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A series of SrZrO3 : Eu3+ nano phosphors synthesized by a modified high‐temperature solid‐state reaction method. The structural, functional vibration groups, optical, morphological, luminescence and quantum yield studies were characterized through XRD, FTIR, UV, 'SEM & HR‐TEM' and PL analyses respectively. The SrZrO3 : Eu3+ phosphor has a perovskite orthorhombic structure and emits intense red emission around 612 nm when it is excited under 465 nm and covers NUV light range. The calculated average lifetime indicates the nature of the allowed emission transition in Eu3+ (2.44 μs). The calculated colour purity and Commission International del' Eclairagethe (CIE) chromaticity coordinates are 97.9 % and (0.5894, 0.4031) respectively. The observed quantum yield and thermal stability for the SrZrO3 : Eu3+ (9 mol %) phosphor are 22 % and 87 % at 423 K, respectively. These obtained results suggest that SrZrO3 : Eu3+ (9 mol %) phosphor would meliorate for red‐emitting phosphor in profound RGB‐based pc‐WLED applications. [ABSTRACT FROM AUTHOR]

Ti, V, Cr, Mn, Co, and Cu, have been investigated as a third dopant in NiFe sulfide for enhanced oxygen evolution reaction (OER)/oxygen reduction reaction (ORR). The effects of dopant on surface electronic structure, conductivity, and thermodynamic barrier of reaction are addressed and discussed. For the OER, X‐ray photoelectron spectroscopy analysis shows that electron transferring from the Ni to the dopants enhances the catalytic performance of the sulfide. Cu doped NiFe sulfide exhibits the best OER performance. For the ORR, density functional theory calculation indicates that Ti, V, Mn, Co, and Cu upshift the d‐band center (ɛd), while Cr downshifts the ɛd. Among the dopants, V leads to optimized electronic structure modification, giving optimized adsorption energy of *O on the Ni, the lowest rate determining step ΔG1, and the best ORR activity. By considering E10‐E1/2 together with the maximum current density of the OER and limited diffusion current density of the ORR, NiFeVS exhibits the best OER/ORR bifunctionality. The performance of NiFeVS as a cathodic catalyst has also been evaluated in a zinc air battery, demonstrating a specific capacity of 698 mAh g−1, maximum power density of 190 mW cm−2, and a superior cycle stability of 2400 cycles (400 h). [ABSTRACT FROM AUTHOR]

Climate change poses a significant threat to humanity. Achieving net-zero emissions is a key goal in many countries. Among various energy resources, solar power generation is one of the prominent renewable energy sources. Previous studies have demonstrated that post-processing techniques such as bias correction can enhance the accuracy of solar power forecasting based on numerical weather prediction (NWP) models. To improve the post-processing technique, this study proposes a new day-ahead forecasting framework that integrates weather research and forecasting solar (WRF-Solar) irradiances and the total solar power generation measurements for five cities in northern, central, and southern Taiwan. The WRF-Solar irradiances generated by the Taiwan Central Weather Bureau (CWB) were first subjected to bias correction using the decaying average (DA) method. Then, the effectiveness of this correction method was verified, which led to an improvement of 22% in the forecasting capability from the WRF-Solar model. Subsequently, the WRF-Solar irradiances after bias correction using the DA method were utilized as inputs into the transformer model to predict the day-ahead total solar power generation. The experimental results demonstrate that the application of bias-corrected WRF-Solar irradiances enhances the accuracy of day-ahead solar power forecasts by 15% compared with experiments conducted without bias correction. These findings highlight the necessity of correcting numerical weather predictions to improve the accuracy of solar power forecasts. [ABSTRACT FROM AUTHOR]

Low temperature rechargeable batteries are important to life in cold climates, polar/deep-sea expeditions, and space explorations. Here, this work reports 3.5-4 V rechargeable lithium/chlorine (Li/Cl 2 ) batteries operating down to -80 °C, employing Li metal negative electrode, a novel carbon dioxide (CO 2 ) activated porous carbon (KJCO 2 ) as the positive electrode, and a high ionic conductivity (≈5-20 mS cm -1 from -80 °C to room-temperature) electrolyte comprised of aluminum chloride (AlCl 3 ), lithium chloride (LiCl), and lithium bis(fluorosulfonyl)imide (LiFSI) in low-melting-point (-104.5 °C) thionyl chloride (SOCl 2 ). Between room-temperature and -80 °C, the Li/Cl 2 battery delivers up to ≈29 100-4500 mAh g -1 first discharge capacity (based on carbon mass) and a 1200-5000 mAh g -1 reversible capacity over up to 130 charge-discharge cycles. Mass spectrometry and X-ray photoelectron spectroscopy probe Cl 2 trapped in the porous carbon upon LiCl electro-oxidation during charging. At -80 °C, Cl 2 /SCl 2 /S 2 Cl 2 generated by electro-oxidation in the charging step are trapped in porous KJCO 2 carbon, allowing for reversible reduction to afford a high discharge voltage plateau near ≈4 V with up to ≈1000 mAh g -1 capacity for SCl 2 /S 2 Cl 2 reduction and up to ≈4000 mAh g -1 capacity at ≈3.1 V plateau for Cl 2 reduction., (© 2023 Wiley-VCH GmbH.)