3D ultralong nanowire arrays with a tailored hydrogen titanate phase as binder-free anodes for Li-ion capacitors
Well-ordered, self-supported ultralong nanowire arrays (NWAs) with a 3D structure and tailored hydrogen titanate (HTO) phase have been synthesized viaa facile template-free hydrothermal method and subsequent calcination and utilized as anodes in Li-ion capacitors (LICs) directly without any ancillar...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2016, Vol.4 (22), p.8716-8723 |
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Sprache: | eng |
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Zusammenfassung: | Well-ordered, self-supported ultralong nanowire arrays (NWAs) with a 3D structure and tailored hydrogen titanate (HTO) phase have been synthesized viaa facile template-free hydrothermal method and subsequent calcination and utilized as anodes in Li-ion capacitors (LICs) directly without any ancillary materials. The 3D structure constructed from ultralong nanowires and a rooftop network is beneficial to structural stability, electrolyte penetration, rich electro-active sites and short Li-ion transport paths. Moreover, the tailored HTO phase can introduce stronger and more effective Li-ion diffusion channels for the fast Li-ion insertion/extraction reaction. These merits from morphological and crystal structural design yield superior electrochemical performance in terms of high capacity, excellent rate capability and ultralong lifespan. The LIC assembled with a HTO NWA anode and activated carbon (AC) cathode achieves an attractive energy storage of 93.8 W h kg super(-1) and a capacitance retention of 78.8% after 3000 cycles at a high current density of 5.0 A g super(-1) within 0.0-3.0 V. Even at a rapid charging rate within 8.0 s, an excellent energy density of 33.3 W h kg super(-1) and a high power density of 15 kW kg super(-1) can be retained. Therefore, the HTO NWAs//AC LIC is a promising candidate as an energy storage system for high-energy and high-power applications. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/c6ta02413k |