New lithium halide solid-electrolyte materials, Li YCl and Li YBr , are found to exhibit high lithium-ion conductivity, high deformability, and high chemical and electrochemical stability, which are required properties for all-solid-state battery (ASSB) applications, particularly for large-scale deployment. The lithium-ion conductivities of cold-pressed powders surpass 1 mS cm at room temperature without additional intergrain or grain boundary resistances. Bulk-type ASSB cells employing these new halide solid electrolyte materials exhibit coulombic efficiencies as high as 94% with an active cathode material of LiCoO without any extra coating. These superior electrochemical characteristics, as well as their material stability, indicate that lithium halide salts are another promising candidate for ASSB solid electrolytes in addition to sulfides or oxides.

We report the observation of photocurrent in silicon nanowires induced by nonradiative resonant energy transfer (NRET) from adjacent layers of lead sulfide nanocrystal quantum dots using time-resolved photocurrent measurements. This demonstration supports the feasibility of a new solar cell paradigm (Lu, S.; Madhukar, A. Nano Lett. 2007, 7, 3443-3451) that exploits NRET between efficient photon absorbers and adjacent nanowire/quantum well high-mobility charge transport channels and could offer a viable alternative to the limitations of carrier transport and collection faced by excitonic solar cells.

Currently lattice mismatch strain-driven three-dimensional coherent island based quantum dots, dubbed self-assembled quantum dots (SAQDs), constitute the most developed class of quantum dots with successful applications to lasers and considerable potential for infrared detectors in the 1–12 μm regime. This is in no small part a consequence of the extensive studies on the formation and control of the islands and on their capping by appropriate overlayer materials under optimal growth conditions. By contrast, surprisingly few studies have been reported on the presence and nature of the deep levels in SAQD structures, much less direct studies of the impact of deep levels on SAQD based device characteristics. The latter is of particular significance to devices such as detectors that require large numbers of SAQD layers [i.e., multiple quantum dot (MQD) structures] and are thus increasingly prone to accumulating strain-induced defect formation with increasing numbers of quantum dot layers. In this paper, we report the results of a study of the density, energy profile, and spatial profile of deep levels in different regions of GaAs(001)/InAs/InGaAs/GaAs SAQD structures in which the InGaAs/GaAs capping layers have been grown at different growth conditions. Different types of deep levels are found in different regions and, as expected, their densities are found to increase in the presence of the SAQDs. The study shows that it is the density of deep levels in the GaAs capping layer, forced to be grown at the low temperature of ∼500 °C to suppress In outdiffusion, which has a significant adverse impact on quantum dot device characteristics. Their density can be reduced by growth conditions such as migration enhanced epitaxy that permit high quality overgrowths at temperatures as low as ∼350 °C. Nevertheless, the ultimate performance limitation of thick MQD based devices resides in the ability to realize low density of the deep levels relative to the density of SAQDs.

All‐solid‐state batteries (ASSBs) with inorganic solid electrolytes (SEs) have attracted significant interest as next‐generation energy storage. Halides such as Li3YCl6 are promising candidates for SE because they combine high oxidation stability and deformability. However, the ionic conductivities of halide SEs are not as high as those of other SEs, especially sulfides. Here, we discover new lithium‐metal‐oxy‐halide materials, LiMOCl4 (M=Nb, Ta). They exhibit extremely high ionic conductivities of 10.4 mS cm−1 for M=Nb and 12.4 mS cm−1 for M=Ta, respectively, even in cold‐pressed powder forms at room temperature, which are comparable to or surpass those of organic liquid electrolytes used in lithium‐ion batteries. Bulk‐type ASSB cells using the oxyhalides as the cathode SE demonstrate an outstanding rate capability with a capacity retention of 80 % at 5 C/0.1 C. We believe that the proposed oxyhalides are promising SE candidates for the practical applications of ASSBs.

We demonstrate high efficiency triple junction solar cells with submillimeter dimensions in an all-back-contact architecture. 550 × 550 μm2 cells flash at 41.3% efficiency under the air mass 1.5 direct normal spectrum at 50 W/cm2 at 25 °C. Compared to standard size production cells, the micro cells have reduced performance at 1-sun due to perimeter recombination, but the performance gap closes at higher concentrations. Micro cells integrated with lens arrays were tested on-sun with an efficiency of 34.7%. All-back-contact architecture and submillimeter dimensions are advantageous for module integration and heat dissipation, allowing for high-performance, compact, lightweight, and cost-effective concentrated photovoltaic modules.