TY - JOUR
T1 - Regulating the Grain Orientation and Surface Structure of Primary Particles through Tungsten Modification to Comprehensively Enhance the Performance of Nickel-Rich Cathode Materials
AU - Li, Wenjin
AU - Zhang, Jian
AU - Zhou, Yunan
AU - Huang, Wei
AU - Liu, Xianghuan
AU - Li, Zhao
AU - Gao, Min
AU - Chang, Zenghua
AU - Li, Ning
AU - Wang, Jiantao
AU - Lu, Shigang
AU - Li, Xiaolong
AU - Wen, Wen
AU - Zhu, Daming
AU - Lu, Yan
AU - Zhuang, Weidong
N1 - Publisher Copyright:
©
PY - 2020/10/21
Y1 - 2020/10/21
N2 - Nickel-rich layered oxides, as the most promising commercial cathode material for high-energy density lithium-ion batteries, experience significant surface structural instabilities that lead to severe capacity deterioration and poor thermal stability. To address these issues, radially aligned grains and surface LixNiyWzO-like heterostructures are designed and obtained with a simple tungsten modification strategy in the LiNi0.91Co0.045Mn0.045O2 cathode. The formation of radially aligned grains, manipulated by the WO3 modifier during synthesis, provides a fast Li+ diffusion channel during the charge/discharge process. Moreover, the tungsten tends to enter into the lattice of the primary particle surface, and the armor-type tungsten-rich heterostructure protects the bulk material from microcracks, structural transformations, and surface side reactions. First-principles calculations indicate that oxygen is more stable in the surface tungsten-rich heterostructure than elsewhere, thus triggering an improved surface structural stability. Consequently, the 2 wt % WO3-modified LiNi0.91Co0.045Mn0.045O2 (NCM@2W) material shows outstanding prolonged cycling performance (capacity retention of 80.85% after 500 cycles) and excellent rate performance (5 C, 188.4 mA h g-1). In addition, its layered-to-rock salt phase transition temperature is increased by 80 °C compared with that of the pristine cathode. This work provides a novel surface modification approach and an in-depth understanding of the overall performance enhancement of nickel-rich layered cathodes.
AB - Nickel-rich layered oxides, as the most promising commercial cathode material for high-energy density lithium-ion batteries, experience significant surface structural instabilities that lead to severe capacity deterioration and poor thermal stability. To address these issues, radially aligned grains and surface LixNiyWzO-like heterostructures are designed and obtained with a simple tungsten modification strategy in the LiNi0.91Co0.045Mn0.045O2 cathode. The formation of radially aligned grains, manipulated by the WO3 modifier during synthesis, provides a fast Li+ diffusion channel during the charge/discharge process. Moreover, the tungsten tends to enter into the lattice of the primary particle surface, and the armor-type tungsten-rich heterostructure protects the bulk material from microcracks, structural transformations, and surface side reactions. First-principles calculations indicate that oxygen is more stable in the surface tungsten-rich heterostructure than elsewhere, thus triggering an improved surface structural stability. Consequently, the 2 wt % WO3-modified LiNi0.91Co0.045Mn0.045O2 (NCM@2W) material shows outstanding prolonged cycling performance (capacity retention of 80.85% after 500 cycles) and excellent rate performance (5 C, 188.4 mA h g-1). In addition, its layered-to-rock salt phase transition temperature is increased by 80 °C compared with that of the pristine cathode. This work provides a novel surface modification approach and an in-depth understanding of the overall performance enhancement of nickel-rich layered cathodes.
KW - morphology control
KW - nickel-rich cathode
KW - surface stability
KW - thermal stability
KW - tungsten modification
UR - http://www.scopus.com/inward/record.url?scp=85094221183&partnerID=8YFLogxK
U2 - 10.1021/acsami.0c12893
DO - 10.1021/acsami.0c12893
M3 - Article
C2 - 32975928
AN - SCOPUS:85094221183
SN - 1944-8244
VL - 12
SP - 47513
EP - 47525
JO - ACS applied materials & interfaces
JF - ACS applied materials & interfaces
IS - 42
ER -