阴极
电化学
电极
储能
化学工程
钒
钾
纳米技术
纤维素
材料科学
化学
无机化学
有机化学
功率(物理)
物理化学
工程类
物理
量子力学
作者
Qingfeng Fu,Chi Peng,Wang Zhou,Xiangni Zhang,Keke Yang,L.B. Chen,Ying Mo,Jian‐Fang Wu,Peng Gao,Changling Fan,Chaohe Xu,Zhaohui Wang,Jilei Liu
标识
DOI:10.1073/pnas.2301622120
摘要
Potassium vanadium fluorophosphate (KVPO 4 F) is regarded as a promising cathode candidate for potassium-ion batteries due to its high working voltage and satisfactory theoretical capacity. However, the usage of electrochemically inactive binders and redundant current collectors typically results in inferior electrochemical performance and low energy density, thus implying the important role of rational electrode structure design. Herein, we have reported a scalable and cost-effective synthesis of a cellulose-derived KVPO 4 F self-supporting electrode, which features a special surface hydroxyl chemistry, three-dimensional porous and conductive framework, as well as super flexible and stable architecture. The cellulose not only serves as a flexible substrate, a pore-forming agent, and a versatile binder for KVPO 4 F/conductive carbon but also enhances the K-ion migration ability. Benefiting from the special hydroxyl chemistry-induced storage mechanism and electrode structural stability, the flexible freestanding KVPO 4 F cathode exhibits high-rate performance (53.0% capacity retention with current densities increased 50-fold, from 0.2 C to 10 C) and impressive cycling stability (capacity retention up to 74.9% can be achieved over 1,000 cycles at a rate of 5 C). Such electrode design and surface engineering strategies, along with a deeper understanding of potassium storage mechanisms, provide invaluable guidance for better electrode design to boost the performance of potassium-ion energy storage systems.
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