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ITO Surface (ito + surface)

Distribution by Scientific Domains

Polymers and Materials Science	50%
Chemistry	50%

Selected Abstracts

Real Time Electrochemical Monitoring of DNA/PNA Dissociation by Melting Curve Analysis

ELECTROANALYSIS, Issue 14 2009
Xiaoteng Luo
Abstract An immobilization-free electrochemical method is reported for real-time monitoring of the DNA hybrid dissociation between a ferrocene labeled peptide nucleic acid (PNA) and a fully-complementary or single-base-mismatched DNA. This method takes advantages of electrostatic charge characteristics and interactions among the neutrally charged PNA, the negatively charged DNA and the negatively charged electrode surface made of indium tin oxide (ITO). When a ferrocene labeled PNA (Fc-PNA) sequence is hybridized to a complementary DNA strand, electrostatic repulsion between the negatively charged PNA/DNA hybrid and the negative ITO surface retards the diffusion of the electroactive Fc to the electrode, resulting in a much reduced electrochemical signal. On the other hand, when the Fc-PNA is dissociated from the hybrid at elevated temperatures, the neutrally charged Fc-PNA easily diffuses to the electrode with an enhanced electrochemical signal. Therefore, an electrochemical melting curve of the Fc-PNA/DNA hybrid can be obtained by measuring the Fc signal with the increasing temperature. This strategy allows monitoring of the dissociation of the DNA hybrid in real time, which might lead to a simple detection method for single nucleotide polymorphism (SNP) analysis. [source]

Anode Interfacial Tuning via Electron-Blocking/Hole-Transport Layers and Indium Tin Oxide Surface Treatment in Bulk-Heterojunction Organic Photovoltaic Cells

ADVANCED FUNCTIONAL MATERIALS, Issue 4 2010
Alexander W. Hains
Abstract The effects of anode/active layer interface modification in bulk-heterojunction organic photovoltaic (OPV) cells is investigated using poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) and/or a hole-transporting/electron-blocking blend of 4,4,-bis[(p -trichlorosilylpropylphenyl)-phenylamino]biphenyl (TPDSi2) and poly[9,9-dioctylfluorene- co - N -[4-(3-methylpropyl)]-diphenylamine] (TFB) as interfacial layers (IFLs). Current,voltage data in the dark and AM1.5G light show that the TPDSi2:TFB IFL yields MDMO-PPV:PCBM OPVs with substantially increased open-circuit voltage (Voc), power conversion efficiency, and thermal stability versus devices having no IFL or PEDOT:PSS. Using PEDOT:PSS and TPDSi2:TFB together in the same cell greatly reduces dark current and produces the highest Voc (0.91,V) by combining the electron-blocking effects of both layers. ITO anode pre-treatment was investigated by X-ray photoelectron spectroscopy to understand why oxygen plasma, UV ozone, and solvent cleaning markedly affect cell response in combination with each IFL. O2 plasma and UV ozone treatment most effectively clean the ITO surface and are found most effective in preparing the surface for PEDOT:PSS deposition; UV ozone produces optimum solar cells with the TPDSi2:TFB IFL. Solvent cleaning leaves significant residual carbon contamination on the ITO and is best followed by O2 plasma or UV ozone treatment. [source]

Efficient Charge Injection from the S2 Photoexcited State of Special-Pair Mimic Porphyrin Assemblies Anchored on a Titanium-Modified ITO Anode

CHEMISTRY - A EUROPEAN JOURNAL, Issue 31 2006
Mitsuhiko Morisue Dr.
Abstract A novel surface fabrication methodology has been accomplished, aimed at efficient anodic photocurrent generation by a photoexcited porphyrin on an ITO (indium,tin oxide) electrode. The ITO electrode was submitted to a surface sol,gel process with titanium n -butoxide in order to deposit a titanium monolayer. Subsequently, porphyrins were assembled as monolayers on the titanium-treated ITO surface via phosphonate, isophthalate, and thiolate groups. Slipped-cofacial porphyrin dimers, the so-called artificial special pair at the photoreaction center, were organized through imidazolyl-to-zinc complementary coordination of imidazolylporphyrinatozinc(II) units, which were covalently immobilized by ring-closing olefin metathesis of allyl side chains. The modified surfaces were analyzed by means of X-ray photoelectron spectroscopy. Photoirradiation of the porphyrin dimer generated a large anodic photocurrent in aqueous electrolyte solution containing hydroquinone as an electron sacrificer, due to the small reorganization energy of the dimer. The use of different linker groups led to significant differences in the efficiencies of anodic photocurrent generation. The apparent flat-band potentials evaluated from the photocurrent properties at various pH values and under biased conditions imply that the band structure of the ITO electrode is modified by the anchoring species. The quantum yield for the anodic photocurrent generation by photoexcitation at the Soret band is increased to 15,%, a surprisingly high value without a redox cascade structure on the ITO electrode surface, while excitation at the Q band is not so significant. Extensive exploration of the photocurrent properties has revealed that hot injection of the photoexcited electron from the S2 level into the conduction band of the ITO electrode takes place before internal conversion to the S1* state, through the strong electronic communication of the phosphonyl anchor with the sol,gel-modified ITO surface. [source]

Rapid Microfluidic Generation of Patterned Aldehydes from Hydroxy-Terminated Self-Assembled Monolayers for Ligand and Cell Immobilization on Optically Transparent Indium Tin Oxide Surfaces

ADVANCED MATERIALS, Issue 30 2009
Abigail Pulsipher
Selective immobilization of a wide range of ligands on an indium tin oxide (ITO) surface is demonstrated. A chemoselective immobilization strategy to tailor ITO surfaces is developed by selectively oxidizing hydroxyl-terminated phosphonate self-assembled monolayers (SAMs) to aldehyde-presenting SAMs using microfluidic channels and then reacting with oxyamine-containing ligands , all on a chip. [source]