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1.
Nano Lett ; 13(10): 4857-61, 2013 Oct 09.
Artículo en Inglés | MEDLINE | ID: mdl-24000961

RESUMEN

We have combined hard X-ray photoelectron spectroscopy with angular dependent O K-edge and V L-edge X-ray absorption spectroscopy to study the electronic structure of metallic and insulating end point phases in 4.1 nm thick (14 units cells along the c-axis of VO2) films on TiO2(001) substrates, each displaying an abrupt MIT centered at ~300 K with width <20 K and a resistance change of ΔR/R > 10(3). The dimensions, quality of the films, and stoichiometry were confirmed by a combination of scanning transmission electron microscopy with electron energy loss spectroscopy, X-ray spectroscopy, and resistivity measurements. The measured end point phases agree with their bulk counterparts. This clearly shows that, apart from the strain induced change in transition temperature, the underlying mechanism of the MIT for technologically relevant dimensions must be the same as the bulk for this orientation.


Asunto(s)
Conductividad Eléctrica , Metales/química , Óxidos/química , Compuestos de Vanadio/química , Transición de Fase , Espectroscopía de Fotoelectrones , Propiedades de Superficie , Espectroscopía de Absorción de Rayos X
2.
Science ; 365(6452): 482-487, 2019 08 02.
Artículo en Inglés | MEDLINE | ID: mdl-31371612

RESUMEN

Collagen is the primary component of the extracellular matrix in the human body. It has proved challenging to fabricate collagen scaffolds capable of replicating the structure and function of tissues and organs. We present a method to 3D-bioprint collagen using freeform reversible embedding of suspended hydrogels (FRESH) to engineer components of the human heart at various scales, from capillaries to the full organ. Control of pH-driven gelation provides 20-micrometer filament resolution, a porous microstructure that enables rapid cellular infiltration and microvascularization, and mechanical strength for fabrication and perfusion of multiscale vasculature and tri-leaflet valves. We found that FRESH 3D-bioprinted hearts accurately reproduce patient-specific anatomical structure as determined by micro-computed tomography. Cardiac ventricles printed with human cardiomyocytes showed synchronized contractions, directional action potential propagation, and wall thickening up to 14% during peak systole.


Asunto(s)
Bioimpresión/métodos , Colágeno , Ventrículos Cardíacos/anatomía & histología , Modelos Anatómicos , Miocitos Cardíacos , Impresión Tridimensional , Matriz Extracelular , Humanos , Hidrogeles , Concentración de Iones de Hidrógeno , Microvasos , Neovascularización Fisiológica , Microtomografía por Rayos X
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