scholarly journals Simulation of bi-layer cathode materials with experimentally validated parameters to improve ion diffusion and discharge capacity

2021 ◽  
Vol 5 (4) ◽  
pp. 1103-1119
Author(s):  
Ridwanur Chowdhury ◽  
Aayan Banerjee ◽  
Yan Zhao ◽  
Xinhua Liu ◽  
Nigel Brandon

Simulation shows that higher electrode utilization (next to current collector) and first discharge capacity can be achieved at high C-rates with bi-layer design compare to conventional electrodes, alongside an increase in energy-power density.

Materials ◽  
2020 ◽  
Vol 14 (1) ◽  
pp. 122
Author(s):  
Renwei Lu ◽  
Xiaolong Ren ◽  
Chong Wang ◽  
Changzhen Zhan ◽  
Ding Nan ◽  
...  

Lithium-ion hybrid capacitors (LICs) are regarded as one of the most promising next generation energy storage devices. Commercial activated carbon materials with low cost and excellent cycling stability are widely used as cathode materials for LICs, however, their low energy density remains a significant challenge for the practical applications of LICs. Herein, Na0.76V6O15 nanobelts (NaVO) were prepared and combined with commercial activated carbon YP50D to form hybrid cathode materials. Credit to the synergism of its capacitive effect and diffusion-controlled faradaic effect, NaVO/C hybrid cathode displays both superior cyclability and enhanced capacity. LICs were assembled with the as-prepared NaVO/C hybrid cathode and artificial graphite anode which was pre-lithiated. Furthermore, 10-NaVO/C//AG LIC delivers a high energy density of 118.9 Wh kg−1 at a power density of 220.6 W kg−1 and retains 43.7 Wh kg−1 even at a high power density of 21,793.0 W kg−1. The LIC can also maintain long-term cycling stability with capacitance retention of approximately 70% after 5000 cycles at 1 A g−1. Accordingly, hybrid cathodes composed of commercial activated carbon and a small amount of high energy battery-type materials are expected to be a candidate for low-cost advanced LICs with both high energy density and power density.


2012 ◽  
Vol 159 (12) ◽  
pp. A2135-A2142 ◽  
Author(s):  
Stefano Meini ◽  
Michele Piana ◽  
Hans Beyer ◽  
Jan Schwämmlein ◽  
Hubert A. Gasteiger

2011 ◽  
Vol 485 ◽  
pp. 115-118
Author(s):  
Atsushi Fujita ◽  
Fuminari Isobe ◽  
Takayuki Kodera ◽  
Takashi Ogihara

C/LiMnPO4 materials were synthesized by the complex polymerized method. An orthorhombic olivine type structure was obtained by calcination at temperatures over 973 K under an argon/hydrogen (5%) atmosphere. Differential thermogravimetric analysis showed that the carbon content of C/LiMnPO4 was about 65 wt%. The initial discharge capacity of C/LiMnPO4 calcined at 973 K was 135 mAh/g at 0.1 C and 60 mAh/g at 1 C.


Author(s):  
Xiao Yu ◽  
Zhiyong Yu ◽  
Jishen Hao ◽  
Hanxing Liu

Electrolyte additive tris(trimethylsilyl) phosphite (TMSPi) was used to promote the electrochemical performances of LiNi[Formula: see text]Co[Formula: see text]Mn[Formula: see text]O2 (NCM523) at elevated voltage (4.5 V) and temperature (55[Formula: see text]C). The NCM523 in 2.0 wt.% TMSPi-added electrolyte exhibited a much higher capacity (166.8 mAh/g) than that in the baseline electrolyte (118.3 mAh/g) after 100 cycles under 4.5 V at 30[Formula: see text]C. Simultaneously, the NCM523 with 2.0 wt.% TMSPi showed superior rate capability compared to that without TMSPi. Besides, after 100 cycles at 55[Formula: see text]C under 4.5 V, the discharge capacity retention reached 87.4% for the cell with 2.0 wt.% TMSPi, however, only 24.4% of initial discharge capacity was left for the cell with the baseline electrolyte. A series of analyses (TEM, XPS and EIS) confirmed that TMSPi-derived solid electrolyte interphase (SEI) stabilized the electrode/electrolyte interface and hindered the increase of interface impedance, resulting in obviously enhanced electrochemical performances of NCM523 cathode materials under elevated voltage and/or temperature.


2019 ◽  
Vol 10 ◽  
pp. 281-293 ◽  
Author(s):  
Donghui Zheng ◽  
Man Li ◽  
Yongyan Li ◽  
Chunling Qin ◽  
Yichao Wang ◽  
...  

Developing a facile and environmentally friendly approach to the synthesis of nanostructured Ni(OH)2 electrodes for high-performance supercapacitor applications is a great challenge. In this work, we report an extremely simple route to prepare a Ni(OH)2 nanopetals network by immersing Ni nanofoam in water. A binder-free composite electrode, consisting of Ni(OH)2 nanopetals network, Ni nanofoam interlayer and Ni-based metallic glass matrix (Ni(OH)2/Ni-NF/MG) with sandwich structure and good flexibility, was designed and finally achieved. Microstructure and morphology of the Ni(OH)2 nanopetals were characterized. It is found that the Ni(OH)2 nanopetals interweave with each other and grow vertically on the surface of Ni nanofoam to form an “ion reservoir”, which facilitates the ion diffusion in the electrode reaction. Electrochemical measurements show that the Ni(OH)2/Ni-NF/MG electrode, after immersion in water for seven days, reveals a high volumetric capacitance of 966.4 F/cm3 at a current density of 0.5 A/cm3. The electrode immersed for five days exhibits an excellent cycling stability (83.7% of the initial capacity after 3000 cycles at a current density of 1 A/cm3). Furthermore, symmetric supercapacitor (SC) devices were assembled using ribbons immersed for seven days and showed a maximum volumetric energy density of ca. 32.7 mWh/cm3 at a power density of 0.8 W/cm3, and of 13.7 mWh/cm3 when the power density was increased to 2 W/cm3. The fully charged SC devices could light up a red LED. The work provides a new idea for the synthesis of nanostructured Ni(OH)2 by a simple approach and ultra-low cost, which largely extends the prospect of commercial application in flexible or wearable devices.


2020 ◽  
Vol 30 (28) ◽  
pp. 2000473 ◽  
Author(s):  
Huangxu Li ◽  
Ming Xu ◽  
Zhian Zhang ◽  
Yanqing Lai ◽  
Jianmin Ma

CrystEngComm ◽  
2019 ◽  
Vol 21 (3) ◽  
pp. 399-402
Author(s):  
Yanli Fu ◽  
Liqiong Wu ◽  
Shengang Xu ◽  
Shaokui Cao ◽  
Xinheng Li

LiNi0.5Mn1.5O4 microcubes grown from nanowires delivered an initial discharge capacity of 123 mAh g−1 at 1C and maintained 95% of the capacity after 50 cycles due to interfacial effect.


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