Highly Efficient Blue-Emitting CsPbBr3 Perovskite Nanocrystals through Neodymium Doping.

Colloidal CsPbX3 (X = Br, Cl, and I) perovskite nanocrystals exhibit tunable bandgaps over the entire visible spectrum and high photoluminescence quantum yields in the green and red regions. However, the lack of highly efficient blue-emitting perovskite nanocrystals limits their development for optoelectronic applications. Herein, neodymium (III) (Nd3+) doped CsPbBr3 nanocrystals are prepared through the ligand-assisted reprecipitation method at room temperature with tunable photoemission from green to deep blue. A blue-emitting nanocrystal with a central wavelength at 459 nm, an exceptionally high photoluminescence quantum yield of 90%, and a spectral width of 19 nm is achieved. First principles calculations reveal that the increase in photoluminescence quantum yield upon doping is driven by an enhancement of the exciton binding energy due to increased electron and hole effective masses and an increase in oscillator strength due to shortening of the Pb-Br bond. Putting these results together, an all-perovskite white light-emitting diode is successfully fabricated, demonstrating that B-site composition engineering is a reliable strategy to further exploit the perovskite family for wider optoelectronic applications

All-inorganic perovskite-based distributed feedback resonator

Halide perovskite materials have rapidly emerged as outstanding optoelectronic materials for solar cells, light-emitting diodes (LEDs), and lasers. Compared to hybrid organic-inorganic perovskites, all-inorganic perovskites have shown unique merits that may contribute to the ultimate goal of developing electrically-pumped lasers. In this paper, we demonstrate a distributed feedback (DFB) resonator using an all-inorganic perovskite thin film as the gain medium. The film has a gain coefficient of 161.1 cm−1 and a loss coefficient of 30.9 cm−1. Excited by picosecond pulses, the microstructured all-inorganic perovskite film exhibits a single-mode emission at 654 nm with a threshold of 33 μJ/cm2. The facile fabrication process provides a promising route towards low-cost single-mode visible lasers for many practical applications

X-ray photoelectron spectroscopy studies of indium-tin-oxide treated via oxygen plasma immersion ion implantation

Surface modification was performed on the indium-tin-oxide (ITO) thin films by oxygen inductive coupling plasma (O-ICP) and oxygen plasma immersion ion implantation (O-PIII). The electronic states of ITO surfaces were characterized by X-ray photoelectron spectroscopy (XPS). The observed peak shifts of O 1s, In 3d5/2 and Sn d5/2 core levels showed that the work function of ITO can be further enhanced by O-PIII treatment, compared with that of untreated and O-ICP treated surfaces. The deconvolution of O 1s spectrum and calculation of stoichiometry showed that the work function improvement should be attributed to the increase of effective oxygen content, namely, the elimination of oxygen vacancies. In addition, the measurement of Kelvin probe confirmed that an increment of the ITO work function by 1.1 eV was obtained on O-PIII treated sample and the results sustained our proposal