21 results match your criteria: "and Center for Nanoscale Materials[Affiliation]"

Multiscale porous elastomer substrates for multifunctional on-skin electronics with passive-cooling capabilities.

Proc Natl Acad Sci U S A

January 2020

Department of Biomedical, Biological, and Chemical Engineering, University of Missouri, Columbia, MO 65211;

In addition to mechanical compliance, achieving the full potential of on-skin electronics needs the introduction of other features. For example, substantial progress has been achieved in creating biodegradable, self-healing, or breathable, on-skin electronics. However, the research of making on-skin electronics with passive-cooling capabilities, which can reduce energy consumption and improve user comfort, is still rare.

View Article and Find Full Text PDF

The effect of Zr modification on the catalytic activity of Co/SiO was investigated for nonoxidative propane dehydrogenation. Isolated Zr on SiO surface sites were prepared by organometallic synthesis using Zr(O Bu) as a precursor. The resulting Zr/SiO support was functionalized with Co ions via strong electrostatic adsorption.

View Article and Find Full Text PDF

Herein we describe the fabrication and characterization of Ag and Au bimetallic plasmonic crystals as a system that exhibits improved capabilities for quantitative, bulk refractive index (RI) sensing and surface-enhanced Raman spectroscopy (SERS) as compared to monometallic plasmonic crystals of similar form. The sensing optics, which are bimetallic plasmonic crystals consisting of sequential nanoscale layers of Ag coated by Au, are chemically stable and useful for quantitative, multispectral, refractive index and spectroscopic chemical sensing. Compared to previously reported homometallic devices, the results presented herein illustrate improvements in performance that stem from the distinctive plasmonic features and strong localized electric fields produced by the Ag and Au layers, which are optimized in terms of metal thickness and geometric features.

View Article and Find Full Text PDF

Parasitic Reactions in Nanosized Silicon Anodes for Lithium-Ion Batteries.

Nano Lett

March 2017

Chemical Science and Engineering Division, ‡X-ray Science Division, Advanced Photon Source, and §Center for Nanoscale Materials, Argonne National Laboratory , Lemont, Illinois 60439, United States.

When designing nano-Si electrodes for lithium-ion batteries, the detrimental effect of the c-LiSi phase formed upon full lithiation is often a concern. In this study, Si nanoparticles with controlled particle sizes and morphology were synthesized, and parasitic reactions of the metastable c-LiSi phase with the nonaqueous electrolyte was investigated. The use of smaller Si nanoparticles (∼60 nm) and the addition of fluoroethylene carbonate additive played decisive roles in the parasitic reactions such that the c-LiSi phase could disappear at the end of lithiation.

View Article and Find Full Text PDF

Single-Crystalline SrRuO3 Nanomembranes: A Platform for Flexible Oxide Electronics.

Nano Lett

January 2016

Materials Science Division, ‡Advanced Photon Source, and §Center for Nanoscale Materials, Argonne National Laboratory , Argonne, Illinois 60439, United States.

The field of oxide electronics has benefited from the wide spectrum of functionalities available to the ABO3 perovskites, and researchers are now employing defect engineering in single crystalline heterostructures to tailor properties. However, bulk oxide single crystals are not conducive to many types of applications, particularly those requiring mechanical flexibility. Here, we demonstrate the realization of an all-oxide, single-crystalline nanomembrane heterostructure.

View Article and Find Full Text PDF

Sub-Picosecond Singlet Exciton Fission in Cyano-Substituted Diaryltetracenes.

Angew Chem Int Ed Engl

July 2015

Department of Chemistry and Argonne-Northwestern Solar Energy Research (ANSER) Center, Northwestern University, 2145 Sheridan Road, Evanston, IL 60208 (USA).

Thin films of 5,11-dicyano-6,12-diphenyltetracene (TcCN) have been studied for their ability to undergo singlet exciton fission (SF). Functionalization of tetracene with cyano substituents yields a more stable chromophore with favorable energetics for exoergic SF (2E(T1)-E(S1)=-0.17 eV), where S1 and T1 are singlet and triplet excitons, respectively.

View Article and Find Full Text PDF

Thermoresponsive Micelles from Double LCST-Poly(3-methyl--vinylcaprolactam) Block Copolymers for Cancer Therapy.

ACS Macro Lett

March 2015

Department of Chemistry and Center for Nanoscale Materials and Biointegration, University of Alabama at Birmingham, Birmingham, Alabama, 35294, United States.

We present synthesis and assembly of novel thermoresponsive block copolymers with double LCST precisely controlled within the physiological temperature range. Two separate phase transition temperatures were achieved by RAFT polymerization of structurally similar monomers with varied hydrophobicity. The LCST1 was varied from 19 to 27 °C by copolymerization of -vinylcaprolactam with a novel hydrophobic monomer, 3-methyl--vinylcaprolactam, while the LCST2 at 41-42 °C was attained by copolymerization of -vinylcaprolactam with hydrophilic -vinylpyrrolidone.

View Article and Find Full Text PDF

Direct measurement of lattice dynamics and optical phonon excitation in semiconductor nanocrystals using femtosecond stimulated Raman spectroscopy.

Phys Rev Lett

September 2013

Department of Chemistry, Northwestern University, Evanston, Illinois 60208-3113, USA and Center for Nanoscale Materials, Argonne National Laboratory, Argonne, Illinois 60439, USA.

We report femtosecond stimulated Raman spectroscopy measurements of lattice dynamics in semiconductor nanocrystals and characterize longitudinal optical (LO) phonon production during confinement-enhanced, ultrafast intraband relaxation. Stimulated Raman signals from unexcited CdSe nanocrystals produce a spectral shape similar to spontaneous Raman signals. Upon photoexcitation, stimulated Raman amplitude decreases owing to experimentally resolved ultrafast phonon generation rates within the lattice.

View Article and Find Full Text PDF

Investigation of the redox chemistry of anthraquinone derivatives using density functional theory.

J Phys Chem A

September 2014

Materials Science Division, ‡Joint Center for Energy Storage (JCESR), and §Center for Nanoscale Materials, Argonne National Laboratory , Argonne, Illinois 60439, United States.

Application of density functional calculations to compute electrochemical properties such as redox windows, effect of substitution by electron donating and electron withdrawing groups on redox windows, and solvation free energies for ∼50 anthraquinone (AQ) derivatives are presented because of their potential as anolytes in all-organic redox flow batteries. Computations suggest that lithium ions can increase (by ∼0.4 V) the reduction potential of anthraquinone due to the lithium ion pairing by forming a Lewis base-Lewis acid complex.

View Article and Find Full Text PDF

Correlating interfacial octahedral rotations with magnetism in (LaMnO3+δ)N/(SrTiO3)N superlattices.

Nat Commun

July 2014

1] Hefei National Laboratory for Physical Sciences at the Microscale, Department of Physics, University of Science and Technology of China, Hefei, Anhui 230026, China [2] Synergetic Innovation Center of Quantum Information and Quantum Physics, University of Science and Technology of China, Hefei, Anhui 230026, China.

Lattice distortion due to oxygen octahedral rotations have a significant role in mediating the magnetism in oxides, and recently attracts a lot of interests in the study of complex oxides interface. However, the direct experimental evidence for the interrelation between octahedral rotation and magnetism at interface is scarce. Here we demonstrate that interfacial octahedral rotation are closely linked to the strongly modified ferromagnetism in (LaMnO3+δ)N/(SrTiO3)N superlattices.

View Article and Find Full Text PDF

Bioelectrochemical sensing based on single stranded deoxyribonucleic acid-carbon nanotubes covalently attached on gold electrodes.

J Nanosci Nanotechnol

April 2009

Department of Chemistry and Center for Nanoscale Materials, University of Puerto Rico, Rio Piedras Campus, P.O. Box 23346, San Juan, Puerto Rico 00931-3346.

A biosensor based on single-stranded deoxyribonucleic acid-functionalized carbon nanotubes covalently attached to a self-assembled monolayer of 11-amino-1-undecanethiol on gold has been prepared. The preparation of the deoxyribonucleic acid sensor was followed using cyclic voltammetry. Single-walled carbon nanotubes, covalently attached to the gold surface present a nanoelectrode array behavior.

View Article and Find Full Text PDF

DNA-functionalized carbon nanotubes for biosensing applications.

J Nanosci Nanotechnol

April 2009

Department of Chemistry, Institute for Functional Nanomaterials and Center for Nanoscale Materials, University of Puerto Rico, Rio Piedras Campus, PO. Box 23346, San Juan, Puerto Rico 00931-3346.

Carbon nanotubes (CNTs) have been broadly studied due to their exceptional structural, electronic and mechanical properties, and their use have been proposed for many applications. The number of biosensing applications of CNTs has increased in the past few years. Nevertheless, in order to use CNTs as standard materials in the biosensing field and to take full advantage of their unique properties, several problems must be solved.

View Article and Find Full Text PDF

Surface plasmon polaritons (SPPs) and diffraction effects such as Rayleigh anomalies (RAs) play key roles in the transmission of light through periodic subwavelength hole arrays in metal films. Using a combination of theory and experiment we show how refractive index (RI) sensitive transmission features arise from hole arrays in thin gold films. We show that large transmission amplitude changes occur over a narrow range of RI values due to coupling between RAs and SPPs on opposite sides of the metal film.

View Article and Find Full Text PDF

Palladium nanostructures and nanoparticles from molecular precursors on highly ordered pyrolytic graphite.

Langmuir

November 2006

Department of Chemistry and Center for Nanoscale Materials, University of Puerto Rico, Rio Piedras Campus, San Juan, Puerto Rico 00931-3346.

Nanostructures and nanoparticles of palladium assembled on highly ordered pyrolytic graphite (HOPG) by the adsorption of palladium molecular precursors (MPs), in dichloromethane solutions, have been prepared. Self-assemblies of palladium nanostructures on HOPG were characterized by scanning electron microscopy (SEM), Auger electron spectroscopy (AES), transmission electron microscopy (TEM), and atomic force microscopy (AFM) techniques. In this work, palladium rings had a wide variety of sizes in the nanometer range, and the ring/tube structures were preserved after a reductive process in which palladium metallic nanoparticles were formed.

View Article and Find Full Text PDF

Single two-dimensional planar silver arrays and one-dimensional linear gold chains of nanoparticles were investigated by dark-field surface plasmon spectroscopy and studied as a function of interparticle distance, particle size, and number of particles. In agreement with recent theoretical predictions, a red shift of the surface plasmon resonance occurring in two-dimensional arrays was found for lattice spacings below 200 nm. This red shift is associated with a significant broadening of the resonance and is attributed to the onset of near-field interactions.

View Article and Find Full Text PDF

The formation of a self-assembled monolayer (SAM) of 4-aminothiophenol (4-ATP) on polycrystalline platinum electrodes has been characterized by surface analysis and electrochemistry techniques. The 4-ATP monolayer was characterized by cyclic voltammetry (CV), linear sweep voltammetry, Raman spectroscopy, reflection-absorption infrared (RAIR) spectroscopy, and X-ray photoelectron spectroscopy (XPS). CV was used to study the dependence of the adsorption time and 4-ATP solution concentration on the relative degree of coverage of 4-ATP monolayers on polycrystalline Pt electrodes.

View Article and Find Full Text PDF

Light emission resulting from two-photon excited gold nanoparticles has been proposed to originate from the radiative decay of surface plasmon resonances. In this vein, we investigated luminescence from individual gold nanorods and found that their emission characteristics closely resemble surface plasmon behavior. In particular, we observed spectral similarities between the scattering spectra of individual nanorods and their photoluminescence emission.

View Article and Find Full Text PDF

Surface plasmon rainbow jets.

Opt Lett

April 2005

Chemistry Division and Center for Nanoscale Materials, Argonne National Laboratory, Argonne, Illinois 60439, USA.

A new method for optically exciting and visualizing surface plasmons in thin metal films is described. The technique relies on the use of a high-numerical-aperture objective lens to locally launch a broad wavelength spectrum of surface waves and to detect the leaky radiative modes associated with them. We used this approach to obtain a direct visualization of the plasmon intensity distributions, e.

View Article and Find Full Text PDF

Ligand effect on the growth and the digestion of Co nanocrystals.

J Am Chem Soc

March 2005

Chemistry Division, Materials Science Division, and Center for Nanoscale Materials, Argonne National Laboratory, Argonne, Illinois 60439, USA.

The reaction product of cobalt carbonyl decomposition depends on the concentration of the oleic acid ligand. With a low concentration of ligand, nanocrystals nucleate and grow to large ferromagnetic particles through the process of Ostwald ripening and coalescence coarsening. With a high concentration of ligand, stable cluster complexes are formed.

View Article and Find Full Text PDF
Article Synopsis
  • The study explores how to modify ultrananocrystalline diamond (UNCD) films by using electrochemical techniques to attach organic molecules to their surface.
  • The process involves creating aryl radicals from diazonium cations, which form stable chemical bonds with the UNCD, enhancing its functionality.
  • Different functional groups can be attached, making the surface either hydrophobic or hydrophilic, with a high surface coverage that allows for the binding of biological molecules like DNA or proteins.
View Article and Find Full Text PDF