Rechargeable Research Articles

High Energy Conversion Efficiency and Cycle Durability of Solar-Powered Self-Sustaining Light-Assisted Rechargeable Zinc–Air Batteries System

The issue of energy supply in outdoor and remote areas has become a significant challenge. Solar-powered self-sustaining rechargeable zinc-air batteries (RZABs) offer a viable energy solution for off-grid regions. However, there has been no specific study on the technical compatibility and adaptability of the solar power generation system and RZABs system, as well as the efficiency of energy conversion and storage in such solar-powered RZABs systems. To address these challenges, this study developed a solar-powered self-sustaining photo-assisted RZABs system based on a photo-responsive polyterthiophene (pTTh) cathode. This system employs pTTh with photo-responsive properties as the cathode catalyst for RZABs, which not only significantly reduces the overpotential of the cathode but also enhances the performance of the RZABs and the overall energy conversion efficiency (reaching 16.2%). In practical applications, the system exhibits excellent stability, operating continuously within a wide temperature range of -15 to 40°C, and demonstrating a stable cycling operation capability of up to 33 days. It provides reliable, low-cost power support for electronic devices such as mobile phones, flashlights, GPS units, and small pollutant detection systems, greatly improving the practicality of these devices in off-grid areas.

Alkyl-Ether Group-Modified Anthraquinone-Based Negative Electrode for Enhanced Electrochemical Performance of All Solid-State Rechargeable Air Batteries

Alkyl-Ether Group-Modified Anthraquinone-Based Negative Electrode for Enhanced Electrochemical Performance of All Solid-State Rechargeable Air Batteries

Regulating the Zn electrode/electrolyte interface with lactose additive for high performance Zn anode

The practical utilization of rechargeable aqueous zinc metal batteries (AZMBs) has been constrained by the formation of zinc dendrites and other associated issues. This article introduces lactose, a compound rich in hydroxyl groups, as an electrolyte additive into the aqueous solution of the electrolyte with the objective of suppressing the harmful growth of zinc dendrites. The lactose additive, with its strong zincophilicity, robust intermolecular hydrogen bonding, and a large number of exposed high electronegativity hydroxyl groups, enables lactose to effectively modulate the electrode/electrolyte interface in a dynamic manner, thereby achieving the stability and reversibility of the zinc anode. The findings presented in this work demonstrate the uniform deposition and stripping of zinc in a 2 M ZnSO4 electrolyte with the addition of lactose, thereby enhancing the cycling performance of Zn||Zn batteries. The alteration of the zinc ion environment on the surface of the zinc electrode, in conjunction with the dynamic modulation of the Gouy-Chapman-Stern (GCS) layer by lactose, increases the nucleation overpotential, thereby facilitating to a uniform deposition morphology in lieu of the formation of large-scale dendrites. Furthermore, the formation of hydrogen bonds serves to prevent the occurrence of side reactions. These factors act in concert to enhance the electrochemical performance of AZMBs. The addition of lactose to the electrolyte has resulted in a significant enhancement in the Coulombic efficiency of the card-type Zn||Cu asymmetric battery, reaching 99.7 %. The biodegradability of lactose and the sustainability of its source make this research conducive to the development of environmentally friendly battery electrolyte additives.

Enhanced bifunctional electrocatalysis of Co5.47N nanocrystals in porous carbon nanofibers for high-efficiency zinc-air batteries

As a promising energy conversion and storage device, recently, rechargeable zinc-air batteries (ZABs) have developed rapidly, and the exploitation of excellent electrode catalysts to improve the energy efficiency and long-term performance of ZABs has become a focus of current research. Herein, the Co5.47N nanocrystals embedded in porous carbon nanofibers (Co5.47N PCNFs) were designed to act as a bifunctional electrocatalyst for the oxygen reduction reaction (ORR) and iodide oxidation reaction (IOR), which occur on the electrode in the charging-discharging process of ZABs. The electrochemistry results showed that the ORR activity of Co5.47N PCNFs is comparable to the commercial Pt/C electrocatalyst, and the IOR activity and stability are higher than those of the Pt/C electrocatalyst. Importantly, Co5.47N PCNFs electrocatalyst endows ZABs with a low charge–discharge voltage difference (0.49 V), a high round-trip energy efficiency (72.1 %), as well as a large specific capacity (791.5 mAh gZn−1), surpassing the performance of Pt/C electrocatalyst. Density functional theory calculation demonstrates that Co5.47N PCNFs have lower Gibbs free energy for the formation of IOR intermediate species, thereby displaying outstanding IOR catalytic performance compared to that of Pt/C electrocatalyst. These findings offer crucial insights into the rational design of cobalt nitride-based electrocatalysts for application in ZABs with high energy efficiency.

Selenic Acid Etching Assisted Atomic Engineering for Designing Metal-Semimetal Dual Single-Atom Catalysts for Enhanced CO2 Electroreduction.

Single-atom catalysts are promising for electrocatalytic CO2 conversion but face challenges in controllable syntheses. Herein, a facile selenic acid etching-assisted strategy has been developed to fabricate a hybrid metal-semimetal dual single-atom catalyst for electrocatalytic CO2 reduction. This strategy enables the simultaneous generation of monodisperse active sites and hierarchical morphologies with hollow nanostructures. The as-obtained catalyst with Fe-Se dual single-atom sites supported by porous nitrogen-doped carbon (FeSe-NC) shows exceptional catalytic activity and CO selectivity, delivering a Faradaic efficiency (FE) of >97% with industrially comparable jCO, superior to the Fe single-atom catalyst. Moreover, the FeSe-NC-based rechargeable Zn-CO2 battery delivers a high power density (2.01 mW cm-2) and outstanding FECO (>90%), as well as excellent cycling stability. Experimental results together with theoretical calculations reveal that the etching-induced defects and the Se-modulated Fe centers with asymmetrical polarized charge distributions synergistically facilitate the key intermediate *CO desorption and thus accelerate the CO2-to-CO conversion.

Polymer Electrolytes with High Ionic Conductivities at Freezing Temperature for Aqueous Hybrid Batteries.

Rechargeable and flexible aqueous batteries (ABs) have emerged as one of promising energy devices which is primarily due to the safety, environmental friendliness and economic efficiency. However, because of the freezing behavior of aqueous electrolytes, most ABs possess poor performance when the working temperature drops below zero. To solve this problem, a gel polymer electrolyte (GPE) with high ionic conductivity (IC) and frost-resistance is designed for aqueous Zn-Li hybrid batteries by a biomass-based polymers complex consisting of carboxyl modified sodium alginate (SA) and zwitterionic betaine (BA). Introducing iminodiacetic acid to enrich -COOH groups along the SA main chains could improve IC of the prepared GPEs to 41.27 and 20.96 mS cm-1 at 20 and -20 oC, respectively. At -20 oC, the discharge capacity of the resultant cell is two times higher than that of the liquid electrolyte-based cell, and the cell presents a capacity retention of 91.6% after 300 charge/discharge cycles at 1 C. This proposed strategy greatly improve the IC of GPEs at freezing temperature, which is expected to broaden the practical application of GPEs in wide range of temperature.

Synergetic bifunctional Cu-In alloy interface enables Ah-level Zn metal pouch cells

Rechargeable aqueous zinc-metal batteries, considered as the possible post-lithium-ion battery technology for large-scale energy storage, face severe challenges such as dendrite growth and hydrogen evolution side reaction (HER) on Zn negative electrode. Herein, a three-dimensional Cu-In alloy interface is developed through a facile potential co-replacement route to realize uniform Zn nucleation and HER anticatalytic effect simultaneously. Both theoretical calculations and experimental results demonstrate that this bifunctional Cu-In alloy interface inherits the merits of low Zn-nucleation overpotential and high HER overpotential from individual copper and indium constituents, respectively. Moreover, the dynamical self-reconstruction during cycling leads to an HER-anticatalytic and zincophilic gradient hierarchical structure, enabling highly reversible Zn chemistry with dendrite-free Zn (002) deposition and inhibited HER. Moreover, the improved interface stability featured by negligible pH fluctuations in the diffusion layer and suppressed by-product formation is evidenced by in-situ scanning probe technology, Raman spectroscopy, and electrochemical gas chromatography. Consequently, the lifespan of the CuIn@Zn symmetric cell is extended to more than one year with a voltage hysteresis of 6 mV. Importantly, the CuIn@Zn negative electrode is also successfully coupled with high-loading iodine positive electrode to fabricate Ah-level (1.1 Ah) laminated pouch cell, which exhibits a capacity retention of 67.9% after 1700 cycles.

Modifying d–p orbital hybridization of Ni/Fe[sbnd]O species by high-valence ruthenium doping to enhance oxygen evolution performance

The electron distribution of catalysts can be modulated by high-valence metal doping, thus enhancing the intrinsic activity. Herein, we adopt Ru modification to adjust the d–p orbital hybridization of Ni-Fe oxyhydroxides, significantly increasing the oxygen evolution reaction (OER) activity. The amorphous NiFe0.5Ru0.1OxHy catalyst synthesized by sol–gel method exhibits excellent OER activity, far superior to commercial RuO2. In situ Raman and XPS results confirm that the NiOOH/FeOOH active species gradually form with increasing applied voltage. Density functional theory (DFT) calculations reveal that high-valence Ru dopants can effectively regulate the hybridization of d–p orbital of Ni/FeO, significantly increase the electron density around Fermi level, promote charge transfer, make them have more anti-bonding orbitals, enhance the binding ability of active sites to intermediates, reduce the reaction energy barrier of the rate-determining step (H2O → *OH), and thus improve the OER activity. In addition, NiFeRuOxHy as a cathode catalyst in a rechargeable zinc-air battery shows an outstanding cycle life of 600 h. This study provides a promising hybrid orbital method for designing high-performance OER catalysts for water splitting and rechargeable zinc-air batteries.

Cutting-Edge Energy Storage System and Battery Management Technology

Cutting-Edge Energy Storage System and Battery Management Technology

Optimal scheduling of smart home appliances with a stochastic power outage: a two-stage stochastic programming approach

This study primarily concentrates on enhancing the scheduling of electric appliances within a smart home equipped with a photovoltaic solar array and a storage battery capable of redistributing excess electricity to the grid. Furthermore, the investigation takes into consideration the unpredictability of a power outage, analyzing the scheduling of these appliances to minimize consumer electricity expenses. To tackle this issue, a two-stage stochastic programming methodology is developed to effectively model the uncertainty surrounding both the onset time and duration of power outages. Additionally, a sample average approximation algorithm (SAA) is devised to efficiently address the problem. Through extensive computational experiments, the outcomes demonstrate that the SAA yields shorter CPU processing times, albeit without guaranteeing optimal solutions. The total average percent deviation of the SAA's upper bound from its lower bound and the optimal solution stands at 4.16% and 4.5%, respectively. Moreover, it is demonstrated that utilizing the stochastic approach, as opposed to the deterministic one, can enhance solution quality by 6.2%. Furthermore, a comprehensive sensitivity analysis is provided, focusing on probability distribution functions of outage start time and duration, alongside an analysis of the solar panel and battery storage capacities. It is revealed that when adopting a Normal distribution instead of a Uniform distribution, the performance of the SAA experiences a slight decline.

Vulvar lichen sclerosus in girls and adult females: A single-center retrospective study of 744 patients in China.

Vulvar lichen sclerosus (VLS) is a chronic, inflammatory disease which is accompanied by itching and pain, affecting the patient's daily life and sexual activity. However, the disease characteristics of children and adults are not completely the same. Currently, there are few studies in China that compare the characteristics of VLS between girls and adult female patients. The aim of this study was to compare the epidemiology, clinical features, and combined autoimmune diseases of VLS patients between girls and adult females, and to help clinicians better understand VLS in different age groups. We enrolled 744 female patients for analysis, divided by age into a child group (<18 years) and an adult group (≥18 years). Among girl patients, 94.6% had preadolescent onset, while among adult female patients, only 4.6% had preadolescent onset, which was a statistically significant difference. The highest percentage of adult female patients had onset during their child-bearing period (75.4%), while 20% had postmenopausal onset, with a significant difference when the three onset states were compared. White patches were equally common in both girl and adult female patients' external genital area, while mossy lesions and labia minora atrophy were more common in adult female patients. Involvement of the clitoris, labia minora, and vaginal opening area were more common in adult patients. The perianal area was more commonly involved in girl patients. We found eight cases (1.2%) of secondary squamous cell carcinoma in adult female patients. We also found that 13 patients had concurrent lichen sclerosus lesions on the vulva and extragenital region, including two girls and 11 adult females. Extragenital lichen sclerosus (EGLS) occurred mostly in the torso. Clinicians should be aware of these differences so that early diagnosis and treatment of the disease can be achieved, to avoid irreversible anatomical alterations and the risk of cancer.

Dramatic enhancement in lithium-ion battery capacity through synergistic effects of electronic transitions in light-assisted organic coordination cathode material Co(bpy)(dhbq)2

Integration of photoactive and lithium storing units into a single cathode endows it with notable capacity in the presence of suitable light. However, the interfacial effect between the two materials causes significant loss of photogenerated electrons during their transfer which is one of the biggest obstacles in the development of current photo-assisted rechargeable batteries. In this paper, a bifunctional cobalt-coordinated organic cathode is fabricated by combining 2,2′-bpy and DHBQ via Co by adopting the spin evaporation technique. It optimizes the pristine interfaces of photoactive and lithium storage units into a photoactive unit-metal interface and a metal-lithium storage unit interface through application of Co. In the presence of light, Co causes a strong metal-ligand charge transfer. Meanwhile, ligand-ligand charge transfer also takes place between the multi-ligands. The synergistic effect of these two phenomena offers a discharge capacity of 387 mAh g -1 which is significantly higher than that of 316 mAh g -1 recorded in the absence of light. The demonstrated design of bifunctional metal-ligand cathode by incorporation of photoactive ligands into lithium storage ligands through applications of metal centers can open the pathways for establishing a new type of photo-assisted lithium-ion batteries with higher efficiency and lower cost.

Advanced Carbon Sphere-Based Hybrid Materials Produced by Innovative Aerosol Process for High-Efficiency Rechargeable Batteries

Advanced Carbon Sphere-Based Hybrid Materials Produced by Innovative Aerosol Process for High-Efficiency Rechargeable Batteries

Emerging trends and innovations in all-solid-state lithium batteries: A comprehensive review

All-solid-state lithium batteries, which utilize solid electrolytes, are regarded as the next generation of energy storage devices. Recent breakthroughs in this type of rechargeable battery have significantly accelerated their path towards becoming commercially viable. Nevertheless, the development of such devices is impeded by various obstacles, including limitations in ion transfer capability, interfacial hurdles, and chemical and electrochemical stability. This paper provides a comprehensive review of the latest advancements in all-solid-state lithium-based batteries. The main emphasis is on the fabrication techniques, novel solid electrolytes, and the application of advanced cathode and anode materials to expedite research and development in this field. Moreover, the feasibility of large-scale manufacturing of solid-state batteries has been evaluated. Finally, the most practical and effective approaches for the advancement of these batteries have been proposed and examined.

The cobalt and nickel enrichment in base metal sulfides from the Xiarihamu Cu-Ni-Co deposit, China: Constrained by in-situ mineral geochemistry of sulfides

Rapidly growing demand for cobalt and nickel in rechargeable battery industry promotes research on metallogenic theory of magmatic Cu-Ni-Co sulfide deposits. Xiarihamu Cu-Ni-Co deposit, one of the lately discovered Co-rich magmatic sulfide deposits in China, is typical of distribution in orogenic belts, rather than in divergent tectonic settings as many deposits of the same type. In-situ elemental and sulfur isotopic analyses of base metal sulfides (BMS; pyrrhotite, pentlandite, and chalcopyrite) from Xiarihamu were conducted in this study. The strongly negative correlation between Fe and Co + Ni reveals the major occurrence of Co and Ni as isomorphism states in pentlandite and pyrrhotite. The δ34S values of pentlandite and pyrrhotite generally increase with Co contents and Co/Ni ratios, indicating that the Co enrichment within BMS accompanied with enhanced contamination of crustal sulfur. Zinc, Cd, Sb, and Te are significantly and preferentially fractionated into intermediate sulfide solution (ISS) from which chalcopyrite exsolved. The Se contents and Se/S ratios of pentlandite and pyrrhotite in lherzolite/harzburgite are much higher than those of BMS from gabbro, which has systematically higher δ34S values. Combined with the partially overlapped Sb/Se and As/Se ratios of BMS from lherzolite and gabbro, as well as similar calculated R factors of ore-hosting peridotite and gabbro, it is proposed that the studied Xiarihamu gabbro was crystallized from a separate pulse of Co-Ni-enriched, Se-depleted and intensively contaminated mafic parent magma, rather than evolved from ultramafic magma through crystallization fractionation. The lack of olivine and spinel in gabbro also promoted more Co and Ni into sulfide liquid. Based on Se/Te ratios, the pentlandite and pyrrhotite from drill core XH1E01S was originated from sulfide liquid, which suffered higher degree of crystallization fractionation of monosulfide solution (MSS). While pentlandite and pyrrhotite that crystallized from less evolved parent sulfide liquid bear less cobalt, such as those collected from drill core XH1109. This study strengthens the potential importance of crustal contamination and crystallization fractionation of MSS from sulfide liquid during Co enrichment within BMS (pentlandite and pyrrhotite).

Optimised scheduling of a cogenerative subnetwork based on a micro gas turbine and thermal storage with the addition of an innovative solar assisted heat pump and Ni-Zn battery

The Innovative Energy Systems (IES) laboratory at the University of Genoa features a plant configuration comprising a micro gas turbine, latent heat thermal energy storage, an innovative heat pump system connected to solar façade panels, and a NiZn battery. This study presents the optimization of four distinct sub-plant configurations, focusing on their economic and environmental performance across different seasons (January, April, July, and October) under two market scenarios (no selling price or selling price equal to buying price). A genetic algorithm-based tool is developed for the optimized energy scheduling of these configurations, taking into account the operational characteristics of programmable, non-programmable energy sources and energy storage devices. The analysis highlighted that when the selling price is equal to zero, the system is optimised to improve sell-consumption. The addition of the battery or the heat pump to the system always lead to reduction of operational costs compared to the baseline case with only the micro gas turbine and thermal energy storage. Notably, the heat pump alone provides greater cost benefits than the battery, although the combined use of both systems yields the highest cost reductions ranging, depending on the month, up to −16.9% in the “no selling” scenario and up to −12.3% when selling and buying prices are equal. Regarding the CO2 emissions, both components lead to an emission reduction in the “no selling scenario” while only the HP guarantees an emission reduction during the “selling equal to buying” scenario, in both cases up to −20.5% less. This analysis highlights the economic and environmental advantages of integrating NiZn battery storage and a solar-assisted heat pump into the energy system, demonstrating cost savings and emission reductions across various market conditions and seasonal demands.

Optimizing Interface Chemistry with Novel Covalent Molecule for Highly Sustainable and Kinetics-Enhanced Sodium Metal Batteries

Metallic sodium has attracted increasing attention as an ideal anode material for next-generation high energy density and low-cost secondary batteries. However, it is highly desired yet remains challenging to improve their cycling stability and safety due to unstable solid electrolyte interphase and dendrite growth. Herein, a hybrid interface layer composed of Na2Se and Na3P is constructed on the surface of Na (Na@NPS) via in situ spontaneous reaction. The hybrid interface layer with merits of high sodiophilicity and high Na-ion conductivity can effectively induce homogeneous Na-ion flux distribution, accelerate the reaction kinetics and suppress decomposition of electrolyte components. Benefitting from the above advantages, the Na@NPS symmetric cell delivers a long cycle life (1000 h at 1 mA cm–2 and 1 mAh cm–2). Furthermore, the full cell coupling with Na3V2(PO4)3-based cathode provides an exceptionally long lifespan (1500 cycles) at 20 C with a capacity retention of 98.2% and high energy density (226 Wh kg–1). Therefore, the enhanced electrochemical performance illustrates the feasibility of the covalent molecule derived hybrid multifunctional interfaces in solving the irregular deposition of Na-ion and expediting reaction kinetics in Na metal batteries.

The Complex and Spatially Heterogeneous Nature of Degradation in Heavily Cycled Li-ion Cells

As service lifetimes of electric vehicle (EV) and grid storage batteries continually improve, it has become increasingly important to understand how cells perform after extensive cycling. The multifaceted nature of degradation in Li-ion cells can lead to complex behavior that may be difficult for battery management systems or operators to model. Accurate characterization of heavily cycled cells is critical for developing accurate models, especially for cycle-intensive applications like second-life grid storage or vehicle-to-grid charging. In this study, we use operando synchrotron x-ray diffraction (SR-XRD) to characterize a commercially manufactured polycrystalline NMC622 pouch cell that was cycled for more than 2.5 years. Using spatially resolved synchrotron XRD, the complex kinetics and spatially heterogeneous behavior of such cells are mapped and characterized under both near-equilibrium and non-equilibrium conditions. The resulting data is complex and multifaceted, requiring a different approach to analysis and modelling than what has been used in the literature. To show how material selection can impact the extent of degradation, we compare the results from polycrystalline NMC622 cells to an extensively cycled single-crystal NMC532 cell with over 20,000 cycles—equivalent to a total EV traveled distance of approximately 8 million km (5 million miles) over six years.

Capacity planning of storage batteries for remote island microgrids with physical energy storage with CO2 phase changes

Energy storage devices based on the CO2 thermal cycle (CTC) lose competitiveness in cold regions because of the decreased energy volume density and charge–discharge efficiency at low ambient temperatures. The CO2 hybrid thermal cycle (CHS) combines the CTC with the CO2 hydrate thermal cycle (CHT) to maintain a high energy volume density and charge–discharge efficiency regardless of the ambient temperature. The CHS-based energy storage system has been shown to have an energy volume density of 80–140 kWh/m3 and charge–discharge efficiency of 60 %–106 %. However, the economic feasibility of this system has not been considered. In this study, a numerical analysis was performed on the practical application and economic feasibility of CHS-based energy storage for the 100 % renewable energy microgrid of a pair of remote islands. In a case analysis of CHS installation in a microgrid for a remote island with 100 % renewable energy, the construction cost of CHS was 2/3 of that of pumped storage; the equipment cost reduction of CHS strongly depends on the type and amount of renewable energy to be interconnected, and therefore, the overall optimization of the power system is necessary.

La1−xSrxF3−x: A Solid-State Electrolyte for Fluoride Ion Battery with High Ionic Conductivity and Wide Electrochemical Potential Window

Fluoride ion conductors are developed for use as solid-state electrolytes in fluoride ion batteries which are one of promising candidates for next-generation storage batteries. Ba-doped LaF3 (La0.9Ba0.1F2.9: LBF) is mainly used as a solid-state electrolyte in fluoride ion batteries. However, room temperature conductivity of LBF is considerably low, on the order of 10−6 S cm−1 and it is still unclear the optimal elements to be doped to LaF3. In this study, we have explored La0.9Sr x Ba0.1−x F2.9 system (x = 0, 0.01, 0.025, 0.05, 0.1), in which Ba in LBF is substituted for Sr and investigated the composition dependence of ionic conductivity. We elucidate that the higher concentration of Sr without Ba can significantly improve the ionic conductivity, and the maximum ionic conductivity of La0.9Sr0.1F2.9 is 1.5 × 10−5 S cm−1 at room temperature, which is one order of magnitude larger than that of LBF. The higher ionic conductivity of LSF is due to the larger grain size and higher sintering density of LSF compared to LBF, which results in lower grain boundary resistance. The LSF total ionic conductivity of 10−4 S cm−1 can be achieved at 350 K, which significantly lowers operating temperature of fluoride ion batteries down to 350 K.