Abstract

It is reported that olivine-type lithium iron phosphate (LFP) for Li-ion batteries is one of the most widely utilized cathode materials, but its high-power applications are limited due to its intrinsically poor ion transfer rate and conductivity. Therefore, it is highly desired to fabricate LFP Li-ion capacitors (LICs) with high power performance and excellent cyclic reversibility, especially in safe, low cost and environmentally friendly aqueous electrolytes. Here, we fabricate LFP/expanded graphite (EG) nanocomposites by a one-step process, in which polyethylene glycol (PEG) is used as the particle growth inhibitor combined with vacuum infiltration of the LFP precursor into EG as a conductive sub-phase, and further investigate their high-power performance in aqueous LICs. Embedding spherical LFP nanoparticles with well-controlled size and agglomeration into the pores of EG and wrapping LFP nanoparticles by EG films contribute to the rapid electron and ion diffusion in LFP/EG composites, resulting in excellent cyclic reversibility and rate performance of LFP/EG composites. The aqueous LFP/EG//active carbon (AC) LICs were assembled in LiNO3 electrolytes with LFP/EG composites and AC as the positive and negative electrodes, respectively. The optimal LIC shows a power density of 2367.9 W kg−1 at an energy density of 6.5 W h kg−1, dramatically favorable rate characteristics and excellent cycle life with 82.1% capacitance retention of its primary capacitance at 2 A g−1 after 6000 cycles, markedly higher than those of the commercial LFP LIC. The presented aqueous LFP/EG//AC LICs with excellent electrochemical performance are expected to have broad high-power appliances that are cost-sensitive and highly secure.

Highlights

  • With the high-speed development of the world economy, environmental contamination is increasing and fossil fuel is being consumed in large quantities

  • From the point of application, it is highly desired that LFP/ expanded graphite (EG) composites with small particle size and high electrical conductivity can be fabricated by a simple one-step method and it will greatly contribute to high power performance of LFP Li-ion capacitors (LICs)

  • A new diffraction peak at 2q 1⁄4 26.6, attributing to the (002) peak of EG, occurs in the LFP/EG composites (S1 and S3) compared with standard LFP. These demonstrate that LFP/EG composites have been successfully prepared and the introduction of EG has no effect on the structure of LFP phase

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Summary

Introduction

Paper display higher power density than LIBs. At present, the organic electrolyte-based LICs have been investigated extensively, while the aqueous electrolyte-based LICs have received a little attention. From the point of application, it is highly desired that LFP/ EG composites with small particle size and high electrical conductivity can be fabricated by a simple one-step method and it will greatly contribute to high power performance of LFP LICs. The assembly process of LICs is crucial for achieving signi cant power and energy density.[32,33] In the process of the charge or discharge, the amount of electrical charge stored or released in the negative and positive electrodes is equal. For the assembled aqueous LFP/EG//active carbon (AC) LICs with LiNO3 electrolytes, through adjusting the mass ratio of the positive and negative electrodes, the cut-off voltage and the electrolyte concentration, we obtain the optimal LFP/EG//AC LIC with a power density of 2367.9 W kgÀ1 at an energy density of 6.5 W h kgÀ1, dramatically good rate characteristics and high cycle life with 82.1% capacitance retention of its primary capacitance at 2 A gÀ1 a er 6000 cycles, markedly higher than the commercial LFP//AC LIC. Our results illustrate a large prospect of our one-step method and aqueous LFP LICs, which are applicable for high-power situations that require low cost and high security

Experimental
Preparation of electrodes
Preparation of LICs
Measurements
XRD analysis
Morphology analysis
AC impedance analysis
Electrochemical performance of Li-ion capacitors
Conclusions

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