This paper reports highly bright and efficient CsPbBr perovskite light-emitting diodes (PeLEDs) fabricated by simple one-step spin-coating of uniform CsPbBr polycrystalline layers on a self-organized buffer hole injection layer and stoichiometry-controlled CsPbBr precursor solutions with an optimized concentration. The PeLEDs have maximum current efficiency of 5.39 cd A and maximum luminance of 13752 cd m . This paper also investigates the origin of current hysteresis, which can be ascribed to migration of Br anions. Temperature dependence of the electroluminescence (EL) spectrum is measured and the origins of decreased spectrum area, spectral blue-shift, and linewidth broadening are analyzed systematically with the activation energies, and are related with Br anion migration, thermal dissociation of excitons, thermal expansion, and electron-phonon interaction. This work provides simple ways to improve the efficiency and brightness of all-inorganic polycrystalline PeLEDs and improves understanding of temperature-dependent ion migration and EL properties in inorganic PeLEDs.

An urgent need in chemodynamic therapy (CDT) is to achieve high Fenton catalytic efficiency at small doses of CDT agents. However, simple general promotion of the Fenton reaction increases the risk of damaging normal cells along with the cancer cells. Therefore, a tailored strategy to selectively enhance the Fenton reactivity in tumors, for example, by taking advantage of the characteristics of the tumor microenvironment (TME), is in high demand. Herein, a heterogeneous CDT system based on copper−iron peroxide nanoparticles (CFp NPs) is designed for TME-mediated synergistic therapy. CFp NPs degrade under the mildly acidic conditions of TME, selfsupply H 2 O 2 , and the released Cu and Fe ions, with their larger portions at lower oxidation states, cooperatively facilitate hydroxyl radical production through a highly efficient catalytic loop to achieve an excellent tumor therapeutic efficacy. This is distinct from previous heterogeneous CDT systems in that the synergism is closely coupled with the Cu + -assisted conversion of Fe 3+ to Fe 2+ rather than their independent actions. As a result, almost complete ablation of tumors at a minimal treatment dose is demonstrated without the aid of any other therapeutic modality. Furthermore, CFp NPs generate O 2 during the catalysis and exhibit a TME-responsive T 1 magnetic resonance imaging contrast enhancement, which are useful for alleviating hypoxia and in vivo monitoring of tumors, respectively.

Control of structure and morphology in electrode design is crucial for creating efficient transport pathways of ions and electrons in high-performance energy storage devices. Here we report the fabrication of high-performance anode materials for lithium-ion batteries based on a 3D heterostructured architecture consisting of Co(3)O(4) nanoparticles deposited onto porous graphene surfaces. A combination of replication and filtration processes - a simple and general method - allows a direct assembly of 2D graphene sheets into 3D porous films with large surface area, porosity, and mechanical stability. The polystyrene spheres are employed as sacrificial templates for an embossing technique that yields porous structures with tunable pore sizes ranging from 100 nm to 2 μm. Co(3)O(4) nanoparticles with high-energy storage capacity can be easily incorporated into the pore surfaces by a simple deposition strategy, thereby creating a 3D heterogeneous Co(3)O(4)/graphene film. In particular, we exploit the 3D Co(3)O(4)/graphene composite films as anode materials for lithium ion batteries in order to resolve the current issues of rate capability and cycling life. This unique heterogeneous 3D structure is capable of delivering excellent Li(+) ion storage/release and displays the following characteristics: a high rate capability of 71% retention even at a high current rate of 1000 mA g(-1) and a good cycling performance with 90.6% retention during 50 cycles. The versatile and simple nature of preparing 3D heterogeneous graphene films with various functional nanoparticles can be extended to overcome the major challenges that exist for many electrochemical devices.

Copper electrodes with a micromesh/nanomesh structure were fabricated on a polyimide substrate using UV lithography and wet etching to produce flexible transparent conducting electrodes (TCEs). Well-defined mesh electrodes were realized through the use of high-quality Cu thin films. The films were fabricated using radio-frequency (RF) sputtering with a single-crystal Cu target—a simple but innovative approach that overcame the low oxidation resistance of ordinary Cu. Hybrid Cu mesh electrodes were fabricated by adding a capping layer of either ZnO or Al-doped ZnO. The sheet resistance and the transmittance of the electrode with an Al-doped ZnO capping layer were 6.197 ohm/sq and 90.657%, respectively, and the figure of merit was 60.502 × 10–3/ohm, which remained relatively unchanged after thermal annealing at 200 °C and 1,000 cycles of bending. This fabrication technique enables the mass production of large-area flexible TCEs, and the stability and high performance of Cu mesh hybrid electrodes in harsh environments suggests they have strong potential for application in smart displays and solar cells.

Y 2 O 3 : Eu 3+ and Li-doped Y2O3:Eu3+ luminescent thin films have been grown on sapphire substrates using pulsed-laser deposition. The films grown under different deposition conditions have been characterized using microstructural and luminescent measurements. The photoluminescence (PL) brightness data obtained from Li-doped Y2O3:Eu3+ films grown under optimized conditions have indicated that sapphire is a promising substrate for the growth of high-quality Li-doped Y2O3:Eu3+ thin-film red phosphor. In particular, the incorporation of Li+ ions into Y2O3 lattice could induce a remarkable increase of PL. The highest emission intensity was observed with LiF-doped Y1.84Li0.08Eu0.08O3, whose brightness was increased by a factor of 2.7 in comparison with that of Y2O3:Eu3+ films. This phosphor may promise for application to the flat panel displays.