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1.
Chem Rec ; 22(8): e202200084, 2022 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-35815949

RESUMEN

Hollow nanostructures of transition metal phosphate are of immense interest in the existing and evolving areas of technology, due to their high surface area, presence of hollow void, and easy tuning of compositions and dimensions. Emerging synthesis methods such as template-free methods, hard-templating, and soft-templating are discussed in this review. Applications of these hollow metal phosphates dominate in energy storage and conversions, with specific advantages as supercapacitor materials. Other applications, including drug delivery, water splitting, catalysis, and adsorption, are reviewed. Finally, additional perspectives on the progress of these nanostructures, and their existing challenges related to the current synthesis routes are covered. Therefore, with the strategic modifications of the unique properties of these hollow metal phosphates, broader application requirements are fulfilled.


Asunto(s)
Nanoestructuras , Elementos de Transición , Adsorción , Catálisis , Sistemas de Liberación de Medicamentos/métodos , Nanoestructuras/química , Fosfatos
2.
Soft Matter ; 18(41): 7975-7980, 2022 Oct 26.
Artículo en Inglés | MEDLINE | ID: mdl-36218035

RESUMEN

A synthetic strategy for fabricating colloidal particles with spatially segregated amine-functionalized lobes enables regioselective coating with gold to afford metallodielectric particles with a variety of shapes and lobe sizes. This approach can produce either dissymmetric dumbbell-shaped two-lobed Au-TPM particles (Au-T) or dissymmetric or symmetric three-lobed particles with gold coating on one (Au-T-T and T-Au-T) or two lobes (Au-T-Au). Dielectrophoretic (DEP) forces exerted by an AC field confined between two opposing electrodes generate aggregates ranging from 1D chains to 2D close-packed lattices, depending on the particle shape and lobe arrangement. The aggregate structures reflect the lowest energy configurations resulting from the induced dipole moments created in particle lobes within the confined electric field.

3.
Acc Mater Res ; 5(3): 249-258, 2024 Mar 22.
Artículo en Inglés | MEDLINE | ID: mdl-38544905

RESUMEN

For the past decade, the field of colloidal science has expanded the collection of colloidal particles to include an entire library of subunits that can be isotropic or anisotropic in terms of structural morphology or chemical composition. Using anisotropic subunits, the field has assembled a variety of static and dynamic structures. For this Account, we use the umbrella term "dynamic colloids" to describe subunits capable of movement, shape-shifting, or any other type of action in response to a stimulus and "static colloids" to describe those that are unresponsive to such stimuli. We view dynamic colloids as an access point to colloidal machines, a unique and emerging subfield of machines, and colloidal science. The assembly of dynamic subunits into colloidal machines differs from traditional self-assembly only in the final structures assembled, not the methods used. Dynamic assemblies have the capacity to interact with their environment in ways that traditional anisotropic self-assemblies do not. Here, we present the current state of the field of colloidal science toward the introduction of the next wave of colloidal machines. Machines are ubiquitous in nature and synthetic systems, governing every aspect of life. In mechanics, a machine is a device that transmits or modifies force or motion. In biology, nature's machines such as kinesin or ATP synthetase are essential to life. In the synthetic realm, molecular machines and nanomachines, recognized with the Nobel prize, include diverse systems, such as molecular rotors and elevators fabricated using bottom-up synthetic methods. On the microscale, microscopic motors based on microelectromechanical systems (MEMs) have been achieved via top-down methods such as micromachining. On the colloidal scale, machines are conspicuously absent due, in part, to the difficulty in navigating combinatory design spaces. We view colloidal machines (100 nm to 10 µm) as the next line of miniaturization in machines. Due to the bottom-up fabrication methods generally used in creating dynamic colloids, one can achieve complexity at a smaller scale than possible with top-down approaches. The introduction of colloidal scale machines would bridge the gap between the microscopic world with its macroscopic counterparts, the nanoworld with its molecular machines, and the biological world with nature's machinery. Reported colloidal machines to date are apparatuses that consist of multiple components of a single composition of dynamic subunits that come together to perform some work. The next step toward complex colloidal machines is systems containing multiple dynamic colloidal scale components that come together to act in tandem to perform some work on the surrounding environment. We envision repurposing a library of dynamic particles originally intended to be used as anisotropic subunits into dynamic components of a colloidal machine. Computationally, the idea of colloidal machines has been extensively explored; however, synthetically, there has been limited exploration. In order to implement this existing library into colloidal machines, the key next step is the development of synthetic combinatorial design spaces.

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