The capacity of fluorescent colloidal semiconductor nanocrystals for commercial application has led to the development of nanocrystals with nontoxic constituent elements as replacements for the currently available Cd- and Pb-containing systems. CuInS2 is a good candidate material because of its direct band gap in the near-infrared spectral region and large optical absorption coefficient. The ternary nature, flexible stoichiometry, and different crystal structures of CuInS2 lead to a range of optoelectronic properties, which have been challenging to elucidate. In this Perspective, the optoelectronic properties of CuInS2 nanocrystals are described and what is known of their origin is discussed. We begin with an overview of their synthesis, structure, and mechanism of formation. A complete discussion of the tunable luminescence properties and the radiative decay mechanism of this system is then presented. Finally, progress toward application of these "green" nanocrystals is summarized.

Gold growth on CdS nanorods and on seeded CdSe/CdS nanorods with and without illumination at different temperatures was studied. Two competing mechanisms were identified: thermal and light-induced growth. The thermal mechanism leads to growth of small gold particles at defects along the rod body and can be suppressed at lower temperatures. This control is attributed to a phase transition of the alkyl chains of the surface amine ligands to a static phase at lower temperatures, blocking the Au precursor's access to the nanorod surfaces. While a long-chain (C18) amine shows effective blocking at 293 K, a shorter chain (C12) amine shows the same result only at 273 K; however, in the case of a bulky trialkylamine, defect growth was observed even at 273 K. Light-induced growth leads to selective deposition of gold on one end of the rods. The tip was shown to grow on sulfur-rich facets of the nanorod, producing end-on and angled tip orientations. Growth under illumination with decreased temperature provides a highly selective synthesis of hybrid semiconductor nanorods with a single gold tip. Such anisotropic semiconductor-metal hybrids are of interest for self-assembly and photocatalysis and as building blocks in optoelectronic devices.

The use of thiol ligands as a sulfur source for nanocrystal synthesis has recently come en vogue, as the products are often high quality. A comparative study was performed of dodecanethiol-capped Cu2S prepared with elemental sulfur and thiol sulfur reagents. XPS and TGA-MS provide evidence for differing binding modes of the capping thiols. Under conditions where the thiol acts only as a ligand, the capping thiols are "surface-bound" and bond to surface cations in low coordination number sites. In contrast, when thiols are used as a sulfur source, "crystal-bound" thiols result that sit in high coordination sites and are the terminal S layer of the crystal. A (1)H NMR study shows suppressed surface reactivity and ligand exchange with crystal-bound thiols, which could limit further application of the particles. To address the challenge and opportunity of nonlabile ligands, dodecyl-3-mercaptopropanoate, a molecule possessing both a thiol and an ester, was used as the sulfur source for the synthesis of Cu2S and CuInS2. A postsynthetic base hydrolysis cleaves the ester, leaving a carboxylate corona around the nanocrystals and rendering the particles water-soluble.

Cage structures exhibit inherent high symmetry and beauty, and both naturally occurring and synthetic molecular-scale cages have been discovered. Their characteristic high surface area and voids have led to their use as catalysts and catalyst supports, filtration media and gas storage materials. Nanometre-scale cage structures have also been synthesized, notably noble-metal cube-shaped cages prepared by galvanic displacement with promising applications in drug delivery and catalysis. Further functionality for nanostructures in general is provided by the concept of hybrid nanoparticles combining two disparate materials on the same system to achieve synergistic properties stemming from unusual material combinations. We report the integration of the two powerful concepts of cages and hybrid nanoparticles. A previously unknown edge growth mechanism has led to a new type of cage-structured hybrid metal-semiconductor nanoparticle; a ruthenium cage was grown selectively on the edges of a faceted copper(I) sulphide nanocrystal, contrary to the more commonly observed facet and island growth modes of other hybrids. The cage motif was extended by exploiting the open frame to achieve empty cages and cages containing other semiconductors. Such previously unknown nano-inorganic cage structures with variable cores and metal frames manifest new chemical, optical and electronic properties and demonstrate possibilities for uses in electrocatalysis.

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