کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1284058 | 1497967 | 2014 | 8 صفحه PDF | دانلود رایگان |

• LiNi0.5Co0.2Mn0.3O2 is designed to double-shelled structure.
• Double-shelled material exhibits improved cycleability and thermal stability.
• Double-shelled sample displays more excellent rate capability.
• The improved performances are probably attributed to the stable and porous outer shell.
LiNi0.5Co0.2Mn0.3O2 is redesigned into a new core-shelled Li[(Ni0.8Co0.1Mn0.1)2/7]core[(Ni1/3Co1/3Mn1/3)3/14]inner-shell[(Ni0.4Co0.2Mn0.4)1/2]outer-shellO2, in which LiNi0.8Co0.1Mn0.1O2 may deliver high capacity and LiNi0.4Co0.2Mn0.4O2 provides structural and thermal stability. To achieve such designed structure, double-shelled hydroxide precursors are firstly prepared via a co-precipitation route. Scanning electron microscope (SEM) shows that all precursors are of 6–10 μm spherical secondary particles developed from nanosheet-shaped primary particles. Energy disperse X-ray spectrum (EDS) on the surface of precursors, in combination with increase of particles size from core to shell during co-precipitation process, confirms the formation of core–shell structure as designed. The spherical morphology is preserved after lithiation at different temperatures from 800 °C to 900 °C while the morphology of primary particles changes from nano-sized plate to micron-sized rectangular-like shapes. EDS surface composition analysis of lithiated compounds also strongly suggests the formation of core–shell structure; nevertheless, diffusion of transition metal ions between the core and shell occurs and becomes severe with increase of sintering temperature. Consequently, the double-shelled materials especially prepared at 850 °C display the remarkably improved cycleability, rate capability, and thermal stability in contrast to normal one. The enhancement of those properties may be ascribed to structurally stable double shell components, especially outer shell.
Journal: Journal of Power Sources - Volume 265, 1 November 2014, Pages 174–181