| 1. |
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- 2019
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Tidskriftsartikel (refereegranskat)
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| 2. |
- Sun, Jinhua, 1987, et al.
(författare)
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Critical Role of Functional Groups Containing N, S, and O on Graphene Surface for Stable and Fast Charging Li-S Batteries
- 2021
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Ingår i: Small. - : Wiley. - 1613-6810 .- 1613-6829. ; 17:17
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Tidskriftsartikel (refereegranskat)abstract
- Lithium‐sulfur (Li‐S) batteries are considered one of the most promising energy storage technologies, possibly replacing the state‐of‐the‐art lithium‐ion (Li‐ion) batteries owing to their high energy density, low cost, and eco‐compatibility. However, the migration of high‐order lithium polysulfides (LiPs) to the lithium surface and the sluggish electrochemical kinetics pose challenges to their commercialization. The interactions between the cathode and LiPs can be enhanced by the doping of the carbon host with heteroatoms, however with relatively low doping content (<10%) in the bulk of the carbon, which can hardly interact with LiPs at the host surface. In this study, the grafting of versatile functional groups with designable properties (e.g., catalytic effects) directly on the surface of the carbon host is proposed to enhance interactions with LiPs. As model systems, benzene groups containing N/O and S/O atoms are vertically grafted and uniformly distributed on the surface of expanded reduced graphene oxide, fostering a stable interface between the cathode and LiPs. The combination of experiments and density functional theory calculations demonstrate improvements in chemical interactions between graphene and LiPs, with an enhancement in the electrochemical kinetics, power, and energy densities.
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| 3. |
- Agostini, Marco, 1987, et al.
(författare)
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Minimizing the Electrolyte Volume in Li–S Batteries: A Step Forward to High Gravimetric Energy Density
- 2018
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Ingår i: Advanced Energy Materials. - : Wiley. - 1614-6840 .- 1614-6832. ; 8:26
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Tidskriftsartikel (refereegranskat)abstract
- Sulfur electrodes confined in an inert carbon matrix show practical limitations and concerns related to low cathode density. As a result, these electrodes require a large amount of electrolyte, normally three times more than the volume used in commercial Li-ion batteries. Herein, a high-energy and high-performance lithium–sulfur battery concept, designed to achieve high practical capacity with minimum volume of electrolyte is proposed. It is based on deposition of polysulfide species on a self-standing and highly conductive carbon nanofiber network, thus eliminating the need for a binder and current collector, resulting in high active material loading. The fiber network has a functionalized surface with the presence of polar oxygen groups, with the aim to prevent polysulfide migration to the lithium anode during the electrochemical process, by the formation of S–O species. Owing to the high sulfur loading (6 mg cm−2) and a reduced free volume of the sulfide/fiber electrode, the Li–S cell is designed to work with as little as 10 µL cm−2of electrolyte. With this design the cell has a high energy density of 450 Wh kg−1, a lifetime of more than 400 cycles, and the possibility of low cost, by use of abundant and eco-friendly materials.
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| 4. |
- Ahmed, Mohammad Shamsuddin, et al.
(författare)
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Multiscale Understanding of Covalently Fixed Sulfur–Polyacrylonitrile Composite as Advanced Cathode for Metal–Sulfur Batteries
- 2021
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Ingår i: Advanced Science. - : Wiley. - 2198-3844 .- 2198-3844. ; 8:21
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Forskningsöversikt (refereegranskat)abstract
- Metal–sulfur batteries (MSBs) provide high specific capacity due to the reversible redox mechanism based on conversion reaction that makes this battery a more promising candidate for next-generation energy storage systems. Recently, along with elemental sulfur (S8), sulfurized polyacrylonitrile (SPAN), in which active sulfur moieties are covalently bounded to carbon backbone, has received significant attention as an electrode material. Importantly, SPAN can serve as a universal cathode with minimized metal–polysulfide dissolution because sulfur is immobilized through covalent bonding at the carbon backbone. Considering these unique structural features, SPAN represents a new approach beyond elemental S8 for MSBs. However, the development of SPAN electrodes is in its infancy stage compared to conventional S8 cathodes because several issues such as chemical structure, attached sulfur chain lengths, and over-capacity in the first cycle remain unresolved. In addition, physical, chemical, or specific treatments are required for tuning intrinsic properties such as sulfur loading, porosity, and conductivity, which have a pivotal role in improving battery performance. This review discusses the fundamental and technological discussions on SPAN synthesis, physicochemical properties, and electrochemical performance in MSBs. Further, the essential guidance will provide research directions on SPAN electrodes for potential and industrial applications of MSBs.
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| 5. |
- Jiao, Xingxing, et al.
(författare)
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Multi-Physical Field Simulation: A Powerful Tool for Accelerating Exploration of High-Energy-Density Rechargeable Lithium Batteries
- 2023
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Ingår i: Advanced Energy Materials. - 1614-6840 .- 1614-6832. ; In Press
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Forskningsöversikt (refereegranskat)abstract
- To meet the booming demand of high-energy-density battery systems for modern power applications, various prototypes of rechargeable batteries, especially lithium metal batteries with ultrahigh theoretical capacity, have been intensively explored, which are intimated with new chemistries, novel materials and rationally designed configurations. What happens inside the batteries is associated with the interaction of multi-physical field, rather than the result of the evolution of a single physical field, such as concentration field, electric field, stress field, morphological evolution, etc. In this review, multi-physical field simulation with a relatively wide length and timescale is focused as formidable tool to deepen the insight of electrodeposition mechanism of Li metal and the electro-chemo-mechanical failure of solid-state electrolytes based on Butler-Volmer electrochemical kinetics and solid mechanics, which can promote the future development of state-of-the-art Li metal batteries with satisfied energy density as well as lifespan.
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| 6. |
- Kang, Hyokyeong, et al.
(författare)
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Relaxation of Stress Propagation in Alloying-Type Sn Anodes for K-Ion Batteries
- 2024
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Ingår i: Small Methods. - 2366-9608. ; 8:1
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Tidskriftsartikel (refereegranskat)abstract
- Alloying-type metallic tin is perceived as a potential anode material for K-ion batteries owing to its high theoretical capacity and reasonable working potential. However, pure Sn still face intractable issues of inferior K+ storage capability owing to the mechanical degradation of electrode against large volume changes and formation of intermediary insulating phases K4Sn9 and KSn during alloying reaction. Herein, the TiC/C–carbon nanotubes (CNTs) is prepared as an effective buffer matrix and composited with Sn particles (Sn–TiC/C–CNTs) through the high-energy ball-milling method. Owing to the conductive and rigid properties, the TiC/C–CNTs matrix enhances the electrical conductivity as well as mechanical integrity of Sn in the composite material and thus ultimately contributes to performance supremacy in terms of electrochemical K+ storage properties. During potassiation process, the TiC/C–CNTs matrix not only dissipates the internal stress toward random radial orientations within the Sn particle but also provides electrical pathways for the intermediate insulating phases; this tends to reduce microcracking and prevent considerable electrode degradation.
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| 7. |
- Lee, Suyeong, et al.
(författare)
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High-Energy and Long-Lifespan Potassium–Sulfur Batteries Enabled by Concentrated Electrolyte
- 2022
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Ingår i: Advanced Functional Materials. - : Wiley. - 1616-3028 .- 1616-301X. ; 32:46
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Tidskriftsartikel (refereegranskat)abstract
- Potassium–sulfur (K–S) batteries are emerging as low-cost and high-capacity energy-storage technology. However, conventional K–S batteries suffer from two critical issues that have not yet been successfully resolved: the dissolution of potassium polysulfides (KPS) into the liquid electrolyte and the formation of K dendrites on the K metal anode, which lead to inadequate cycling efficiencies with a low reversible capacity. Herein, a high-capacity and long cycle-life K–S battery consisting of a highly concentrated electrolyte (HCE) (4.34 mol kg−1 potassium bis(fluorosulfonyl)imide in a 1,2-Dimethoxyethane) and a sulfurized polyacrylonitrile (SPAN) cathode is presented The application of a HCE efficiently suppresses the dendritic growth of K, as evidenced by operando optical imaging and phase field modeling, owing to the reduced K-ion depletion on the electrode surface and a uniform Faradaic current density over the K metal anode surface. Additionally, because S is covalently bonded to the C backbone of PAN in the SPAN structure, the SPAN cathode inhibits the dissolution of KPS. These features generate synergy that the proposed K–S battery can provide a practical areal capacity of 2.5 mAh cm−2 and unprecedented lifetimes with high Coulombic efficiencies over 700 cycles.
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| 8. |
- Park, Jimin, et al.
(författare)
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A Dual-Functional Electrolyte Additive for High-Performance Potassium Metal Batteries
- 2023
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Ingår i: Advanced Functional Materials. - 1616-3028 .- 1616-301X. ; 33:48
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Tidskriftsartikel (refereegranskat)abstract
- Potassium metal batteries (KMBs) coupled with layered transition metal oxides as cathode materials are a promising energy−storage technology owing to low cost and high capacity. However, uncontrollable dendritic growth in the K−metal anode and chemical reactivity of the layered transition metal oxide cathode against the electrolyte solution cause KMBs to suffer from low Coulombic efficiency, rapid capacity fading, and critical safety issues. In this study, an electrolyte engineering strategy is introduced by introducing adiponitrile (ADN) as a dual−functional electrolyte additive containing an electron−rich nitrile group (C≡N) in its molecule structure. Thus, the addition of 1 wt.% ADN can alter the chemical properties of the electrolyte solution, thereby improving the anode−electrolyte and cathode−electrolyte interfacial stabilities in KMBs. The formation of a potassiophilic compound with C≡N in the solid electrolyte interphase layer can guide the uniform electrodeposition of K and suppress the dendritic growth in the K−metal. Moreover, C≡N forms a strong coordination bond with the oxidized transition metal, leading the reversible redox reactions by mitigating the undesirable disproportionation reaction and improving the thermal stability of the layered transition metal oxide cathode. Computational calculations and experimental characterizations are used to verify the role of ADN additive in enhancing the electrochemical properties of KMBs.
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| 9. |
- Park, Jimin, et al.
(författare)
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Regulating the Solvation Structure of Electrolyte via Dual–Salt Combination for Stable Potassium Metal Batteries
- 2023
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Ingår i: Advanced Science. - 2198-3844 .- 2198-3844. ; 10:16
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Tidskriftsartikel (refereegranskat)abstract
- Batteries using potassium metal (K-metal) anode are considered a new type of low-cost and high-energy storage device. However, the thermodynamic instability of the K-metal anode in organic electrolyte solutions causes uncontrolled dendritic growth and parasitic reactions, leading to rapid capacity loss and low Coulombic efficiency of K-metal batteries. Herein, an advanced electrolyte comprising 1 M potassium bis(fluorosulfonyl)imide (KFSI) + 0.05 M potassium hexafluorophosphate (KPF6) dissolved in dimethoxyethane (DME) is introduced as a simple and effective strategy of regulated solvation chemistry, showing an enhanced interfacial stability of the K-metal anode. Incorporating 0.05 M KPF6 into the 1 M KFSI in DME electrolyte solution decreases the number of solvent molecules surrounding the K ion and simultaneously leads to facile K+ de-solvation. During the electrodeposition process, these unique features can lower the exchange current density between the electrolyte and K-metal anode, thereby improving the uniformity of K electrodeposition, as well as potentially suppressing dendritic growth. Even under a high current density of 4 mA cm−2, the K-metal anode in 0.05 M KPF6-containing electrolyte ensures high areal capacity and an unprecedented lifespan with stable Coulombic efficiency in both symmetrical half-cells and full-cells employing a sulfurized polyacrylonitrile cathode.
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| 10. |
- Park, Jimin, et al.
(författare)
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Stable Solid Electrolyte Interphase for Long-Life Potassium Metal Batteries
- 2022
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Ingår i: ACS Energy Letters. - : American Chemical Society (ACS). - 2380-8195. ; 7:1, s. 401-409
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Tidskriftsartikel (refereegranskat)abstract
- Potassium (K) is considered to be the most suitable anode material for rechargeable K batteries because of its high theoretical capacity (686 mAh g(-1)) and low redox potential (-2.93 V vs SHE). However, uneven electrodeposition of K during cycling usually leads to the growth of dendrites, resulting in low Coulombic efficiency and compromising battery safety. Herein, we develop a strategy for stabilizing K metal through simple interface control. The conductive passivation layer can be controllably designed by a spontaneous chemical reaction when a K metal foil is kept in contact with a liquid-phase potassium-polysulfide (PPS); this guides the formation of an electronically and ionically conductive solid electrolyte interphase layer including K2S compound, enabling dense K plating with a dendrite-free morphology. Compared to the bare K metal anode, the PPS-treated K metal anode demonstrates superior cycling stability in symmetric half cells and full cells using a TiS2 cathode under practical constraints.
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