TY - JOUR
T1 - Dental Resin Monomer Enables Unique NbO2/Carbon Lithium-Ion Battery Negative Electrode with Exceptional Performance
AU - Ji, Qing
AU - Gao, Xiangwen
AU - Zhang, Qiuju
AU - Jin, Liyu
AU - Wang, Da
AU - Xia, Yonggao
AU - Yin, Shanshan
AU - Xia, Senlin
AU - Hohn, Nuri
AU - Zuo, Xiuxia
AU - Wang, Xiaoyan
AU - Xie, Shuang
AU - Xu, Zhuijun
AU - Ma, Liujia
AU - Chen, Liang
AU - Chen, George Z.
AU - Zhu, Jin
AU - Hu, Binjie
AU - Müller-Buschbaum, Peter
AU - Bruce, Peter G.
AU - Cheng, Ya Jun
N1 - Publisher Copyright:
© 2019 The Authors. Published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2019/10/1
Y1 - 2019/10/1
N2 - Niobium dioxide (NbO2) features a high theoretical capacity and an outstanding electron conductivity, which makes it a promising alternative to the commercial graphite negative electrode. However, studies on NbO2 based lithium-ion battery negative electrodes have been rarely reported. In the present work, NbO2 nanoparticles homogeneously embedded in a carbon matrix are synthesized through calcination using a dental resin monomer (bisphenol A glycidyl dimethacrylate, Bis-GMA) as the solvent and a carbon source and niobium ethoxide (NbETO) as the precursor. It is revealed that a low Bis-GMA/NbETO mass ratio (from 1:1 to 1:2) enables the conversion of Nb (V) to Nb (IV) due to increased porosity induced by an alcoholysis reaction between the NbETO and Bis-GMA. The as-prepared NbO2/carbon nanohybrid delivers a reversible capacity of 225 mAh g−1 after 500 cycles at a 1 C rate with a Coulombic efficiency of more than 99.4% in the cycles. Various experimental and theoretical approaches including solid state nuclear magnetic resonance, ex situ X-ray diffraction, differential electrochemical mass spectrometry, and density functional theory are utilized to understand the fundamental lithiation/delithiation mechanisms of the NbO2/carbon nanohybrid. The results suggest that the NbO2/carbon nanohybrid bearing high capacity, long cycle life, and low gas evolution is promising for lithium storage applications.
AB - Niobium dioxide (NbO2) features a high theoretical capacity and an outstanding electron conductivity, which makes it a promising alternative to the commercial graphite negative electrode. However, studies on NbO2 based lithium-ion battery negative electrodes have been rarely reported. In the present work, NbO2 nanoparticles homogeneously embedded in a carbon matrix are synthesized through calcination using a dental resin monomer (bisphenol A glycidyl dimethacrylate, Bis-GMA) as the solvent and a carbon source and niobium ethoxide (NbETO) as the precursor. It is revealed that a low Bis-GMA/NbETO mass ratio (from 1:1 to 1:2) enables the conversion of Nb (V) to Nb (IV) due to increased porosity induced by an alcoholysis reaction between the NbETO and Bis-GMA. The as-prepared NbO2/carbon nanohybrid delivers a reversible capacity of 225 mAh g−1 after 500 cycles at a 1 C rate with a Coulombic efficiency of more than 99.4% in the cycles. Various experimental and theoretical approaches including solid state nuclear magnetic resonance, ex situ X-ray diffraction, differential electrochemical mass spectrometry, and density functional theory are utilized to understand the fundamental lithiation/delithiation mechanisms of the NbO2/carbon nanohybrid. The results suggest that the NbO2/carbon nanohybrid bearing high capacity, long cycle life, and low gas evolution is promising for lithium storage applications.
KW - lithium-ion negative electrodes
KW - methacrylate
KW - nanoparticles
KW - niobium dioxide/carbon nanohybrids
KW - thermal polymerization
UR - http://www.scopus.com/inward/record.url?scp=85070762005&partnerID=8YFLogxK
U2 - 10.1002/adfm.201904961
DO - 10.1002/adfm.201904961
M3 - Article
AN - SCOPUS:85070762005
SN - 1616-301X
VL - 29
JO - Advanced Functional Materials
JF - Advanced Functional Materials
IS - 43
M1 - 1904961
ER -