M.Sc. Cansu Kök

The efficient and selective extraction of lithium ions from aqueous media is crucial for resource recovery, yet remains challenging due to the chemical similarity of coexisting alkali ions, such as sodium. In this study, we report a two-step electrochemical strategy that utilizes tailored MXene electrodes for lithium ion extraction with enhanced selectivity and extraction rates. By preintercalating hexadecylamine (HDA) and decyltrimethylammonium (C10), which are long-chain organic molecules, into the Ti3C2Tx MXene structure, we tailored the interlayer environment to favor lithium ions over sodium ions. The HDA-intercalated MXene demonstrated high Li+/Na+ selectivity with a lithium ion uptake of 2.2 mmol/L and a suppressed sodium ion uptake (<0.2 mmol/L). Extended cycling revealed that molecular preintercalation modulates ion transport pathways and influences structural and electrochemical stability. Both HDA-Ti3C2Tx and C10-Ti3C2Tx maintained a lithium ion purity of nearly 100% over 50 cycles.

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)3 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)3 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)3 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.

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)3 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)3 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)3 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.

The growing demand for lithium batteries in various applications has increased lithium production from multiple sources, including ores, brines, and spent batteries. Traditional extraction methods such as mining and evaporation ponds have significant environmental risks, such as air pollution and loss of habitats for aquatic and terrestrial animals. Furthermore, they cannot meet the ever-increasing demand for lithium in the global market. Consequently, industries have been exploring rapid and sustainable lithium recovery methods from these sources. Similar to what shale did for oil industry, Direct Lithium Extraction (DLE) represents a promising approach poised to enhance lithium production efficiency. This method not only reduces operation time but also brings added sustainability benefits. Various DLE methods have been proposed, such as adsorption, ion exchange, membranes, direct carbonation, and electrochemical processes. This paper comprehensively analyzes DLE technologies, including their fundamentals, principles, and applications. The focus is on various techniques used in DLE, highlighting their respective strengths and limitations. The study explores the potential of DLE for efficient and sustainable lithium recovery, considering the growing demand for lithium in the energy sector. Furthermore, the analysis examines the challenges associated with DLE, including cost, environmental impact, and scalability. This paper contributes to a greater understanding of the opportunities and limitations of DLE to inspire future crucial research efforts in this strategically important emerging technology.

The demand for electronic devices that utilize lithium is steadily increasing in this rapidly advancing technological world. Obtaining high-purity lithium in an environmentally friendly way is challenging by using commercialized methods. Herein, we propose the first fuel cell system for continuous lithium-ion extraction using a lithium superionic conductor membrane and advanced electrode. The fuel cell system for extracting lithium-ion has demonstrated a twofold increase in the selectivity of Li+/Na+ while producing electricity. Our data show that the fuel cell with a titania-coated electrode achieves 95% lithium-ion purity while generating 10.23 Wh of energy per gram of lithium. Our investigation revealed that using atomic layer deposition improved the electrode's uniformity, stability, and electrocatalytic activity. After 2000 cycles determined by cyclic voltammetry, the electrode preserved its stability.

Electrochemical desalination shows promise for ion-selective, energy-efficient water desalination. This work reviews performance metrics commonly used for electrochemical desalination. We provide a step-by-step guide on acquiring, processing, and calculating raw desalination data, emphasizing informative and reliable figures of merit. A typical experiment uses calibrated conductivity probes to relate measured conductivity to concentration. Using a standard electrochemical desalination cell with activated carbon electrodes, we demonstrate the calculation of desalination capacity, charge efficiency, energy consumption, and ion selectivity metrics. We address potential pitfalls in performance metric calculations, including leakage current (charge) considerations and aging of conductivity probes, which can lead to inaccurate results. The relationships between pH, temperature, and conductivity are explored, highlighting their influence on final concentrations. Finally, we provide a checklist for calculating performance metrics and planning electrochemical desalination tests to ensure accuracy and reliability. Additionally, we offer simplified spreadsheet tools to aid data processing, system design, estimations, and upscaling.