Coupling Liquid Electrochemical TEM and Mass‐Spectrometry to Investigate Electrochemical Reactions Occurring in a Na‐Ion Battery Anode

Author:

Gallegos‐Moncayo Kevyn12,Folastre Nicolas12,Toledo Milan1,Tonnoir Hélène12,Rabuel François12,Gachot Grégory12,Huo Da12,Demortière Arnaud123ORCID

Affiliation:

1. Laboratoire de Réactivité et Chimie des Solides (LRCS) CNRS UMR 7314 UPJV Hub de l'Energie 15 rue Baudelocque Amiens Cedex 80039 France

2. Réseau sur le Stockage Electrochimique de l'Energie (RS2E) CNRS FR 3459 Hub de l'Energie 15 Rue Baudelocque Amiens Cedex 80039 France

3. ALISTORE‐European Research Institute CNRS FR 3104 Hub de l'Energie Rue Baudelocque Amiens Cedex 80039 France

Abstract

AbstractA novel approach for investigating the formation of solid electrolyte interphase (SEI) in Na‐ion batteries (NIB) through the coupling of in situ liquid electrochemical transmission electron microscopy (ec‐TEM) and gas‐chromatography mass‐spectrometry (GC/MS) is proposed. To optimize this coupling, experiments are conducted on the sodiation of hard carbon materials (HC) using two setups: in situ ec‐TEM holder and ex situ setup. Electrolyte (NP30) is intentionally degraded using cyclic voltammetry (CV), and the recovered liquid product is analyzed using GC/MS. Solid product (µ‐chip) is analyzed using TEM techniques in a post‐mortem analysis. The ex situ experiments served as a reference to for insertion of Na+ ions in the HC, SEI size (389 nm), SEI composition (P, Na, F, and O), and Na plating. The in situ TEM analysis reveals a cyclability limitation, this issue appears to be caused by the plating of Na in the form of a “foam” structure, resulting from the gas release during the reaction of Na with DMC/EC electrolyte. The foam structure, subsequently transformes into a second SEI, is electrochemically inactive and reduces the cyclability of the battery. Overall, the results demonstrate the powerful synergy achieved by coupling in situ ec‐TEM and GC/MS techniques.

Funder

Agence Nationale de la Recherche

Publisher

Wiley

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