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This research elucidates novel insights into the electrochemical properties and degradation phenomena of propylene carbonate (PC)-based supercapacitors at a large-scale 18650 cylindrical jelly-roll cell level. Central to our findings is the identification of 2-ethyl-4-methyl-1,3-dioxolane (EMD) as a hitherto undocumented decomposition by-product, highlighting the nuanced complexity of PC electrolyte stability. We further demonstrate that elevated operational voltages precipitate accelerated electrolyte degradation, underscoring the criticality of defining the operational voltage window for maximizing device longevity. Employing advanced analytical techniques, including gas chromatography-mass spectrometry (GC-MS), this study meticulously analyzes electrolyte decomposition mechanisms. The outcomes offer pivotal insights into the operational constraints and chemical resilience of PC-based supercapacitors, contributing significantly to the optimization of supercapacitor design and application. By delineating a specific decomposition pathway, this investigation enriches the understanding of electrochemical dynamics in supercapacitor systems, providing a foundation for future research and technological advancement in energy storage devices., (© 2024 Wiley-VCH GmbH.)

The pursuit of high-performing cathode materials for next-generation lithium ion batteries has focused on increasing the nickel content of the material. However, this study reveals that particle size uniformity is a more decisive factor in battery performance than the nickel content alone. Using in operando X-ray diffraction, in situ gas evolution, and Atlung intercalant diffusion, we compared two promising cathode materials: LiNi 0.8 Mn 0.1 Co 0.1 O 2 (NMC80) and LiNi 0.9 Mn 0.05 Co 0.05 O 2 (NMC90). We found that the NMC90 cell, with its more uniform particle size, exhibits a remarkable accumulation energy density of 558 kW h kg NMC -1 , which is 22% higher than that of the NMC80 cell. Also, the NMC90 cell unexpectedly has a 20% better capacity retention, a 50-fold higher discharge capacity at the 5C rate, and an Atlung lithium diffusion coefficient that is one order of magnitude higher after 1000 cycles. In situ gas analysis at a high voltage of 4.5 V reveals that the NMC80 cell generates 1.75 times more CO 2 than the NMC90 cell. These findings illuminate the intricate relationship between the nickel content, particle size uniformity, and battery performance. They offer vital insights for optimizing cathode materials in future lithium ion batteries., Competing Interests: The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (This journal is © The Royal Society of Chemistry.)

The demand for lithium-ion batteries has significantly increased due to the increasing adoption of electric vehicles (EVs). However, these batteries have a limited lifespan, which needs to be improved for the long-term use needs of EVs expected to be in service for 20 years or more. In addition, the capacity of lithium-ion batteries is often insufficient for long-range travel, posing challenges for EV drivers. One approach that has gained attention is using core-shell structured cathode and anode materials. That approach can provide several benefits, such as extending the battery lifespan and improving capacity performance. This paper reviews various challenges and solutions by the core-shell strategy adopted for both cathodes and anodes. The highlight is scalable synthesis techniques, including solid phase reactions like the mechanofusion process, ball-milling, and spray-drying process, which are essential for pilot plant production. Due to continuous operation with a high production rate, compatibility with inexpensive precursors, energy and cost savings, and an environmentally friendly approach that can be carried out at atmospheric pressure and ambient temperatures. Future developments in this field may focus on optimizing core-shell materials and synthesis techniques for improved Li-ion battery performance and stability., (© 2023 Wiley-VCH GmbH.)

Li-S batteries with a sulphur loading content of 5 mg cm -2 were produced as large-scale 18 650 cylindrical cells. We have found that a key failure mode of cylindrical Li-S battery cells is the severe capacity fading during the galvanostatic charge-discharge process due to the corrosion of the electrodes, the electrolyte decomposition, and the severe polysulphide shuttling effect.

This study investigates the use of a hierarchical porous carbon electrode derived from oil palm leaves in a "water-in-salt" supercapacitor. The impact of anion identity on the electrical performance of the carbon electrode was also explored. The results show that the prepared carbon had a hierarchical porous structure with a high surface area of up to 1840 m 2 g -1 . When a 20 m LiTFSI electrolyte was used, the carbon electrode had a specific capacitance of 176 F g -1 with a wider potential window of about 2.6 V, whereas the use of a cheaper 20 m LiCl electrolyte showed a higher specific capacitance of 331 F g -1 due to the smaller size of the Cl - anion, which enabled inner capacitance. Therefore, the anion identity has an effect on the electrochemical performance of porous carbon, and this research contributes to the understanding of using "water-in-salt" electrolytes in carbon-based supercapacitors. The study's findings provide insights into developing low-cost, high-performance supercapacitors that can operate in a wider voltage range., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

This manuscript presents the design and facile production of screen-printed arrays (SPAs) for the internally validated determination of raised levels of serum procalcitonin (PCT). The screen-printing methodology produced SPAs with six individual working electrodes that exhibit an inter-array reproducibility of 3.64% and 5.51% for the electrochemically active surface area and heterogenous electrochemical rate constant respectively. The SPAs were modified with antibodies specific for the detection of PCT through a facile methodology, where each stage simply uses droplets incubated on the surface, allowing for their mass-production. This platform was used for the detection of PCT, achieving a linear dynamic range between 1 and 10 ng mL -1 with a sensor sensitivity of 1.35 × 10 -10 NIC%/ng mL -1 . The SPA produced an intra- and inter-day %RSD of 4.00 and 5.05%, with a material cost of £1.14. Internally validated human serum results (3 sample measurements, 3 control) for raised levels of PCT (>2 ng mL -1 ) were obtained, with no interference effects seen from CRP and IL-6. This SPA platform has the potential to offer clinicians vital information to rapidly begin treatment for "query sepsis" patients while awaiting results from more lengthy remote laboratory testing methods. Analytical ranges tested make this an ideal approach for rapid testing in specific patient populations (such as neonates or critically ill patients) in which PCT ranges are inherently wider. Due to the facile modification methods, we predict this could be used for various analytes on a single array, or the array increased further to maintain the internal validation of the system., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2023 The Authors. Published by Elsevier B.V. All rights reserved.)

Potassium-based energy storage devices are attracting increasing attention as an alternative to lithium and sodium systems. In addition, metal-organic frameworks (MOFs) can be considered as promising electrode materials for this type of device due to their advantageous properties. Herein, the anionic MOF JUMP-1 and its analog with pre-loading of potassium cations, namely JUMP-1(K), were synthesized and characterized. The anionic framework of JUMP-1 is found to be extremely stable towards the exchange of the dimethylammonium cations by potassium ions. These MOFs were tested in composite electrodes in combination with conventional organic electrolytes as anode materials in a potassium-based system, including the full cell assembly of a potassium ion capacitor (KIC). The results show the significant improvement in capacity between the pristine JUMP-1 and the potassium-exchanged analog JUMP-1(K) as electrode materials. KICs containing JUMP-1(K) coupled with activated carbon (AC) display a promising stability over 4000 cycles. According to the results from these studies, the composite MOF electrode with the potassium-exchange analog JUMP-1(K) presents a promising approach, for which the electrochemical performance compared to the pristine anionic MOF is significantly enhanced., Competing Interests: There are no conflicts to declare., (This journal is © The Royal Society of Chemistry.)

The rapidly increasing adoption of electric vehicles (EVs) worldwide is causing high demand for production of lithium-ion batteries (LIBs). Tremendous efforts have been made to develop different components of LIBs in addition to design of battery pack architectures as well as manufacturing processes to make better batteries with affordable prices. Nonetheless, sustainable use of LIBs relies on the availability and cost of rare metals, which are naturally concentrated in a few countries. In addition, toxic electrolytes used in LIBs pose concerns on environmental impacts if LIBs are not handled properly after decommissioned from EVs. Therefore, it is paramount to realize effective utilization of spent LIBs, where their remaining capacities can be reused in less demanding applications. Finally, electrode materials and other valuable components of LIBs can be recovered via recycling, completing their circular life cycle. In this review, available options of LIBs after their retirement from EV applications, including battery second use, repair of electrode materials by direct regeneration, and material recovery by hydrometallurgical or pyrometallurgical processes are discussed. Throughout the review, the discussion is based around current available technologies, their environmental impacts, and economic feasibility as well as provided examples of pilot and industrial scale adoption of the processes., Competing Interests: The authors declare no conflict of interest., (© 2023 The Authors. Global Challenges published by Wiley‐VCH GmbH.)

Zero-emission hydrogen and oxygen production are critical for the UK to reach net-zero greenhouse gasses by 2050. Electrochemical techniques such as water splitting (electrolysis) coupled with renewables energy can provide a unique approach to achieving zero emissions. Many studies exploring electrocatalysts need to "electrically wire" to their material to measure their performance, which usually involves immobilization upon a solid electrode. We demonstrate that significant differences in the calculated onset potential for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) can be observed when using screen-printed electrodes (SPEs) of differing connection lengths which are immobilized with a range of electrocatalysts. This can lead to false improvements in the reported performance of different electrocatalysts and poor comparisons between the literature. Through the use of electrochemical impedance spectroscopy, uncompensated ohmic resistance can be overcome providing more accurate Tafel analysis., Competing Interests: There are no conflicts of interest to declare.

There is a controversial issue based on the particle cracking of the Ni-rich layered oxide cathode materials whether it occurs at the primary particles or the grain boundary. Herein, we found that the microcracking of NMC811 does not occur at single crystalline primary particles even abused at a severe upper cell voltage of 4.7 V having a lot of gas evolution since the single-crystal NMC811 has superior mechanical stability. The capacity retentions determined at 1C rate and a 100% state of charge (SOC) are 80% and 50% after 1000 cycles for single crystal and polycrystal NMC811, respectively.

Although the LiMn 2 O 4 cathode can provide high nominal cell voltage, high thermal stability, low toxicity, and good safety in Li-ion batteries, it still suffers from capacity fading caused by the combination of structural transformation and transition metal dissolution. Herein, a carbon-coated LiMn 2 O 4 cathode with core@shell structure (LMO@C) was therefore produced using a mechanofusion method. The LMO@C exhibits higher cycling stability as compared to the pristine LiMn 2 O 4 (P-LMO) due to its high conductivity reducing impedance growth and phase transition. The carbon shell can reduce direct contact between the electrolyte and the cathode reducing side reactions and Mn dissolution. Thus, the cylindrical cell of LMO@C//graphite provides higher capacity retention after 900 cycles at 1 C. The amount of dissoluted Mn for the LMO@C is almost 2 times lower than that of the P-LMO after 200 cycles. Moreover, the LMO@C shows smaller change in lattice parameter or phase transition than P-LMO, indicating to the suppression of λ-MnO 2 phase from the mixed phase of Li 1-δ Mn 2 O 4  + λ-MnO 2 when Li-delithiation at highly charged state leading to an improved cycling reversibility. This work provides both fundamental understanding and manufacturing scale demonstration for practical 18650 Li-ion batteries., (© 2022. The Author(s).)

The safety of Li-ion batteries is one of the most important factors, if not the most, determining their practical applications. We have found that free carbonate-based solvent molecules in the hybrid electrolyte system can cause severe safety concerns. Mixing ionic liquids with a carbonate-based solvent as the co-solvent at a fixed salt concentration of 1 M LiPF 6 can lead to free carbonate-based molecules causing poor charge storage performance and safety concerns.

The specific cell capacitance, equivalent series resistance (ESR) and equivalent distributed resistance (EDR) of porous carbon-based supercapacitors linearly depend on the cationic molecular length of room-temperature ionic liquids.