阳极
材料科学
多孔性
水溶液
化学工程
碳纤维
金属
生物量(生态学)
兴奋剂
涂层
电偶阳极
电化学
锌
水溶液中的金属离子
离子
无机化学
冶金
复合数
纳米技术
化学
阴极保护
复合材料
电极
有机化学
海洋学
光电子学
物理化学
工程类
地质学
作者
Wenjing Zheng,Lin Zhu,Hang Huang,Zhongti Sun,Hao Zhou,Kan Zhang
出处
期刊:ACS Sustainable Chemistry & Engineering
[American Chemical Society]
日期:2024-05-15
卷期号:12 (21): 8070-8082
被引量:4
标识
DOI:10.1021/acssuschemeng.4c00436
摘要
Aqueous zinc-ion batteries (AZIBs) have significant potential as a large-scale energy storage device due to their low cost and high safety. However, the formation of zinc dendrites during repeated plating and stripping and complicated side reactions has seriously hindered the development of AZIBs. Herein, a N, P dual-doped biomass carbon was constructed by a simple hydrothermal and pyrolysis strategy. In this case, N and P heteroatoms increased the defects of biomass carbon and made it easier to form a uniform and stable interface with the zinc metal. On the other hand, the interfacial interactions between Zn2+ and the biomass carbon surface were enhanced by the introduction of zincophilic groups, which lowered the energy barriers required for zinc nucleation, resulting in uniform zinc deposition. Therefore, symmetric batteries assembled with Zn anodes based on N and P dual-doped biomass carbon exhibited outstanding cycling stability (2000 h) and relatively small voltage hysteresis (45 mV) at a current density of 1 mA cm–2 and an area capacity of 0.15 mAh cm–2. Besides, with a VO2 cathode to compose a full battery, the capacity of the NPBC@Zn//VO2 battery was 132.2 mAh g–1 after 1500 cycles at 5 A g–1, with 76.8% capacity retention. It is much higher than the 27.7% of the Zn//VO2 battery. This work demonstrates a novel two-element-doped biomass carbon/Zn anode interface modification strategy to achieve dendrite-free Zn anodes in AZIBs.
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