Gradient-coated P-doped Si3N4 with dual functions for silicon anodes: stress buffering and charge transport enhancement

Abstract

To address the challenges of silicon anodes, including large volume changes and low ion mobility in Li-ion batteries, we propose a novel strategy: directly forming P-Si3N4 protective layers on Si particles. This coating mitigates structural degradation during cycling while enhancing electrical conductivity. Additionally, integrating pitch creates a conductive network, leveraging the high carrier concentration of P-Si3N4 for efficient electron transfer at high current densities. The N,P-Si@PC composite exhibits exceptional stability and capacity retention. Even after 800 cycles at current densities of 1 A g−1 and 3 A g−1, it maintains high capacities of 695 mAh g−1 and 427 mAh g−1, respectively. To elucidate the underlying mechanisms, we performed elasticity tensor analysis and Density Functional Theory (DFT) calculations. These studies reveal that P-Si3N4 enhances mechanical resilience, effectively reducing stress-induced fractures and limiting Solid Electrolyte Interphase (SEI) growth. Furthermore, DFT results indicate that phosphorus doping narrows the band gap, increasing carrier concentration and improving the conductivity of the protective layer. These alternative versions offer varied perspectives on addressing challenges with silicon-based Li-ion battery anodes through innovative coating strategies and theoretical insights into their mechanisms of action.

Graphical abstract: Gradient-coated P-doped Si3N4 with dual functions for silicon anodes: stress buffering and charge transport enhancement

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Article information

Article type
Paper
Submitted
07 Mar 2025
Accepted
05 Jun 2025
First published
12 Jun 2025

Sustainable Energy Fuels, 2025, Advance Article

Gradient-coated P-doped Si3N4 with dual functions for silicon anodes: stress buffering and charge transport enhancement

Y. Zhong, B. Yu, L. Xu, Y. Huang, Y. Zheng, J. Li and Z. Huang, Sustainable Energy Fuels, 2025, Advance Article , DOI: 10.1039/D5SE00347D

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