Carbon-incorporated NaTi2(PO4)3 on carbon cloth as a binder-free anode material for high-performance aqueous sodium-ion hybrid capacitors

IF 2.5 4区 材料科学 Q2 CHEMISTRY, APPLIED
Peng Zhao, Xulin Yang, Qiancheng Liu, Jie Zhu, Sudong Yang, Lin Chen, Qian Zhang
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Abstract

NaTi2(PO4)3, as one of sodium superionic conductor (NASICON)-type anode materials, has been extensively concerned by researchers in Na-storage technologies due to their unique three-dimensional structure for Na+ insertion/deinsertion. However, the low conductivity of NaTi2(PO4)3 seriously hinders its electrochemical kinetics, which has been a major obstacle to further application. Herein, a facile strategy is proposed to synthesize carbon-incorporated NaTi2(PO4)3 nanoparticles on carbon cloth (NTP/C@CC) as a binder-free anode for aqueous sodium-ion hybrid capacitors (SIHCs). The amorphous carbon as a continuous conductive network can improve the electronic conductivity and restrict the particle growth of NaTi2(PO4)3. The small-sized NaTi2(PO4)3 nanoparticles embedded in the carbon network could increase the electrolyte/electrode interfacial area and shorten the Na+ transport path, resulting in increased electrochemical performance. Meanwhile, the carbon matrix can buffer the volume expansion during cycling and stabilize the structure of active materials. Consequently, the NTP/C@CC anode possesses a high specific capacity (0.416 mAh cm− 2 at 2 mA cm− 2), considerable rate capability (0.172 mAh cm− 2 at 30 mA cm− 2, 41.3% capacitance retention), and good long-term stability (83.2% capacitance retention after 5000 cycles at 30 mA cm− 2). In addition, an assembled SIHC device with P-doped porous carbon cloth (PPCC) as the cathode shows a capacity of 0.205 mAh cm− 2. The SIHC cell also acquires a superior energy density of 2.82 mWh cm− 3 and 81.5% capacity retention over 5000 cycles. This work may offer a viable way for constructing binder-free electrode materials for hybrid capacitors.

Abstract Image

碳布上的碳掺杂 NaTi2(PO4)3 作为高性能钠离子水混合电容器的无粘结剂阳极材料
NaTi2(PO4)3作为钠超离子导体(NASICON)型阳极材料之一,因其独特的Na+插入/脱出三维结构而受到储钠技术研究人员的广泛关注。然而,NaTi2(PO4)3 的低电导率严重阻碍了其电化学动力学的发展,成为其进一步应用的主要障碍。本文提出了一种在碳布(NTP/C@CC)上合成碳包合 NaTi2(PO4)3 纳米粒子的简便策略,作为钠离子混合水电容器(SIHC)的无粘结剂阳极。无定形碳作为一种连续的导电网络,可以提高电子导电性并限制 NaTi2(PO4)3 粒子的生长;嵌入碳网络中的小尺寸 NaTi2(PO4)3 纳米粒子可以增加电解质/电极界面面积并缩短 Na+ 传输路径,从而提高电化学性能。同时,碳基质可以缓冲循环过程中的体积膨胀,稳定活性材料的结构。因此,NTP/C@CC 阳极具有很高的比容量(2 mA cm- 2 时为 0.416 mAh cm- 2)、相当可观的速率能力(30 mA cm- 2 时为 0.172 mAh cm- 2,电容保持率为 41.3%)和良好的长期稳定性(30 mA cm- 2 循环 5000 次后电容保持率为 83.2%)。此外,以掺杂 P 的多孔碳布(PPCC)为阴极的组装 SIHC 器件显示出 0.205 mAh cm- 2 的容量。该 SIHC 电池还获得了 2.82 mWh cm- 3 的超高能量密度和超过 5000 次循环的 81.5% 容量保持率。这项研究为构建混合电容器的无粘结剂电极材料提供了一种可行的方法。
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来源期刊
Journal of Porous Materials
Journal of Porous Materials 工程技术-材料科学:综合
CiteScore
4.80
自引率
7.70%
发文量
203
审稿时长
2.6 months
期刊介绍: The Journal of Porous Materials is an interdisciplinary and international periodical devoted to all types of porous materials. Its aim is the rapid publication of high quality, peer-reviewed papers focused on the synthesis, processing, characterization and property evaluation of all porous materials. The objective is to establish a unique journal that will serve as a principal means of communication for the growing interdisciplinary field of porous materials. Porous materials include microporous materials with 50 nm pores. Examples of microporous materials are natural and synthetic molecular sieves, cationic and anionic clays, pillared clays, tobermorites, pillared Zr and Ti phosphates, spherosilicates, carbons, porous polymers, xerogels, etc. Mesoporous materials include synthetic molecular sieves, xerogels, aerogels, glasses, glass ceramics, porous polymers, etc.; while macroporous materials include ceramics, glass ceramics, porous polymers, aerogels, cement, etc. The porous materials can be crystalline, semicrystalline or noncrystalline, or combinations thereof. They can also be either organic, inorganic, or their composites. The overall objective of the journal is the establishment of one main forum covering the basic and applied aspects of all porous materials.
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