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首页> 外文期刊>Advanced energy materials >Enhanced Potassium Ion Battery by Inducing Interlayer Anionic Ligands in MoS_(1.5)Se_(0.5) Nanosheets with Exploration of the Mechanism
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Enhanced Potassium Ion Battery by Inducing Interlayer Anionic Ligands in MoS_(1.5)Se_(0.5) Nanosheets with Exploration of the Mechanism

机译:通过探索机构,通过诱导MOS_(1.5)SE_(0.5)纳米片中的层间阴离子配体增强钾离子电池

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摘要

The strategy of inducing interlayer anionic ligands in 2D MoS1.5Se0.5 nanosheets is employed to consolidate the interlayer band gap and optimize the electronic structure for the potassium ion battery. It combines complementary advantages from two kinds of anionic ligands with high conductivity and good affinity with potassium ions. The potassium ion diffusion rate is accelerated as well by an optimized lower energy barrier for ion diffusion pathways, with the formation of highly reversible KMo3Se3 crystal other than K0.4MoS2/K2MoS4, which encounters a much slower electro/ion diffusion rate upon discharging. These advances deliver enhanced potassium storage properties with excellent cycling stability, with retained specific capacity of 531.6 mAh g(-1) at a current density of 200 mA g(-1) even after 1000 cycles, and high rate capability with specific capacity of 270.1 mAh g(-1) at 5 A g(-1). The insertion and conversion mechanism are also elucidated by a combination of density functional theory computations and in situ synchrotron measurements.
机译:采用诱导2D MOS1.5Se0.5纳米片中的中间层阴离子配体的策略来巩固层间带隙并优化钾离子电池的电子结构。它结合了两种阴离子配体的互补优点,具有高导电性和与钾离子的良好亲和力。通过用于离子扩散途径的优化的较低能量屏障,钾离子扩散速率加速,具有除K0.4MOS2 / K2MOS4之外的高度可逆的KMO3Se3晶体,其在放电时遇到了更慢的电频/离子扩散速率。这些前进提供了具有优异的循环稳定性的增强钾储存性能,即使在1000次循环之后,电流密度为200mA g(-1)的储存比容量为531.6mAhg(-1),以及具有270.1的特定容量的高速率能力MAH G(-1)在5A(-1)。插入和转换机构也通过密度函数理论计算和原位同步测量的组合来阐明。

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