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单层TiSi₂P₄作为钠离子电池的高性能阳极。

Monolayer TiSi2P4as a high-performance anode for Na-ion batteries.

作者信息

Peng Jie, Wang Zhi-Yong

机构信息

School of Physical Science and Technology, Southwest University, Chongqing 400715, People's Republic of China.

Chongqing Key Laboratory of Micro-Nano Structure Optoelectronics, Chongqing 400715, People's Republic of China.

出版信息

J Phys Condens Matter. 2023 Aug 10;35(45). doi: 10.1088/1361-648X/acecf2.

DOI:10.1088/1361-648X/acecf2
PMID:37531965
Abstract

Exploring anode materials with overall excellent performance remains a great challenge for rechargeable Na-ion battery technologies. Herein, we have identified that monolayer TiSi2P4is just such a prospective anode candidate via first-principles calculations. It is showed to be dynamically, thermally, mechanically, and energetically stable, which provides feasibility for experimental realization. The Na diffusion on the its surface is proved to be ultrafast, with a migration energy barrier as low as 73 meV. Electronic structure confirms that the pristine system undergoes a transition from the semiconductor to metal during the whole sodiation process, which is a significant advantage to the electrode conductivity. More excitingly, monolayer TiSi2P4can accommodate up to double-sided five-layer adatoms, resulting in an ultrahigh theoretical capacity of 1176 mA h gand a low average open-circuit voltage of 0.195 V. Moreover, the maximally sodiated electrode monolayer yields rather small in-plane lattice expansion of only 1.40%, which ensures reversible deformation and excellent cycling stability as further corroborated by structural relaxation andmolecular dynamics simulation. Overall, all of these results point to the potential that monolayer TiSi2P4can serve as a promising anode candidate for application in high-performance low-cost Na-ion batteries.

摘要

对于可充电钠离子电池技术而言,探索具有整体优异性能的负极材料仍然是一项巨大的挑战。在此,我们通过第一性原理计算确定单层TiSi₂P₄正是这样一种有前景的负极候选材料。结果表明它在动力学、热学、力学和能量方面均具有稳定性,这为实验实现提供了可行性。经证实,Na在其表面的扩散速度极快,迁移能垒低至73 meV。电子结构表明,在整个钠化过程中,原始体系从半导体转变为金属,这对电极导电性而言是一个显著优势。更令人兴奋的是,单层TiSi₂P₄最多可容纳双面五层吸附原子,理论比容量高达1176 mA h g,平均开路电压低至0.195 V。此外,完全钠化的电极单层的面内晶格膨胀仅为1.40%,非常小,这确保了可逆变形和优异的循环稳定性,结构弛豫和分子动力学模拟进一步证实了这一点。总体而言,所有这些结果表明单层TiSi₂P₄有潜力成为高性能低成本钠离子电池应用中有前景的负极候选材料。

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