Issue 32, 2021

Black phosphorene/blue phosphorene van der Waals heterostructure: a potential anode material for lithium-ion batteries

Abstract

Van der Waals (vdW) heterostructure-based electrodes have invoked tremendous research interest due to their intriguing properties and their capability to break the limitations of the restricted properties of single-material systems. Herein, based on first-principles approaches, we propose that the black phosphorene/blue phosphorene (BLK-P/BLE-P) vdW heterostructure can be a capable anode material for power-driving lithium-ion batteries (LIBs), as it exhibits a large theoretical capacity, together with a relatively strong binding strength compared with the individual BLK-P and BLE-P monolayers. Our calculation results show that the Li adatom prefers to intercalate into the interlayer of the BLK-P/BLE-P vdW heterostructure due to the synergistic interfacial effect, resulting in a high binding strength and a diffusivity comparable to the BLK-P and BLE-P monolayers. Subsequently, the theoretical specific capacity is found to be as high as 552.8 mA h gāˆ’1, which can be attributed to the much higher storage capacity of Li adatoms in the BLK-P/BLE-P vdW heterostructure. Furthermore, electronic structure calculations reveal that a large amount of charge transfer assists in semiconductor to metallic transition upon lithiation, which would ensure good electrical conductivity. These simulations prove that the BLK-P/BLE-P heterostructure has great potential in LIBs and is essential for future battery design.

Graphical abstract: Black phosphorene/blue phosphorene van der Waals heterostructure: a potential anode material for lithium-ion batteries

Supplementary files

Article information

Article type
Paper
Submitted
07 Apr 2021
Accepted
09 Jul 2021
First published
13 Jul 2021

Phys. Chem. Chem. Phys., 2021,23, 17392-17401

Black phosphorene/blue phosphorene van der Waals heterostructure: a potential anode material for lithium-ion batteries

N. Muhammad, M. U. Muzaffar and Z. J. Ding, Phys. Chem. Chem. Phys., 2021, 23, 17392 DOI: 10.1039/D1CP01509E

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