Recently, CuSbS 2 has been proposed as an alternative earth-abundant absorber material for thin film solar cells. However, no systematic study on the chemical, optical, and electrical properties of CuSbS 2 has been reported. Using density functional theory (DFT) calculations, we showed that CuSbS 2 has superior defect physics with extremely low concentration of recombination-center defects within the forbidden gap, espeically under the S rich condition. It has intrinsically p-type conductivity, which is determined by the dominant Cu vacancy (V Cu ) defects with the a shallow ionization level and the lowest formation energy. Using a hydrazine based solution process, phase-pure, highly crystalline CuSbS 2 film with large grain size was successfully obtained. Optical absorption investigation revealed that our CuSbS 2 has a direct band gap of 1.4 eV. Ultraviolet photoelectron spectroscopy (UPS) study showed that the conduction band and valence band are located at 3.85 eV and −5.25 eV relative to the vacuum level, respectively. As the calculations predicted, a p-type conductivity is observed in the Hall effect measurements with a hole concentration of ∼10 18 cm −3 and hole mobility of 49 cm 2 /(V s). Finally, we have built a prototype FTO/CuSbS 2 /CdS/ZnO/ZnO:Al/Au solar cell and achieved 0.50% solar conversion efficiency. Our theoretical and experimental investigation confirmed that CuSbS 2 is indeed a very promising absorber material for solar cell application.
Flat panel displays enjoy 100 billion‐dollar markets with significant penetration in daily life, which require efficient, color‐saturated blue, green, and red light‐emitting diodes (LEDs). The recently emerged halide perovskites have demonstrated low‐cost and outstanding performance for potential LED applications. However, the performance of blue perovskite LEDs (PeLEDs) lags far behind red and green cousins, particularly for color coordinates approaching (0.131, 0.046) that fulfill the Rec. 2020 specification for blue emitters. Here, a high‐efficiency, lead‐free perovskite, CsEuBr3, is reported that exhibits bright blue exciton emission centered at 448 nm with a color coordinates of (0.15, 0.04), contributed from Eu‐5d→Eu‐4f/Br‐4p transition with an optical band gap of 2.85 eV. Further optical characterizations reveal its short excited‐state lifetime of 151 ns, excellent exciton diffusion diffusivity of 0.0227 cm2 s−1, and high quantum yield of ≈69%. Inspired by these findings, deep‐blue PeLEDs based on all‐vacuum processing methods, which have been demonstrated as the most successful approach for the organic LED industry, are constructed. The devices show a maximum external quantum efficiency of 6.5% with an operating half‐lifetime of 50 mins at an initial brightness of 15.9 cd m−2. It is anticipated that this work will inspire further research on lanthanide‐based perovskites for next‐generation LED applications.
An ionic liquid polymer, poly (1-alkyl-3-(acryloyloxy)hexylimidazolium iodide), was employed as an iodine-free electrolyte in all-solid-state dye-sensitized solar cells with an overall conversion efficiency of 5.29% under AM 1.5 simulated solar light (100 mW cm(-2)) illumination.
SignificanceInferring connections forms a critical step toward understanding large and diverse complex networks. To date, reliable and efficient methods for the reconstruction of network topology from measurement data remain a challenge due to the high complexity and nonlinearity of the system dynamics. These obstacles also form a bottleneck for analyzing and controlling the dynamic structures (e.g., synchrony) and collective behavior in such complex networks. The novel contribution of this work is to develop a unified data-driven approach to reliably and efficiently reveal the dynamic topology of complex networks in different scales—from cells to societies. The developed technique provides guidelines for the refinement of experimental designs toward a comprehensive understanding of complex heterogeneous networks.
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