The ability to guide the assembly of nanosized objects reversibly with external stimuli, in particular light, is of fundamental importance, and it contributes to the development of applications as diverse as nanofabrication and controlled drug delivery. However, all the systems described to date are based on nanoparticles (NPs) that are inherently photoresponsive, which makes their preparation cumbersome and can markedly hamper their performance. Here we describe a conceptually new methodology to assemble NPs reversibly using light that does not require the particles to be functionalized with light-responsive ligands. Our strategy is based on the use of a photoswitchable medium that responds to light in such a way that it modulates the interparticle interactions. NP assembly proceeds quantitatively and without apparent fatigue, both in solution and in gels. Exposing the gels to light in a spatially controlled manner allowed us to draw images that spontaneously disappeared after a specific period of time.

The chemical behaviour of molecules can be significantly modified by confinement to volumes comparable to the dimensions of the molecules. Although such confined spaces can be found in various nanostructured materials, such as zeolites, nanoporous organic frameworks and colloidal nanocrystal assemblies, the slow diffusion of molecules in and out of these materials has greatly hampered studying the effect of confinement on their physicochemical properties. Here, we show that this diffusion limitation can be overcome by reversibly creating and destroying confined environments by means of ultraviolet and visible light irradiation. We use colloidal nanocrystals functionalized with light-responsive ligands that readily self-assemble and trap various molecules from the surrounding bulk solution. Once trapped, these molecules can undergo chemical reactions with increased rates and with stereoselectivities significantly different from those in bulk solution. Illumination with visible light disassembles these nanoflasks, releasing the product in solution and thereby establishes a catalytic cycle. These dynamic nanoflasks can be useful for studying chemical reactivities in confined environments and for synthesizing molecules that are otherwise hard to achieve in bulk solution.

Active control over the shape, composition, and crystalline habit of nanocrystals has long been a goal. Various methods have been shown to enable postsynthesis modification of nanoparticles, including the use of the Kirkendall effect, galvanic replacement, and cation or anion exchange, all taking advantage of enhanced solid-state diffusion on the nanoscale. In all these processes, however, alteration of the nanoparticles requires introduction of new precursor materials. Here we show that for cesium lead halide perovskite nanoparticles, a reversible structural and compositional change can be induced at room temperature solely by modification of the ligand shell composition in solution. The reversible transformation of cubic CsPbX3 nanocrystals to rhombohedral Cs4PbX6 nanocrystals is achieved by controlling the ratio of oleylamine to oleic acid capping molecules. High-resolution transmission electron microscopy investigation of Cs4PbX6 reveals the growth habit of the rhombohedral crystal structure is composed of a zero-dimensional layered network of isolated PbX6 octahedra separated by Cs cation planes. The reversible transformation between the two phases involves an exfoliation and recrystalliztion process. This scheme enables fabrication of high-purity monodispersed Cs4PbX6 nanoparticles with controlled sizes. Also, depending on the final size of the Cs4PbX6 nanoparticles as tuned by the reaction time, the back reaction yields CsPbX3 nanoplatelets with a controlled thickness. In addition, detailed surface analysis provides insight into the impact of the ligand composition on surface stabilization that, consecutively, acts as the driving force in phase and shape transformations in cesium lead halide perovskites.

Despite the recent surge of interest in lead halide perovskite nanocrystals, there are still significant gaps in the understanding of nucleation and growth processes involved in their formation. Using CsPbX 3 as a model system, we systematically study the formation mechanism of cubic CsPbX 3 nanocrystals, their growth via oriented attachment into larger nanostructures, and the associated phase transformations. We found evidence to support that the formation of CsPbX 3 NCs occurs through the seed-mediated nucleation method, where Pb°NPs formed during the course of reaction act as seeds. Further growth occurs through self-assembly and oriented attachment. The polar environment is a major factor in determining the structure and shape of the resulting nanoparticles, as confirmed by experiments with aged seed reaction mixtures, and by addition of polar additives. These results provide a fundamental understanding of the influence of the environment polarity on self-assembly, self-healing, and the ability to control the morphology and structure over the perovskite structures. As a result of this understanding, we were able to extend the synthesis to produce other materials such as CsPbBr 3 nanowires and orthorhombic CsPbI 3 nanowires with tunable length ranging from 200 nm to several microns.

"Catching" metals in the nonmetallic form in solution, as they grow to bulk, is one of the most exciting areas of contemporary materials research. A new kind of stabilization to catch the nonmetallic form of noble metals with small thiols has evolved as an exciting area of synthesis during the past decade. Gold clusters stay in the frontline of this research, yielding new "molecules" composed of a few to several hundreds of atoms. By taking guidelines from gold cluster research, various new protocols for silver nanoclusters were developed. In this Perspective, we highlight the recent advances on the synthesis of atomically precise silver, gold, and their alloy clusters with a special emphasis on silver. As a result of intense efforts of the recent past, clusters such as Ag7,8(SR)7,8, Ag7(-S-R-S-)4, Ag9(SR)7, Ag32(SR)19, Ag44(SR)30, Ag140(SR)53, Ag280(SR)140, and Ag152(SR)60 (SR and S-R-S refer to thiolate and dithiolate ligands, respectively) were added to the literature. Moreover, "silver-covered" and "gold-covered" alloy clusters have also been synthesized. Early reports of the crystallization of such clusters are available. Several of these clusters are shown to act as sensors, catalysts, and pesticide degradation agents, which suggests that these materials may find applications in daily life in the foreseeable future.