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Li-CO2 batteries (LCBs) have emerged as promising solutions for energy storage, with the added benefit of contributing to carbon neutrality by capturing and utilizing CO2 during operation. In this study, a high-performance LCB was developed using a Ge-doped LiAlGeTi (PO4)3 (LAGTP) solid electrolyte, which was synthesized via a solution-based method by doping Ge into NASICON-type LATP. The ionic conductivity of the LAGTP pellets was measured as 1.04 × 10−3 S/cm at 25 °C. The LCB utilizing LAGTP and an MWCNT/Ru cathode maintained a stable cycling performance over 200 cycles at a current density of 100 mA/g, with a cut-off capacity of 500 mAh/g. Post-cycle analysis confirmed the reversible electrochemical reactions at the cathode. The integration of LAGTP as a solid electrolyte effectively enhanced the ionic conductivity and improved the cycle life and performance of the LCB. This study highlights the potential of Ge-doped NASICON-type solid electrolytes for advanced energy-storage technologies and offers a pathway for developing sustainable and high-performance LCBs. [ABSTRACT FROM AUTHOR]

Li–S batteries are promising large-scale energy storage systems but currently suffer from performance issues; a major reason is the dissolution of polysulfides in electrolytes. To this end, we report a high-energy-density Lithium–Sulfur (Li–S) battery that combines a catholyte and a sulfur-free carbon nanofiber (CNF) cathode. The cathode was synthesized by carbonizing binder-free polyacrylonitrile (PAN) nanofibers, affording a high surface area. In the catholyte, added polysulfides acted as both conductive Li salts and active materials. Investigating the electrochemical performance of this concept in both Swagelok- and pouch-type cells afforded energy densities exceeding 3 mAh cm−2 at a discharge rate of 0.1 C. This combination could also be utilized in high-capacity pouch cells with capacities of up to 250 mAh g−1. Both cell types exhibited good cycle performance. Adding LiNO3 to the electrolyte suppressed the redox shuttle reactions. Moreover, the cathode being binder-free increased the energy density and simplified cathode fabrication. Characterizing the cathode before and after cycling revealed that deposition was reversible, and that cell reactions at least partially formed sulfur as the end product, resulting in high sulfur amounts in the cell. We expect our concept to greatly aid in the development of practically applicable Li–S cells. [ABSTRACT FROM AUTHOR]

We developed an automated microregistration method that enables repeated in vivo skin microscopy imaging of the same tissue microlocation and specific cells over a long period of days and weeks with unprecedented precision. Applying this method in conjunction with an in vivo multimodality multiphoton microscope, the behavior of human skin cells such as cell proliferation, melanin upward migration, blood flow dynamics, and epidermal thickness adaptation can be recorded over time, facilitating quantitative cellular dynamics analysis. We demonstrated the usefulness of this method in a skin biology study by successfully monitoring skin cellular responses for a period of two weeks following an acute exposure to ultraviolet light. [ABSTRACT FROM AUTHOR]

This study reports an integrated device in which a lithium-ion battery (LIB) and Si solar cells are interconnected. The LIB is fabricated using the Li(Ni0.65Co0.15Mn0.20)O2 (NCM622) cathode and the Li4Ti5O12 (LTO) anode. The surface and shape morphologies of the NCM and LTO powders were investigated by field emission scanning electron microscopy (FE-SEM). In addition, the structural properties were thoroughly examined by X-ray diffraction (XRD). Further, their electrochemical characterization was carried out on a potentiostat. The specific discharge capacity of the NCM cathode (half-cell) was 188.09 mAh/g at 0.1 C current density. In further experiments, the NCM-LTO full-cell has also shown an excellent specific capacity of 160 mAh/g at a high current density of 1 C. Additionally, the capacity retention was outstanding, with 99.63% at 1 C after 50 cycles. Moreover, to meet the charging voltage requirements of the NCM-LTO full-cell, six Si solar cells were connected in series. The open-circuit voltage (VOC) and the short-circuit photocurrent density (JSC) for the Si solar cells were 3.37 V and 5.42 mA/cm2. The calculated fill factor (FF) and efficiency for the Si solar cells were 0.796 and 14.54%, respectively. Lastly, the integrated device has delivered a very high-power conversion-storage efficiency of 7.95%. [ABSTRACT FROM AUTHOR]

Commercial lithium-ion batteries using liquid electrolytes are still a safety hazard due to their poor chemical stability and other severe problems, such as electrolyte leakage and low thermal stability. To mitigate these critical issues, solid electrolytes are introduced. However, solid electrolytes have low ionic conductivity and inferior power density. This study reports the optimization of the synthesis of sodium superionic conductor-type Li1.5Al0.3Si0.2Ti1.7P2.8O12 (LASTP) solid electrolyte. The as-prepared powder was calcined at 650 °C, 700 °C, 750 °C, and 800 °C to optimize the synthesis conditions and yield high-quality LASTP powders. Later, LASTP was sintered at 950 °C, 1000 °C, 1050 °C, and 1100 °C to study the dependence of the relative density and ionic conductivity on the sintering temperature. Morphological changes were analyzed using field-emission scanning electron microscopy (FE-SEM), and structural changes were characterized using X-ray diffraction (XRD). Further, the ionic conductivity was measured using electrochemical impedance spectroscopy (EIS). Sintering at 1050 °C resulted in a high relative density and the highest ionic conductivity (9.455 × 10−4 S cm−1). These findings corroborate with the activation energies that are calculated using the Arrhenius plot. Therefore, the as-synthesized superionic LASTP solid electrolytes can be used to design high-performance and safe all-solid-state batteries. [ABSTRACT FROM AUTHOR]

This study reports an integrated device of a lithium-ion battery (LIB) connected with Si solar cells. A Li(Ni0.65Co0.15Mn0.20)O2 (NCM) cathode and a graphite (G) anode were used to fabricate the lithium-ion battery (LIB). The surface and shape morphologies of NCM and graphite powder were characterized by field emission scanning electron microscopy (FE-SEM). The structural properties of NCM and graphite powder were determined by X-ray diffraction (XRD) analysis. XRD patterns of powders were well matched with those of JCPDS data. To investigate the electrochemical characteristics of NCM and graphite, cycling tests were performed after assembling the NCM-Li, the G-Li half-cell, and the NCM-G full-cell. The discharge capacity of the NCM cathode at 0.1C was 189.82 mAh/g−1. The NCM-graphite full-cell showed 98.25% cycle retention at 1C after 50 cycles. To obtain enough charging voltage for the LIB connected with solar cells in an integrated device, eight single Si solar cells were connected in a series. The short-circuit photocurrent density for Si solar cells was 4.124 mA/cm2. The fill factor and the open circuit voltage were 0.78 and 4.5 V, respectively. These Si solar cells showed a power conversion efficiency of 14.45%. The power conversion andstorage efficiency of the integrated device of the NCM battery and Si solar cells was 7.74%. Charging of the integrated device could be as effective as charging with a battery cycler. [ABSTRACT FROM AUTHOR]

This study demonstrates the use of perovskite solar cells for fabrication of self-charging lithium-ion batteries (LIBs). A LiFePO4 (LFP) cathode and Li4Ti5O12 (LTO) anode were used to fabricate a LIB. The surface morphologies of the LiFePO4 and Li4Ti5O12 powders were examined using field emission scanning electron microscopy. The structural properties of the two powders were investigated using X-ray diffraction. The electrochemical properties of the LiFePO4-Li and Li4Ti5O12-Li half cells and of the full cell were investigated. The LiFePO4-Li4Ti5O12 full cell showed an excellent Coulombic efficiency of 99.3% after 100 cycles. CH3NH3PBI3 (MAPbI3) perovskite solar cells (PSCs) were fabricated using a spin coating technique. A single PSC showed a power conversion efficiency of 12.95%. In order to develop a self-charging system for LIBs, four single PSCs connected in series were used as an LFP-LTO battery. The integrated PSC system showed a power conversion efficiency of 12.44%. The PSC-LIB coupled device showed excellent overall self-charging conversion and a storage efficiency of 9.25%. [ABSTRACT FROM AUTHOR]

The constant effectiveness of a policy instrument was a major lacuna in energy policy for a long time. However, selecting and mixing appropriate policy instruments has become crucial in the era of climate change. The aim of this paper is to investigate the renewable portfolio standard (RPS) system as a sustainable policy instrument for promoting new and renewable energy. To answer the research question, we utilized the latent growth model by applying the data on 27 types of new and renewable energy production from 2014, 2015, and 2016. Our empirical analysis concluded that the effectiveness of the RPS as a policy instrument decreased linearly each year, and its effectiveness is expected to decrease in the long term from 2017 to 2023. Profound debates and evidence from other RPS-adopting countries should be additionally conducted to bolster this theme of sustainable energy policy instruments [ABSTRACT FROM AUTHOR]