Iron-Loaded Carbon Spherogels as Sustainable Electrode Materials for High-Performance Lithium-Ion Batteries

The increasing demand for sustainable energy storage drives the development of advanced lithium-ion battery (LIB) materials that combine high performance, cost efficiency, and environmental sustainability. Carbon spherogels, characterized by high surface area, interconnected porosity, and high conductivity, are promising electrode candidates; however, they suffer from low specific capacities when used alone. This study presents iron-loaded carbon spherogels as next-generation LIB electrodes, leveraging iron's high theoretical capacity, abundance, and eco-friendliness. A scalable and tailorable synthesis method enabled the integration of tunable iron contents (15-40 mass %) into the carbon framework, forming robust porous networks with uniformly distributed iron nanoparticles. Electrochemical characterization revealed high specific capacities (up to 1190 mAh g<sup>-1</sup>) and high cycling stability (>99% Coulombic efficiency over 300 cycles). Post-mortem analysis highlighted the synergistic interaction between iron redox activity and carbon matrix stability. The medium (27 mass %) iron-loaded carbon spherogel sample achieved the best balance between capacity and durability. These findings position iron-loaded carbon spherogels as sustainable, high-performance LIB electrodes, offering a cobalt-free and nickel-free alternative that addresses key challenges of conversion-type materials, such as volume expansion and capacity fading.

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Publication Details

Journal
Chemistry of Materials
Published
2026-01-29
DOI
https://doi.org/10.1021/acs.chemmater.5c02442
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Iron-Loaded Carbon Spherogels as Sustainable Electrode Materials for High-Performance Lithium-Ion Batteries

Gregor A. Zickler, Stefanie Arnold, Michael S. Elsaesser, A Quade et al.
Chemistry of Materials
Advancements in Battery Materials
article

Iron-Loaded Carbon Spherogels as Sustainable Electrode Materials for High-Performance Lithium-Ion Batteries

Gregor A. Zickler, Stefanie Arnold, Michael S. Elsaesser, A Quade, Le Thi Thao, Saeed Borhani, Volker Presser
article en

Abstract

The increasing demand for sustainable energy storage drives the development of advanced lithium-ion battery (LIB) materials that combine high performance, cost efficiency, and environmental sustainability. Carbon spherogels, characterized by high surface area, interconnected porosity, and high conductivity, are promising electrode candidates; however, they suffer from low specific capacities when used alone. This study presents iron-loaded carbon spherogels as next-generation LIB electrodes, leveraging iron's high theoretical capacity, abundance, and eco-friendliness. A scalable and tailorable synthesis method enabled the integration of tunable iron contents (15-40 mass %) into the carbon framework, forming robust porous networks with uniformly distributed iron nanoparticles. Electrochemical characterization revealed high specific capacities (up to 1190 mAh g<sup>-1</sup>) and high cycling stability (>99% Coulombic efficiency over 300 cycles). Post-mortem analysis highlighted the synergistic interaction between iron redox activity and carbon matrix stability. The medium (27 mass %) iron-loaded carbon spherogel sample achieved the best balance between capacity and durability. These findings position iron-loaded carbon spherogels as sustainable, high-performance LIB electrodes, offering a cobalt-free and nickel-free alternative that addresses key challenges of conversion-type materials, such as volume expansion and capacity fading.

Chemistry of MaterialsVol. 38(5)
University of Salzburg (AT), Leibniz Institute for Plasma Science and Technology (DE), Leibniz-Institute for New Materials (DE), Saarland University (DE)
Universität des Saarlandes, Universität Salzburg, Leibniz-Gemeinschaft
Responsible consumption and production
Openalex Percentile: Top 73%
Advancements in Battery Materials
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