Publications by authors named "Nina Heinig"

As an intermediate form of matter between a single atom or molecule and the bulk, nanoclusters (NCs) provide novel properties because of their high surface area-to-volume ratios and distinct physical and electronic structures. These ultrasmall NCs offer a new approach to advance charge-spin manipulation for novel devices, including spintronics and magnetic tunneling junctions. Here, we deposit monosized ZrO NCs over a large area by using gas-phase aggregation followed by size selection by a quadrupole mass filter.

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Resist-based ion beam lithography has been studied by exposing different species of ions (He, Si, Ga and Au) on 700 and 2000 Å thick poly(methyl methacrylate) (or PMMA) films supported on Si substrates. By comparing the resist sensitivities to different ions and the cross-sectional shapes of the developed features with the simulation outputs from the TRIM (TRansport of Ions in Matter) software, long-chain scissoring in PMMA can be largely attributed to ion-initiated electron cascades (as evaluated by ion energy loss to the electrons) and recoil atom cascades (as evaluated by vacancy distribution in TRIM). The ion-initiated electron cascades contribute more to the resist sensitivity for the lighter ions, while the recoil atom cascades are more important for the heavier ions.

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Hybrid metallic nanowire-embedded, highly conductive poly(3,4-ethylenedioxy thiophene):polystyrenesulfonate (PEDOT:PSS) with synergetic properties is indispensable for enhancing the performances of conductive polymer-based electronic devices. Here, we report embedment of silver nanowires (AgNWs), with diameter ∼100 nm and a high concentration (500 mg/mL) of nanowires dispersed in either ethanol or isopropanol, in PEDOT:PSS and compare the effects of the nanowire-dispersing solvents as well as its thicker diameter and high concentration on the overall properties and particularly its charge transfer characteristics and planar heterojunction solar cell (HSC) properties. Furthermore, electrostatic force microscopy is applied to elucidate the direct charge transfer from AgNWs to the PEDOT:PSS matrix.

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Embedding nanowires, such as silver nanowires (AgNWs), in a transparent conductive polymer poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) to enhance its conductivity is technologically important for improving the performances of devices comprising transparent conductive layers. Addition of nanowires in the highly conducting form of cosolvent (ethylene glycol) or mixed-cosolvent (ethylene glycol and methanol) modified PEDOT:PSS could change the nanowire structure and significantly alter the conductivity. Here, we report a simple method to embed AgNWs in PEDOT:PSS efficiently to improve its conductivity.

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The theoretical and practical realization of memristive devices has been hailed as the next step for nonvolatile memories, low-power remote sensing, and adaptive intelligent prototypes for neuromorphic and biological systems. However, the active materials of currently available memristors need to undergo an often destructive high-bias electroforming process in order to activate resistive switching. This limits their device performance in switching speed, endurance/retention, and power consumption upon high-density integration, due to excessive Joule heating.

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Formation of nanoclusters has attracted a lot of attention in recent years because of their distinct properties from isolated atoms and bulk solids. Here, we focus on the catalytic properties of supported transition metal oxide nanoclusters, such as TaO, with a well-defined size distribution below 10 nm. We show that their catalytic performance can be greatly enhanced by introducing a reaction promoter such as Pt.

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Solar cells depend on effectively absorbing light and converting it into electrical current. It is therefore essential to increase conductivity and to limit both reflection and parasitic absorbance to achieve higher photoconversion efficiency. Here, we examine the effect of post-treatment on the absorbance and conductivity of hybrid solar cells comprised of p-type poly(3,4-ethylene-dioxythiophene) poly(styrenesulfonate) (PEDOT:PSS) on an n-type silicon substrate.

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Unlabelled: Hybrid solar cells made of poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (

Pedot: PSS) and appropriate amounts of a cosolvent and a fluorosurfactant on planar n-type silicon substrates showed a photoconversion efficiency (PCE) of above 13%. These cells also exhibited stable, reproducible, and high external quantum efficiency (EQE) that was not sensitive to light-bias intensity (LBI). In contrast, solar cells made of pristine

Pedot: PSS showed low PCE and high EQE only under certain measurement conditions.

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Nanoclusters (NCs) are of great interest because they provide the link between the distinct behavior of atoms and nanoparticles and that of bulk materials. Here, we report precisely controlled deposition of size-selected TiO2 NCs produced by gas-phase aggregation in a special magnetron sputtering system. Carefully optimized aggregation length and Ar gas flow are used to control the size distribution, while a quadrupole mass filter provides precise in situ size selection (from 2 to 15 nm).

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Conducting p-type polymer layers on n-type Si have been widely studied for the fabrication of cost-effective hybrid solar cells. In this work, time-of-flight secondary ion mass spectrometry (TOF-SIMS) is used to provide three-dimensional chemical imaging of the interface between poly(3,4-ethylene-dioxythiophene):polystyrenesulfonate (PEDOT:PSS) and SiOx/Si in a hybrid solar cell. To minimize structural damage to the polymer layer, an Ar cluster sputtering source is used for depth profiling.

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Determination of the concentration of ascorbic acid in a solution has attracted intense recent interest. Here we demonstrate the feasibility of electro-oxidation of ascorbic acid on spherical cobalt core-shell nanoparticles (10-50 nm dia.) prepared by electrochemical deposition on a H-terminated Si(100) substrate.

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Spherical Au-Pt alloy nanoparticles of 10 nm average size have been prepared on a H-terminated Si(100) substrate by an extremely simple method of dip-coating. X-ray photoelectron spectroscopy and glancing-incidence X-ray diffraction confirm the formation of Au-Pt alloy. The Au(3+) ions are first reduced on the Si substrate upon dipping, and the freshly formed Au nuclei then work as a "catalyst" by promoting the reduction of PtCl(6)(2-) ions on the Au nuclei.

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Self-assembly of thiol-modified oligonucleotides on Au films has great importance for biosensor applications. Prior to the self-assembly, a piranha treatment (PT) is commonly used to clean the Au surface. Here we report that near-surface oxidized sulfur modifications on Au thin films by PT for longer than 60 s have serious effects on the self-assembled monolayer (SAM) formation of thiol-modified single-stranded thrombin binding aptamer (s-TBA), and a PT time of 10-30 s is optimal for s-TBA SAM formation.

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Aim: Decalcification remains a serious problem when treating patients with a multibracket appliance. The objective of this study was to classify patients with decalcification in terms of where it occurs, and to compare its potential reduction using a smooth surface sealant with a control group with no sealant. We also aimed to discover whether this enamel sealant would affect the incidence of bracket loss.

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