Ternary composites of Ni–polyaniline–graphene as counter electrodes for dye-sensitized solar cells

Dye-sensitized solar cells (DSSCs), different in principle from the conventional solar cells based on p–n junctions, are competitively cost-effective. For development of this kind of emerging solar cell, it is very significant to reduce their cost and improve their energy conversion efficiency to the maximum extent. In this article, ternary composites (Ni–PANI–G composites) consisting of nickel nanoparticles, polyaniline (PANI), and graphene (G) were prepared for the first time and used as counter electrodes to replace the noble metal Pt in DSSCs. In the case of PANI, the introduction of Ni nanoparticles can improve the electrocatalytic ability for the reduction of triiodide ions in the counter electrode, while in the meantime, the addition of graphene in the Ni–PANI–G composites can increase the electrical conductivity of the counter electrode. The optimized DSSCs fabricated by using the Ni–PANI–G composites as the counter electrode exhibit an overall power conversion efficiency of 5.80% compared to 5.30% for reference platinum (Pt) counter-electrodes. Electrochemical impedance spectra (EIS) show that the charge-transfer resistance at the interface between electrolyte and counter-electrode in the case of the ternary composite is obviously decreased. These results are significant to develop low-cost counter electrode materials for DSSCs.

In this article, ternary composites (Ni–PANI–G composites) consisting of nickel nanoparticles, polyaniline (PANI), and graphene (G) were prepared for the first time and used as counter electrodes to replace the noble metal Pt in DSSCs.     

Humidity sensor based on poly(lactic acid)/PANI–ZnO composite electrospun fibers

The electrospinning technique has been successfully used to prepared micro-fibers of the poly(lactic acid)/polyaniline–zinc oxide (PLA/PANI–ZnO) composite. The polyaniline–zinc oxide (PANI–ZnO) nanocomposites are synthesized by hydrothermal and in situ polymerization methods. X-ray diffraction techniques are used to study the structural properties of the PLA/PANI–ZnO composite fibers and the PANI–ZnO nanocomposite. The average crystallite size of the PANI–ZnO nanocomposite is found to be 36 nm. The morphology and diameter of the composite fibers are analyzed by scanning electron microscopy (SEM). The average fiber diameter of the pure poly(lactic acid) (PLA) fiber is around 2.5 μm and that of the PLA/PANI–ZnO composite fiber is around 1.4 μm. Differential scanning calorimetry (DSC) provides the thermal properties of the PLA/PANI–ZnO composite fibers. The melting temperature (T_m) for the pure PLA is observed at 149.3 °C, and it is shifted to 153.0 °C for the PLA/PANI–ZnO composite fibers. The enhanced thermal properties of the composite fibers are due to the interaction between the polymer and the nanoparticles. The water contact angle measurements probe the surface hydrophilicity of the PLA/PANI–ZnO composite fibers. The role of the PANI–ZnO nanocomposite on the sensing behavior of PLA fibers has also been investigated. The humidity sensing properties of the composite fiber based sensor are studied in the relative humidity (RH) range of 20–90% RH. The experimental results show that the composite fiber exhibited good response (85 s) and recovery (120 s) times. These results indicate that the one-dimensional (1D) fiber structure enhances the humidity sensing properties.

The electrospinning technique has been successfully used to prepared micro-fibers of the poly(lactic acid)/polyaniline–zinc oxide (PLA/PANI–ZnO) composite for humidity sensor application.     

Au–Ag and Pt–Ag bimetallic nanoparticles@halloysite nanotubes: morphological modulation,improvement of thermal stability and catalytic performance

In this study, Au–Ag and Pt–Ag bimetallic nanocages were loaded on natural halloysite nanotubes (HNTs) via galvanic exchange based on Ag@HNT. By changing the ratio of Au to Ag or Pt to Ag in exchange processes, Au–Ag@HNT and Pt–Ag@HNT with different nanostructures were generated. Both Au–Ag@HNT and Pt–Ag@HNT systems showed significantly improved efficiency as peroxidase-like catalysts in the oxidation of o-phenylenediamine compared with monometallic Au@HNT and Pt@HNT, although inert Ag is dominant in the composition of both Au–Ag and Pt–Ag nanocages. On the other hand, loading on HNTs enhanced the thermal stability for every system, whether monometallic Ag nanoparticles, bimetallic Au–Ag or Pt–Ag nanocages. Ag@HNT sustained thermal treatment at 400 °C in nitrogen with improved catalytic performance, while Au–Ag@HNT and Pt–Ag@HNT maintained or even had slightly enhanced catalytic efficiency after thermal treatment at 200 °C in nitrogen. This study demonstrated that natural halloysite nanotubes are a good support for various metallic nanoparticles, improving their catalytic efficiency and thermal stability.

Bimetallic Au–Ag@HNT and Pt–Ag@HNT nanocages showed significantly improved efficiency in the oxidation of o-phenylenediamine as peroxidase-like catalyst compared with corresponding monometallic nanoparticles.     

Epoxy-matrix polyaniline/p-phenylenediamine-functionalised graphene oxide coatings with dual anti-corrosion and anti-fouling performance

This research work reports on the anti-corrosion and anti-fouling properties of epoxy (E) coatings reinforced with polyaniline (PANI)/p-phenylenediamine-functionalised graphene oxide (PGO) composites. The mass ratio of graphene oxide/p-phenylenediamine in any PGO was assumed to be 1 : 1, but different PANI–PGO composites containing various loadings of PGO were prepared. An ultrasonic-assisted in situ polymerization method was employed to produce PANI–PGO at low temperature (0 °C). Several analytical and microscopical techniques, i.e., Fourier-transfer infrared (FTIR) spectroscopy, X-ray diffraction (XRD), and field emission scanning electron microscopy (FESEM), were used to confirm that PANI–PGO composites were successfully synthesized. The epoxy-based coatings (E/PANI–PGO (x), x = 0.05–0.4 g) were applied by brushing them onto carbon steel substrates, which exhibited dual anti-corrosion and anti-fouling performance. Electrochemical impedance spectroscopy (EIS) results show that E/PANI–PGO (0.2) has the highest corrosion resistance (8.87 × 10⁶ Ω cm²) after 192 h of immersion in 3.5 wt% NaCl amongst all the coatings compared with neat epoxy (1.00 × 10⁴ Ω cm²) and E/PANI (6.82 × 10³ Ω cm²). Efficient antifouling performance at the macroscopic level under simulated marine conditions was observed for the epoxy-based PANI–PGO coatings with a range of PGO compositions, in particular for the 0.1 and 0.2 g PGO coatings.

Graphene oxide (GO), GO-functionalised using p-phenylenediamine (PGO) and polyaniline (PANI)-PGO composites were successfully prepared for use in epoxy-matrix coatings for anti-corrosion and anti-fouling applications.     

Efficient nickel or copper oxides decorated graphene–polyaniline interface for application in selective methanol sensing

Graphene sheets decorated with nickel or copper oxides that were anchored on polyaniline (denoted as PANI-graphene/NiO and PANI-graphene/CuO) were prepared by a simple, easy to-control electrochemical method and applied as novel materials for sensitive and selective methanol sensing. The fabricated sensors exhibited good electrocatalytic activity, appropriate dynamic linear range (20–1300 mM), sensitivity (0.2–1.5 μA mM⁻¹ cm⁻²) and excellent selectivity towards methanol. It should be highlighted from the selectivity tests that no significant interference was observed from ethanol and other alcohols. To our best knowledge, using inexpensive but efficient transition metals like Ni, Cu instead of Pt, Pd and their composites with PANI, graphene would be scientifically novel and practically feasible approach for sensor fabrication that could be potentially used to identify methanol adulteration in counterfeit alcoholic beverages.

PANI/graphene/NiO or PANI/graphene/CuO were prepared by a simple, easy to-control electrochemical method and applied as novel materials for sensitive and selective methanol sensing.     

Investigation of the structural,optical and gas sensing properties of PANI coated Cu–ZnS microsphere composite

Polyaniline (PANI)/Cu–ZnS composites with porous microspheres are prepared by a hydrothermal and in situ polymerization method. The structural, optical, and morphological properties are characterized by X-ray powder diffraction, FTIR, UV-vis, scanning electron microscope, transmission electron microscope. The XRD results confirmed that the PANI/Cu–ZnS composite is formed. The morphological analyses exhibited that the PANI/Cu–ZnS composite comprises the porous microspherical structures. The emission peaks obtained in photoluminescence spectra confirm the presence of surface defects in the prepared composite. The UV-DRS study shows that the bandgap of the samples is found to decrease for the PANI/Cu–ZnS composite compared to the pure Cu–ZnS sample. The calculated band gap (E_g) value of PANI/Cu–ZnS composite is 2.47 eV. Furthermore, the fabricated gas sensor based on PANI/Cu–ZnS can perform at room temperature and exhibits good gas sensing performance toward CO₂ gas. In particular, PANI/Cu–ZnS sensor shows good response (31 s) and recovery time (23 s) upon exposure to CO₂ gas. The p/n heterojunction, surface defects, and porous nature of the PANI/Cu–ZnS composite microsphere enhanced sensor performance.

Polyaniline (PANI)/Cu–ZnS composites with porous microspheres are prepared by a hydrothermal and in situ polymerization method.     

Nitrogen–sulfur dual-doped porous carbon spheres/sulfur composites for high-performance lithium–sulfur batteries

A nitrogen–sulfur dual-doped porous carbon spheres/sulfur composite (PCS-NS/S) sample was prepared by a simple hydrothermal method with starch and l-methionine as carbon and nitrogen–sulfur resources, respectively. XRD, XPS, and N₂ adsorption–desorption tests were used to characterize the crystal and pore structure of the PCS-NS/S sample. The morphology and weight ratio of sulfur were investigated by SEM, TEM, and TG analyses. The sample was used as the positive electrode for lithium–sulfur batteries and found to exhibit excellent electrochemical performance.

Simultaneously introduced nitrogen–sulfur through one reagent. The as-prepared PCS-NS/S composites exhibited excellent electrochemical performance as positive electrode for Li–S battery.     

Vitamin C assisted synthesis of rGO–Ag/PANI nanocomposites for improved photocatalytic degradation of pharmaceutical wastes

A highly efficient visible light active polyaniline (PANI)/Ag composites grafted reduced graphene oxide (rGO–Ag/PANI) was prepared for the efficient photocatalytic degradation of paracetamol. The structural, morphological, and light absorption properties of the as-synthesized rGO–Ag/PANI were characterized by UV-Visible (UV-Vis) spectroscopy, Fourier transform infrared (FTIR) spectroscopy, powder X-ray diffraction (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). Paracetamol was taken as a model water pollutant to investigate the photocatalytic degradation efficiency of the rGO–PANI/Ag nanocomposites under visible light radiation. The result shows the degradation of paracetamol to be 99.6% in the acidic medium (pH 5) and 75.76% in the basic medium (pH 9), respectively. The enhanced degradation efficiency is attributed to the synergetic effect of rGO, PANI, and Ag NPs in the nanocomposites. This synergy of the rGO–Ag/PANI is explained by the strong adsorption efficiency, charge separation, and light absorption in the visible region.

A highly efficient visible light active polyaniline (PANI)/Ag composites grafted reduced graphene oxide (rGO–Ag/PANI) was prepared for the efficient photocatalytic degradation of paracetamol.     

Cyanide-free electrolyte for Au/Co–Au nano-multilayer electrodeposition utilising 5,5-dimethylhydantoin as a complexing agent

A novel cyanide-free electrolyte was used in electrodepositing Au/Co–Au nano-multilayers. Firstly, an optimised electrolyte for Au–Co alloy electrodeposition was obtained from orthogonal experiments. The effect of current density and potential values on the deposited composition was investigated. Results showed that low current density and over-potential value promoted Au deposition. A large current density and high over-potential value resulted in high cobalt concentration. The co-deposition of gold and cobalt in this study system was canonical. When the electrode potential was positive (−0.6 V, −0.7 V vs. saturated calomel electrode (SCE)), only gold was deposited; when the potential was negative (−0.8 V vs. SCE), gold and cobalt were co-deposited. Using an optimised cyanide-free electrolyte produced Au/94.07 at% Co–Au multi-layers with a gold layer of approximately 20 nm and a 94.07 at% Co–Au alloy layer of approximately 90 nm in the 5,5-dimethylhydantoin-containing, cyanide-free system.

Cross-section of Au/Co-rich nano-multilayer.     

Deposition of an ultra-thin polyaniline coating on a TiO2 surface by vapor phase polymerization for electrochemical glucose sensing and photocatalytic degradation

Here, we have synthesized an ultra-thin coating of polyaniline on a TiO₂ nanoparticle surface (PANI–TiO₂) using a simple vapor phase polymerization method. By this method, an ultra-thin layer of PANI is obtained selectively on the TiO₂ surface. This ultra-thin coating exhibits the properties of both the parent materials due to the composite surface causing an effective synergistic effect. SEM, TEM, and EDX studies and elemental mapping confirmed the formation of ultra-thin films on the TiO₂ surface. TGA, UV/Vis and XRD studies were also done for further characterization. The composite has been used as a biosensor for glucose detection by immobilization of the enzyme glucose oxidase (GOx). Cyclic voltammetry, electrochemical impedance spectroscopy and amperometry studies were performed for glucose sensing. The linear range was observed from 20 to 140 μM glucose concentration from the amperometric analysis. The LOD of the biosensor was found to be 5.33 μM. The composite has also been used for photocatalytic degradation of the cationic dye Rhodamine B (RB). The order of degradation efficiency of RB is found to be PANI < TiO₂ < PANI–TiO₂. The synergetic effect of PANI and TiO₂ is the reason for the enhanced degradation efficiency of the composite PANI–TiO₂.

Here, we have synthesized an ultra-thin coating of polyaniline on a TiO₂ nanoparticle surface (PANI–TiO₂) using a simple vapor phase polymerization method.     

A photoelectrochemical glucose sensor based on gold nanoparticles as a mimic enzyme of glucose oxidase

This work reports the first construction of the ternary layers of ITO/PbS/SiO₂/AuNPs nanostructure for development of photoelectrochemical (PEC) glucose sensor. Herein, the thioglycolic acid-capped PbS quantum dots was employed as a PEC active probe, which is very sensitive to oxygen. The small gold nanoparticles (AuNPs) were act as nanozyme (mimic enzyme of glucose oxidase) to catalytically oxidize glucose in the presence of oxygen, meanwhile consumed oxygen and then resulted in the decrease of cathodic photocurrent. The insertion layer of SiO₂ nanoparticles between PbS and AuNPs could reduce efficiently the base current due to its low electroconductivity, which improved the detection limit. The proposed PEC sensor exhibited high sensitivity and gold selectivity towards glucose. The linear response of glucose concentrations ranged from 1.0 μM to 1.0 mM with detection limit of 0.46 μM (S/N = 3). The results suggest the potential of design and development of numerous nanozyme-based PEC biosensors with the advantage of the simplicity, stability, and efficiency.

This work reports the first construction of the ternary layers of ITO/PbS/SiO₂/AuNPs nanostructure for development of photoelectrochemical (PEC) glucose sensor.     

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.     

New advances on Au–magnetic organic hybrid core–shells in MRI,CT imaging,and drug delivery

Magnetic nanoparticles have been widely studied for various scientific and technological applications such as magnetic storage media, contrast agents for magnetic resonance imaging (MRI), biolabelling, separation of biomolecules, and magnetic-targeted drug delivery. A new strategy on Au–magnetic nano-hybrid core–shells was applied in MRI, CT imaging, and drug delivery, which has been received much attention nowadays. Herein, the designing of different magnetic core–shells with Au in MRI and cancer treatment is studied.

Magnetic nanoparticles have been studied for scientific and technological applications such as magnetic storage media, contrast agents for magnetic resonance imaging, biolabelling, separation of biomolecules, and magnetic-targeted drug delivery.     

Sensitive impedimetric detection of troponin I with metal–organic framework composite electrode

Metal–organic frameworks (MOFs) are promising materials for biosensing applications due to their large surface to volume ratio, easy assembly as thin films, and better biocompatibility than other nanomaterials. Their application in electrochemical biosensing devices can be realized by integrating them with other conducting materials, like polyaniline (PANI). In the present research, a composite of a copper-MOF (i.e., Cu₃(BTC)₂) with PANI has been explored to develop an impedimetric sensor for cardiac marker troponin I (cTnI). The solvothermally synthesized Cu₃(BTC)₂/PANI composite has been coated as a thin layer on the screen-printed carbon electrodes (SPE). This electroconductive thin film was conjugated with anti-cTnI antibodies. The above formed immunosensor has allowed the impedimetric detection of cTnI antigen over a clinically important concentration range of 1–400 ng mL⁻¹. The whole process of antigen analysis could be completed within 5 min. The detection method was specific to cTnI even in the co-presence of other possibly interfering proteins.

A Cu-MOF/PANI modified screen-printed electrode based immunosensing technique is described for the sensitive detection of cardiac troponin I. The sensor provides detection over a wide concentration range with a limit of detection of 0.8 ng mL⁻¹.     

CNT–TiO2 core–shell structure: synthesis and photoelectrochemical characterization

Porous composite coatings, made of a carbon nanotube (CNT)–TiO₂ core–shell structure, were synthesized by the hybrid CVD-ALD process. The resulting TiO₂ shell features an anatase crystalline structure that covers uniformly the surface of the CNTs. These composite coatings were investigated as photoanodes for the photo-electrochemical (PEC) water splitting reaction. The CNT–TiO₂ core–shell configuration outperforms the bare TiO₂ films obtained using the same process regardless of the deposited anatase thickness. The improvement factor, exceeding 400% in photocurrent featuring a core–shell structure, was attributed to the enhancement of the interface area with the electrolyte and the electrons fast withdrawal. The estimation of the photo-electrochemically effective surface area reveals that the strong absorption properties of CNT severely limit the light penetration depth in the CNT–TiO₂ system.

CNT–TiO₂ core–shell nanostructured coatings were made using a hybrid CVD/ALD process. The evaluation of these films as photoanodes for the photoelectrochemical water splitting reaction reveals a clear benefit from the involvement of CNTs.     

Hybrid ZnO–graphene electrode with palladium nanoparticles on Ni foam and application to self-powered nonenzymatic glucose sensing

A self-powered nonenzymatic glucose sensor electrode boasts the advantages of both a glucose sensor and fuel cell. Herein, an electrode composed of ZnO–graphene hybrid materials on nickel foam (NF) is prepared by electrodeposition of Pd NPs. The electrode is characterized systematically and the dependence of electrocatalytic oxidation of glucose on the concentrations of KOH and glucose, temperature, and potential limit in the anodic direction is investigated. The Pd/NF-ZnO–G electrode shows high catalytic activity, sensitivity, stability, and selectivity in glucose detection, as exemplified by an electrocatalytic glucose oxidation current of 222.2 mA cm⁻² under alkaline conditions, high linearity in the glucose concentration range from 5 μM to 6 mM (R² = 0.98), and high sensitivity of 129.44 μA mM⁻¹⁻¹ cm⁻². The Pd/NF-ZnO–G electrode which exhibits superior electrocatalytic activity under alkaline conditions has large potential in nonenzymatic glucose sensing and direct glucose fuel cells and is suitable for miniaturized self-powered nonenzymatic glucose sensing.

A self-powered nonenzymatic glucose sensor electrode boasts the advantages of both a glucose sensor and fuel cell.     

Au–Ag core–shell composite nanoparticles as a selective and sensitive plasmonic chemical probe for l-cysteine detection in Lens culinaris (lentils)

The present work reported is a simple and selective method for the colorimetrical detection of l-cysteine in Lens culinaris (or lentils) using Au–Ag core–shell (Au core Ag shell) composite nanoparticles as a chemical probe. The phenomenon is based on the color change of composite nanoparticles from yellowish brown to light blue, followed by a shift of the localized surface plasmon resonance (LSPR) absorption band in the UV-visible region (i.e., 200–800 nm) with the addition of l-cysteine into the solution of bimetallic nanoparticles. The mechanism for the detection of l-cysteine is based on the electrostatic interaction of the metal ion with the thiol group of the amino acid, which causes the red shift of the LSPR band at 685 nm. The size distribution, morphology, composition and optical properties of the Au–Ag core–shell composite nanoparticles were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS), energy dispersive X-ray diffraction (EDX), UV-visible spectrophotometer and Fourier transform infrared spectroscopy (FTIR) techniques. An excellent linearity range for the present method was observed in the range of 20–140 μg mL⁻¹ with a limit of detection at 1.95 μg mL⁻¹ and correlation coefficient (R²) of 0.986. A good% recovery of 4.0% showed the selectivity of the method for l-cysteine determination from sample matrices. The advantageous features of the present method are being simple, rapid, low cost and selectivity towards the determination of l-cysteine in lentils.

The present work reported is a simple and selective method for the colorimetrical detection of l-cysteine in Lens culinaris (or lentils) using Au–Ag core–shell (Au core Ag shell) composite nanoparticles as a chemical probe.     

Developing a screen-printed graphite–polyurethane composite electrode modified with gold nanoparticles for the voltammetric determination of dopamine

A screen-printed electrode (SPGPUE) was prepared with graphite–polyurethane composite ink containing gold nanoparticles (AuNPs), resulting in a screen-printed graphite–polyurethane composite electrode modified with gold nanoparticles (SPGPUE–AuNPs). Gold nanoparticles were prepared by the citrate method and extracted from the water medium since polyurethane is not compatible with humidity. After extraction to chloroform, they were characterized via transmission electron microscopy (TEM). The presence of gold on the SPGPUE–AuNP surface was confirmed via SEM and EDX analyses, while thermogravimetry revealed the presence of approximately 3.0% (m/m) gold in the composite. An electrochemical pretreatment in 0.10 mol L⁻¹ phosphate buffer (pH 7.0) with successive cycling between −1.0 V and 1.0 V (vs. pseudo-Ag/AgCl) under a scan rate of 200 mV s⁻¹ and 150 cycles was required in order to provide a suitable electrochemical response for the voltammetric determination of dopamine. After the optimization of the parameters of differential pulse voltammetry (DPV), an analytical curve was obtained within a linear dynamic range of 0.40–60.0 μmol L⁻¹ and detection limit (LOD) of 1.55 ×10⁻⁸ mol L⁻¹ for dopamine at the SPGPUE–AuNP. A non-modified SPGPUE was used for comparison and a linear range was obtained between 2.0 and 10 μmol L⁻¹ with an LOD of 2.94 × 10⁻⁷ mol L⁻¹. During the dopamine determination in cerebrospinal synthetic fluid (CSF), recoveries between 89.3 and 103% were achieved. There were no significant interferences from ascorbic acid and uric acid, but some from epinephrine due to the structural similarity.

A screen-printed modified composite electrode (SPGPUE) was prepared with graphite–polyurethane ink containing gold nanoparticles (AuNPs), resulting in a sensor with improved sensitivity regarding the unmodified device in dopamine determination.     

Electrospun acellular scaffolds for mimicking the natural anisotropy of the extracellular matrix

In tissue engineering, the use of scaffolds helps establish a synergistic relationship between the scaffolds and the tissues by improving cell–scaffold interaction. This interaction is enhanced when physiologically relevant biophysical cues are replicated in the artificial scaffolds. Here, we present a novel scaffold that mimics the natural anisotropy of the native extracellular matrix of tissues, fabricated by electrospinning a combination of three polymers: polycaprolactone (PCL), polyvinylidene fluoride (PVDF) and polyaniline (PANI). The scaffolds were characterized for their morphology, surface and mechanical properties. Rat cardiomyoblast (H9c2) cells, cultured on the PCL–PANI–PVDF scaffold, demonstrated cell alignment, penetration and proliferation across the entire surface area of the scaffold without any external chemical or physical stimuli. The PCL–PANI–PVDF scaffold, unlike other scaffolds, does not require post-processing or specific temperature conditions of storage, prior to use. These acellular scaffolds fabricated through polymer blending, open new avenues for research on functional acellular scaffolds for tissue engineering, based on synthetic materials.

Co-axial electrospinning of three immiscible polymers by sequentially blending in solvents of different boiling points to obtain biomimetic scaffolds.     

Hot electron transfer in Zn–Ag–In–Te nanocrystal–methyl viologen complexes enhanced with higher-energy photon excitation

The dynamics of hot electron transfer from Zn–Ag–In–Te (ZAITe) nanocrystals (NCs) to adsorbed methyl viologen (MV²⁺) were investigated by transient absorption spectroscopy. The bleaching of the exciton peak in the ZAITe NC–MV²⁺ complexes evolved faster than that of ZAITe NCs. The hot electron transfer efficiency increased from 45% to 72% with increasing excitation photon energy.

Zn–Ag–In–Te nanocrystals exhibited hot electron transfer to adsorbed methyl viologen, the efficiency being enhanced from 45% to 72% with an increase in the excitation photon energy.