Chiral nanographenes with pyrene and m-terphenyl groups were developed. The two nanographenes displayed opposite induced circular dichroism spectra due to the opposite chirality of the basal planes. Density functional theory calculations s...

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In Situ Synthesis of Amorphous GeSe/CNT Composite via Defective‐carbon‐mediated Chemical Bonding for Ultrastable Na Ion Storage
Von Wiley-VCH zur Verfügung gestellt
Structural defects in CNTs play a crucial role in the chemical bonding and bonding strength in GeSe/CNTs composites. Remarkably, the strong chemical bonding between GeSe and CNTs significantly weakens Ge−Se bonds and promotes amorphization of GeSe, thus facilitating a reversible conversion reaction and enhancing Na-ion diffusion.
Abstract
Herein, we report the in-situ synthesis of amorphous GeSe/CNT composite via defective-carbon-mediated chemical bonding for ultrastable Na-ion storage. Structural defects in CNTs play a crucial role in the chemical bonding and bonding strength in GeSe/CNTs composites. Specifically, the bonding strength tends to increase with increasing defect concentrations of CNTs. Remarkably, the strong chemical bonding between GeSe and CNTs significantly weakens Ge−Se bonds and promotes amorphization of GeSe, thus facilitating a reversible conversion reaction and enhancing Na-ion diffusion. Consequently, GeSe/CNTs composite exhibits outstanding cyclability of 87.9% even after 1000 cycles at 1 A g−1 and a high-rate capability of 288.3 mA h g−1 at 10 A g−1. Our work presents a promising approach for the amorphization of electrode materials enabled by the defective-carbon-mediated strong chemical bonding for Li-, Na-, and K-ion batteries.
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