Large-Scale Synthesis and Lithium Storage Performance of Multilayer TiO2 Nanobelts

2019 ◽  
Vol 72 (6) ◽  
pp. 473 ◽  
Author(s):  
Zongkai Yue ◽  
Yaozu Kang ◽  
Tianyu Mao ◽  
Mengmeng Zhen ◽  
Zhiyong Wang

Titanium dioxide (TiO2) has been widely investigated as the electrode material for lithium ion batteries (LIBs), due to its low cost, small volume expansion, and high environmental friendliness. However, the fading capacity and short cycle life during the cycling process lead to poor cycling performance. Herein, multilayer TiO2 nanobelts with a high specific surface area and with many pores between nanoparticles are constructed via a simple and large-scale approach. Benefiting from the multilayer nanobelt structure, as-prepared TiO2 nanobelts deliver a high reversible capacity, strong cycling stability, and ultra-long cycle life (~185mAhg−1 at 500mAg−1 after 500 cycles) as electrode materials for LIBs.

2020 ◽  
Vol 12 (4) ◽  
pp. 486-491
Author(s):  
Jinlei Wang ◽  
Na Cao ◽  
Huiling Du ◽  
Xian Du ◽  
Hai Lu ◽  
...  

Metal-organic frameworks (MOFs) have recently emerged as promising electrode materials for lithium-ion batteries (LIBs). However, poor electrical conductivity in most MOFs limits their electrochemical performance. In this work, the integration of flaky cobalt 1,4-benzenedicarboxylate (Co-BDC) MOF with conductive polypyrrole (PPy) nanofibers via in-situ growth strategy was explored for developing novel anode materials for LIBs. Electrochemical studies showed that PPy/Co-BDC composites exhibited enhanced cycling performance (a reversible capacity of ca. 364 mA h g–1 at a current density of 50 mA g–1 after 100 cycles) and rate capability, com- pared with the pristine Co-BDC. The well dispersion of Co-BDC on polypyrrole nanofibers and the decrease in charge-transfer resistance of the composite electrodes accounted for the improvement of electrochemical properties.


2011 ◽  
Vol 197-198 ◽  
pp. 1113-1116 ◽  
Author(s):  
Wen Li Yao ◽  
Jin Qing Chen ◽  
An Yun Li ◽  
Xin Bing Chen

The platelike Co3O4/carbon nanofiber (CNF) composite materials were synthesized by the calcination of β-Co(OH)2/CNF precursor prepared by a surfactant-free hydrothermal method. As negative electrode materials for lithium-ion batteries, the platelike Co3O4/CNF composites can deliver a high reversible capacity of 900 mAh g-1 for a life extending over hundreds of cycles at a current density of 100 mA g-1. The high Li-storage capacity and excellent cycling performance for Co3O4/CNF composite materials may mainly attribute to the beneficial effect of the CNFs addition on enhancing structural stability and electrical conductivity of Co3O4 platelets.


Materials ◽  
2019 ◽  
Vol 12 (12) ◽  
pp. 1952 ◽  
Author(s):  
Santanu Mukherjee ◽  
Shakir Bin Mujib ◽  
Davi Soares ◽  
Gurpreet Singh

Sodium ion batteries (SIBs) are being billed as an economical and environmental alternative to lithium ion batteries (LIBs), especially for medium and large-scale stationery and grid storage. However, SIBs suffer from lower capacities, energy density and cycle life performance. Therefore, in order to be more efficient and feasible, novel high-performance electrodes for SIBs need to be developed and researched. This review aims to provide an exhaustive discussion about the state-of-the-art in novel high-performance anodes and cathodes being currently analyzed, and the variety of advantages they demonstrate in various critically important parameters, such as electronic conductivity, structural stability, cycle life, and reversibility.


Nanomaterials ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 695 ◽  
Author(s):  
Yijun Liu ◽  
Ying He ◽  
Elif Vargun ◽  
Tomas Plachy ◽  
Petr Saha ◽  
...  

To improve Li storage capacity and the structural stability of Ti3C2 MXene-based electrode materials for lithium-ion batteries (LIBs), a facile strategy is developed to construct three-dimensional (3D) hierarchical porous Ti3C2/bimetal-organic framework (NiCo-MOF) nanoarchitectures as anodes for high-performance LIBs. 2D Ti3C2 nanosheets are coupled with NiCo-MOF nanoflakes induced by hydrogen bonds to form 3D Ti3C2/NiCo-MOF composite films through vacuum-assisted filtration technology. The morphology and electrochemical properties of Ti3C2/NiCo-MOF are influenced by the mass ratio of MOF to Ti3C2. Owing to the interconnected porous structures with a high specific surface area, rapid charge transfer process, and Li+ diffusion rate, the Ti3C2/NiCo-MOF-0.4 electrode delivers a high reversible capacity of 402 mAh g−1 at 0.1 A g−1 after 300 cycles; excellent rate performance (256 mAh g−1 at 1 A g−1); and long-term stability with a capacity retention of 85.7% even after 400 cycles at a high current density, much higher than pristine Ti3C2 MXene. The results highlight that Ti3C2/NiCo-MOF have great potential in the development of high-performance energy storage devices.


MRS Advances ◽  
2019 ◽  
Vol 4 (33-34) ◽  
pp. 1861-1868 ◽  
Author(s):  
Hui Wang ◽  
Youning Gong ◽  
Delong Li ◽  
Qiang Fu ◽  
Chunxu Pan

ABSTRACTIn this study, a novel brick-like NiCo2O4 material was synthesized via a facile hydrothermal method. The as-prepared NiCo2O4 material possessed high porosity with the BET specific surface area of 58.33 m2/g, and its pore size distribution was in a range of 5-15 nm with a dominant pore diameter of 10.7 nm. The electrochemical performance of the NiCo2O4 was further investigated as anode material for lithium-ion battery. The NiCo2O4 anode possessed a high lithium storage capacity up to 2353.0 mAh/g at the current density of 100 mA/g. Even at the high rate of 1 A/g, a reversible capacity of ∼600 mAh/g was still retained, and an average discharge capacity of ∼1145 mAh/g could be recovered when the current density was reduced back to 150 mA/g. Due to the simple and cost-effective process, the NiCo2O4 bricks anode material shows great potential for further large-scale applications on the area of lithium-ion battery.


2022 ◽  
Vol 6 (1) ◽  
Author(s):  
Tian Carey ◽  
Abdelnour Alhourani ◽  
Ruiyuan Tian ◽  
Shayan Seyedin ◽  
Adrees Arbab ◽  
...  

AbstractThe scalable production of two-dimensional (2D) materials is needed to accelerate their adoption to industry. In this work, we present a low-cost in-line and enclosed process of exfoliation based on high-shear mixing to create aqueous dispersions of few-layer graphene, on a large scale with a Yw ~ 100% yield by weight and throughput of ϕ ~ 8.3 g h−1. The in-line process minimises basal plane defects compared to traditional beaker-based shear mixing which we attribute to a reduced Reynolds number, Re ~ 105. We demonstrate highly conductive graphene material with conductivities as high as σ ∼ 1.5 × 104 S m−1 leading to sheet-resistances as low as Rs ∼ 2.6 Ω □−1 (t ∼ 25 μm). The process is ideal for formulating non-toxic, biocompatible and highly concentrated (c ∼ 100 mg ml−1) inks. We utilise the graphene inks for inkjet printable conductive interconnects and lithium-ion battery anode composites that demonstrate a low-rate lithium storage capability of 370 mAh g−1, close to the theoretical capacity of graphite. Finally, we demonstrate the biocompatibility of the graphene inks with human colon cells and human umbilical vein endothelial cells at high c ∼ 1 mg ml−1 facilitating a route for the use of the graphene inks in applications that require biocompatibility at high c such as electronic textiles.


Author(s):  
Xinhui Zhao ◽  
Qingqing Ren

Abstract Low-cost Fe-based electrode materials for Li-ion energy storage devices attract lots of attention. In this work, porous Fe2O3 nanoparticles are synthesized by a simple route. Firstly, their lithium storage performance is investigated by assembling half-cell configurations with Li foil as the counter electrode. During initial dozens of cycles, capacities of Fe2O3 nanoparticles fall off rapidly, which is related to continuous growth of solid electrolyte interphase (SEI). Amazingly, the capacities show an upturn in extended cycles. The pseudocapacitance of activated capacities is revealed by executing cyclic voltammetry (CV) tests at various scan rates on 500-cycled Fe2O3 electrodes. Based on electrochemical results, we speculate this special cycling performance of Fe2O3 nanoparticles may be associated with reversible electrochemical processes of SEI under the catalysis of nano-size Fe. Further, 500-cycled Fe2O3 anodes are reassembled with activated carbon cathodes for Li-ion capacitors (LICs). The LICs show energy densities of 110 Wh kg−1 at power densities of 136 W kg−1, and 72.8% capacity retention after 3000 cycles at 2 A g−1. We report an interesting electrochemical behavior of porous Fe2O3 nanoparticles, and a high-performance LIC based on activated Fe2O3 as an anode. This work may offer a new understanding for lithium storage capacities of metal oxide anodes.


2014 ◽  
Vol 07 (06) ◽  
pp. 1440008 ◽  
Author(s):  
Linlin Wang ◽  
Kaibin Tang ◽  
Min Zhang ◽  
Xiaozhu Zhang ◽  
Jingli Xu

Particle size effects on the electrochemical performance of the CuO particles toward lithium are essential. In this work, a low-cost, large-scale production but simple approach has been developed to fabricate CuO nanoparticles with an average size in ~ 130 nm through thermolysis of Cu ( OH )2 precursors. As anode materials for lithium ion batteries (LIBs), the CuO nanoparticles deliver a high reversible capacity of 540 mAh g-1 over 100 cycles at 0.5 C. It also exhibits a rate capacity of 405 mAh g-1 at 2 C. These results suggest that the facile synthetic method of producing the CuO nanoparticles can enhance cycle performance, superior to that of some different sizes of the CuO nanoparticles and many reported CuO -based anodes.


2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Enze Xu ◽  
Pengcheng Li ◽  
Junjie Quan ◽  
Hanwen Zhu ◽  
Li Wang ◽  
...  

AbstractRecently, abundant resources, low-cost sodium-ion batteries are deemed to the new-generation battery in the field of large-scale energy storage. Nevertheless, poor active reaction dynamics, dissolution of intermediates and electrolyte matching problems are significant challenges that need to be solved. Herein, dimensional gradient structure of sheet–tube–dots is constructed with CoSe2@CNTs–MXene. Gradient structure is conducive to fast migration of electrons and ions with the association of ether electrolyte. For half-cell, CoSe2@CNTs–MXene exhibits high initial coulomb efficiency (81.7%) and excellent cycling performance (400 mAh g−1 cycling for 200 times in 2 A g−1). Phase transformation pathway from crystalline CoSe2–Na2Se with Co and then amorphous CoSe2 in the discharge/charge process is also explored by in situ X-ray diffraction. Density functional theory study discloses the CoSe2@CNTs–MXene in ether electrolyte system which contributes to stable sodium storage performance owing to the strong adsorption force from hierarchical structure and weak interaction between electrolyte and electrode interface. For full cell, CoSe2@CNTs–MXene//Na3V2 (PO4)3/C full battery can also afford a competitively reversible capacity of 280 mAh g−1 over 50 cycles. Concisely, profiting from dimensional gradient structure and matched electrolyte of CoSe2@CNTs–MXene hold great application potential for stable sodium storage.


Scanning ◽  
2018 ◽  
Vol 2018 ◽  
pp. 1-7 ◽  
Author(s):  
Xuzi Zhang ◽  
Zhihong Chen ◽  
Lingling Shui ◽  
Chaoqun Shang ◽  
Hua Liao ◽  
...  

Sodium-ion batteries (SIBs), owning to the low cost, abundant resources, and similar physicochemical properties with lithium-ion batteries (LIBs), have earned much attention for large-scale energy storage systems. In this article, we successfully synthesize flexible freestanding carbon nanofiber-embedded TiO2 nanoparticles (CNF-TiO2) and then apply it directly as anode in SIBs without binder or current collector. Taking the advantage of flexible CNF and high structural stability, this anode exhibits high reversible capacity of 614 mAh·g−1 (0.27 mAh·cm−2) after almost 400 cycles and excellent capacity retention ability of ~100%


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