Acid-Free Electrochemical Regeneration of Sandrose-like Aluminum Layered Double Hydroxide Electrodes for Selective Lithium-Ion Recovery in Mixed Ion Solution

The demand for lithium production has seen a significant rise, with the growing electric vehicle and stationary battery markets requiring further development of sustainable and scalable extraction methods. Direct lithium extraction technologies have been developed to address potential shortages, with adsorption emerging as a key method due to its efficiency and low environmental impact. Given that Al-(OH)<sub>3</sub> is already utilized as an adsorbent in various industrial applications, the practical importance of Al-based alternative systems for lithium ion extraction is increasing, yet lithium ion recovery requires harsh chemicals. In this study, we report a novel lithium extraction method combining chemical adsorption and electrochemical release using a synthesized aluminum layered double hydroxide (Al-LDH) material, developed under mild reaction conditions. The performance of the Al-LDH electrode was evaluated against a commercial Al-(OH)<sub>3</sub> adsorbent. Comprehensive characterization using techniques such as X-ray diffraction, Fourier-transform infrared spectroscopy, and scanning electron microscopy revealed detailed insights into the crystalline structure, particle size distribution, and surface morphology of the materials. The Al-LDH electrode exhibited a lithium ion adsorption capacity, achieving an average chemical uptake of lithium ions of 57.6 mg/g. In contrast, lithium-ion uptake capacity for Al-(OH)<sub>3</sub> was 1.0 mg/g over 15 cycles. Notably, this method operates under pH-neutral conditions, eliminating the need for harsh acidic or basic eluents. As a result, it prevents structural degradation and minimizes secondary pollution for potential future applications of lithium-ion recovery. The material's layered structure selectively allowed lithium ion intake while blocking sodium ions, demonstrating its high selectivity and utility in lithium ion recovery processes. The integration of pH-neutral regeneration and high selectivity shows that Al-LDH electrodes as viable candidates for next-generation, green lithium extraction technologies.

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Publication Details

Journal
ACS Sustainable Chemistry & Engineering
Published
2025-10-31
DOI
https://doi.org/10.1021/acssuschemeng.5c08261
Primary Topic
Extraction and Separation Processes
Type
article
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article

Acid-Free Electrochemical Regeneration of Sandrose-like Aluminum Layered Double Hydroxide Electrodes for Selective Lithium-Ion Recovery in Mixed Ion Solution

Antje Quade, Volker Presser, Prisciliano Hernández, Cansu Kök et al.
ACS Sustainable Chemistry & Engineering
Extraction and Separation Processes
article

Acid-Free Electrochemical Regeneration of Sandrose-like Aluminum Layered Double Hydroxide Electrodes for Selective Lithium-Ion Recovery in Mixed Ion Solution

Antje Quade, Volker Presser, Prisciliano Hernández, Cansu Kök, Jean G. A. Ruthes, Oliver Janka
article en

Abstract

The demand for lithium production has seen a significant rise, with the growing electric vehicle and stationary battery markets requiring further development of sustainable and scalable extraction methods. Direct lithium extraction technologies have been developed to address potential shortages, with adsorption emerging as a key method due to its efficiency and low environmental impact. Given that Al-(OH)<sub>3</sub> is already utilized as an adsorbent in various industrial applications, the practical importance of Al-based alternative systems for lithium ion extraction is increasing, yet lithium ion recovery requires harsh chemicals. In this study, we report a novel lithium extraction method combining chemical adsorption and electrochemical release using a synthesized aluminum layered double hydroxide (Al-LDH) material, developed under mild reaction conditions. The performance of the Al-LDH electrode was evaluated against a commercial Al-(OH)<sub>3</sub> adsorbent. Comprehensive characterization using techniques such as X-ray diffraction, Fourier-transform infrared spectroscopy, and scanning electron microscopy revealed detailed insights into the crystalline structure, particle size distribution, and surface morphology of the materials. The Al-LDH electrode exhibited a lithium ion adsorption capacity, achieving an average chemical uptake of lithium ions of 57.6 mg/g. In contrast, lithium-ion uptake capacity for Al-(OH)<sub>3</sub> was 1.0 mg/g over 15 cycles. Notably, this method operates under pH-neutral conditions, eliminating the need for harsh acidic or basic eluents. As a result, it prevents structural degradation and minimizes secondary pollution for potential future applications of lithium-ion recovery. The material's layered structure selectively allowed lithium ion intake while blocking sodium ions, demonstrating its high selectivity and utility in lithium ion recovery processes. The integration of pH-neutral regeneration and high selectivity shows that Al-LDH electrodes as viable candidates for next-generation, green lithium extraction technologies.

ACS Sustainable Chemistry & EngineeringVol. 13(44)
Leibniz Institute for Plasma Science and Technology (DE), Leibniz-Institute for New Materials (DE), Saarland University (DE)
Openalex Percentile: Top 67%
Extraction and Separation Processes
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