the Suzuki–Miyaura cross-coupling reactions, as an efficient heterogeneous catalytic system. Concisely, the inherent magnetic property of VPMP (30 emu g⁻¹) provides a great possibility for separation of the catalyst particles from the reaction mixture with great ease. In addition, high heterogeneity and high structural stability are obtained by this composition resulting in remarkable recyclability (ten times successive use). As the main catalytic sites, palladium nanoparticles (Pd NPs) are finely distributed onto the VPMP@CLS structure. To catalyze the Suzuki–Miyaura cross-coupling reactions producing biphenyl pharmaceutical derivatives, the present Pd NPs were reduced from chemical state Pd²⁺ to Pd⁰. In this regard, a plausible mechanism is submitted in the context as well. As the main result of the performed analytical methods (including FT-IR, EDX, VSM, TGA, FESEM, TEM, BTE, and XPS), it is shown that the spherical-shaped nanoscale Pd particles have been well distributed onto the surfaces of the porous laminate-shaped VPMP. However, the novel designed VPMP@CLS-Pd catalyst is used for facilitating the synthetic reactions of biphenyls, and high reaction yields (∼98%) are obtained in a short reaction time (10 min) by using a small amount of catalytic system (0.01 g), under mild conditions (room temperature).

An efficient natural-based catalyst constructed of volcanic pumice, cellulose polymeric chains, and palladium nanoparticles is presented for Suzuki–Miyaura coupling reaction.     

Carbonylative Suzuki–Miyaura cross-coupling by immobilized Ni@Pd NPs supported on carbon nanotubes

In this study, a novel carbon nanotube (CNT) based nanocatalyst (Ni@Pd/CNT) was synthesized by modifying CNTs using Ni@Pd core–shell nanoparticles (NPs). Ni@Pd/CNT was used in catalytic carbonylative cross-coupling between 4-iodoanisole and phenylboronic acid. The Ni@Pd NPs possessed a magnetic nickel (Ni) core with a palladium (Pd) structural composite shell. Thus, the use of Ni had led to a reduced consumption of Pd without sacrificing the overall catalytic performance, simultaneously making it reusable as it could be conveniently recovered from the reaction mixture by using an external magnetic field. Immobilization of the Ni@Pd NPs on carbon nanotubes not only prevented their aggregation, but also significantly enhanced the accessibility of the catalytically active sites. The abovementioned approach based on carbon nanotubes and Ni@Pd NPs provided a useful platform for the fabrication of noble-metal-based nanocatalysts with easy accessibility and low cost, which may allow for an efficient green alternative for various catalytic reductions.

In this study, a novel carbon nanotube (CNT) based nanocatalyst (Ni@Pd/CNT) was synthesized by modifying CNTs using Ni@Pd core–shell nanoparticles (NPs).     

Efficient photocatalytic degradation of dyes using photo-deposited Ag nanoparticles on ZnO structures: simple morphological control of ZnO

In this work, morphology-controlled ZnO structures were prepared via a hydrothermal method by simple adjustments in the NaOH concentration. The NaOH concentration variation from 0.2 to 1.2 M resulted in the formation of ZnO structures in shapes such as walnut, spherical flower, flower, rod, and urchin-like. The extent of OH⁻ ions is the main factor influencing the growth of ZnO structures. Well-defined morphologies, good crystallinity, and optical properties were obtained for all ZnO structures. Among these ZnO structures, ZnOsf (spherical flower-like) structure showed a greater percentage of photodegradation of methyl orange and rhodamine B dyes. Surface plasmon resonance was achieved by modifying the surface of ZnO with Ag nanoparticles. ZnOsf was loaded with Ag nanoparticles by a facile photo-deposition method. Ag–ZnOsf showed superior photoactivity and recyclability for the degradation of methyl orange and rhodamine B. Therefore, modification of different ZnO structures can help realize potential catalysts for future environmental applications.

Morphology control of ZnO structures were fabricated by hydrothermal method with simple adjustments of NaOH concentration and Ag–ZnO composite showed superior photoactivity and recyclability for the degradation of MO and RhB.     

Simultaneous detection of acetaminophen and 4-aminophenol with an electrochemical sensor based on silver–palladium bimetal nanoparticles and reduced graphene oxide

In this paper, Ag–Pd bimetallic nanoparticles uniformly distributed on reduced graphene oxide (rGO) were synthesized by redox reaction between Pd²⁺, Ag⁺and GO, and were characterized by X-ray diffractometry, field emission scanning electron microscopy, electrochemical impedance spectroscopy and thermal gravimetric analyses. A novel electrochemical sensor was constructed based on these nanocomposites using glassy carbon as a substrate. Under optimal conditions, the linear ranges were 0.50–300.00 μM for PA and 1.00–300.00 μM for 4-AP, with the detection limits of 0.23 μM for PA and 0.013 μM for 4-AP, respectively. This sensor was successfully applied to the determination of PA in pharmaceutical formulations and gave satisfactory results with a lower detection limit, wider linear range and good reproducibility.

Simultaneous detection of acetaminophen and 4-aminophenol with a highly sensitive electrochemical sensor based on silver–palladium bimetal nanoparticles and reduced graphene oxide.     

Ag–Au bimetallic nanocomposites stabilized with organic–inorganic hybrid microgels: synthesis and their regulated optical and catalytic properties

Herein, we present the synthesis of Ag–Au bimetallic nanocomposites stabilized with organic–inorganic hybrid microgels. The aim is to get both the surface plasmon resonance (SPR) and catalytic performance of the composite material can be changed in response to external stimuli. Ag@poly(N-isopropylacrylamide-co-3-methacryloxypro-pyltrimethoxysilane) (Ag@P(NIPAM-co-MAPTMS)) hybrid microgels were synthesized by seed-emulsion polymerization using Ag nanoparticles (NPs) as the core and NIPAM/MAPTMS as monomers. Ag–Au@P(NIPAM-co-MAPTMS) bimetallic hybrid microgels were prepared by a galvanic replacement (GR) reaction between Ag NPs and HAuCl₄, with the composition and structure of these bimetallic nanocomposites being determined by the amount of added HAuCl₄. The highly porous organic–inorganic microgel layer provided confined space for the GR reaction, effectively preventing the aggregation of Ag–Au NPs. The shell layer of P(NIPAM-co-MAPTMS) three-dimensional network chains not only enhanced nanocomposite dispersity and stability, but also provided highly porous gel microdomains that could increase the diffusion of the substrate and hence enhanced catalytic activity. Additionally, the SPR and catalytic properties of Ag–Au@P(NIPAM-co-MAPTMS) are reversibly sensitive to external temperature. With increase of temperature, the maximum absorption peak of bimetallic nanocomposites shifted to longer wavelengths, and the catalytic activity of these composites for the reduction of 4-nitrophenol by NaBH₄ remarkably increased. The features above mentioned are related to presence of the thermosensitive PNIPAM chains and the highly porous structure constructed by rigid MAPTMS segments intersected between NIPAM chains.

Ag–Au bimetallic nanocomposites stabilized with organic–inorganic hybrid microgels allowed the mass transfer of reactants to be controlled by temperature modulation.     

Counterion coupled (COCO) gemini surfactant capped Ag/Au alloy and Ag@Au core–shell nanoparticles for cancer therapy

Hybrid silver (Ag)–gold (Au) nanoparticles (NPs) with different sizes and compositions were synthesized. Ag/Au alloy and Ag@Au core–shell type NPs were prepared from Ag and Au with various ratios using the COCO gemini surfactant, 1,6-bis (N,N-hexadecyldimethylammonium) adipate (COCOGS), 16-6-16 as a stabilizer. The formation of the Ag/Au alloy and Ag@Au core–shell was confirmed by UV-visible absorption spectroscopy, high-resolution transmission electron microscopy (HRTEM), energy-dispersive X-ray spectroscopy (EDX) and selected area electron diffraction (SAED) patterns. Depending on the composition of the Ag/Au alloy NPs, the λ_max values varied from 408 nm to 525 nm. FTIR measurements were used to evaluate the adsorption of the COCO gemini surfactant (16-6-16) on the Ag/Au alloy and Ag@Au core–shell surface. In this present work, we study how to achieve the stability and activity of the COCO gemini surfactant (16-6-16) capped Ag/Au alloy and Ag@Au core–shell NPs for developing novel anti-cancer agents by evaluating their potentials in the Hep-2 cell line model. Thus the developed core–shell NPs were possibly involved in inducing cytotoxicity followed by inhibition of cell proliferation to the cancer cells with apoptosis induction. The developed core–shell NPs might serve as highly applicable agents in the development of next-generation cancer chemotherapeutic agents.

In this work hybrid silver (Ag)–gold (Au) nanoparticles (NPs) with different sizes and compositions were synthesized and applied for anticancer evaluations and which is effectively involved in cancer cell apoptosis through DNA damage.     

Physical process-aided fabrication of periodic Au–M (M = Ag,Cu, Ag–Cu) alloyed nanoparticle arrays with tunable localized surface plasmon resonance and diffraction peaks

Periodic alloyed (Au–Ag, Au–Cu, Au–Ag–Cu) nanoparticle (NP) arrays with uniform size, controllable composition and center-to-center spacing were fabricated by a novel and facile strategy based on physical vapor deposition on a monolayer colloidal crystal template and further heat treatment. The composition and center-to-center spacing were manipulated by adjusting the sputtering target in the deposition process and the size of colloidal spheres of the template, respectively. The shadow effect and a dewetting model were employed to analyze the whole process of evolution from a metallic thin film to spherical nanoparticles with uniform size. The localized surface plasmon resonance (LSPR) and diffraction peaks of these alloyed arrays were systematically measured. The dielectric constant has an important influence on LSPR peaks and diffraction peaks. Both the LSPR and diffraction peaks of Au–Ag alloyed NPs arrays exhibit a blue shift due to their lower dielectric constant than that of pure Au NPs. However, compared with Au, Cu possesses a higher dielectric constant, leading to a red shift of the LSPR and diffraction peaks of Au–Cu alloyed NPs arrays. With the increase of NP size, the diffraction peaks of both binary alloyed NPs exhibit a slight red shift. Moreover, the LSPR absorption peaks were more sensitive to the composition of the NPs than the diffraction peaks. This work would open up a novel strategy in the production of alloyed NP arrays with tunable LSPR peaks and diffraction peaks, which would be very helpful to improve their practical applications in various fields.

An interesting and facile physical route is proposed to fabricate multi-elemental alloyed nanoparticle arrays with controllable size, composition and periodicity.     

Cobalt-modified palladium nanocatalyst on nitrogen-doped reduced graphene oxide for direct hydrazine fuel cell

Nitrogen-doped reduced graphene oxide-supported palladium–cobalt nanoparticles (PdCo NPs/NrGO NSs) are synthesized and used as a high-performance and low-cost anodic catalyst for direct hydrazine–hydrogen peroxide fuel cells. The SEM and TEM images of PdCo NPs/NrGO NSs show the uniform metal nanoparticle distribution on the NrGO NSs. The reduction of the oxygen functional groups and the doping of the nitrogen atoms in the GO framework are confirmed by FT-IR and XRD spectroscopic studies. The Pd catalysts modified by Co exhibit a higher catalytic activity, lower onset potential, better durability, and lower impedance values than unmodified Pd catalysts for the electro-oxidation of hydrazine. The kinetic studies show a first-order reaction with an activation energy of 12.51 kJ mol⁻¹. A direct hydrazine–hydrogen peroxide fuel cell with PdCo NPs/NrGO NSs as anode and Pt/C as cathode provides an open circuit voltage of 1.76 V and a maximum power density of 148.58 mW cm⁻² at 60 °C, indicating that the PdCo NPs/NrGO NSs are an economical, high performance and reliable anode catalyst for the direct hydrazine–hydrogen peroxide fuel cell.

The superior catalytic activity and stability of a novel anodic PdCo NPs/NrGO NSs for HzOR are confirmed by half and signal cell investigations.     

Fabrication,characterization and high photocatalytic activity of Ag–ZnO heterojunctions under UV-visible light

Pure ZnO and Ag–ZnO nanocomposites were fabricated via a sol–gel route, and the obtained photocatalysts were characterized by XRD, SEM, TEM, BET, XPS, PL and DRS. The results showed that Ag⁰ nanoparticles deposit on the ZnO surface and Ag modification has negligible impact on the crystal structure, surface hydroxyl group content and surface area of ZnO. However, the recombination of photogenerated electrons and holes was suppressed effectively by Ag loading. The photocatalytic activity was investigated by evaluating the degradation of MB under xenon lamp irradiation as the UV-visible light source, and the results show that the photocatalytic activity of ZnO significantly improved after Ag modification. Ag–ZnO photocatalysts exhibit higher photocatalytic activity than commercial photocatalyst P25. The degradation degree of MB for 1%Ag–ZnO was 97.1% after 15 min. ˙O₂⁻ radicals are the main active species responsible for the photodegradation process, and Ag–ZnO heterojunctions generate more ˙O₂⁻ radicals, which is the primary reason for the improved photocatalytic performance.

Ag–ZnO heterojunction promotes the separation of photogenerated pairs and thus exhibits high catalytic activity under UV-visible light.     

Green synthesis of palladium nanoparticles using lentinan for catalytic activity and biological applications

The green synthesis of palladium nanoparticles (Pd NPs) for catalysis and biological applications has been gaining great interest. To replace complex plant extracts, lentinan (LNT) may be a good reducing and stabilizing agent. In this work, a simple and green method using LNT to reduce and stabilize palladium Pd NPs was verified. The resulting LNT stabilized palladium nanoparticles (Pd_n-LNT NPs) were characterized by UV-Vis spectroscopy, DLS, TEM, and XPS. The results indicated that Pd NPs inside of Pd_n-LNT NPs had a small size (2.35–3.32 nm). Pd_n-LNT NPs were stable in solution for 7 days. In addition, Pd_n-LNT NPs had higher catalytic activity towards the reduction of 4-nitrophenol than other catalysts. More importantly, Pd_n-LNT NPs had negligible cytotoxicity towards cells and showed good antioxidant activity. Taken together, the prepared Pd_n-LNT NPs have great potential bio-related applications.

Lentinan stabilized palladium nanoparticles had high catalytic activity, negligible cytotoxicity and good antioxidant activity.     

Sulfonic-acid-functionalized carbon fiber from waste newspaper as a recyclable carbon based solid acid catalyst for the hydrolysis of cellulose

Waste newspaper is one of the most common cellulosic materials. Therefore, effective utilization of this commonly available biomass resource to prepare high-value carbon-based solid acid catalysts is an interesting and meaningful task. In this study we propose a new route for waste newspaper valorization, in which sulfonic-acid-functionalized carbon fiber can be directly produced from waste newspaper as a recyclable carbon based solid acid catalyst (WCSA) for the hydrolysis of cellulose. The as-prepared sulfonic-acid-functionalized carbon fiber contained –SO₃H, –COOH, and phenolic –OH groups and exhibited good catalytic activity for the hydrolysis of cellulose. WCSA prepared under sulfonation conditions at a temperature of 100 °C and for a duration of 10 h has a higher sulfonic acid content. A total reducing sugars (TRS) yield of 58.2% was obtained with a catalyst/microcrystalline cellulose (MCC) ratio of 4 at 150 °C using a reaction time of 6 h. The recycling performance of the WCSA catalyst indicated that the TRS remained almost stable for five cycles during the hydrolysis of cellulose.

Waste newspaper is one of the most common cellulosic materials.     

Cadmium oxide nanoparticles/graphene composite: synthesis,theoretical insights into reactivity and adsorption study

Graphene-based metal oxide nanocomposites are interesting and promising kinds of nanocomposites due to their large specific area, fast kinetics, and specific affinity towards heavy metal contaminants. In this work, a facile and cost-effective route was used to synthesize CdO nanoparticles (CdO NPs) and graphene-based CdO nanocomposite (G–CdO). The prepared nanomaterials were characterized and explored for lead removal from water. Both CdO NPs and G–CdO composite exhibited excellent sorption capacity of 427 and 398 mg g⁻¹, respectively, at pH 4.8 and T = 298 K, which was superior to individual graphene and many other adsorbents. The results indicated that the recovered nanomaterials endure 4 times recyclability retaining up to 89% lead uptake efficiency. To complement the experimental study, DFT calculations were performed to investigate the stability of the formed G–CdO composite compared to CdO NPs; the reactivity of G–CdO compared to plain graphene as well as the interaction insights between graphene and CdO clusters were studied using natural-bond-orbital (NBO), electron-localization-function (ELF) and reduced-density-gradient (RDG) analyses.

Graphene-based metal oxide nanocomposites are interesting and promising kinds of nanocomposites due to their large specific area, fast kinetics, and specific affinity towards heavy metal contaminants.