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1.
Proc Natl Acad Sci U S A ; 118(15)2021 04 13.
Artigo em Inglês | MEDLINE | ID: mdl-33833057

RESUMO

Structural characterization of biologically formed materials is essential for understanding biological phenomena and their enviro-nment, and for generating new bio-inspired engineering concepts. For example, nacre-the inner lining of some mollusk shells-encodes local environmental conditions throughout its formation and has exceptional strength due to its nanoscale brick-and-mortar structure. This layered structure, comprising alternating transparent aragonite (CaCO3) tablets and thinner organic polymer layers, also results in stunning interference colors. Existing methods of structural characterization of nacre rely on some form of cross-sectional analysis, such as scanning or transmission electron microscopy or polarization-dependent imaging contrast (PIC) mapping. However, these techniques are destructive and too time- and resource-intensive to analyze large sample areas. Here, we present an all-optical, rapid, and nondestructive imaging technique-hyperspectral interference tomography (HIT)-to spatially map the structural parameters of nacre and other disordered layered materials. We combined hyperspectral imaging with optical-interference modeling to infer the mean tablet thickness and its disorder in nacre across entire mollusk shells from red and rainbow abalone (Haliotis rufescens and Haliotis iris) at various stages of development. We observed that in red abalone, unexpectedly, nacre tablet thickness decreases with age of the mollusk, despite roughly similar appearance of nacre at all ages and positions in the shell. Our rapid, inexpensive, and nondestructive method can be readily applied to in-field studies.


Assuntos
Exoesqueleto/química , Gastrópodes/metabolismo , Nácar/análise , Imagem Óptica/métodos , Exoesqueleto/metabolismo , Animais , Gastrópodes/citologia , Imagem Óptica/instrumentação , Imagem Óptica/normas , Sensibilidade e Especificidade
2.
Proc Natl Acad Sci U S A ; 116(52): 26402-26406, 2019 Dec 26.
Artigo em Inglês | MEDLINE | ID: mdl-31848248

RESUMO

Thermal emission is the process by which all objects at nonzero temperatures emit light and is well described by the Planck, Kirchhoff, and Stefan-Boltzmann laws. For most solids, the thermally emitted power increases monotonically with temperature in a one-to-one relationship that enables applications such as infrared imaging and noncontact thermometry. Here, we demonstrated ultrathin thermal emitters that violate this one-to-one relationship via the use of samarium nickel oxide (SmNiO3), a strongly correlated quantum material that undergoes a fully reversible, temperature-driven solid-state phase transition. The smooth and hysteresis-free nature of this unique insulator-to-metal phase transition enabled us to engineer the temperature dependence of emissivity to precisely cancel out the intrinsic blackbody profile described by the Stefan-Boltzmann law, for both heating and cooling. Our design results in temperature-independent thermally emitted power within the long-wave atmospheric transparency window (wavelengths of 8 to 14 µm), across a broad temperature range of ∼30 °C, centered around ∼120 °C. The ability to decouple temperature and thermal emission opens a gateway for controlling the visibility of objects to infrared cameras and, more broadly, opportunities for quantum materials in controlling heat transfer.

3.
Langmuir ; 37(30): 9222-9231, 2021 Aug 03.
Artigo em Inglês | MEDLINE | ID: mdl-34279965

RESUMO

Functionalization of diamond surfaces with TEMPO and other surface paramagnetic species represents one approach to the implementation of novel chemical detection schemes that make use of shallow quantum color defects such as silicon-vacancy (SiV) and nitrogen-vacancy (NV) centers. Yet, prior approaches to quantum-based chemical sensing have been hampered by the absence of high-quality surface functionalization schemes for linking radicals to diamond surfaces. Here, we demonstrate a highly controlled approach to the functionalization of diamond surfaces with carboxylic acid groups via all-carbon tethers of different lengths, followed by covalent chemistry to yield high-quality, TEMPO-modified surfaces. Our studies yield estimated surface densities of 4-amino-TEMPO of approximately 1.4 molecules nm-2 on nanodiamond (varying with molecular linker length) and 3.3 molecules nm-2 on planar diamond. These values are higher than those reported previously using other functionalization methods. The ζ-potential of nanodiamonds was used to track reaction progress and elucidate the regioselectivity of the reaction between ethenyl and carboxylate groups and surface radicals.

4.
Nanotechnology ; 20(25): 255304, 2009 Jun 24.
Artigo em Inglês | MEDLINE | ID: mdl-19487804

RESUMO

We present a low-cost overlay alignment metrology solution for nanoimprint lithography that uses optical microscopy, displacement-sensing algorithms, and specially-designed imprint molds that include shallow alignment marks that are visible to the optical system but do not pattern the wafer. This innovation reduces measurement distances to near zero, the optimal distance for displacement-sensing algorithms, and allows for alignment marks to occupy the same piece of wafer real estate without interfering in any way, thus saving silicon area. Additionally, the method we present does not require the comparison of alignment marks between the wafer and the mold, thus removing process variations as a variable. We fabricate the shallow-mark molds, show that the shallow alignment marks indeed do not leave a mark on the wafer, and, implementing our nDSE (nanoscale displacement sensing and estimation) techniques, we demonstrate nanoscale alignment to a precision of 35 nm, 1-sigma. Given sufficient engineering refinement, we would fully anticipate achieving alignment errors down to the 1 nm range using these methods.

5.
Nano Lett ; 8(11): 3865-9, 2008 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-18837563

RESUMO

We introduce the concept of wafer bowing to affect nanoimprinting. This approach allows a design that can fit the key imprinting mechanism into a compact module, which we have constructed and demonstrated with an overlay and resolution of <0.5 microm and <10 nm, respectively. In the short term, this wafer bowing approach makes nanoimprint lithography much more accessible to a broad range of researchers. More importantly, this approach eliminates machine movement other than wafer bowing and shortens the mechanical path; these will enable the achievement of excellent patterning and overlay at a much lower cost. In the long term, wafer bowing is extensible to step-and-repeat printing for volume manufacturing.

6.
Nano Lett ; 6(3): 351-4, 2006 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-16522021

RESUMO

High density metal cross bars at 17 nm half-pitch were fabricated by nanoimprint lithography. Utilizing the superlattice nanowire pattern transfer technique, a 300-layer GaAs/AlGaAs superlattice was employed to produce an array of 150 Si nanowires (15 nm wide at 34 nm pitch) as an imprinting mold. A successful reproduction of the Si nanowire pattern was demonstrated. Furthermore, a cross-bar platinum nanowire array with a cell density of approximately 100 Gbit/cm(2) was fabricated by two consecutive imprinting processes.

7.
Phys Rev Lett ; 94(19): 196101, 2005 May 20.
Artigo em Inglês | MEDLINE | ID: mdl-16090189

RESUMO

The successful design of nanofluidic devices for the manipulation of biopolymers requires an understanding of how the predictions of soft condensed matter physics scale with device dimensions. Here we present measurements of DNA extended in nanochannels and show that below a critical width roughly twice the persistence length there is a crossover in the polymer physics.


Assuntos
DNA Viral/química , Nanotubos/química , Bacteriófago lambda/química , Bacteriófago lambda/genética , DNA Viral/imunologia , Nanotecnologia/métodos , Dióxido de Silício/química
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