ABSTRACT
N-doped mesoporous carbon-capped MoO2 nanobelts (designated as MoO2 @NC) were synthesized and applied to lithium-ion storage. Owing to the stable core-shell structural framework and conductive mesoporous carbon matrix, the as-prepared MoO2 @NC shows a high specific capacity of around 700â mA h g-1 at a current of 0.5â A g-1 , excellent cycling stability up to 100â cycles, and superior rate performance. The N-doped mesoporous carbon can greatly improve the conductivity and provide uninhibited conducting pathways for fast charge transfer and transport. Moreover, the core-shell structure improved the structural integrity, leading to a high stability during the cycling process. All of these merits make the MoO2 @NC to be a suitable and promising material for lithium ion battery.
ABSTRACT
The rational design and controlled synthesis of a smart device with flexibly tailored response ability is all along desirable for bioapplication but long remains a considerable challenge. Here, a pH-stimulated valve system with a visualized "on-off" mode is constructed through a dual-shell fluorescence resonance energy transfer (FRET) strategy. The dual shells refer to carbon dots and fluorescent molecules embedded polymethacrylic acid (F-PMAA) layers successively coating around a SiO2 core (ca. 120 nm), which play the roles as energy donor and acceptor, respectively. The total thickness of the dual-shell in the solid composite is ca. 10 nm. The priorities of this dual-shell FRET nanovalve stem from three facts: (1) the thin shell allows the formation of efficient FRET system without chemical bonding between energy donor and acceptor; (2) the maximum emission wavelength of CD layer is tunable in the range of 400-600 nm, thus providing a flexible energy donor for a wide variety of energy acceptors; (3) the outer F-PMAA shell with a pH-sensitive swelling-shrinking (on-off) behavior functions as a valve for regulating the FRET process. As such, a sensitive and stable pH ratiometric sensor with a working pH range of 3-6 has been built by simply encapsulating pH-responsive fluorescein isothiocyanate (FITC) into PMAA; a pH-dependent swelling-shrinking shuttle carrier with a finely controllable molecule-release behavior has been further fabricated using rhodamine B isothiocyanate (RBITC) as the energy donor and model guest molecule. Significantly, the controlled releasing process is visually self-monitorable.
ABSTRACT
Yolk-shell (Y-S) structured Fe3O4@void@CdS nanoparticles (NPs) are synthesized through a one-pot coating-etching process with Fe3O4@SiO2 as the core, where the coating of an outer CdS shell from a chemical bath deposition (CBD) process is simultaneously accompanied by the gradual etching of an inner SiO2 shell. The as-prepared Fe3O4@void@CdS NPs (ca. 200 nm) possess good monodispersity and a uniform CdS shell of ca.15 nm. This composite exhibits excellent photo-Fenton (ph-F) activity toward the degradation of methylene blue (MB) in a wide pH working range of 4.5-11 under the visible light irradiation. A series of control experiments demonstrate the unique Y-S structure contributes to the enhanced activity, where the separation of hole-electron pair from CdS and the reduction of Fe(2+) from Fe(3+) are mutually promoted. The similar efficiency can also be achieved when the shell component changes to TiO2 or CeO2, demonstrating a general strategy for the design of robust ph-F agent.
ABSTRACT
The Stöber process is revisited using vinyltriethoxysilane as the precursor, where a kinetics-controlled condensation of vinylsilanols, free from external fluorogens, unprecedentedly produces hydrophilic diamond-structured organosilica nanocrystals (ca. 2-6 nm) with finely tunable fluorescence (460-625 nm). The key to the synthesis lies in a slow successful condensation of vinylsilanols triggered and guided by the π-π stacking interaction of vinyl groups.
