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      3D hierarchical graphene matrices enable stable Zn anodes for aqueous Zn batteries

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          Abstract

          Metallic zinc anodes of aqueous zinc ion batteries suffer from severe dendrite and side reaction issues, resulting in poor cycling stability, especially at high rates and capacities. Herein, we develop two three-dimensional hierarchical graphene matrices consisting of nitrogen-doped graphene nanofibers clusters anchored on vertical graphene arrays of modified multichannel carbon. The graphene matrix with radial direction carbon channels possesses high surface area and porosity, which effectively minimizes the surface local current density, manipulates the Zn 2+ ions concentration gradient, and homogenizes the electric field distribution to regulate Zn deposition. As a result, the engineered matrices achieve a superior coulombic efficiency of 99.67% over 3000 cycles at 120 mA cm −2, the symmetric cells with the composite zinc anode demonstrates 2600 h dendrite-free cycles at 80 mA cm −2 and 80 mAh cm −2. The as-designed full cell exhibits an inspiring capacity of 16.91 mAh cm −2. The Zn capacitor matched with activated carbon shows a superior long-term cycle performance of 20000 cycles at 40 mA cm −2. This strategy of constructing a 3D hierarchical structure for Zn anodes may open up a new avenue for metal anodes operating under high rates and capacities.

          Abstract

          Uncontrolled dendrite growth and severe side reactions at high capacities and rates impede its practical application for zinc metal anodes. Here, the authors propose a composite zinc anode with 3D hierarchical graphene matrix as a multifunctional host to regulate zinc deposition for aqueous zinc batteries.

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          Most cited references39

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          Long-life and deeply rechargeable aqueous Zn anodes enabled by a multifunctional brightener-inspired interphase

          A brightener-inspired polymer interphase enables highly reversible aqueous Zn anodes via suppressing side-reactions and manipulating the nucleation process. Aqueous Zn anodes have been revisited for their intrinsic safety, low cost, and high volumetric capacity; however, deep-seated issues of dendrite growth and intricate side-reactions hindered their rejuvenation. Herein, a “brightener-inspired” polyamide coating layer which elevates the nucleation barrier and restricts Zn 2+ 2D diffusion is constructed to effectively regulate the aqueous Zn deposition behavior. Importantly, serving as a buffer layer that isolates active Zn from bulk electrolytes, this interphase also suppresses free water/O 2 -induced corrosion and passivation. With this synergy effect, the polymer-modified Zn anode produces reversible, dendrite-free plating/stripping with a 60-fold enhancement in running lifetime (over 8000 hours) compared to the bare Zn, and even at an ultrahigh areal capacity of 10 mA h cm −2 (10 mA cm −2 for 1 h, 85% depth of discharge). This efficient rechargeability for Zn anodes enables a substantially stable full-cell paired with a MnO 2 cathode. The strategy presented here is straightforward and scalable, representing a stark, but promising approach to solve the anode issues in advanced Zn batteries.
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            Manipulating the ion-transfer kinetics and interface stability for high-performance zinc metal anodes

            We report a new class of Zn anodes modified by a three-dimensional nanoporous ZnO architecture (Zn@ZnO-3D), which can accelerate the kinetics of Zn 2+ transfer and deposition, inhibit dendrite growth, and reduce the side-reactions. The zinc metal is recognized as one of the most promising anodes for Zn-based batteries in an energy-storage system. However, the deposition and transfer of bivalent Zn 2+ into the host structure suffer from sluggish kinetics accompanying the side-reactions at the interface. Herein, we report a new class of Zn anodes modified by a three-dimensional (3D) nanoporous ZnO architecture coating on a Zn plate (designated as Zn@ZnO-3D) prepared by in situ Zn(OH) 4 2− deposition onto the surface. This novel structure has been proven to accelerate the kinetics of Zn 2+ transfer and deposition via the electrostatic attraction toward Zn 2+ rather than the hydrated one in the electrical double layer. As a consequence, it achieves an average 99.55% Zn utilization and long-time stability for 1000 cycles. Meanwhile, the Zn@ZnO-3D/MnO 2 cell shows no capacity fading after 500 cycles at 0.5 A g −1 with a specific capacity of 212.9 mA h g −1 . We believe that the mechanistic insight into the kinetics and thermodynamic properties of the Zn metal and the understanding of structure–interface–function relationships are very useful for other metal anodes in aqueous systems.
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              The Three‐Dimensional Dendrite‐Free Zinc Anode on a Copper Mesh with a Zinc‐Oriented Polyacrylamide Electrolyte Additive

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                Author and article information

                Contributors
                zhaots@sustech.edu.cn
                zengl3@sustech.edu.cn
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                14 July 2023
                14 July 2023
                2023
                : 14
                : 4205
                Affiliations
                [1 ]GRID grid.263817.9, ISNI 0000 0004 1773 1790, Shenzhen Key Laboratory of Advanced Energy Storage, , Southern University of Science and Technology, ; Shenzhen, 518055 China
                [2 ]GRID grid.263817.9, ISNI 0000 0004 1773 1790, Department of Mechanical and Energy Engineering, , Southern University of Science and Technology, ; Shenzhen, 518055 China
                [3 ]GRID grid.263817.9, ISNI 0000 0004 1773 1790, SUSTech Energy Institute for Carbon Neutrality, , Southern University of Science and Technology, ; Shenzhen, 518055 China
                [4 ]GRID grid.263488.3, ISNI 0000 0001 0472 9649, College of Chemistry and Environmental Engineering, Shenzhen University, ; Shenzhen, 518060 China
                Author information
                http://orcid.org/0000-0002-0510-1754
                Article
                39947
                10.1038/s41467-023-39947-8
                10349079
                07aea0d4-1870-4657-9062-f33cd7ab74cb
                © The Author(s) 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 22 November 2022
                : 6 July 2023
                Funding
                Funded by: Shenzhen Key Laboratatory of Advanced Energy Storage:20220815094504001
                Categories
                Article
                Custom metadata
                © Springer Nature Limited 2023

                Uncategorized
                mechanical and structural properties and devices,batteries
                Uncategorized
                mechanical and structural properties and devices, batteries

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