Harvesting abundant and renewable sunlight in energy production and environmental remediation is an emerging research topic. Indeed, research on solar-driven heterogeneous photocatalysis based on surface plasmon resonance has seen rapid growth and potentially opens a technologically promising avenue that can benefit the sustainable development of global energy and the environment. This review briefly summarizes recent advances in the synthesis and photocatalytic properties of plasmonic composites (e.g., hybrid structures) formed by noble metal (e.g., gold, silver) nanoparticles dispersed on a variety of substrates that are composed of metal oxides, silver halides, graphene oxide, among others. Brief introduction of surface plasmon resonance and the synthesis of noble metal-based composites are given, followed by highlighting diverse applications of plasmonic photocatalysts in mineralization of organic pollutants, organic synthesis and water splitting. Insights into surface plasmon resonancemediated photocatalysis not only impact the basic science of heterogeneous photocatalysis, but generate new concepts guiding practical technologies such as wastewater treatment, air purification, selective oxidation reactions, selective reduction reactions, and solar-to-hydrogen energy conversion in an energy efficient and environmentally benign approach. This review ends with a summary and perspectives.

Photodegradation of rhodamine B in the presence of H2O2 by visible light over α‐Fe2O3 architectures has been investigated (see picture; left to right: 1D nanorods, 2D nanoplates, 3D nanocubes). A link between the exposed facets of α‐Fe2O3 architectures and their photoreactivity is established, following {110}>{012}≫{001}.

Photocatalytic reactions on TiO 2 have recently gained an enormous resurgence because of various new strategies and findings that promise to drastically increase efficiency and specificity of such reactions by modifications of the titania scaffold and chemistry. In view of geometry, in particular, anodic TiO 2 nanotubes have attracted wide interest, as they allow a high degree of control over the separation of photogenerated charge carriers not only in photocatalytic reactions but also in photoelectrochemical reactions. A key advantage of ordered nanotube arrays is that nanotube modifications can be embedded site specifically into the tube wall; that is, cocatalysts, doping species, or junctions can be placed at highly defined desired locations (or with a desired regular geometry or pattern) along the tube wall. This allows an unprecedented level of engineering of energetics of reaction sites for catalytic and photocatalytic reactions, which target not only higher efficiencies but also the selectivity of reactions. Many recent tube alterations are of a morphologic nature (mesoporous structures, designed faceted crystallites, hybrids, or 1D structures), but a number of color-coded (namely, black, blue, red, green, gray) modifications have attracted wide interest because of the extension of the light absorption spectrum of titania in the visible range and because unique catalytic activity can be induced. The present Perspective gives an overview of TiO 2 nanotubes in photocatalysis with an emphasis on the most recent advances in the use of nanotube arrays and discusses the underlying concepts in tailoring their photocatalytic reactivity.

Visible light (λ > 420 nm) induced photocatalytic degradation of rhodamine B (RhB) in the presence of H2O2 by one-dimensional (1D) nanorods of goethite (α-FeOOH) and hematite (α-Fe2O3) has been investigated, and results were compared to those of micrometer-sized rods. α-FeOOH nanorods were self-assembled by oriented attachment of α-FeOOH primary nanoparticles, while porous α-Fe2O3 rods were prepared by thermal dehydration of respective α-FeOOH precursors via a topotactic transformation. The as-prepared samples were characterized by powder X-ray diffraction, micro-Raman spectroscopy, diffuse reflectance UV−visible spectroscopy, X-ray photoelectron spectroscopy, nitrogen adsorption−desorption, high-angle annular dark-field scanning transmission electron microscopy, transmission electron microscopy, and high-resolution transmission electron microscopy. Nanosized α-FeOOH and α-Fe2O3 particles appeared to be more active than microsized ones in terms of surface area normalized reaction rate, suggesting intrinsic photocatalytic properties of nanorods as compared to microrods in both α-FeOOH and α-Fe2O3. In addition, α-Fe2O3 nanorods exhibited the greatest activity among the as-prepared samples. The observed photocatalytic performance by iron oxide particles was attributed to the synergetic effects of the particle composition, size, porosity, and the variations of local structure. The results from current study will be potentially applicable to a range of naturally abundant semiconducting minerals and compounds (e.g., metal oxyhydroxides and metal oxides).