Cotton-derived cellulose film as a dendrite-inhibiting separator to stabilize the zinc metal anode of aqueous zinc ion batteries
TL;DR: In this paper, a cotton-derived cellulose film was used as the separator for aqueous zinc-ion batteries (Zn-MnO2), which can effectively inhibit zinc dendrites and harmful side reactions.
About: This article is published in Energy Storage Materials.The article was published on 2022-01-01. It has received 138 citations till now. The article focuses on the topics: Separator (oil production) & Zinc.
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TL;DR: In this article , a separator (UiO-66-GF) modified by Zr-based metal organic framework for robust zinc-ion batteries is proposed, which effectively enhances the transport ability of charge carriers and demonstrates preferential orientation of (002) crystal plane, which is favorable for corrosion resistance and dendrite-free zinc deposition.
Abstract: Aqueous zinc-ion batteries (AZIBs) are one of the promising energy storage systems, which consist of electrode materials, electrolyte, and separator. The first two have been significantly received ample development, while the prominent role of the separators in manipulating the stability of the electrode has not attracted sufficient attention. In this work, a separator (UiO-66-GF) modified by Zr-based metal organic framework for robust AZIBs is proposed. UiO-66-GF effectively enhances the transport ability of charge carriers and demonstrates preferential orientation of (002) crystal plane, which is favorable for corrosion resistance and dendrite-free zinc deposition. Consequently, Zn|UiO-66-GF-2.2|Zn cells exhibit highly reversible plating/stripping behavior with long cycle life over 1650 h at 2.0 mA cm-2, and Zn|UiO-66-GF-2.2|MnO2 cells show excellent long-term stability with capacity retention of 85% after 1000 cycles. The reasonable design and application of multifunctional metal organic frameworks modified separators provide useful guidance for constructing durable AZIBs.
92 citations
TL;DR: In this article , a charge-enriched strategy through MXene-based polypyrrole (MXene•mPPy) layers is explored toward dendrite-free Zn metal anode.
Abstract: Although zinc metal anodes have some intrinsic advantages for aqueous zinc ion batteries, the notorious dendrites hamper its practical applications. Herein, a charge‐enriched strategy through MXene‐based polypyrrole (MXene‐mPPy) layers is explored toward dendrite‐free Zn metal anode. The MXene‐mPPy layers composed of mesoporous PPy on both sides of Ti3C2Tx‐MXene exhibit an exceptional charge enrichment ability (149 F g−1, 5 mV s−1), which is beneficial not onlying terms of accumulating the charge levels, but also to homogenize the dispersions of electric field and ion flux as used as an artificial interface on a Zn anode. Thus, a dendrite‐free Zn anode with an ultralong cycling lifespan up to 2500 h and superior rate capability is achieved, which is further applied as an anode for aqueous zinc ion batteries with a long‐term span over 3000 cycles at 10 A g−1.
83 citations
TL;DR: In this paper , a hierarchical confinement strategy is proposed to design zincophilic and spatial traps through a host of porous Co-embedded carbon cages (denoted as CoCC), which enables a dendrite-free behavior with excellent kinetics.
Abstract: Zn-based aqueous batteries (ZABs) have been regarded as promising candidates for safe and large-scale energy storage in the "post-Li" era. However, kinetics and stability problems of Zn capture cannot be concomitantly regulated, especially at high rates and loadings. Herein, a hierarchical confinement strategy is proposed to design zincophilic and spatial traps through a host of porous Co-embedded carbon cages (denoted as CoCC). The zincophilic Co sites act as preferred nucleation sites with low nucleation barriers (within 0.5 mA h cm-2), and the carbon cage can further spatially confine Zn deposition (within 5.0 mA h cm-2). Theoretical simulations and in situ/ex situ structural observations reveal the hierarchical spatial confinement by the elaborated all-in-one network (within 12 mA h cm-2). Consequently, the elaborate strategy enables a dendrite-free behavior with excellent kinetics (low overpotential of ca. 65 mV at a high rate of 20 mA cm-2) and stable cycle life (over 800 cycles), pushing forward the next-generation high-performance ZABs.
70 citations
TL;DR: In this paper , a freestanding, lightweight, and zincophilic MXene/nanoporous oxide heterostructure engineered separator is designed to stabilize a Zn metal anode.
Abstract: Aqueous zinc (Zn)-ion batteries are regarded as promising candidates for large-scale energy storage systems because of their high safety, low cost, and environmental benignity. However, the dendrite issue of Zn anode hinders their practical application. Herein, a freestanding, lightweight, and zincophilic MXene/nanoporous oxide heterostructure engineered separator is designed to stabilize a Zn metal anode. The nanoporous oxides prepared by a one-step vacuum distillation technique afford the advantages of large surface area, high porosity, and homogeneous porous structure. The zincophilic MXene@oxides layer can homogenize the electric field distribution, facilitate ion diffusion kinetics, reduce local current density, and promote even Zn ionic flux, which will regulate uniform Zn deposition and suppress side reactions. Accordingly, dendrite-free Zn anodes with stable cyclability are achieved for over 500 h at an ultrahigh area capacity of 10 mAh cm-2. Besides, flexible, long-lifespan, and high-rate N/S-doped three-dimensional MXene@MnO2||Zn full cells are constructed with the engineered separator. Moreover, this strategy can be successfully extended to lithium, sodium, potassium, and magnesium metal batteries, indicating that separator regulation is a universal approach to overcome the challenges of metal batteries.
62 citations
TL;DR: In this article , the authors discuss solutions to the above problems to protect the zinc anode, including the improvement of zinc anodes materials, modification of the anode-electrolyte interface, and optimization of the electrolyte.
Abstract: Zinc-ion batteries (ZIBs) have been extensively investigated and discussed as promising energy storage devices in recent years owing to their low cost, high energy density, inherent safety, and low environmental impact. Nevertheless, several challenges remain that need to be prioritized before realizing the widespread application of ZIBs. In particular, the development of zinc anodes has been hindered by many challenges, such as inevitable zinc dendrites, corrosion passivation, and the hydrogen evolution reaction (HER), which have severely limited the practical application of high-performance ZIBs. This review starts with a systematic discussion of the origins of zinc dendrites, corrosion passivation, and the HER, as well as their effects on battery performance. Subsequently, we discuss solutions to the above problems to protect the zinc anode, including the improvement of zinc anode materials, modification of the anode–electrolyte interface, and optimization of the electrolyte. In particular, this review emphasizes design strategies to protect zinc anodes from an integrated perspective with broad interest rather than a view with limited focus. In the final section, comments and perspectives are provided for the future design of high-performance zinc anodes.
44 citations
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TL;DR: In this article, a vanadium oxide bronze was used as the positive electrode for a Zn cell with reversible intercalation of Zn ions in a layered Zn0.25V2O5⋅nH2O-based positive electrode.
Abstract: Although non-aqueous Li-ion batteries possess significantly higher energy density than their aqueous counterparts, the latter can be more feasible for grid-scale applications when cost, safety and cycle life are taken into consideration. Moreover, aqueous Zn-ion batteries have an energy storage advantage over alkali-based batteries as they can employ Zn metal as the negative electrode, dramatically increasing energy density. However, their development is plagued by a limited choice of positive electrodes, which often show poor rate capability and inadequate cycle life. Here we report a vanadium oxide bronze pillared by interlayer Zn2+ ions and water (Zn0.25V2O5⋅nH2O), as the positive electrode for a Zn cell. A reversible Zn2+ ion (de)intercalation storage process at fast rates, with more than one Zn2+ per formula unit (a capacity up to 300 mAh g−1), is characterized. The Zn cell offers an energy density of ∼450 Wh l−1 and exhibits a capacity retention of more than 80% over 1,000 cycles, with no dendrite formation at the Zn electrode. High-performing positive electrode materials are crucial for the development of aqueous Zn-ion batteries. Here the authors report a battery based on reversible intercalation of Zn ions in a layered Zn0.25V2O5⋅nH2O-based positive electrode, which exhibits high-capacity and long-term cycling stability.
1,948 citations
TL;DR: This work demonstrates that an aqueous electrolyte based on Zn and lithium salts at high concentrations is a very effective way to address irreversibility issues and brings unprecedented flexibility and reversibility to Zn batteries.
Abstract: Metallic zinc (Zn) has been regarded as an ideal anode material for aqueous batteries because of its high theoretical capacity (820 mA h g–1), low potential (−0.762 V versus the standard hydrogen electrode), high abundance, low toxicity and intrinsic safety. However, aqueous Zn chemistry persistently suffers from irreversibility issues, as exemplified by its low coulombic efficiency (CE) and dendrite growth during plating/ stripping, and sustained water consumption. In this work, we demonstrate that an aqueous electrolyte based on Zn and lithium salts at high concentrations is a very effective way to address these issues. This unique electrolyte not only enables dendrite-free Zn plating/stripping at nearly 100% CE, but also retains water in the open atmosphere, which makes hermetic cell configurations optional. These merits bring unprecedented flexibility and reversibility to Zn batteries using either LiMn2O4 or O2 cathodes—the former deliver 180 W h kg–1 while retaining 80% capacity for >4,000 cycles, and the latter deliver 300 W h kg–1 (1,000 W h kg–1 based on the cathode) for >200 cycles.
1,721 citations
TL;DR: In this article, the authors focus on fundamental aspects of the chemistry of Zn-ion batteries that are the least understood and on which there has been progress over the last few years, and provide guidance for future research regarding (1) the significant challenge of proton/Zn2+ co-intercalation in aqueous media, (2) limitations to conversion chemistry that often accompanies ZIB electrochemistry, (3) positive aspects of facile Zn 2+ (de)intercalations in nonaqueous electrolytes and organic cathode materials, (
874 citations
TL;DR: The challenges in AB fundamental research are presented, focusing on the design of advanced materials and practical applications of whole devices, and a roadmap starting with material design and ending with the commercialization of next-generation reliable ABs is provided.
Abstract: Safety concerns about organic media-based batteries are the key public arguments against their widespread usage. Aqueous batteries (ABs), based on water which is environmentally benign, provide a promising alternative for safe, cost-effective, and scalable energy storage, with high power density and tolerance against mishandling. Research interests and achievements in ABs have surged globally in the past 5 years. However, their large-scale application is plagued by the limited output voltage and inadequate energy density. We present the challenges in AB fundamental research, focusing on the design of advanced materials and practical applications of whole devices. Potential interactions of the challenges in different AB systems are established. A critical appraisal of recent advances in ABs is presented for addressing the key issues, with special emphasis on the connection between advanced materials and emerging electrochemistry. Last, we provide a roadmap starting with material design and ending with the commercialization of next-generation reliable ABs.
847 citations
727 citations