Electrochemical Energy Storage Technologies Research Articles

NANOCARBONS-BASED TRIFUNCTIONAL ELECTROCATALYSTS FOR OVERALL WATER SPLITTING AND METAL-AIR BATTERIES: - METAL-FREE AND HYBRID ELECTROCATALYSTS.

Trifunctional electrocatalysts, an exciting class of materials that can simultaneously catalyze hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR), can significantly enhance the performance and economic viability of electrochemical energy storage and conversion technologies such as water-splitting electrolyzers, metal-air batteries, fuel cells and their integrated devices. Such multifunctional electrocatalysts encompass multiple active sites that can simultaneously catalyze two or more different electrochemical reactions and are feasible routes for addressing global energy and environmental challenges. This review accounts for nanocarbons-based trifunctional electrocatalysts reported for electrolyzers, metal-air batteries and integrated electrolyzer-battery systems, providing a practical perspective. Metal-free and hybrid (hybrids of nanocarbons and transition metals/compounds) trifunctional electrocatalysts are covered. Given the growing importance of green technologies, we discuss biomass-derived carbon-based trifunctional electrocatalysts separately. The collective information provided in the review could help researchers derive more effective and durable trifunctional electrocatalysts suitable for commercial use.

Sodium layered oxide cathodes: properties, practicality and prospects.

Rechargeable sodium-ion batteries (SIBs) have emerged as an advanced electrochemical energy storage technology with potential to alleviate the dependence on lithium resources. Similar to Li-ion batteries, the cathode materials play a decisive role in the cost and energy output of SIBs. Among various cathode materials, Na layered transition-metal (TM) oxides have become an appealing choice owing to their facile synthesis, high Na storage capacity/voltage that are suitable for use in high-energy SIBs, and high adaptivity to the large-scale manufacture of Li layered oxide analogues. However, going from the lab to the market, the practical use of Na layered oxide cathodes is limited by the ambiguous understanding of the fundamental structure-performance correlation of cathode materials and lack of customized material design strategies to meet the diverse demands in practical storage applications. In this review, we attempt to clarify the fundamental misunderstandings by elaborating the correlations between the electron configuration of the critical capacity-contributing elements (e.g., TM cations and oxygen anion) in oxides and their influence on the Na (de)intercalation (electro)chemistry and storage properties of the cathode. Subsequently, we discuss the issues that hinder the practical use of layered oxide cathodes, their origins and the corresponding strategies to address their issues and accelerate the target-oriented research and development of cathode materials. Finally, we discuss several new Na layered cathode materials that show prospects for next-generation SIBs, including layered oxides with anion redox and high entropy and highlight the use of layered oxides as cathodes for solid-state SIBs with higher energy and safety. In summary, we aim to offer insights into the rational design of high-performance Na layered oxide cathode materials towards the practical realization of sustainable electrochemical energy storage at a low cost.

Interfacial regulation engineering in anode‐free rechargeable batteries

AbstractAnode‐free rechargeable batteries (AFRBs), equipped with bare collectors at the anode, are potential electrochemical energy storage technology attributed to their simplified cell configuration, high energy density, and cost reduction. Nevertheless, issues including insufficient Coulombic efficiency as well as the formation of the dendrites restrict their practical implementation. In recent years, various strategies have been proposed to overcome the critical issues of AFRBs. Among which, interfacial properties play key roles for achieving high stable AFRBs. In this review, an overview of AFRBs is discussed in the first part. Then, the main strategies based on interfacial regulation engineering toward high‐performance AFRBs are summarized including designing of current collectors, introducing of surface coating layers, modification of electrolytes, separators engineering, cathode materials regulation, and so forth. In addition, some future perspectives for developing AFRBs are proposed. This review will create new avenues on constructing stable AFRBs for advanced energy storage devices.

Mesophase pitch-derived porous carbon constructed by template/activation synchronous pore-forming technology for electrochemical energy storage

Porous carbon materials with high specific surface area and wide pore size distribution play a crucial role in the energy storage process. In this paper, a mixed sol-gel system of carbon source, chemical activator and salt template agent was constructed using raw pitch, o-xylene soluble substance and their mesophase as carbon source, NaCl as template agent and KOH as activator. After one step process of high temperature treatment, porous carbon materials with high specific surface area (SBET 1969 m2/g) and wide nanopore distribution (0.4–6 nm) were obtained. The electrochemical properties of the prepared mesophase porous carbon materials were tested. At a charge-discharge rate of 80 mA/g, a specific capacitance of 102.5 F/g can be achieved for porous carbon materials obtained from the o-xylene soluble mesophase, indicating the feasibility of preparing porous carbon electrode materials by o-xylene soluble mesophase. The development of template/activation synchronous pore-forming technology can integrate the advantages of the two kinds of pore-forming technologies, reduce the demand for pore size control in porous carbon materials, and promote the one-step realization of porous carbon materials with high specific surface area, wide pore size distribution and controllable pore size.

Design of Multifunctional Electrocatalysts for ORR/OER/HER/HOR: Janus Makes Difference.

Multifunctional electrocatalysts for hydrogen evolution reaction (HER), hydrogen oxidation reaction (HOR), oxygen evolution reaction (OER), and oxygen reduction reaction (ORR) have broad application prospects; However, realization of such kinds of materials remain difficulties because it requires the materials to have not only unique electronic properties, but multiple active centers to deal with different reactions. Here, employing density functional theory (DFT) computations, it is demonstrated that by decorating the Janus-type 2D transition metal dichalcogenide (TMD) of TaSSe with the single atoms, the materials can achieve multifunctionality to catalyze the ORR/OER/HER/HOR. Out of sixteen catalytic systems, Pt-VS (i.e., Pt atom embedded in the sulfur vacancy), Pd-VSe, and Pt-VSe@TaSSe are promising multifunctional catalysts with superior stability. Among them, the Pt-VS@TaSSe catalyst exhibits the highest activity with theoretical overpotentials ηORR = 0.40V, ηOER = 0.39V, and ηHER/HOR = 0.07V, respectively, better than the traditional Pt (111), IrO2 (110). The interplays between the catalyst and the reaction intermediate over the course of the reaction are then systematically investigated. Generally, this study presents a viable approach for the design and development of advanced multifunctional electrocatalysts. It enriches the application of Janus, a new 2D material, in electrochemical energy storage and conversion technology.

Tailoring the Size of Reduced Graphene Oxide Sheets to Fabricate Silicon Composite Anodes for Lithium-Ion Batteries.

The integration of a silicon (Si) anode into lithium-ion batteries (LIBs) holds great promise for energy storage, but challenges arise from unstable electrochemical reactions and volume changes during cycling. This study investigates the influence of reduced graphene oxide (rGO) size on the performance of rGO-protected Si composite (Si@rGO) anodes. Two sizes of graphene oxide (GO(L) and GO(S)) are used to synthesize Si@rGO composites with a core-shell structure by spray drying and thermal reduction. Electrochemical evaluations show the advantages of the Si@rGO(S) anode with improved cycle life and cycling efficiency over Si@rGO(L) and pure Si. The Si@rGO(S) anode facilitates the formation of a stable LiF-rich solid electrolyte interface (SEI) after cycling, ensuring enhanced capacity retention and swelling control. Rate capability tests also demonstrate the superior high-power performance of Si@rGO(S) with low and stable resistances in Si@rGO(S) over extended cycles. This study provides critical insights into the tailoring of graphene-protected Si composites, highlighting the critical role of rGO size in shaping structural and electrochemical properties. The Si material wrapped by graphene with an optimal lateral size of graphene emerges as a promising candidate for high-performance LIB anodes, thereby advancing electrochemical energy storage technologies.

Scanning Electrochemical Microscopy Meets Optical Microscopy: Probing the Local Paths of Charge Transfer Operando in Booster-Microparticles for Flow Batteries.

Understanding the oxidation/reduction dynamics of secondary microparticles formed from agglomerated nanoscale primary particles is crucial for advancing electrochemical energy storage technologies. In this study, the behavior of individual copper hexacyanoferrate (CuHCF) microparticles is explored at both global and local scales combining scanning electrochemical microscopy (SECM), for electrochemical interrogation of a single, but global-scale microparticle, and optical microscopy monitoring to obtain a higher resolution dynamic image of the local electrochemistry within the same particle. Chronoamperometric experiments unveil a multistep oxidation/reduction process with varying dynamics. On the one hand, the global SECM analysis enables quantifying the charge transfer as well as its dynamics at the single microparticle level during the oxidation/reduction cycles by a redox mediator in solution. These conditions allow mimicking the charge storage processes in these particles when they are used as solid boosters in redox flow batteries. On the other hand, optical imaging with sub-particle resolution allows the mapping of local conversion rates and state-of-charge within individual CuHCF particles. These maps reveal that regions of different material loadings exhibit varying charge storage capacities and conversion rates. The findings highlight the significance of porous nanostructures and provide valuable insights for designing more efficient energy storage materials.

Design Strategies for Anti‐Freeze Electrolytes in Aqueous Energy Storage Devices at Low Temperatures

AbstractWith the continuous development of electrochemical energy storage technology, especially in the current pursuit of environmental sustainability and safety, aqueous energy storage devices, due to their high safety, environmental friendliness, and cost‐effectiveness, are becoming an important direction of development in the field of energy storage. Diverse application scenarios require that energy storage systems be capable of continuous power supply under low temperature conditions. However, conventional aqueous electrolytes freeze at extremely low temperatures, causing limited ion transport and slow reaction kinetics, degrading the performance of the energy storage system. The design of low‐temperature anti‐freeze aqueous electrolytes has become an effective way to address this issue. In this review, the deep connection between hydrogen bonds (HBs) interactions in aqueous electrolytes and the liquid‐to‐solid conversion process, and the fundamental principles of the anti‐freeze mechanism is first explored. Subsequently, a systematic categorization and discussion of the design strategies for low‐temperature anti‐freeze aqueous electrolytes are conducted. Finally, potential directions are proposed. This review aims to provide comprehensive scientific guidance and technical reference for the development of anti‐freeze aqueous electrolytes with excellent low‐temperature performance, thereby promoting the application and innovation of aqueous energy storage devices in low‐temperature environments.

Development of Electrolytes under Lean Condition in Lithium-Sulfur Batteries.

Lithium-sulfur (Li-S) batteries stand out as one of the promising candidates for next-generation electrochemical energy storage technologies. A key requirement to realize high-specific-energy Li-S batteries is to implement low amount of electrolyte, often characterized by the electrolyte/sulfur (E/S) ratio. Low E/S ratio aggravates the known challenges for Li-S batteries and introduces new ones originated from the high concentration of polysulfides in limited electrolyte reservoir. In this review, the connections between the fundamental properties of electrolytes and the electrochemical/chemical reactions in Li-S batteries under lean electrolyte condition are elucidated. The emphasis is on how the solvating properties of the electrolyte affect the fate of polysulfides. Built upon the mechanistic analysis, different strategies to design lean electrolytes to improve the overall process of Li-S reactions and Li anode protection are discussed.

Electrochemistry of 2D-materials for the remediation of environmental pollutants and alternative energy storage/conversion materials and devices, a comprehensive review

This review article explores into the complicated relationship between electrochemistry and 2D materials, exploring their mutual influences and the consequential advancements in energy conversion, storage, and environmental applications. Electrochemical reactions, manifested through oxidations and reductions at submerged electrodes, form the linchpin connecting the electrochemistry of 2D materials with their practical utility. Various electrochemical cell topologies are investigated for their role in enhancing material flexibility, operational states, energy conversion efficiency, and device design adaptability. The comprehensive discussion extends to diverse applications, emphasizing the pivotal roles of 2D materials in environmental remediation, alternate energy storage and conversion, and chemical reactivity. Noteworthy applications include pollutant detection, adsorption and absorption of pollutants, elimination of both organic and inorganic pollutants, and photocatalytic degradation. The review also addresses materials synthesis via electrochemical processes, detailing functionalization, handling, and deposition techniques. Particular focus is directed towards local electrochemical techniques enabling the analysis and local alteration of 2D materials. Moreover, this paper concludes the article published in the recent years with this topic and most significant trends observed in 2022 and 2023 with electrochemistry of materials for the remediation of environmental pollutants. While the trends of article publishing increased from 2020 to 2023 with topic alternative energy storage/conversion materials. Finally, offering a comprehensive overview of the synergistic relationship between electrochemistry and 2D materials and their transformative potential in sustainable technologies. Broader contextThe decreasing availability of energy resources and the contamination of the environment are two significant worldwide concerns that need immediate attention. The focus on 2D materials and associated technologies is important for the efficient conversion of solar energy into chemical energy. These materials have diverse applications in fields such as energy (e.g., water splitting), synthesis (e.g., production of valuable chemicals and N2 reduction), and the environment (e.g., CO2 reduction and environmental remediation). Furthermore, Electrochemical energy storage and conversion (EESC) technologies are widely acknowledged as the most viable solutions to address the escalating energy crisis and environmental degradation because to their exceptional energy efficiency and little environmental footprint. Currently, there have been several reports discussing the use of 2D-materials in energy applications and wastewater treatment. However, there is a lack of comprehensive reviews that summarize the electrochemistry of 2D-materials, their preparation strategies, modification techniques, and related properties. Furthermore, there is a need for detailed analysis of the progress in applying 2D-materials for environmental pollution remediation, electrocatalytic performance, energy storage, and conversion technologies and devices. In this paper, we systematically and comprehensively review the electrochemistry of 2D-materials and innovatively analyze the design principles and difficulties of 2D-materials. We discussed comprehensively the remediation of environmental pollutants through 2D-materials in water treatment fields such as photocatylsts, adsorption/absorption and dyes removal as an entry point and provide an in-depth knowledge and outlook on the current status and development potential of specific applications of energy storage and conversion materials and devices.

Dual-Function Electrolyte Additive Design for Long Life Alkaline Zinc Flow Batteries.

Alkaline zinc-based flow batteries (AZFBs) have emerged as a promising electrochemical energy storage technology owing to Zn abundance, high safety, and low cost. However, zinc dendrite growth and the formation of dead zinc greatly impede the development of AZFBs. Herein, a dual-function electrolyte additive strategy is proposed to regulate zinc nucleation and mitigate the hydroxide corrosion of zinc depositions for stable AZFBs. This strategy, as exemplified by urea, introduces an electrolyte additive to coordinate with Zn2+/Zn with proper strength, slowing zinc deposition kinetics to induce uniform nucleation and protecting the deposited zinc surface from attack by hydroxide ions through preferable adsorption. The zincate complexes with urea are identified to be Zn(OH)2(urea)(H2O)2 and Zn2(OH)4(H2O)4(urea), which exhibit slow zinc deposition kinetics, allowing instantaneous nucleation. Calculation results reveal an additional energy barrier of 1.29eV for the subsequent adsorption of an OH- group when a urea molecule absorbs on the zinc cluster, significantly mitigating the formation of dead zinc. Consequently, prolonged cell cycling of the prototype alkaline zinc-iron flow battery demonstrates stable operation for over 130 h and an average coulombic efficiency of 98.5%. It is anticipated that this electrolyte additive strategy will pave the way for developing highly stable AZFBs.

Cellulose nanofiber enabled high-mass loading N-doped porous carbon electrode for zinc-ion supercapacitors

Zinc-ion hybrid supercapacitors (ZHSCs) are among the most promising electrochemical energy storage technologies because of their high energy density, environmental sustainability, low price, and inherent security. High-load, high-capacity cathodes are critical for the practical application of ZHSCs. However, it is challenging to achieve optimal performance of high-loading electrodes due to slow reaction kinetics, retarded ion transport, and structural instability. Herein, a salt-template technique was used to fabricate nitrogen-doped porous carbon (NPC) with large surface area, abundant mesopores, and electroactive nitrogen dopants. When combined with a fibrous network scaffold of carbon nanotubes and cellulose nanofibers (CNT/CNF), the optimized NPC delivered an outstanding specific capacitance of 133.4 mAh g−1 and a remarkable capacity retention of 95.4% after 10,000 cycles. More impressively, we achieved a cathode with high mass-loading of 10 mg cm−2 without significantly sacrificing the electrochemical performance (area capacity of 2.05 mAh cm−2 and good cycling stability with capacity retention of 86.2% after 3000 cycles). The excellent performance can be attributed to the continuous electron/ion conduction pathways of CNT/CNF scaffold and redox-active surface generated by the favorable heteroatom-doped porous carbon. In sum, this work offers a platform for making high mass-loading carbon electrodes for practical ZHSCs.

Unveiling the Potential of Covalent Organic Frameworks for Energy Storage: Developments, Challenges, and Future Prospects

AbstractCovalent organic frameworks (COFs) are porous structures emerging as promising electrode materials due to their high structural diversity, controlled and wide pore network, and amenability to chemical modifications. COFs are solely composed of periodically arranged organic molecules, resulting in lightweight materials. Their inherent properties, such as extended surface area and diverse framework topologies, along with their high proclivity to chemical modification, have positioned COFs as sophisticated materials in the realm of electrochemical energy storage (EES). The modular structure of COFs facilitates the integration of key functions such as redox‐active moieties, fast charge diffusion channels, composite formation with conductive counterparts, and highly porous network for accommodating charged energy carriers, which can significantly enhance their electrochemical performance. However, ascribing intricate porosity and redox‐active functionalities to a single COF structure, while maintaining long‐term electrochemical stability, is challenging. Efforts to overcome these hurdles embrace strategies such as the implementation of reversible linkages for structural flexibility, stimuli‐responsive functionalities, and incorporating chemical groups to promote the formation of COF heterostructures. This review focuses on the recent progress of COFs in EES devices, such as batteries and supercapacitors, through a meticulous exploration of the latest strategies aimed at optimizing COFs as advanced electrodes in future EES technologies.

Boehmite-PVDF-CTFE/F-PI composite separator irradiated by electron beam for high-rate lithium-ion batteries

As an important part of the fields such as renewable energy and electric vehicles, electrochemical energy storage technology faces significant challenges in improving energy density, extending battery life and improving safety. We successfully prepared a composite battery separator of polyvinylidene fluoride-chlorotrifluorinylene (PVDF-CTFE) and fluorinated polyimide (F-PI) -based materials, mixed it with different contents of boehmite nanoparticles, and then modified it by different doses of electron beam irradiation to improve the performance, especially to overcome the problem of maintaining capacity decline in high-speed charging environment. The results showed that the prepared battery separators exhibited outstanding thermal stability, electrochemical properties and ionic conductivity with 12 % boehmite nanoparticles. After 1000 high-speed charge and discharge cycles in current density of 10C, the battery based on the modified separator still maintained a capacity retention rate of 84.4 %, with the initial discharge specific capacity of 111.9 mAhg−1. This means that irradiated separators not only maintain a high energy density in a high-speed charging environment, but also overcome the problem of maintaining capacity decline. Electron beam irradiation further improved the comprehensive performance of the separator. After 1000 and 1500 cycles at the current density of 10C and 15C, the specific discharge capacity of the battery can still retain more than 90 % and 80 % of the initial specific discharge capacity, which provides a longer life in practical applications.

Mixed biomass-derived multi-heteroatom doped carbon-decorated Mn3O4 for a high-performance asymmetric all solid-state supercapacitor

Recently, the development of non-conventional electrochemical energy storage technologies has attracted great attention. Herein, in accordance with green strategies for the producing renewable energy storage systems, eco-friendly electrode was successfully produced from mixed biomass precursors through carbonization and activation processes. Obtained electrode (MB-AC) as a negative and its composite (Mn3O4@MB-AC) as positive electrodes were exhibited excellent electrochemical performance with high specific capacitance of 716.49 Fg−1 at 0.75 Ag−1 and 848.21 Fg−1 at 1.0 Ag−1 respectively, in 3 M KOH electrolyte. Further, for the practical application, flexible asymmetric all-solid-state supercapacitor was made. Which offer high specific capacitance of 266.46 Fg−1 at 2 Ag−1, high energy density of 119.91 Wh kg−1 at a high-power density of 1800.08 W kg−1 within a voltage window of 1.8 V. These prominent electrochemical performances suggest that selected waste biomass materials derived carbon have considerable applications in the field of energy storage technologies.

Metal-Free Electron Donor-Acceptor Pair Enabled Long-Term Stability of Li-CO2 Battery.

The challenges of Lithium-carbon dioxide (Li-CO2) batteries for ensuring long-term cycling stability arise from the thermodynamically stable and electrically insulating discharge products (e.g., Li2CO3), which primarily rely on their interaction with the active materials. To achieve the optimized intermediates, the bifunctional electron donor-acceptor (D-A) pairs are proposed in cathode design to adjust such interactions in the case of B-O pairs. The inclusion of BC2O sites allows for the optimized redistribution of electrons via p-π conjugation. The as-obtained DO-AB pairs endow the enhanced interactions with Li+, CO2, and various intermediates, accompanied by the adjustable growth mode of Li2CO3. The shift from solvation-mediated mode into surface absorption mode in turn manipulates the morphology and decomposition kinetics of Li2CO3. Therefore, the corresponding Li-CO2 battery got twofold improved in both the capacity and reversibility. The cycling prolongs exceed 1300h and well operates at a wide temperature range (20-50°C) and different folding angles (0-180°). Such a strategy of introducing electron donor-acceptor pairs provides a distinct direction to optimize the lifetime of Li-CO2 battery from local structure regulation at the atomic scale, further inspiring in-depth understandings for developing electrochemical energy storage and carbon capture technologies.

Additives for Aqueous Zinc-Ion Batteries: Recent Progress, Mechanism Analysis, and Future Perspectives.

Aqueous zinc-ion batteries (ZIBs) stand out as a promising next-generation electrochemical energy storage technology, offering notable advantages such as high specific capacity, enhanced safety, and cost-effectiveness. However, the application of aqueous electrolytes introduces challenges: Zn dendrite formation and parasitic reactions at the anode, as well as dissolution, electrostatic interaction, and by-product formation at the cathode. In addressing these electrode-centric problems, additive engineering has emerged as an effective strategy. This review delves into the latest advancements in electrolyte additives for ZIBs, emphasizing their role in resolving the existing issues. Key focus areas include improving morphology and reducing side reactions during battery cycling using synergistic effects of modulating anode interface regulation, zinc facet control, and restructuring of hydrogen bonds and solvation sheaths. Special attention is given to the efficacy of amino acids and zwitterions due to their multifunction to improve the cycling performance of batteries concerning cycle stability and lifespan. Additionally, the recent additive advancements are studied for low-temperature and extreme weather applications meticulously. This review concludes with a holistic look at the future of additive engineering, underscoring its critical role in advancing ZIB performance amidst the complexities and challenges of electrolyte additives.

Low-cost H2/K+ hybrid batteries for large-scale energy storage

Rechargeable hydrogen gas batteries are gaining significant attention as a highly reliable electrochemical energy storage technology. However, the high costs of both cathode and anode limit their widespread applications. Here, we demonstrate a low-cost H2/K+ hybrid battery using Fe–Mn-based Prussian white - K2·74Mn[Fe(CN)6]0.90·0.13H2O (KMF) as cathode and non-noble metal high entropy alloy (NNM-HEA) as anode. It demonstrates a high capacity of 146.1 mAh g−1 at 1 A g−1 with excellent rate performance and stability. Even with a ∼7-fold increase in active loading of the KMF cathode, the capacity of the H2/K+ battery remains as high as 100.5 mAh g−1. Furthermore, a low-cost H2/K+ hybrid battery using our newly developed NNM-HEA based hydrogen catalytic anode is successfully fabricated, which shows an extended capacity with a retention of 90% after 1200 cycles. This work will pave the way for designing low-cost electrode materials for high-performance, large-scale energy storage hydrogen gas batteries.

Structural reconstruction of electrocatalysts

Efficient and durable electrocatalysts are essential for achieving high electrocatalytic efficiency in electrocatalytic reactions, forming the bedrock of effective electrochemical energy technologies. Electrocatalysis is a complex process, marked by intricate reaction system and crucial interfacial interactions, leading to diverse degrees of reconstruction changes in electrocatalysts, affecting both catalytic capabilities and structural integrity. This review delves into the development and prospects of electrocatalyst reconstruction within the electrochemical energy conversion and storage technologies. It elucidates the underlying motivation and mechanism driving reconstruction in various oxidation/reduction reaction systems. Moreover, it elucidates the evolution and comprehension of highly effective electrocatalysts that emerge as a result of this reconstruction phenomenon. The characterizations of catalyst reconstruction are thoroughly examined through the cutting-edge imaging/spectroscopy technologies, enabling dynamic reconstruction tracking and identification. Finally, this work highlights the challenges and opportunities associated with advancing reconstructed electrocatalysts. The primary objectives are to fathom the intricacies of reconstruction and its structural evolution for precise catalyst design. Additionally, it aims to regulate the reconstruction process to enhance the electrocatalyst longevity, stabilize catalytic reactions, and ultimately facilitate the implementation of electrochemical technologies.

GUARANTEED ORIGIN OF ELECTRICITY IN THE LOCAL POWER SYSTEM WITH RENEWABLE ENERGY SOURCES

The article is focused on the development of a method for determining the part of electricity generated by renewable energy sources (RES) in the electricity flows in the branches of the electric grid. The method is based on a mathematical model of the electric grid, in which the coefficients of current distribution in the branches of the circuit from RES nodes and nodal voltages are used to determine the electricity flows in the branches of the electric grid. As a result, a matrix of power distribution coefficients of RES generation units to load nodes of the power grid is formed. This way, the component of the load power that depends on the power in the RES nodes is determined. The voltages used to form the RES power distribution matrix are determined based on the results of calculating the steady-state modes of the power grid or on the measurement data of the ACEMS. Since the forming of local electric power systems (LES) based on RES is actual, the article considers LES as a balancing group within the electric power system (EPS), which can operate as an autonomous system according to certain conditions. It is shown that for this purpose, a RES reservation system should be created in the power system due to their dependence on natural conditions and, accordingly, the instability of their electricity generation. When a transmission system operates as part of an EPS, a general system reserve is usually used (mainly maneuverable capacities of thermal and hydroelectric power plants). In order for the LES can operate as an autonomous one, it is proposed to use other means of power reserve available today: electrochemical energy storage, hydrogen and biogas technologies. An effective way is to coordinate the schedules of RES generation in the LES with the load schedules of active consumers. The example shows that in the case of a power deficit in the LES, RES located in the power grid can be used. The values of the necessary power at the LES connection node, power flows in the branches connecting the LES and RES grid, and power losses in them are determined by the offered method.