Photon‐coupling and electron dynamics are the key processes leading to the photocatalytic activity of plasmonic metal‐semiconductor nanohybrids. To better utilize and explore these effects, a facile large‐scale synthesis route to form Ag@AgCl cubic cages with well‐defined hollow interiors is carried out using a water‐soluble sacrificial salt‐crystal‐template process. Theoretical calculations and experimental probes of the electron transfer process are used in an effort to gain insight into the underlying plasmonic properties of the Ag@AgCl materials. Efficient utilization of solar energy to create electron‐hole pairs is attributed to the significant light confinement and enhancement around the Ag/AgCl interfacial plasmon hot spots and multilight‐reflection inside the cage structure. More importantly, an ultrafast electron transfer process (≤150 fs) from Ag nanoparticles to the AgCl surface is detected, which facilitates the charge separation efficiency in this system, contributing to high photocatalytic activity and stability of Ag@AgCl photocatalyst towards organic dye degradation.

The state-of-the-art development of fabrication strategies of multi-dimensional titanate and titania nanostructures is reviewed first. This is followed by an overview of their potential applications in environmental, energy, and biomedical sectors.

Highly crystalline pure brookite and two-phase anatase/brookite TiO 2 nanostructures were synthesized via a simple hydrothermal method with titanium sulfide as the precursors in sodium hydroxide solutions. The control of the phase composition has been demonstrated via solution concentration and reaction time, and the phase transformation mechanism has been elucidated. Photocatalytic activities of the assynthesized two-phase anatase/brookite TiO 2 , pure anatase nanoparticles, and pure brookite nanoplates were appraised via photocatalytic hydrogen evolution in aqueous methanol solution. Results have shown that the photocatalytic activity is higher for the two-phase anatase/brookite TiO 2 and brookite nanoplates as compared to pure anatase nanoparticles despite the lower surface areas of the two-phase anatase/brookite TiO 2 and brookite nanoplates. From the Mott−Schottky analysis, brookite phase is shown to have a more cathodic conduction band edge potential than anatase phase, which leads to more energetically favorable hydrogen reduction. Moreover, femtosecond transient absorption spectroscopy measurements suggests that the photoexcited electrons transfer from brookite to anatase phaseleading to further enhancement of the photocatalytic activity. In comparison with the highly active two-phase commercial benchmark P25, our synthesized two-phase anatase/brookite TiO 2 is 220% more active when measured by the H 2 yield per unit area of the photocatalyst surface.

For the purpose of efficiently utilizing the renewable solar energy, it is of vital importance to understand the key factors that contribute to the performance merits for photocatalysis applications. In this work, we find that anatase titania nanostructures with high efficiency in photoelectrochemical cell (PEC) do not necessarily retain the same good performance when used in direct heterogeneous reaction (DHR). Investigation is carried out to elucidate how the electronic properties of the different nanostructures are correlated with the PEC and DHR efficiencies. Good PEC cell performance is identified to be related to topotactically formed samples with intimately connected particles that facilitate easy charge transfer. Additional benefit for PEC cell is found to be achieved from the vectorial conduction pathway in the pseudo one dimensional structure. On the other hand, high activity of DHR photocatalysis is attributed mainly to the exposed high reactivity crystal facets. The presence of anatase TiO2 {010} facets is identified to enhance electron‐hole separation and create specific surface states that facilitate interactions across the semiconductor/electrolyte interfaces.

Dense and uniform silver halides AgX (X = Cl, Br, I) nanoparticles were successfully fabricated on layered titanate nanowired honeycomb (TNHC) thin films. The growth of AgX nanocrystals was carried out through two steps. Firstly, ion-exchange was employed to incorporate Ag(+) ions into the interlayer of the titanate nanowires. Secondly, hydrogen halide (HX) solution was rapidly injected onto the ion-exchanged silver TNHC surface to generate nanosized AgX particles on TNHC films. The effect of the reaction time, solution pH, and concentration of halide anions on the morphology of the AgX photocatalysts has been studied. Followed by light-irradiation, the optimized Ag/AgX thin films exhibited excellent degradation performance under visible light because of localized surface plasmon resonance effect.

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In situ X-ray diffraction reveals key processes that can be utilized to direct the synthesis of complex inorganic crystals.

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