Abstract

Titanium dioxide (TiO2), as a potential anode material applied for lithium-ion batteries (LIBs), is constrained due to its poor theoretical specific capacity (335 mAh·g−1) and low conductivity (10−7-10−9 S·cm−1). When compared to TiO2, NiO with a higher theoretical specific capacity (718 mAh·g−1) is regarded as an alternative dopant for improving the specific capacity of TiO2. The present investigations usually assemble TiO2 and NiO with a simple bilayer structure and without NiO that is immersed into the inner of TiO2, which cannot fully take advantage of NiO. Therefore, a new strategy was put forward to utilize the synergistic effect of TiO2 and NiO, namely doping NiO into the inner of TiO2. NiO-TiO2 was fabricated into the nanofibers with a higher specific surface area to further improve their electrochemical performance due to the transportation path being greatly shortened. NiO-TiO2 nanofibers are expected to replace of the commercialized anode material (graphite). In this work, a facile one-step electrospinning method, followed by annealing, was applied to synthesize the Ni-doped TiO2 nanofibers. The Ni doping content was proven to be a crucial factor affecting phase constituents, which further determined the electrochemical performance. When the Ni doping content was less than 3 wt.%, the contents of anatase and NiO were both increased, while the rutile content was decreased in the nanofibers. When the Ni doping content exceeded 3 wt.%, the opposite changes were observed. Hence, the optimum Ni doping content was determined as 3 wt.%, at which the highest weight fractions of anatase and NiO were obtained. Correspondingly, the obtained electronic conductivity of 4.92 × 10−5 S⋅cm−1 was also the highest, which was approximately 1.7 times that of pristine TiO2. The optimal electrochemical performance was also obtained. The initial discharge and charge specific capacity was 576 and 264 mAh·g−1 at a current density of 100 mA·g−1. The capacity retention reached 48% after 100 cycles, and the coulombic efficiency was about 100%. The average discharge specific capacity was 48 mAh·g−1 at a current density of 1000 mA·g−1. Approximately 65.8% of the initial discharge specific capacity was retained when the current density was recovered to 40 mA·g−1. These excellent electrochemical results revealed that Ni-doped TiO2 nanofibers could be considered to be promising anode materials for LIBs.

Highlights

  • There will be huge demand for rechargeable energy storage systems ( lithium ion batteries (LIBs)) with the fast-growing energy consumption on earth and the development of renewable energy storage devices in recent years (portable electronics (PEs) and electric vehicles (EVs) and so on).Materials 2020, 13, 1302; doi:10.3390/ma13061302 www.mdpi.com/journal/materialsGraphite is commonly used as the anode material in commercial lithium-ion batteries (LIBs) [1,2,3,4]

  • NiO-TiO2 was fabricated into the nanofibers with a higher specific surface area to further improve their electrochemical performance due to the transportation path being greatly shortened

  • NiO-TiO2 nanofibers are expected to replace of the commercialized anode material

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Summary

Introduction

There will be huge demand for rechargeable energy storage systems ( lithium ion batteries (LIBs)) with the fast-growing energy consumption on earth and the development of renewable energy storage devices in recent years (portable electronics (PEs) and electric vehicles (EVs) and so on). Under the current density of 15, 75, 150, 300, 450, and 750 mA·g−1 , the rate performance test results showed that the discharge specific capacity of TiO2 /graphene was higher than that of pure TiO2. This result was explained in terms of the better conductivity of the composite material, which was conducive to lithium ions deintercalation. The initial discharge/charge specific capacity of NTA reached 297/256 mAh·g−1 at the current density of 0.5 C, while the value was improved to 203/177 mAh·g−1 by introducing NiO into NTA.

Synthesis of Pristine TiO2 and Ni-doped TiO2 Nanofibers
Characterization
Phase and Morphology Characterization of Nanofibers
Gibbs free free energy change
Transmission
Electrochemical
Conclusions
Full Text
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