Zincophilic Sites‐Enriched Carbonized ZIF‐8/MXene Heterostructure Enables Rapid Reaction Kinetics and Interface Stability Toward Ultra‐High Rate Zn Anodes
Source abstract
Abstract
Abstract Though aqueous zinc ion batteries have driven increased attention due to various merits, the challenges of Zn anodes such as Zn dendrites and side reactions still hamper their practical applications. Herein, zincophilic conductive carbonized ZIF‐8 and MXene heterostructures (cZIF@MXene) acting as multifunctional layers on Zn anodes (cZIF@MXene‐Zn) are developed. In the cZIF@MXene, not only abundant nitrogen‐containing functional groups exhibit strong interaction with Zn ions but also the conductive matrix with a large surface area provides a reaction interface, thereby accelerating the reaction kinetics while guiding uniform Zn deposition. Meanwhile, cZIF@MXene exhibits numerous ion diffusion paths, facilitating uniform ion distribution. Moreover, 2D cZIF@MXene heterostructures maintain the stability of the interfacial structure. As a consequence, cZIF@MXene‐Zn shows stability, such as a long cycle life of over 3000 cycles at 10 mA cm −2 and 1 mAh cm −2 , and over 1000 cycles at 5 mA cm −2 and 1 mAh cm −2 .
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Research context
OpenAlex topics: Advanced battery technologies research · Advanced Battery Materials and Technologies · Membrane-based Ion Separation Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Fujian Key Laboratory of Polymer Materials College of Chemistry and Materials Science Fujian Normal University Fuzhou 350007 China
School of Materials Science and Engineering Beihang University Beijing 100191 China
Funding
National Natural Science Foundation of China · Natural Science Foundation of Fujian Province
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