Heat Transfer Fluids as Co‐Diluents in Localized High‐Concentration Electrolytes for High‐Rate Lithium Metal Batteries With Enhanced Safety

D Dominik Weintz (Helmholtz‐Institute Münster (IMD‐4) Forschungszentrum Jülich GmbH Münster Germany) A Adil Aboobacker (Helmholtz‐Institute Münster (IMD‐4) Forschungszentrum Jülich GmbH Münster Germany) A Andrew Dopilka (Energy Technologies and Systems Division, Lawrence Berkeley National Laboratory) F Felix Pfeiffer (Helmholtz-Institut Münster, IMD-4, Forschungszentrum Jülich GmbH 2 , 48149 Münster,) A Anne Hockmann (Institute of Physical Chemistry, University of Münster 1 , Corrensstraße 28/30, 48149 Münster,) U Uta Rodehorst (MEET Battery Research Center University of Münster Münster Germany) C Christian Wölke M Monika Schönhoff (Institute of Physical Chemistry, University of Münster 1 , Corrensstraße 28/30, 48149 Münster,) R Robert Kostecki (Energy Technologies and Systems Division, Lawrence Berkeley National Laboratory) D Diddo Diddens (Helmholtz Institute Münster (IMD-4), Forschungszentrum Jülich GmbH 2 , Münster 48149,) M Martin Winter (Forschungszentrum Jülich GmbH, Helmholtz-Institute Münster (IMD-4), Corrensstraße 46, 48149 Münster, Germany) I Isidora Cekic‐Laskovic (Helmholtz‐Institute Münster (IMD‐4) Forschungszentrum Jülich GmbH Münster Germany)

Abstract

ABSTRACT Localized high‐concentration electrolytes (LHCEs) have been identified as promising electrolyte formulations for lithium metal batteries, due to their effective interphase formation and promotion of compact Li deposition, yet their practical implementation is often limited by reduced ion transport kinetics. In this study, two industrially established fluorinated ethers are identified for the first time in battery research as effective co‐diluents as they combine a broad electrochemical stability window with a low viscosity and intrinsic non‐flammability. Incorporating these components, commonly used as heat transfer fluids, yields safer, less flammable electrolyte formulations with enhanced ion mobilities. In particular, the ternary co‐diluent formulation shows improved ion mobility by reducing the electrolyte's viscosity while limiting excessive ion clustering. Based on the improved electrolyte transport kinetics, lower overvoltages and higher Coulombic efficiencies at current densities ≥ 1 mA cm −2 are achieved with the ternary co‐diluent blend, resulting in markedly extended cycle life in an application‐oriented zero‐excess pouch cell compared with the baseline system. Complementary electrochemical and ex situ analysis of harvested electrodes at moderate current densities reveals no discernible differences in interphase morphology and composition, suggesting enhanced ion mobility as the primary cause of the improved high‐rate performance.

Article Details

Volume / Issue Vol. 1, Issue 1
Published June 16, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (12)

D

Dominik Weintz

Helmholtz‐Institute Münster (IMD‐4) Forschungszentrum Jülich GmbH Münster Germany

A

Adil Aboobacker

Helmholtz‐Institute Münster (IMD‐4) Forschungszentrum Jülich GmbH Münster Germany

A

Andrew Dopilka

Energy Technologies and Systems Division, Lawrence Berkeley National Laboratory

F

Felix Pfeiffer

Helmholtz-Institut Münster, IMD-4, Forschungszentrum Jülich GmbH 2 , 48149 Münster,

A

Anne Hockmann

Institute of Physical Chemistry, University of Münster 1 , Corrensstraße 28/30, 48149 Münster,

U

Uta Rodehorst

MEET Battery Research Center University of Münster Münster Germany

C

Christian Wölke

M

Monika Schönhoff

Institute of Physical Chemistry, University of Münster 1 , Corrensstraße 28/30, 48149 Münster,

R

Robert Kostecki

Energy Technologies and Systems Division, Lawrence Berkeley National Laboratory

D

Diddo Diddens

Helmholtz Institute Münster (IMD-4), Forschungszentrum Jülich GmbH 2 , Münster 48149,

M

Martin Winter

Forschungszentrum Jülich GmbH, Helmholtz-Institute Münster (IMD-4), Corrensstraße 46, 48149 Münster, Germany

I

Isidora Cekic‐Laskovic

Helmholtz‐Institute Münster (IMD‐4) Forschungszentrum Jülich GmbH Münster Germany