Abstract

To explore anode materials with large capacities and high rate performances for the lithium-ion batteries of electric vehicles, defective Ti2Nb10O27.1 has been prepared through a facile solid-state reaction in argon. X-ray diffractions combined with Rietveld refinements indicate that Ti2Nb10O27.1 has the same crystal structure with stoichiometric Ti2Nb10O29 (Wadsley-Roth shear structure with A2/m space group) but larger lattice parameters and 6.6% O2– vacancies (vs. all O2– ions). The electronic conductivity and Li+ion diffusion coefficient of Ti2Nb10O27.1 are at least six orders of magnitude and ~2.5 times larger than those of Ti2Nb10O29, respectively. First-principles calculations reveal that the significantly enhanced electronic conductivity is attributed to the formation of impurity bands in Ti2Nb10O29–x and its conductor characteristic. As a result of the improvements in the electronic and ionic conductivities, Ti2Nb10O27.1 exhibits not only a large initial discharge capacity of 329 mAh g–1 and charge capacity of 286 mAh g–1 at 0.1 C but also an outstanding rate performance and cyclability. At 5 C, its charge capacity remains 180 mAh g–1 with large capacity retention of 91.0% after 100 cycles, whereas those of Ti2Nb10O29 are only 90 mAh g–1 and 74.7%.

Highlights

  • There is a one-electron transfer between Ti4+ and Ti3+ ions and two-electron transfer between Nb5+ and Nb3+ ions

  • TiNb2O7 has a large theoretical capacity of 388 mAh g–1 based on the five-electron transfer per formula unit, and that of Ti2Nb10O29 is 396 mAh g–1 based on its 22-electron transfer

  • For the first time, we have employed the strategy of crystal structure modification to improve the rate performance of Ti2Nb10O29

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Summary

Introduction

There is a one-electron transfer between Ti4+ and Ti3+ ions and two-electron transfer between Nb5+ and Nb3+ ions. In spite of the above advantages, TiNb2O7 and Ti2Nb10O29 suffer from their intrinsically low electronic conductivities and Li+ ion diffusion coefficients, which significantly limit their rate performances. Crystal structure modification (including doping) has been demonstrated as an effective and facile strategy to improve the rate performance of intercalation-type electrode materials due to the resultant improvements of the electronic conductivity and/or Li+ ion diffusion coefficient[5,6].

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