A Ru(3+)-mediated synthesis for the unique Pd concave nanostructures, which can directly harvest UV-to-visible light for styrene hydrogenation, is described. The catalytic efficiency under 100 mW cm(-2) full-spectrum irradiation at room temperature turns out to be comparable to that of thermally (70 °C) driven reactions. The yields obtained with other Pd nanocrystals, such as nanocubes and octahedrons, are lower. The nanostructures reported here have sufficient plasmonic cross-sections for light harvesting in a broad spectral range owing to the reduced shape symmetry, which increases the solution temperature for the reaction by the photothermal effect. They possess a large quantity of atoms at corners and edges where local heat is more efficiently generated, thus providing active sites for the reaction. Taken together, these factors drastically enhance the hydrogenation reaction by light illumination.
black phosphorene (BP) carries a stellar set of physical properties such as conveniently tunable bandgap and extremely high ambiopolar carrier mobility for optoelectronic devices. Herein, we report, for the first time, the judicious design and positioning of BP with tailored thickness as dual-functional nanomaterials to concurrently enhance carrier extraction at both electron transport layer (ETL)/perovskite and perovskite/hole transport layer (HTL) interfaces for high-efficiency and stable perovskite solar cells (PSCs). The synergy of favorable band energy alignment and concerted cascade interfacial carrier extraction, rendered by concurrent positioning of BP, delivered a progressively enhanced power conversion efficiency (PCE) of 19.83% from 16.95% (BP-free). Investigation into interfacial engineering further reveals enhanced light absorption and reduced trap density for improved photovoltaic performance with BP incorporation. This work demonstrates the appealing characteristic of rational implementation of BP as dualfunctional transport material for a diversity of optoelectronic devices, including photodetectors, sensors, light-emitting diodes, etc.
Two-dimensional CdSe nanoplatelets are promising lasing materials. Their large lateral areas reduce the optical gain threshold by increasing the oscillator strength and multiexciton lifetimes but also increase the gain threshold by requiring multiple band-edge excitons (>2) to reach the optical gain. We observe that the optical gain threshold of CdSe nanoplatelets at 4 K is ∼4-fold lower than that at room temperature. Transient absorption spectroscopy measurements indicate that the exciton center-of-mass coherent area is smaller than the lateral size at room temperature and extends to nearly the whole nanoplatelets at 4 K. This suggests that the reduction in the optical gain threshold at a low temperature can be attributed to exciton coherent area extension that reduces the saturation number of band-edge excitons to enable biexciton gain and increases the radiative decay rate, consistent with the giant oscillator strength transition effect. This work demonstrates a new direction for lowering the optical gain threshold of nanomaterials.
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