TY - JOUR
T1 - The solid-state chelation synthesis of LiNi1/3Co1/3Mn1/3O2 as a cathode material for lithium-ion batteries
AU - Jiang, Xuyin
AU - Sha, Yujing
AU - Cai, Rui
AU - Shao, Zongping
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2015.
PY - 2015/5/21
Y1 - 2015/5/21
N2 - A facile solid-state chelation method using citric acid as the solid chelant was investigated for the synthesis of layered LiNi1/3Co1/3Mn1/3O2 as a cathode material for rechargeable lithium-ion batteries. The reaction was promoted by high-energy ball milling. During the synthesis, PVP was used as an additive. For comparison, LiNi1/3Co1/3Mn1/3O2 was also synthesized by a conventional sol-gel method using citric acid as the chelant. The as-prepared samples were characterized by TG-DSC, XRD, FESEM, BET specific surface area and galvanostatic charge-discharge tests. Based on the XPS, TEM and ED results, the sample synthesized by the solid-state chelation method with the PVP as an additive and subsequent calcination at 900 °C for 12 h in air was well indexed to a pure-phase hexagonal α-NaFeO2 structure with the highest crystallinity. The resulting sample showed an initial discharge capacity of 173 mA h g-1 in the potential range of 2.6-4.5 V and at a rate of 0.1 C, higher than that of the sample prepared by the same method without the use of a PVP additive during the synthesis (146 mA h g-1). Moreover, the electrochemical results at different current rates and the cycle performance for 100 cycles at 0.5 C indicated that the sample prepared by the solid-state chelation method exhibited better rate capability and cyclic stability than that prepared by the conventional sol-gel method. This phenomenon promises solid-state chelation as a new universal method for the preparation of functional materials.
AB - A facile solid-state chelation method using citric acid as the solid chelant was investigated for the synthesis of layered LiNi1/3Co1/3Mn1/3O2 as a cathode material for rechargeable lithium-ion batteries. The reaction was promoted by high-energy ball milling. During the synthesis, PVP was used as an additive. For comparison, LiNi1/3Co1/3Mn1/3O2 was also synthesized by a conventional sol-gel method using citric acid as the chelant. The as-prepared samples were characterized by TG-DSC, XRD, FESEM, BET specific surface area and galvanostatic charge-discharge tests. Based on the XPS, TEM and ED results, the sample synthesized by the solid-state chelation method with the PVP as an additive and subsequent calcination at 900 °C for 12 h in air was well indexed to a pure-phase hexagonal α-NaFeO2 structure with the highest crystallinity. The resulting sample showed an initial discharge capacity of 173 mA h g-1 in the potential range of 2.6-4.5 V and at a rate of 0.1 C, higher than that of the sample prepared by the same method without the use of a PVP additive during the synthesis (146 mA h g-1). Moreover, the electrochemical results at different current rates and the cycle performance for 100 cycles at 0.5 C indicated that the sample prepared by the solid-state chelation method exhibited better rate capability and cyclic stability than that prepared by the conventional sol-gel method. This phenomenon promises solid-state chelation as a new universal method for the preparation of functional materials.
UR - http://www.scopus.com/inward/record.url?scp=84928951948&partnerID=8YFLogxK
U2 - 10.1039/c5ta01236h
DO - 10.1039/c5ta01236h
M3 - 文章
AN - SCOPUS:84928951948
SN - 2050-7488
VL - 3
SP - 10536
EP - 10544
JO - Journal of Materials Chemistry A
JF - Journal of Materials Chemistry A
IS - 19
ER -