Compacted mesoporous titania nanosheets anode for pseudocapacitance‐dominated, high‐rate, and high‐volumetric sodium‐ion storage

SmartMat Pub Date : 2023-03-10 DOI:10.1002/smm2.1192
Jiayu Yu, Xiaojuan Huang, Yalin He, Dafu Tang, Ting Huang, Lu Liu, Haobin Wu, D. Peng, Dongyuan Zhao, Kun Lan, Qiulong Wei
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引用次数: 1

Abstract

Surface‐redox pseudocapacitive nanomaterials show promise for fast‐charging energy storage. However, their high surface area usually leads to low density, which is not conducive to achieving both high volumetric capacity and high‐rate capability. Herein, we demonstrate that TiO2 nanosheets (meso‐TiO2‐NSs) with densely packed mesoporous are capable of fast pseudocapacitance‐dominated sodium‐ion storage, as well as high volumetric and gravimetric capacities. Through compressing treatment, the compaction density of meso‐TiO2‐NSs is up to ~1.6 g/cm3, combined with high surface area and high porosity with mesopore channels for rapid Na+ diffusion. The compacted meso‐TiO2‐NSs electrodes achieve high pseudocapacitance (93.6% of total charge at 1 mV/s), high‐rate capability (up to 10 A/g), and long‐term cycling stability (10,000 cycles). More importantly, the space‐efficiently packed structure enables high volumetric capacity. The thick‐film meso‐TiO2‐NSs anode with the mass loading of 10 mg/cm2 delivers a gravimetric capacity of 165 mAh/g and a volumetric capacity of 223 mAh/cm3 at 5 mA/cm2, much higher than those of commercial hard carbon anode (80 mAh/g and 86 mAh/cm3). This work highlights a pathway for designing a dense nanostructure that enables fast charge kinetics for high‐density sodium‐ion storage.
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紧凑的介孔二氧化钛纳米片阳极用于假电容主导,高速率和高容量的钠离子存储
表面氧化还原赝电容纳米材料显示出快速充电储能的前景。然而,它们的高表面积通常导致低密度,这不利于实现高容量和高速率的能力。在此,我们证明了密集排列的介孔TiO2纳米片(meso - TiO2 - NSs)能够快速存储假电容主导的钠离子,以及高容量和重量容量。通过压缩处理,meso - TiO2 - NSs的压实密度可达~1.6 g/cm3,具有高表面积和高孔隙率的介孔通道,有利于Na+的快速扩散。紧凑的介观- TiO2 - NSs电极具有高赝电容(1mv /s时总电荷的93.6%),高速率容量(高达10a /g)和长期循环稳定性(10,000次循环)。更重要的是,高效的空间填充结构实现了高容量。质量负载为10 mg/cm2的厚膜介膜TiO2 - NSs阳极的重量容量为165 mAh/g, 5 mA/cm2时的体积容量为223 mAh/cm3,远高于商用硬碳阳极(80 mAh/g和86 mAh/cm3)。这项工作强调了设计致密纳米结构的途径,该结构可以实现高密度钠离子存储的快速充电动力学。
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