# Nanoscale chemical imaging of pseudocapacitive charge storage in MXenes

## TL;DR

This study uses advanced imaging to reveal how ions interact with MXene materials, showing different chemical reactions for protons and lithium ions.

## Contribution

The paper provides new insights into the chemical mechanisms of pseudocapacitive charge storage in MXenes using nanoscale imaging.

## Key findings

- Proton intercalation reduces titanium atoms in MXene flakes.
- Lithium-ion intercalation oxidizes titanium atoms in MXene flakes.
- Chemical imaging reveals distinct redox and intercalation pseudocapacitive processes.

## Abstract

Pseudocapacitive materials store electrochemical energy through fast and reversible surface charge transfer reactions. Titanium carbide MXenes are two-dimensional materials which have shown redox or intercalation pseudocapacitive properties depending on the electrolyte. Nevertheless, the intrinsic pseudocapacitive charging mechanism in individual MXene flakes remains unresolved. Here, we employ in situ scanning transmission X-ray microscopy (STXM) to map the local chemical changes in individual Ti3C2Tx MXene flakes during spontaneous and electrochemical intercalation of protons and lithium ions in aqueous electrolytes. Our investigations reveal that proton and lithium-ion intercalation induces a reduction and an oxidation, respectively, of the titanium atoms in the MXene. This difference reveals a profoundly different chemical origin between redox and intercalation pseudocapacitive processes. By elucidating the interplay between ion hydration, MXene surface chemistry and flake morphology, our study highlights the relevance of chemical imaging in single entities for the fundamental understanding of electrochemical charge storage mechanisms.

The intercalation of ions in individual Ti3C2Tx MXene flakes is investigated by scanning transmission X-ray microscopy. We reveal an opposite change in the oxidation state of titanium atoms upon proton and solvated lithium ion intercalation.