# Cation-Disordered Rock-Salt Lithium Titanium Oxyfluoride Anode Enabling High-Rate Li-Ion Storage Through a 3D Percolation Network

**Authors:** Jing Gao, Minghao Hua, Junze Lu, Yuying Qin, Shuxian Zhang, Qingyu Li, Lidong Yang, Chengxiang Wang, Xiaohang Lin, Yuanwei Sun, Longwei Yin, Rutao Wang

PMC · DOI: 10.1007/s40820-026-02123-w · 2026-03-10

## TL;DR

A new lithium titanium oxyfluoride anode enables fast and efficient lithium-ion storage with high capacity and performance in batteries.

## Contribution

A novel cation-disordered anode material with a 3D percolation network enables pseudocapacitive Li+ storage at low potentials.

## Key findings

- The DRX-LixTiOF2 anode delivers a high reversible capacity of ~310 mAh g−1 and a rate capability exceeding 64.4 C.
- Monte Carlo simulations show that a 3D percolation network enables fast Li+ migration with low energy barriers.
- A lithium-ion capacitor with this anode achieves 4.0 V cell voltage, 197.9 Wh kg−1 energy density, and 50,000 W kg−1 power density.

## Abstract

A novel low-potential cation-disordered rock-salt lithium titanium oxyfluoride (DRX-LixTiOF2) anode synthesized via electrochemically induced transformation enables pseudocapacitive Li+ storage extending down to 0.1 V vs. Li+/Li and delivers a high reversible capacity of ~ 310 mAh g−1 and an ultrahigh rate capability exceeding 64.4 C.Monte Carlo simulations reveal that the pseudocapacitive characteristics of DRX-LixTiOF2 anode originate from a three-dimensional percolation network that facilitates fast Li+ migration with low energy barriers, enabled by a cation/anion-disordered structure arising from the mixed occupancy of Li/Ti cations and O/F anions.The lithium-ion capacitor assembled with this DRX-LixTiOF2 anode and an activated carbon cathode exhibits exceptional performance: a 4.0 V operating voltage, a high energy density of 197.9 Wh kg−1 and an ultrahigh power density of 50,000 W kg−1.

A novel low-potential cation-disordered rock-salt lithium titanium oxyfluoride (DRX-LixTiOF2) anode synthesized via electrochemically induced transformation enables pseudocapacitive Li+ storage extending down to 0.1 V vs. Li+/Li and delivers a high reversible capacity of ~ 310 mAh g−1 and an ultrahigh rate capability exceeding 64.4 C.

Monte Carlo simulations reveal that the pseudocapacitive characteristics of DRX-LixTiOF2 anode originate from a three-dimensional percolation network that facilitates fast Li+ migration with low energy barriers, enabled by a cation/anion-disordered structure arising from the mixed occupancy of Li/Ti cations and O/F anions.

The lithium-ion capacitor assembled with this DRX-LixTiOF2 anode and an activated carbon cathode exhibits exceptional performance: a 4.0 V operating voltage, a high energy density of 197.9 Wh kg−1 and an ultrahigh power density of 50,000 W kg−1.

The online version contains supplementary material available at 10.1007/s40820-026-02123-w.

Pseudocapacitive materials employ rapid, non-diffusion-limited faradaic processes to store charge, demonstrating significant potential for fast-charging batteries and supercapacitors. However, the high redox potentials of existing pseudocapacitive anodes substantially lower the overall cell voltage and energy density. Here, a cation-disordered rock-salt lithium titanium oxyfluoride (DRX-LixTiOF2, 0 < x < 2) is reported to reversibly accommodate approximately 1.19 mol of Li+ (~ 310 mAh g−1) and delivers high-rate performance (exceeding 64.4 C) via pseudocapacitive Li+ storage within a low potential window extending down to 0.1 V vs. Li+/Li. This pseudocapacitive behavior is characterized by several structural and electrochemical features: the absence of phase transformation during Li+ intercalation, quasi-rectangular cyclic voltammetry curves, sloping charge/discharge profiles and a surface-controlled current response. We further reveal that the pseudocapacitive characteristics originate from a three-dimensional percolation network that facilitates fast Li+ migration with low energy barriers, enabled by a cation/anion-disordered structure arising from the mixed occupancy of Li/Ti cations and O/F anions. Owing to its low operating potential and high-rate capability, DRX-LixTiOF2 allows a lithium-ion capacitor to attain 4.0 V cell voltage and achieve energy and power densities several times higher than those obtained with conventional anodes, such as battery-type Li4Ti5O12 or pseudocapacitive materials like Nb2O5 and TiO2.

The online version contains supplementary material available at 10.1007/s40820-026-02123-w.

## Linked entities

- **Chemicals:** Li+/Li (PubChem CID 16196428), Li+ (PubChem CID 28486), O/F (PubChem CID 6432002), Nb2O5 (PubChem CID 9903420), TiO2 (PubChem CID 26042)

## Full-text entities

- **Genes:** FLI1 (Fli-1 proto-oncogene, ETS transcription factor) [NCBI Gene 2313] {aka BDPLT21, EWSR2, FLI-1, SIC-1}
- **Diseases:** Ti (MESH:D000072676), LICs (MESH:D016864)
- **Chemicals:** 1-methyl-2-pyrrolidinone (MESH:C038678), graphite (MESH:D006108), MoS2 (MESH:C082964), DRX-Li2TiOF2 (-), PTFE (MESH:D011138), tetrabutyl titanate (MESH:C060171), O (MESH:D010100), nitrogen (MESH:D009584), Ti (MESH:D014025), V2O5 (MESH:C066075), AC (MESH:D002244), H2O (MESH:D014867), MnO2 (MESH:C016552), LiF (MESH:C027651), F (MESH:D005461), TiO2 (MESH:C009495), Li (MESH:D008094), Nb2O5 (MESH:C073337), HF (MESH:D006195), MXene (MESH:C000723374), Cu (MESH:D003300), PVDF (MESH:C024865), polyphenylene (MESH:C041325), ethanol (MESH:D000431), Ar (MESH:D001128), B (MESH:D001895), TM (MESH:D028561)
- **Cell lines:** Li2TiOF2 — Mus musculus (Mouse), Finite cell line (CVCL_4977)

## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12976300/full.md

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Source: https://tomesphere.com/paper/PMC12976300