Bo Yan , Yilong Yu , Hao Sun , Xueping Liu , Yahao Li , Lulu Zhang , Xuelin Yang , Shengkui Zhong , Renheng Wang
{"title":"Flexible potassium-ion batteries enabled by encapsulating hollow NiSe/SnSe nanocubes within freestanding N-doped carbon nanofibers","authors":"Bo Yan , Yilong Yu , Hao Sun , Xueping Liu , Yahao Li , Lulu Zhang , Xuelin Yang , Shengkui Zhong , Renheng Wang","doi":"10.1016/j.ensm.2024.103908","DOIUrl":null,"url":null,"abstract":"<div><div>Self-supporting electrode materials are instrumental in accelerating the development of flexible potassium-ion batteries (PIBs). However, the challenge lies in designing self-supporting materials with sophisticated structures and compositions to overcome the sluggish kinetics and volume effect caused by the large size of potassium ions during K-storage. In this work, we present novel flexible anodes synthesized by confining hollow NiSe/SnSe nanocubes within nitrogen-doped carbon nanofibers (H<img>NiSe/SnSe@NC). Leveraging its unique organization and composition, the H<img>NiSe/SnSe@NC anode exhibits impressive initial Coulombic efficiency, excellent rate capability, and exceptional cyclability, even at high mass loadings, outperforming most reported PIBs anodes. Utilizing in-situ XRD and ex-situ TEM techniques, we elucidate the mechanism responsible for its high capacity and gain insights into the K-storage behavior and reaction kinetics through diverse electrochemical measurements. First-principles calculations further clarify the underlying mechanism by which the designed heterostructured anode enhances the adsorption/diffusion of K-ions. Additionally, we integrate this novel anode into full cells, achieving high energy density and extended cycling life. Remarkably, the pouch cell we fabricated delivers high reversible capacity and cyclability even under periodic bending conditions, highlighting its superiority for flexible devices. This research showcases the significance of designing and fabricating advanced self-supporting electrodes for flexible PIBs applications.</div></div>","PeriodicalId":306,"journal":{"name":"Energy Storage Materials","volume":"74 ","pages":"Article 103908"},"PeriodicalIF":18.9000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Energy Storage Materials","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2405829724007347","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Self-supporting electrode materials are instrumental in accelerating the development of flexible potassium-ion batteries (PIBs). However, the challenge lies in designing self-supporting materials with sophisticated structures and compositions to overcome the sluggish kinetics and volume effect caused by the large size of potassium ions during K-storage. In this work, we present novel flexible anodes synthesized by confining hollow NiSe/SnSe nanocubes within nitrogen-doped carbon nanofibers (HNiSe/SnSe@NC). Leveraging its unique organization and composition, the HNiSe/SnSe@NC anode exhibits impressive initial Coulombic efficiency, excellent rate capability, and exceptional cyclability, even at high mass loadings, outperforming most reported PIBs anodes. Utilizing in-situ XRD and ex-situ TEM techniques, we elucidate the mechanism responsible for its high capacity and gain insights into the K-storage behavior and reaction kinetics through diverse electrochemical measurements. First-principles calculations further clarify the underlying mechanism by which the designed heterostructured anode enhances the adsorption/diffusion of K-ions. Additionally, we integrate this novel anode into full cells, achieving high energy density and extended cycling life. Remarkably, the pouch cell we fabricated delivers high reversible capacity and cyclability even under periodic bending conditions, highlighting its superiority for flexible devices. This research showcases the significance of designing and fabricating advanced self-supporting electrodes for flexible PIBs applications.
自支撑电极材料有助于加速柔性钾离子电池(PIB)的开发。然而,如何设计具有复杂结构和成分的自支撑材料,以克服钾离子储存过程中因钾离子尺寸过大而导致的动力学迟缓和体积效应,是一项挑战。在这项工作中,我们介绍了通过将空心镍硒/硒纳米立方体限制在掺氮碳纳米纤维(H-NiSe/SnSe@NC)内合成的新型柔性阳极。利用其独特的组织和成分,H-NiSe/SnSe@NC 阳极即使在高负载情况下也能表现出令人印象深刻的初始库仑效率、出色的速率能力和卓越的循环性,优于大多数已报道的 PIBs 阳极。利用原位 XRD 和原位 TEM 技术,我们阐明了造成其高容量的机理,并通过各种电化学测量深入了解了 K 存储行为和反应动力学。第一性原理计算进一步阐明了所设计的异质结构阳极增强 K 离子吸附/扩散的基本机制。此外,我们还将这种新型阳极集成到全电池中,实现了高能量密度并延长了循环寿命。值得注意的是,即使在周期性弯曲条件下,我们制造的袋式电池也能提供高可逆容量和循环能力,突出了其在柔性设备方面的优越性。这项研究展示了为柔性 PIB 应用设计和制造先进自支撑电极的重要意义。
期刊介绍:
Energy Storage Materials is a global interdisciplinary journal dedicated to sharing scientific and technological advancements in materials and devices for advanced energy storage and related energy conversion, such as in metal-O2 batteries. The journal features comprehensive research articles, including full papers and short communications, as well as authoritative feature articles and reviews by leading experts in the field.
Energy Storage Materials covers a wide range of topics, including the synthesis, fabrication, structure, properties, performance, and technological applications of energy storage materials. Additionally, the journal explores strategies, policies, and developments in the field of energy storage materials and devices for sustainable energy.
Published papers are selected based on their scientific and technological significance, their ability to provide valuable new knowledge, and their relevance to the international research community.