mxene衍生的二氧化钛纳米片/氧化石墨烯异质结构用于优越的钠离子存储

Baosong Li , Dezhuang Ji , Abdallah Kamal Hamouda , Shaohong Luo
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引用次数: 0

摘要

过渡金属氧化物有望成为电池和超级电容器等储能设备的电极材料。然而,获得具有高容量、长期循环稳定性和卓越速率能力的理想电极材料仍然是一个挑战。在这项研究中,我们提出了一种由Ti3C2Tx MXene和还原氧化石墨烯衍生的TiO2纳米片组成的自组装异质结构。这种结构有利于异质结构的形成,同时建立导电网络。在异质结构中重新堆积多孔TiO2纳米片和还原氧化石墨烯可以获得高孔隙率和优异的导电性。由于电子和Na+转移的增强,以及在Na+插入/提取过程中结构稳定性的提高,这种异质结构表现出优异的Na+存储性能。具体来说,它表现出长期的循环稳定性(217 mAh g−1,在10℃,5000次循环)和超高倍率能力(135 mAh g−1,40℃)。电极反应动力学分析表明,Na+在异质结构中的储存主要由表面控制过程控制。我们的研究结果为在先进储能应用中利用自组装异质结构提供了一种有前途的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MXene-derived TiO2 nanosheets/rGO heterostructures for superior sodium-ion storage
Transition metal oxides hold promise as electrode materials for energy-storage devices such as batteries and supercapacitors. However, achieving ideal electrode materials with high capacity, long-term cycling stability, and superb rate capability remains a challenge. In this study, we present a self-assembled heterogeneous structure consisting of TiO2 nanosheets derived from Ti3C2Tx MXene and reduced graphene oxide. This structure facilitates the formation of heterogeneous structures while establishing a conductive network. The restacking of porous TiO2 nanosheets and reduced graphene oxide within the heterostructure results in high porosity and excellent conductivity. Due to enhanced electron and Na+ transfer, as well as improved structural stability during the Na+ insertion/extraction process, this heterogeneous structure exhibited exceptional Na+ storage performance. Specifically, it exhibits a long-term cycling stability (217 mAh g−1 at 10 C, 5000 cycles) and an ultrahigh rate capability (135 mAh g–1, 40 C). Analysis of electrode reaction kinetics suggests that Na+ storage in the heterostructure is predominantly governed by a surface-controlled process. Our results provide a promising strategy for utilizing self-assembled heterostructures in advanced energy storage applications.
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