Influence of Ti/V Cation-Exchange in Na$_2$Ti$_3$O$_7$ on Na-Ion Negative Electrode Performance: an Insight from First-Principles Study

TL;DR

This study uses first-principles calculations to show that exchanging Ti with V in Na2Ti3O7 enhances its capacity and electronic conductivity as a Na-ion battery anode, with minimal volume change.

Contribution

It provides new insights into how Ti/V cation exchange improves Na2Ti3O7's electrochemical performance based on first-principles analysis.

Findings

Na2TiV2O7 shows over 280 mAh g$^{-1}$ capacity.

V substitution lowers voltages and volume expansion.

Electronic transport is significantly improved in V-modified compounds.

Abstract

Sodium-titanate \ce{Na2Ti3O7} (NTO) is regarded as a highly promising anode material with a very low voltage for Na-ion batteries and capacitors, but suffered from relatively low specific capacity and poor electron conductivity. Here we report a first-principles study of electrochemical properties of NTO and its vanadium-modified compounds, \ce{Na2Ti2VO7} and \ce{Na2TiV2O7} (NTVO), offering an insight into their detailed working mechanism and an evidence of enhancing anode performance by Ti/V cation exchange. Our calculations reveal that the specific capacity can increase from 177 mAh g$^{-1}$ in NTO to over 280 mAh g$^{-1}$ in NTVO when using \ce{NaTi_{3-$x$}V_{$x$}O7} ($x$ = 1, 2) as a starting material for Na insertion due to higher oxidation state of \ce{V^{+5}}, together with lower voltages and small volume expansion rates below 3\%. With Ti/V exchange, we obtain slightly higher activation energies for Na ion migrations along the two different pathways, but find an obvious improvement of electronic transport in NTVO.