Two-dimensional (2D) nanomaterials have been the focus of substantial research interest recently owing to their fascinating and excellent properties. However, 2D porous materials have remained quite rare due to the difficulty of creating pores in 2D nanostructures. Here, we have synthesized a novel type of single-layered 2D mesoporous TiO nanosheets with very uniform size and thickness as well as ordered mesostructure from an unprecedented hydrothermal-induced solvent-confined assembly approach. The F127/TiO spherical monomicelles are first formed and redispersed in ethanol and glycerol, followed by a hydrothermal treatment to assemble these subunits into single-layered 2D mesostructure owing to the confinement effect of highly adhered glycerol solvent. The obtained 2D mesoporous TiO nanosheets have a relative mean size at around 500 × 500 nm and can be randomly stacked into a bulk. The TiO nanosheets possess only one layer of ordered mesopores with a pore size of 4.0 nm, a very high surface area of 210 m g and a uniform thickness of 5.5 nm. The thickness can be further manipulated from 5.5 to 27.6 nm via simply tuning precursor concentration or solvent ratio. Due to the well-defined 2D morphology and large mesoporosity as well as crystalline anatase mesopore walls, these uniform TiO nanosheets are capable of providing large accessible voids for sodium ion adsorption and intercalation as well as preventing volume expansion. As expected, these mesoporous TiO nanosheets have exhibited an excellent reversible capacity of 220 mAh g at 100 mA g as sodium-ion battery anodes, and they can retain at 199 mAh g after numerous cycles at different current densities. The capacity is retained at 44 mAh g even at a large current density of 10 A g after 10 000 cycles, demonstrating a remarkable performance for energy storage.
We have demonstrated a facile hydrothermal approach to synthesize a novel type of mesoporous TiO 2 material with highly controllable structure. By regulating the synthetic conditions, the mesoporous TiO 2 can be well controlled with desired crystallites and architectures. The resulting mesoporous TiO 2 exhibits excellent penetration properties and photocatalytic performance. These unique mesoporous TiO 2 microspheres produced at moderate conditions could afford great opportunities in achieving high performance in various practical applications.
Constructing three-dimensional (3-D) hierarchical mesostructures with unique morphology, pore orientation, single-crystal nature, and functionality remains a great challenge in materials science. Here, we report a confined microemulsion self-assembly approach to synthesize an unprecedented type of 3-D highly ordered mesoporous TiO superstructure (Level-1), which consists of 1 spherical core and 12 symmetric satellite hemispheres epitaxially growing out of the core vertices. A more complex and asymmetric TiO superstructure (Level-2) with 13 spherical cores and up to 44 symmetric satellite hemispheres can also be well manipulated by increasing the size or content of impregnated TiO precursor emulsion droplets. The obtained 3-D mesoporous TiO superstructures have well-defined bouquet-posy-like topologies, oriented hexagonal mesochannels, high accessible surface area (134-148 m/g), large pore volume (0.48-0.51 cm/g), and well single-crystalline anatase walls with dominant (001) active facets. More interestingly, all cylindrical mesopore channels are highly interconnected and radially distributed within the whole superstructures, and all TiO nanocrystal building blocks are oriented grown into a single-crystal anatase wall, making them ideal candidates for various applications ranging from catalysis to optoelectronics. As expected, the bouquet-posy-like mesoporous TiO superstructure supported catalysts show excellent catalytic activity (≥99.7%) and selectivity (≥96%) in cis-semihydrogenation of various alkynes, exceeding that of commercial TiO (P25) supported catalyst by a factor of 10. No decay in the activity was observed for 25 cycles, revealing a high stability of the mesoporous TiO superstructure supported catalyst.
Two-dimensional
(2D) heterostructures endowed with mesoporosities
offer exciting opportunities in electrocatalysis, photocatalysis,
energy storage, and conversion technologies due to their integrated
functionalities, abundant active sites and shortened diffusion distance.
However, layered mesostructures have not been combined due to the
immense difficulties by conventional chemical, mechanical exfoliation
or self-assembly approaches. Herein, we explore a bottom-up strategy,
carried out under mild conditions, for the facile synthesis of monolayered
mesoporous-titania–mesoporous-carbon vertical heterostructure
with uniform mesopore size, which enables ultrahigh rate capability
and cycling longevity for pseudocapacitive sodium-ion storage in nonaqueous
electrolyte. Such a brand-new type of heterostructure consists of
well-ordered monolayered mesoporous titania nanosheets and surrounding
two mesoporous carbon monolayers assembled at both sides. Remarkably,
the combination of interconnected large mesoporosity and heterointerface
leads to highly promoted reversible pseudocapacitance (96.4% of total
charge storage at a sweep rate of 1 mV s–1), and
it enables the material to retain strong mechanical stability during
the rapid sodiation and desodiation processes. This study reveals
the importance of incorporating mesopores into heterointerface as
a strategy for enhancing charge storage kinetics of electroactive
materials.
We have demonstrated a confined interfacial monomicelle assembly approach for accurately coating ordered monolayered TiO 2 mesopores on diverse surfaces. By regulating the synthetic conditions, the coated mesoporous TiO 2 layers can be well controlled with desired thickness, mesopore size, and switchable coated surfaces. The resulting monolayered mesoporous TiO 2 exhibit excellent sodiumstorage properties. This unique mesoporous TiO 2 coating strategy affords great potential in constructing multicomponent nanostructures with mesoporosities for advanced technologies.
By introducing a compatible reducing agent (2‐ethylimidazole) into a mono‐micelle assembly process, we present a type of ordered mesoporous TiO2 microspheres that combines radially aligned mesostructure with Ti3+ defects in mesoporous frameworks. Such reductant acts as a building block of mesostructured frameworks and reduces Ti4+ in situ to generate defects during calcination, giving rise to the coexistence of bulk Ti3+ defects and an ordered mesostructure. The mesoporous TiO2 has both excellent mesoporosity (a high surface area of 106 m2 g−1, a mean pore size of 18.4 nm) and stable defects with an extended photoresponse. Such integration of unique mesoscopic architecture and atomic vacancies provide both effective mass transportation and enhanced light utilization, leading to a remarkable increase in H2 generation rate. A maximum H2 evolution rate of 19.8 mmol g−1 h−1 can be achieved, along with outstanding stability under solar light.
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