B-/Si-containing electrolyte additive efficiently establish a stable interface for high-voltage LiCoO cathode and its synergistic effect on LiCoO/graphite pouch cells.

J Colloid Interface Sci

School of Chemistry, South China Normal University, Guangzhou 510006, Guangdong, China; National and Local Joint Engineering Research Center of MPTES in High Energy and Safety LIBs, Engineering Research Center of MTEES (Ministry of Education), and Key Lab. of ETESPG (GHEI), South China Normal Univer

Published: July 2023


Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

An effective electrolyte additive, 3-(tert-Butyldimethylsilyoxy) phenylboronic acid (TBPB), is proposed to significantly improve the cycle stability of high voltage LiCoO (LCO) cathode. Experimental and computational results show that TBPB has a relatively higher oxidation activity than base electrolyte, and preferentially constructs a stable cathode electrolyte interphase (CEI) containing B-/Si- components on LCO surface. Theoretical calculation, XPS and NMR data show that TBPB-derived CEI layer contains B-F species and has the function of eliminating HF. The as-formed CEI effectively inhibits the detrimental side reactions from electrolyte decomposition and LCO surface structure reconstruction. The capacity retention of LCO/Li half-cell increases from 38.92% (base electrolyte) to 83.70% after 150 cycles at 1 C between 3.0 V and 4.5 V by adding 1% TBPB. Moreover, TBPB is also reduced prior to base electrolyte, forming an ionic conducting solid electrolyte interphase (SEI) on graphite surface. Benefiting from the synergistic effect between CEI layer on LCO cathode and SEI layer on graphite anode to effectively decrease the electrolyte decomposition, the capacity retention of commercial LCO/graphite pouch cell with 1% TBPB increases from 10.44% to 76.13% after 400 cycles at 1 C between 3.0 V and 4.5 V. This work demonstrates that TBPB can act as an effective film-forming additive for high energy density LCO cathode at high voltage, and provides novel insights for its commercial application from the aspect of synergistically interfacial stability.

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jcis.2023.03.156DOI Listing

Publication Analysis

Top Keywords

lco cathode
12
base electrolyte
12
electrolyte additive
8
electrolyte
8
high voltage
8
electrolyte interphase
8
lco surface
8
cei layer
8
electrolyte decomposition
8
capacity retention
8

Similar Publications

High-nickel layered oxide LiNiCoMnO (NCM, ≥ 0.8) materials are considered optimal cathodes for lithium-ion power batteries owing to their high energy density, commendable cycling performance, and cost-effectiveness. However, structural collapse and interface instability during cycling result in diminished cycling stability, significantly hindering their commercial viability.

View Article and Find Full Text PDF

Amidst global sustainability imperatives, this study pioneers a solid-state regeneration strategy that transforms spent LiCoO (LCO) cathodes into high-performance materials via amorphous lithium iron phosphate glass (LFPg)-driven structural reconfiguration. Unlike conventional recycling that decomposes cathodes, our approach leverages LFPg's defect-rich framework, high ionic conductivity, and dynamic interfacial activity to directly reconstruct degraded LCO crystals. The LFPg acts as a multifunctional repair agent: creating Li diffusion channels through disorder engineering, eliminating oxygen vacancies via atomic oxygen transfer, scavenging impurities (e.

View Article and Find Full Text PDF

A Hydrogen-Bonded Crossing Binder for High-Voltage Applications of the Lithium Cobalt Oxide Cathode.

ACS Appl Mater Interfaces

September 2025

Jiangsu Key Laboratory of Materials and Technologies for Energy Storage, College of Materials Science and Technology, Nanjing University of Aeronautics and Astronautics, Nanjing 210016, P. R. China.

The inferior cycle capacity of the lithium cobalt oxide (LCO) cathode at high potential hinders the further enhancement of its working voltage. In response to this challenge, an innovative water-based binder (SL-GG) was prepared by employing sodium lignosulfonate (SL) and guar gum (GG) as raw materials to achieve high-potential LiCoO (4.6 V) cathodes with cycling stability.

View Article and Find Full Text PDF

Unlocking the capacity potential of mainstream LiCoO (LCO) cathode materials for stable cycling at a high upper cut-off voltage is undoubtedly one of the most economical approaches to achieving high-energy-density lithium-ion batteries. However, significant polarization issues induced by interfacial and interphase degradation during high-voltage cycling remain well known. This study demonstrates the efficient depolarization effects of cyclic organosiloxane additive 2,4,6,8-tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane (V4D4) at the cathode-electrolyte interface, facilitating interfacial charge transfer and enhancing the capacity of LCO||Li cells to 220 mA h g even at 4.

View Article and Find Full Text PDF

Breaking the 4.6 V Barrier in LiCoO Cathodes: Synergistic Effects of Bulk and Surface Structure Modification.

Small

August 2025

Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Department of Chemistry, College of Smart Materials and Future Energy, Fudan University, Shanghai, 200433, P. R. China.

Overcoming the 4.6 V barrier for LiCoO (LCO) cathodes necessitates concurrent mitigation of bulk structural degradation and interfacial side reactions. Herein, a bulk-surface synergistic stabilization strategy is proposed integrating Fe/F dual-site doping with an ultrathin LiCPON solid electrolyte coating (≈2 nm) deposited via magnetron sputtering.

View Article and Find Full Text PDF