Escalating Catalytic Activity for Hydrogen Evolution Reaction on MoSe@Graphene Functionalization.

Developing highly efficient and durable hydrogen evolution reaction (HER) electrocatalysts is crucial for addressing the energy and environmental challenges. Among the 2D-layered chalcogenides, MoSe possesses superior features for HER catalysis. The attractions and high surface energy, however, stack the MoSe layers, resulting in a loss of edge active catalytic sites.

Rectification Behavior on Polyelectrolyte-Modified Flexible ITO Electrode via Ionic Charge-Selective Electron Transfer.

New types of diodes, such as molecular and ionic diodes, have drawn considerable attention because of their advantages from the viewpoint of potential applications such as the downscaling of electronic devices, ionic circuits, and biological systems. Researchers are motivated to develop a simple, scalable, and promising system that can overcome the existing limitations because this can enable their application in various devices. This study proposes a system that not only integrates the advantages of ionic and single-molecule diodes but also avoids their disadvantages, denoting the rectification behavior due to ionic charge-selective electron transfer between two redox species, i.

Ultrasensitive Fluorescence Detection of Alzheimer's Disease Based on Polyvalent Directed Peptide Polymer Coupled to a Nanoporous ZnO Nanoplatform.

Amyloid-beta 42 (Aβ), the key biomarker of Alzheimer's disease (AD), aggregates to form neurotoxic amyloid plaques. In this work, we modified two fluorescein isothiocyanate-labeled Aβ-targeting peptides and designed an Aβ-specific ultrasensitive polyvalent-directed peptide polymer (PDPP) to enhance AD diagnosis sensitivity. The dissociation constant of Aβ by PDPP was 10-fold higher than the single-site-directed peptide.

Hole transport layer based on conjugated polyelectrolytes for polymer solar cells.

We demonstrate the conjugated polyelectrolytes (CPEs) as efficient hole transport layer (HTL) of polymer solar cells. Replacing poly(3,4-ethylenedioxy-thiophene):poly(styrenesulfonate) (PEDOT:PSS) with a CPEs with narrow bandgap results in both improvements in device efficiency and stability. In spite of their narrow bandgap, thin CPE films (thickness of ∼30 nm) enable sufficient light absorption within the active layer.

Anodically Grown Binder-Free Nickel Hexacyanoferrate Film: Toward Efficient Water Reduction and Hexacyanoferrate Film Based Full Device for Overall Water Splitting.

One of the challenges in obtaining hydrogen economically by electrochemical water splitting is to identify and substitute cost-effective earth-abundant materials for the traditionally used precious-metal-based water-splitting electrocatalysts. Herein, we report the electrochemical formation of a thin film of nickel-based Prussian blue analogue hexacyanoferrate (Ni-HCF) through the anodization of a nickel substrate in ferricyanide electrolyte. As compared to the traditionally used Nafion-binder-based bulk film, the anodically obtained binder-free Ni-HCF film demonstrates superior performance in the electrochemical hydrogen evolution reaction (HER), which is highly competitive with that shown by a Pt-plate electrode.

Novel Solid-State Solar Cell Based on Hole-Conducting MOF-Sensitizer Demonstrating Power Conversion Efficiency of 2.1.

This work reports on designing of first successful MOF-sensitizer based solid-state photovoltaic device, perticularly with a meaningful output power conversion efficiency. In this study, an intrinsically conductive cobalt-based MOFs (Co-DAPV) formed by the coordination between Co (II) ions and a redox active di(3-diaminopropyl)-viologen (i.e.

A self-assembled Ni(cyclam)-BTC network on ITO for an oxygen evolution catalyst in alkaline solution.

A self-assembled Ni(cyclam)-BTC film was formed on ITO in an acidic solution. Ni(cyclam)-BTC exhibited an enhanced electro-catalytic property for the oxygen evolution reaction (OER), which was strongly relevant to the Ni(iii)/Ni(iv) redox reaction activated by the potential dynamic process. A possible formation mechanism of Ni(cyclam)-BTC by self-assembly on ITO was also proposed.

A facile room temperature chemical transformation approach for binder-free thin film formation of AgTe and lithiation/delithiation chemistry of the film.

The present work demonstrates a highly controllable, facile and environmentally friendly aqueous solution based synthetic method for oxide contamination-free AgTe thin films on desired substrates at room temperature using ion exchange induced chemical transformation of Ag/AgO thin films. The films before and after chemical transformation reaction are characterized using an energy dispersive X-ray analyzer, field emission scanning electron microscopy, X-ray photoelectron spectroscopy, thin film X-ray diffraction technique, high resolution transmission electron microscopy, and the selected area electron diffraction analysis technique. The as-deposited AgTe films show a highly crystalline nature even without thermal treatment.

Copper-Organic Framework Fabricated with CuS Nanoparticles: Synthesis, Electrical Conductivity, and Electrocatalytic Activities for Oxygen Reduction Reaction.

To apply electrically nonconductive metal-organic frameworks (MOFs) in an electrocatalytic oxygen reduction reaction (ORR), we have developed a new method for fabricating various amounts of CuS nanoparticles (nano-CuS) in/on a 3D Cu-MOF, [Cu (BTC) ⋅(H O) ] (BTC=1,3,5-benzenetricarboxylate). As the amount of nano-CuS increases in the composite, the electrical conductivity increases exponentially by up to circa 10 -fold, while porosity decreases, compared with that of the pristine Cu-MOF. The composites, nano-CuS(x wt %)@Cu-BTC, exhibit significantly higher electrocatalytic ORR activities than Cu-BTC or nano-CuS in an alkaline solution.

One-Step Catalytic Synthesis of CuO/Cu2O in a Graphitized Porous C Matrix Derived from the Cu-Based Metal-Organic Framework for Li- and Na-Ion Batteries.

The hybrid composite electrode comprising CuO and Cu2O micronanoparticles in a highly graphitized porous C matrix (CuO/Cu2O-GPC) has a rational design and is a favorable approach to increasing the rate capability and reversible capacity of metal oxide negative materials for Li- and Na-ion batteries. CuO/Cu2O-GPC is synthesized through a Cu-based metal-organic framework via a one-step thermal transformation process. The electrochemical performances of the CuO/Cu2O-GPC negative electrode in Li- and Na-ion batteries are systematically studied and exhibit excellent capacities of 887.

Interfacial Engineering for Enhanced Light Absorption and Charge Transfer of a Solution-Processed Bulk Heterojunction Based on Heptazole as a Small Molecule Type of Donor.

In the present study, a solution-processed organic semiconductor based on indolocarbazole derivative (heptazole) is introduced as a p-type donor material for a bulk-heterojunction photovoltaic device. The heptazole has an optical band gap of 2.97 eV, and its highest occupied molecular orbital-lowest unoccupied molecular orbital energy levels are compactable with the PC60BM to construct a donor-acceptor heterojuction for energy harvesting and transfer.

Formation of Semimetallic Cobalt Telluride Nanotube Film via Anion Exchange Tellurization Strategy in Aqueous Solution for Electrocatalytic Applications.

Metal telluride nanostructures have demonstrated several potential applications particularly in harvesting and storing green energy. Metal tellurides are synthesized by tellurization process performed basically at high temperature in reducing gas atmosphere, which makes the process expensive and complicated. The development of a facile and economical process for desirable metal telluride nanostructures without complicated manipulation is still a challenge.

Improved Photoelectrochemical Cell Performance of Tin Oxide with Functionalized Multiwalled Carbon Nanotubes-Cadmium Selenide Sensitizer.

Here we report functionalized multiwalled carbon nanotubes (f-MWCNTs)-CdSe nanocrystals (NCs) as photosensitizer in photoelectrochemical cells, where f-MWCNTs were uniformly coated with CdSe NCs onto SnO2 upright standing nanosheets by using a simple electrodeposition method. The resultant blended photoanodes demonstrate extraordinary electrochemical properties including higher Stern-Volmer constant, higher absorbance, and positive quenching, etc., caused by more accessibility of CdSe NCs compared with pristine SnO2-CdSe photoanode.

Charge Transfer-Induced Molecular Hole Doping into Thin Film of Metal-Organic Frameworks.

Despite the highly porous nature with significantly large surface area, metal-organic frameworks (MOFs) can be hardly used in electronic and optoelectronic devices due to their extremely poor electrical conductivity. Therefore, the study of MOF thin films that require electron transport or conductivity in combination with the everlasting porosity is highly desirable. In the present work, thin films of Co3(NDC)3DMF4 MOFs with improved electronic conductivity are synthesized using layer-by-layer and doctor blade coating techniques followed by iodine doping.

Interfacial Engineering of CdO-CdSe 3D Microarchitectures with in situ Photopolymerized PEDOT for an Enhanced Photovoltaic Performance.

In the present work, porous 3D CdO-microstructured electrode obtained by pyrolysis of 3D CdCO3 microstructures is self-sensitized with CdSe using an ion exchange reaction. After sensitization, an interfacial treatment of the CdO-CdSe interface is performed by depositing a thin film of PEDOT using a photoinduce polymerization route. The microstructured electrode before and after interfacial treatment is characterized using field-emission scanning microscope, energy dispersive X-ray analyzer, contact angle measurement, UV-Visible absorption spectrophotometer and X-ray photoelectron spectrometer.

Optical and structural properties of plasma-treated ZnO nanostructures.

We studied the effect of plasma treatment on the structural and optical properties of ZnO nanostructures prepared by chemical bath deposition in an aqueous solution of Zn(NO3)2 and hexamethylenetetramine. The room-temperature photoluminescence (PL) spectrum of the as-grown ZnO nanostructures exhibited two emission bands due to exciton emission and defect emission. After treating with hydrogen plasma, the treated ZnO nanostructures exhibited stronger exciton emission than the as-grown, untreated ZnO nanostructures in their respective cathodoluminescence and PL spectra.

Highly efficient and stable DSSCs of wet-chemically synthesized MoS2 counter electrode.

A competitive power conversion efficiency of 7.01% is achieved for TiO2-based dye-sensitized solar cells (DSSCs) using a chemically stable and mechanically robust molybdenum di-sulfide (MoS2) counter electrode, synthesized using a simple, scalable and low-temperature wet-chemical process, owing to its good redox reaction stability.

Long-range ordered self-assembly of novel acrylamide-based diblock copolymers for nanolithography and metallic nanostructure fabrication.

Novel acrylamide-based hard-soft hybrid block copolymers generate high-quality nanolithographic patterns satisfying high-resolution, long-range ordering, low defect density, moderate etch selectivity, and easy pattern transfer onto a substrate. The resulting patterns can also be used as a scaffold for metallic nanostructures such as aligned nanowires and nanomeshes with extraordinary structural regularity.

Enhanced photovoltaic performance of Cu-based metal-organic frameworks sensitized solar cell by addition of carbon nanotubes.

In the present work, TiO2 nanoparticle and multi-walled carbon nanotubes composite powder is prepared hydrothermally. After doctor blading the paste from composite powder, the resulted composite film is sensitized with Cu-based metal-organic frameworks using a layer-by-layer deposition technique and the film is characterized using FE-SEM, EDX, XRD, UV/Visible spectrophotometry and photoluminescence spectroscopy. The influence of the carbon nanotubes in photovoltaic performance is studied by constructing a Grätzel cell with I3(-)/I(-) redox couple containing electrolyte.

Current density enhancement in ZnO/CdSe photoelectrochemical cells in the presence of a charge separating SnO2 nanoparticles interfacing-layer.

Photoelectrochemical cells (PECs) of ZnO/CdSe decorated with a charge separating SnO2 nanoparticles (NPs) layer of various thicknesses are prepared and characterized by using scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), UV-visible absorption, energy dispersive X-ray analysis spectroscopy (EDX) and incident photon-to-current conversion efficiency (IPCE) measurements. A uniform coverage of the SnO2 NPs layer over ZnO/CdSe electrode surface is evidenced. The EDX elemental mapping analysis of the ZnO/CdSe/SnO2 PECs demonstrates the presence of Sn and O over the surface.

High-performance air-stable single-crystal organic nanowires based on a new indolocarbazole derivative for field-effect transistors.

A new indolocabazole derivative possessing an extended aromatic core and solubilizing long aliphatic chains effectively self-assembles and crystallizes within the nanoscale channels to form single-crystal nanowires via a direct printing method from an ink solution. Single-crystal organic nanowire transistor arrays based on the π-extended indolocarbazole derivative exhibit an excellent hole mobility of 1.5 cm² V⁻¹ s⁻¹ and outstanding environmental stability.

Rapid dye adsorption via surface modification of TiO2 photoanodes for dye-sensitized solar cells.

A facile method for increasing the reaction rate of dye adsorption, which is the most time-consuming step in the production of dye-sensitized solar cells (DSSCs), was developed. Treatment of a TiO2 photoanode with aqueous nitric acid solution (pH 1) remarkably reduced the reaction time required to anchor a carboxylate anion of the dye onto the TiO2 nanoparticle surface. After optimization of the reaction conditions, the dye adsorption process became 18 times faster than that of the conventional adsorption method.

Low temperature chemically synthesized rutile TiO2 photoanodes with high electron lifetime for organic dye-sensitized solar cells.

Electron lifetime in mesoporous nanostructured rutile TiO2 photoanodes, synthesized via a simple, cost-effective, low temperature (50-55 °C) wet chemical process, annealed at 350 °C for 1 h and not employing any sprayed TiO2 compact layer, was successfully tailored with 0.2 mM TiCl4 surface treatment that resulted in light to electric power conversion efficiency up to 4.4%.

Polythiophene infiltrated TiO2 nanotubes as high-performance supercapacitor electrodes.

We report exceptional electrochemical specific capacitance (640 F g(-1)) for polythiophene (PTh) infiltrated into TiO(2) nanotubes (TNTs) by a controlled electropolymerization route. The resulting PTh-TNTs also exhibit excellent electrochemical behavior with long-term stability. This reproducible and superior performance of PTh-TNT electrodes makes them attractive candidates for energy storage.

Direct detection of sulfide ions [S2-] in aqueous media based on fluorescence quenching of functionalized CdS QDs at trace levels: analytical applications to environmental analysis.

A novel, simple but highly selective fluorescent probe is developed for the direct detection of sulfide ions [S(2-)] based on the fluorescence quenching of the functionalized CdS QDs in aqueous solution at trace levels and successfully applied for quantitation of S(2-) from water samples in a complex matrix exclusive of pretreatment by standard addition method.