Grid-scale Energy Storage Applications Research Articles

A Planar Sodium Nickel Chloride Battery Running at Intermediate Temperatures for Mid-Range Energy Storage

Sodium nickel chloride (Na-NiCl2) battery is one of the most promising candidates for grid scale electricity storage due to its high safety, long lifetime and demonstrated performance. The battery comprises molten Na and NiCl2 as negative and positive electrodes, respectively, in its charged state, separating them by a β”-Al2O3 solid electrolyte (BASE). In order to facilitate fast sodium ion transport in the cathode compartment, molten catholyte (NaAlCl4) is infiltrated into the cathode granule made of Ni and NaCl powders. The battery typically operates at 250-300oC so as to maximize the ionic flux in the cathode and through the solid electrolyte, and to minimize the dissolution of NiCl2 into the catholyte. However, this efficient battery is yet to be widely used in grid scale energy storage applications since it is still expensive mainly due to its use of expensive sealing technologies.The presentation introduces international collaborative efforts to develop a lower temperature operating planar Na-NiCl2 battery towards commercialization for the mid-range energy storage. Since the novel battery runs at 180oC, it can be fabricated at an ultra low manufacturing cost by adopting simpler and inexpensive polymer sealing and by introducing a planar cell design that can eliminate a number of unnecessary cell components. Starting with stating problems in traditional sodium beta-alumina batteries, their possible corresponding solutions are described. Challenges and progress in materializing the 6Ah class proto-type unit cell and its serially stacked cells will be discussed with related core technologies, including a cell design, highly toughened planar solid electrolyte, enhanced wetting, and semi-automated cell manufacturing platform.

Rechargeable Hydrogen Gas Batteries: Fundamentals, Principles, Materials, and Applications.

The growing demand for renewable energy sources has accelerated a boom in research on new battery chemistries. Despite decades of development for various battery types, including lithium-ion batteries, their suitability for grid-scale energy storage applications remains imperfect. In recent years, rechargeable hydrogen gas batteries (HGBs), utilizing hydrogen catalytic electrode as anode, have attracted extensive academic and industrial attention. HGBs, facilitated by appropriate catalysts, demonstrate notable attributes such as high power density, high capacity, excellent low-temperature performance, and ultralong cycle life. This review presents a comprehensive overview of four key aspects pertaining to HGBs: fundamentals, principles, materials, and applications. First, detailed insights are provided into hydrogen electrodes, encompassing electrochemical principles, hydrogen catalytic mechanisms, advancements in hydrogen catalytic materials, and structural considerations in hydrogen electrode design. Second, an examination and future prospects of cathode material compatibility, encompassing both current and potential materials, are summarized. Third, other components and engineering considerations of HGBs are elaborated, including cell stack design and pressure vessel design. Finally, a techno-economic analysis and outlook offers an overview of the current status and future prospects of HGBs, indicating their orientation for further research and application advancements.

Thermodynamically and Dynamically Boosted Electrocatalytic Iodine Conversion with Hydroxyl Groups for High-Efficiency Zinc-Iodine Batteries.

Rechargeable zinc-iodine (Zn-I2) batteries have shown immense potential for grid-scale energy storage applications, but there remain challenges of improving efficiency and cycling stability due to the sluggish iodine reduction reaction (IRR) kinetics and serious shuttle problem of polyiodides. We herein demonstrate an efficient metal-free hydroxyl (-OH)-functionalized carbon catalyst that effectively boosts the performance of Zn-I2 batteries. It has been found that the obtained electrocatalytic performance is strongly correlated with the surface oxygen chemical environment in the carbon matrix. Both theoretical calculations and experimental measurements have uncovered that the -OH group, rather than carbonyl (-C═O) and carboxyl (-COOH), provides the active electrocatalytic site for IRR, improves the iodine redox kinetics and the electrochemical reversibility, and facilitates I2 nucleation. As confirmed by a series of in situ and ex situ spectroscopy techniques, due to the favorable reaction thermodynamics and the lowered energy barrier for I3- dissociation, the O-H···I channels can effectively trigger the direct transformation of I2/I- and avoid the formation of stable polyiodides. As a result, the as-assembled battery of I2/oxygen-functionalized carbon cloth (I2/OCC-2)//Zn exhibits a high capacity of 2.27 mA h cm-2 at 1 mA cm-2, outstanding rate capability with 89.0% capacity retention at 20 mA cm-2, and long-term stability of 10,000 cycles.

Modulating Interfacial Zn2+ Desolvation and Transport Kinetics through Coordination Interaction toward Stable Anodes in Aqueous Zn-Ion Batteries.

Aqueous Zn-ion batteries (AZIBs) are promising candidates for grid-scale energy-storage applications, but uneven Zn2+ flux distribution and undesirable water-related interfacial side reactions seriously hinder their practical application. Herein, a strategy of regulating the coordination interaction between Zn2+ and artificial interphase layers (AILs) to modulate the interfacial Zn2+ desolvation/transport behaviors and relieve side reactions for building stable Zn anodes is proposed. By selectively choosing appropriate polymers with different functional groups, it is shown that compared with the strong interaction offered by aryl groups in polystyrene-based AILs, cyano groups in polyacrylonitrile (PAN)-based AILs provide a moderate coordination interaction with Zn2+, which not only accelerates interfacial Zn2+desolvation kinetics but also enables efficient Zn2+ transport within AILs. Moreover, the Zn2+ transport kinetics of PAN-based AILs can be further enhanced with the incorporation of an ionic conductor, zinc phosphate (ZP). Because of these advantages, the Zn anodes decorated with the hybrid AILs composed of PAN and ZP can steadily operate for >2000h at 0.2mA cm-2 and >350h at a high current density of 10mA cm-2. This work provides a valuable guideline for selective design of AILs at the molecular level for durable AZIBs.

(Invited) Development of Mildly Acidic Aqueous Zinc Batteries: Anode, Cathode, and Electrolyte

Aqueous zinc batteries use earth abundant materials and has stable supply chains, making them one of the promising battery technologies for grid-scale energy storage applications. However, the limited cycle life because of the dendrite formation of zinc anodes, poor reversibility of cathodes, and consumption of electrolyte has greatly hampered its practical application. Recently, extensive research effort has been made on the development of rechargeable alkaline batteries and mildly acidic zinc ion batteries. Novel structured zinc anodes, intercalation cathode materials and new electrolytes have been developed to improve the performance. Here, we would like to present our effort towards aqueous zinc batteries under practical conditions. Zinc alloy anodes, organic cathode materials, and the use of new binders and electrolyte additives will be discussed.

Perspectives on Advanced Lithium-Sulfur Batteries for Electric Vehicles and Grid-Scale Energy Storage.

Intensive increases in electrical energy storage are being driven by electric vehicles (EVs), smart grids, intermittent renewable energy, and decarbonization of the energy economy. Advanced lithium-sulfur batteries (LSBs) are among the most promising candidates, especially for EVs and grid-scale energy storage applications. In this topical review, the recent progress and perspectives of practical LSBs are reviewed and discussed; the challenges and solutions for these LSBs are analyzed and proposed for future practical and large-scale energy storage applications. Major challenges for the shuttle effect, reaction kinetics, and anodes are specifically addressed, and solutions are provided on the basis of recent progress in electrodes, electrolytes, binders, interlayers, conductivity, electrocatalysis, artificial SEI layers, etc. The characterization strategies (including in situ ones) and practical parameters (e.g., cost-effectiveness, battery management/modeling, environmental adaptability) are assessed for crucial automotive/stationary large-scale energy storage applications (i.e., EVs and grid energy storage). This topical review will give insights into the future development of promising Li-S batteries toward practical applications, including EVs and grid storage.

Screening Ultra-Stable (Phenazine)dioxyalkanocic Acids with Varied Water-Solubilizing Chain Lengths for High-Capacity Aqueous Redox Flow Batteries.

Aqueous redox flow batteries (ARFBs) hold great potential for large-scale energy storage. Recently, research on aqueous flow batteries has shifted toward water-soluble organic molecules with redox capabilities to reduce the use of mineral resources. The chemical and electrochemical stabilities of organic compounds are heavily influenced by their functional groups and reaction sites. In this study, we present a low-cost synthesis of the O-alkyl-carboxylate-functionalized derivatives of 2,3-dihydroxyphenazine, namely, phenazine-(2,3-diyl) dioxy dibutyric acid (DBEP) and phenazine-(2,3-diyl)dioxy diacetic acid (DAEP), which serve as negolytes and exhibit good reversibility and high redox kinetics. The evidence is provided to clarify the capacity degradation mechanisms of DAEP and DBEP by a series of comprehensive characterizations. Similar to anthraquinones functionalized with alkyl chains, the main degradation mechanism of DAEP modified with acetic acid is due to side chain loss. Longer side chains are more stable and can withstand long-term electrochemical reactions. DBEP modified with butyric acid exhibits superior chemical and electrochemical stability. Our results demonstrate that rational molecular design and suitable membranes, such as the alkaline ARFBs based on DBEP negolyte, potassium ferrocyanide (K4Fe(CN)6) posolyte, and custom sulfonated poly(ether ether ketone) membrane, can deliver a high open-circuit voltage of 1.17 V and high capacity retention of 99.997% per cycle for over 1000 cycles at 50 mA cm-2. This study highlights the importance of not only considering the modification position of the molecules but also focusing on the influence of various side chains on the redox core's stability toward sustainable grid-scale energy storage applications.

Revealing the Dominance of the Dissolution-Deposition Mechanism in Aqueous Zn-MnO2 Batteries.

Zn-MnO2 batteries have attracted extensive attention for grid-scale energy storage applications, however, the energy storage chemistry of MnO2 in mild acidic aqueous electrolytes remains elusive and controversial. Using α-MnO2 as a case study, we developed a methodology by coupling conventional coin batteries with customized beaker batteries to pinpoint the operating mechanism of Zn-MnO2 batteries. This approach visually simulates the operating state of batteries in different scenarios and allows for a comprehensive study of the operating mechanism of aqueous Zn-MnO2 batteries under mild acidic conditions. It is validated that the electrochemical performance can be modulated by controlling the addition of Mn2+ to the electrolyte. The method is utilized to systematically eliminate the possibility of Zn2+ and/or H+ intercalation/de-intercalation reactions, thereby confirming the dominance of the MnO2 /Mn2+ dissolution-deposition mechanism. By combining a series of phase and spectroscopic characterizations, the compositional, morphological and structural evolution of electrodes and electrolytes during battery cycling is probed, elucidating the intrinsic battery chemistry of MnO2 in mild acid electrolytes. Such a methodology developed can be extended to other energy storage systems, providing a universal approach to accurately identify the reaction mechanism of aqueous aluminum-ion batteries as well.

Electrochemical Storage Behavior of a High-Capacity Mg-Doped P2-Type Na2/3Fe1-yMnyO2 Cathode Material Synthesized by a Sol-Gel Method.

Grid-scale energy storage applications can benefit from rechargeable sodium-ion batteries. As a potential material for making non-cobalt, nickel-free, cost-effective cathodes, earth-abundant Na2/3Fe1/2Mn1/2O2 is of particular interest. However, Mn3+ ions are particularly susceptible to the Jahn-Teller effect, which can lead to an unstable structure and continuous capacity degradation. Modifying the crystal structure by aliovalent doping is considered an effective strategy to alleviate the Jahn-Teller effect. Using a sol-gel synthesis route followed by heat treatment, we succeeded in preparing an Mg-doped Na2/3Fe1-yMnyO2 cathode. Its electrochemical properties and charge compensation mechanism were then studied using synchrotron-based X-ray absorption spectroscopy and in situ X-ray diffraction techniques. The results revealed that Mg doping reduced the number of Mn3+ Jahn-Teller centers and alleviated high voltage phase transition. However, Mg doping was unable to suppress the P2-P'2 phase transition at a low voltage discharge. An initial discharge capacity of about 196 mAh g-1 was obtained at a current density of 20 mAh g-1, and 60% of rate capability was maintained at a current density of 200 mAh g-1 in a voltage range of 1.5-4.3 V. This study will greatly contribute to the ongoing search for advanced and efficient cathodes from earth-abundant elements for rechargeable sodium-ion batteries operable at room temperature.

Advances in 2D Ultrathin Nanosheets of a2FeSiO4 (A= Li, Na, K) for Next-Generation Alkali-Ion Batteries

Although lithium-ion batteries (LIBs) have become ubiquitous in various applications, the limited resource of Li and increasing cost hinder their scalability for grid-scale energy storage applications. Thus, alternative rechargeable batteries that use more earth-abundant elements such as sodium and potassium have received significant attention. However, the distinct different properties of Li+, Na+, and K+ ions hinder the extensive development of universal host materials for alkali metal ions. Polyanion-type electrode materials, which contain polyanionic groups (XO4)n −, (XO4F)n −, and (XmO2m+1)n − (X = P, Si, S, etc.), have garnered significant interest owing to their remarkable structural stability and adjustable electrode potential; this properties make them excellent candidates as cathode materials in sodium-ion batteries (SIBs) and potassium-ion batteries (KIBs). Among these, A2FeSiO4 (AFS) (A= Li, Na, K) is highlighted as a promising cathode material due to its abundant Fe resources, low cost, and non-toxicity. The crystal structure, transport pathways, and synthesis techniques of Li2FeSiO4 (LFS) have been extensively explored whereas research on Na2FeSiO4 (NFS) as a cathode material is still in the process of maturing and research on K2FeSiO4 (KFS) is very rare. The large ionic radius of sodium and potassium presents a significant challenge to effective ion-intercalation reactions for energy storage in electrodes, destabilizing the crystal structures of host materials. In addition, orthosilicates exhibit poor electronic conductivity, greatly limiting its practical application. To address this issue, various techniques have been explored, which include nanostructuring, coating with conductive polymers, and metal doping. In this study, a facile solvothermal technique for the fabrication of ultrathin 2D AFS nanosheets by hydrothermal transformation and propose the reaction mechanism for this chemical transformation. The as-obtained AFS nanosheets are highly exfoliated using oxalic acid as the exfoliating agent to improve their electrochemical performance. These nanosheets are designed to mitigate the diffusion limitations encountered by alkali ions when traversing the densely packed structure of AFS. The highly exfoliated AFS 2D nanosheets greatly improve the electrochemical performance and cyclability of the cathode. The nanosheets exhibit a specific discharge capacity of 149 mAh g-1 for Li+, 99 mAh g-1 for Na+, and 88 mAh g-1 for K+ when operated at a current density of 100 mA g-1. Moreover, the nanosheets display exceptional capacity retention, with a retention rate of 75% for Li+, 99% for Na+, and 65% for K+ after 100 charge/discharge cycles for each of the cathodes. This study demonstrates the potential of 2D nanosheets for stabilizing the silicate-based cathode materials against structural and volume changes, and for improving their electrochemical performance in SIBs and KIBs. Figure 1

Some facets of the Mg/Na3VCr0.5Fe0.5(PO4)3 battery

Magnesium rechargeable batteries (MRBs) present opportunities for grid-scale energy storage applications as a complement to Li-ion batteries (LIBS). The major challenges are the low reversible capacity, inferior cycling stability and unsatisfactory energy densities. Na3VCr0.5Fe0.5(PO4)3 with a well-defined NASION-type structure is used as cathode in Mg cell. Two-electrons reaction (∼116 mAh/g), 1.5 V average voltage and 65% of capacity retention over 100 cycles are accomplished. Mg is inserted by a biphasic reaction with the participation of V3+/V4+/V5+ redox couples in the electrochemical reaction while the non-active redox couples such as Cr3+/Cr4+ and Fe2+/Fe3+ served as stabilizer to buffer the volume variation. A thermal stability up to ∼412 °C is also exhibited. Therefore, incorporating a mixture of three transition metal (V/Cr/Fe) in this type of structures will broaden new perspectives for realizing high performance cathodes for MRBs.

Extending phase-variation voltage zones in P2-type sodium cathodes through high-entropy doping for enhanced cycling stability and rate capability

P2-type layered sodium oxides hold great promise for grid-scale energy storage applications owing to their low-cost merit, while their detrimental structural and chemical transition lead to low reversible capacities and poor cycling stability. Herein, we leverage a high-entropy (HE) doping strategy to stabilize the P2-type Na0.667Mn0.667Ni0.167Co0.167O2 (NMNC) cathode. A novel Na0.667Mn0.667Ni0.167Co0.117Ti0.01Mg0.01Cu0.01Mo0.01Nb0.01O2 (HE-NMNC) composite, with five equal content (1 at %) of cation substitution and exhibiting a pure P63/mmc space group structure, is proposed. Interestingly, a reversible P2-type phase variation is identified for HE-NMNC at high degrees of charge, but such phase variation occurs in a wider voltage region and is much slower than that in the NMNC baseline. It is demonstrated that the HE-NMNC delivers outstanding rate capability and cycling stability under a charging cutoff voltage of 4.5 V, achieving a reversible capacity of 111 mAh/g at 5 C and retaining around 130 mAh/g after 100 cycles at 1 C. Apart from the charge compensation of main transition metals (Ni, Co, and Mn), the reversible redox of lattice oxygen also contributes to the capacity of HE-NMNC upon cycling. The proposed high-entropy doping strategy and reaction mechanism may provide new insights for developing advanced cathode materials.

A Universal Additive Design Strategy to Modulate Solvation Structure and Hydrogen Bond Network toward Highly Reversible Fe Anode for Low-Temperature All-Iron Flow Batteries.

Aqueous all-iron redox flow batteries (RFBs) are promising competitors for next-generation grid-scale energy storage applications. However, the high-performance operation of all-iron RFBs in a wider temperature range is greatly hindered by inferior iron plating/stripping reaction and low solid-liquid transition temperature at Fe anode. Herein, a universal electrolyte additive design strategy for all-iron RFBs is reported, which realizes a highly reversible and dendrite-free Fe anode at low temperatures. Quantum chemistry calculations first screen several organic molecules with oxygen-containing functional groups and identify N,N-Dimethylacetmide (DMAc) as a potential candidate with low cost, high solubility, and strong interactions with Fe2+ and H2 O. Combined experimental characterizations and theoretical calculations subsequently demonstrate that adding DMAc into the FeCl2 solution effectively reshapes the primary solvation shell of Fe2+ via the Fe2+ -O (DMAc) bond and breaks hydrogen-bonding network of water through intensified H-bond interaction between DMAc and H2 O, thereby affording the Fe anode with enhanced Fe/Fe2+ reversibility and lower freezing point. Consequently, the assembled all-iron RFB achieves an excellent combination of high power density (25mWcm-2 ), long charge-discharge cycling stability (95.59% capacity retention in 103h), and preeminent battery efficiency at -20°C (95% coulombic efficiency), which promise a future for wider temperature range operation of all-iron RFBs.

C-H···π interactions disrupt electrostatic interactions between non-aqueous electrolytes to increase solubility.

Grid-scale energy storage applications, such as redox flow batteries, rely on the solubility of redox-active organic molecules. Although redox-active pyridiniums exhibit exceptional persistence in multiple redox states at low potentials (desirable properties for energy storage applications), their solubility in non-aqueous media remains low, and few practical molecular design strategies exist to improve solubility. Here we convey the extent to which discrete, attractive interactions between C-H groups and π electrons of an aromatic ring (C-H···π interactions) can describe the solubility of N-substituted pyridinium salts in a non-aqueous solvent. We find a direct correlation between the number of C-H···π interactions for each pyridinium salt and its solubility in acetonitrile. The correlation presented in this work highlights a consequence of disrupting strong electrostatic interactions with weak dispersion interactions, showing how minimal structural change can dramatically impact pyridinium solubility.

Vine shoot-derived hard carbons as promising anodes for sodium-ion batteries: valorization of pig manure as HTC solvent

Sodium-ion batteries (SIBs) are one of the most promising candidates to replace lithium-ion batteries (LIBs) in grid-scale energy storage applications. The design of high-performance anodes and the fully understanding of the sodium storage mechanisms are the main bottleneck to overcome. Herein, a vine shoot-based hard carbon anode was synthesized via hydrothermal carbonization followed by a pyrolysis step (800 to 1200 °C). In addition to water, pig manure and diluted hydrochloric acid were tested as reaction media.

Ultrafast Electrical Pulse Synthesis of Highly Active Electrocatalysts for Beyond-Industrial-Level Hydrogen Gas Batteries.

The high reliability and proven ultra-longevity make aqueous hydrogen gas (H2 ) batteries ideal for large-scale energy storage. However, the low alkaline hydrogen evolution and oxidation reaction (HER/HOR) activities of expensive platinum catalysts severely hamper their widespread applications in H2 batteries. Here, cost-effective, highly active electrocatalysts, with a model of ruthenium-nickel alloy nanoparticles in ≈3nm anchored on carbon black (RuNi/C) as an example, are developed by an ultrafast electrical pulse approach for nickel-hydrogen gas (NiH2 ) batteries. Having a competitive low cost of about one fifth of Pt/C benckmark, this ultrafine RuNi/C catalyst displays an ultrahigh HOR mass activity of 2.34 A mg-1 at 50 mV (vs RHE) and an ultralow HER overpotential of 19.5 mV at a current density of 10 mA cm-2 . As a result, the advanced NiH2 battery can efficiently operate under all-climate conditions (from -25 to +50 °C) with excellent durability. Notably, the NiH2 cell stack achieves an energy density up to 183Wh kg-1 and an estimated cost of ≈49 $ kWh-1 under an ultrahigh cathode Ni(OH)2 loading of 280mg cm-2 and a low anode Ru loading of ≈62.5µg cm-2 . The advanced beyond-industrial-level hydrogen gas batteries provide great opportunities for practical grid-scale energy storage applications.

Highly Soluble Dimethoxymethyl Tetrathiafulvalene with Excellent Stability for Non-Aqueous Redox Flow Batteries.

Non-aqueous redox flow batteries (RFBs) are highly attractive for grid-scale energy storage applications because of their independent design of energy and power, high energy density and efficiency, easy maintenance, and potentially low cost. In order to develop active molecules with large solubility, excellent electrochemical stability, and high redox potential for a non-aqueous RFB catholyte, herein, two flexible methoxymethyl groups had been attached to a famous redox-active tetrathiafulvalene (TTF) core. The strong intermolecular packing of the rigid TTF unit was effectively depressed, leading to a dramatically improved solubility of up to 3.1 M in conventional carbonate solvents. The performance of the obtained dimethoxymethyl TTF (DMM-TTF) was studied in a semi-solid RFB system with Li foil as the counter electrode. When using porous Celgard as the separator, the hybrid RFB with 0.1 M DMM-TTF had two high discharge plateaus at 3.20 and 3.52 V and a low capacity retention of 30.7% after 100 cycles at 5 mA cm-2. Replacing Celgard with a permselective membrane, the capacity retention was increased to 85.4%. Further increasing the concentration of DMM-TTF to 1.0 M and current density to 20 mA cm-2, the hybrid RFB exhibited a high volumetric discharge capacity of 48.5 A h L-1 and an energy density of 154 W h L-1. The capacity was maintained at 72.2% after 100 cycles (10.7 days). The great redox stability of DMM-TTF was revealed by UV-vis and 1H NMR tests and verified by density functional theory calculations. Therefore, the methoxymethyl group is an excellent group to increase the solubility while maintaining the redox capability of TTF for high-performance non-aqueous RFBs.

Ultrastable Cu2+ Intercalation Chemistry Based on a Niobium Sulfide Nanosheet Cathode for Advanced Aqueous Storage Devices

Exploring stable and durable cathodes for cost-effective reversible aqueous batteries is highly desirable for grid-scale energy storage applications, but significant challenges remain. Herein, we disclosed an ultrastable Cu2+ intercalation chemistry in mass-produced exfoliated NbS2 nanosheets to build ultralong lifespan aqueous batteries with cost advantages. Anisotropic interplanar expansion of NbS2 lattices balanced dynamic Cu2+ incorporation and the highly reversible redox reaction of Nb4+/Nb(4-δ)+ couple were illuminated by operando synchrotron X-ray diffraction and energy dispersive X-ray absorption spectroscopy, affording an extraordinary capacity of approximately 317 mAh g-1 at 1 A g-1 and a good stability of 92.2% capacity retention after 40000 cycles at 10 A g-1. Impressively, a budget NbS2||Fe hybrid ion cell involving an aqueous electrolyte/Fe-metal anode is established and provides a reliable energy supply of 225.4 Wh kg-1 at 750 W kg-1, providing insights for building advanced aqueous battery systems for large-scale applications.

Private and External Costs and Benefits of Replacing High-Emitting Peaker Plants with Batteries

Falling costs of lithium-ion (Li-ion) batteries have made them attractive for grid-scale energy storage applications. Energy storage will become increasingly important as intermittent renewable generation and more frequent extreme weather events put stress on the electricity grid. Environmental groups across the United States are advocating for the replacement of the highest-emitting power plants, which run only at times of peak demand, with Li-ion battery systems. We analyze the life-cycle cost, climate, and human health impacts of replacing the 19 highest-emitting peaker plants in California with Li-ion battery energy storage systems (BESS). Our results show that designing Li-ion BESS to replace peaker plants puts them at an economic disadvantage, even if facilities are only sized to meet 95% of the original plants' load events and are free to engage in arbitrage. However, five of 19 potential replacements do achieve a positive net present value after including monetized climate and human health impacts. These BESS cycle far less than typical front-of-the-meter batteries and rely on the frequency regulation market for most of their revenue. All projects offer net air pollution benefits but increase net greenhouse gas emissions due to electricity demand during charging and upstream emissions from battery manufacturing.

Pom-Pom Flower-like Morphology of δ-MnO2 with Superior Electrochemical Performances for Rechargeable Aqueous Zinc Ion Batteries

A rechargeable aqueous zinc-ion battery is an encouraging alternative for grid-scale energy storage applications, owing to its advantages of high safety, low cost, and environmental benignity. Since MnO2 is found to be one of the most efficient intercalation cathode materials for ZIBs, the layered type δ-MnO2 polymorph exhibits reversible intercalation/de-intercalation of Zn2+ ions with a high capacity. Unfortunately, the δ-MnO2 cathode suffers from poor cyclability, low-rate capability, and structural degradation during charge–discharge cycles. Therefore, δ-MnO2 with Pom-Pom Flower-like morphology have been synthesized using a facile hydrothermal method. The unique morphology of δ-MnO2 provides a high surface area with numerous reaction sites, leading to excellent electrochemical performance. The obtained results revealed that the δ-MnO2 electrode retained ~99% of its initial capacity even after 250 cycles, which can be ascribed to the reversible Zn2+ insertion/de-insertion from the current unique morphology of the layered δ-MnO2 nanostructure. In addition, the electrochemical and structural investigation also indicates a two-step co-insertion of H+ and Zn2+ ions into the interlayer of δ-MnO2 during the discharge process. Thus, the superior electrochemical performances of the δ-MnO2 cathode paves a way for the high capacity and a long lifespan of zinc-ion batteries.