Martin Grützke

Ion chromatography electrospray ionization mass spectrometry method development and investigation of lithium hexafluorophosphate-based organic electrolytes and their thermal decomposition products

A method based on the coupling of ion chromatography (IC) and electrospray ionization mass spectrometry (ESI-MS) for the separation and determination of thermal decomposition products of LiPF6-based organic electrolytes is presented. The utilized electrolytes, LP30 and LP50, are commercially available and consist of 1mol/l LiPF6 dissolved in ethylene carbonate/dimethyl carbonate and ethylene carbonate/ethyl methyl carbonate, respectively. For the separation method development three ion chromatographic columns with different capacity and stationary phase were used and compared. Besides the known hydrolysis products of lithium hexafluorophosphate, several new organophosphates were separated and identified with the developed IC-ESI-MS method during aging investigations of the electrolytes. The chemical structures were elucidated with IC-ESI-MS/MS.

Identification of alkylated phosphates by gas chromatography–mass spectrometric investigations with different ionization principles of a thermally aged commercial lithium ion battery electrolyte

The thermal aging process of a commercial LiPF6 based lithium ion battery electrolyte has been investigated in view of the formation of volatile phosphorus-containing degradation products. Aging products were analyzed by GC-MS. Structure determination of the products was performed by support of chemical ionization MS in positive and negative modes. A fraction of the discovered compounds belongs to the group of fluorophosphates (phosphorofluoridates) which are in suspect of potential toxicity. This is well known for relative derivatives, e.g. diisopropyl fluorophosphate. Another fraction of the identified compounds belongs to the group of trialkyl phosphates. These compounds may provide a positive impact on the thermal and electrochemical performance of Li-based batteries as repeatedly described in the literature.

Two-dimensional ion chromatography for the separation of ionic organophosphates generated in thermally decomposed lithium hexafluorophosphate-based lithium ion battery electrolytes.

A two-dimensional ion chromatography (IC/IC) technique with heart-cutting mode for the separation of ionic organophosphates was developed. These analytes are generated during thermal degradation of three different commercially available Selectilyte™ lithium ion battery electrolytes. The composition of the investigated electrolytes is based on 1M lithium hexafluorophosphate (LiPF6) dissolved in ethylene carbonate/dimethyl carbonate (50:50wt%, LP30), ethylene carbonate/diethyl carbonate (50:50wt%, LP40) and ethylene carbonate/ethyl methyl carbonate (50:50wt%, LP50). The organophosphates were pre-separated from PF6(-) anion on the low capacity A Supp 4 column, which was eluted with a gradient step containing acetonitrile. The fraction containing analytes was retarded on a pre-concentration column and after that transferred to the high capacity columns, where the separation was performed isocratically. Different stationary phases and eluents were applied on the 2nd dimension for the investigation of retention times, whereas the highly promising results were obtained with a high capacitive A Supp 10 column. The organophosphates generated in LP30 and LP40 electrolytes could be separated by application of an aqueous NaOH eluent providing fast analysis time within 35min. For the separation of the organophosphates of LP50 electrolyte due to its complexity a NaOH eluent containing a mixture of methanol/H2O was necessary. In addition, the developed two dimensional IC method was hyphenated to an inductively coupled plasma mass spectrometer (ICP-MS) using aqueous NaOH without organic modifiers. This proof of principle measurement was carried out for future quantitative investigation regarding the concentration of the ionic organophosphates. Furthermore, the chemical stability of several ionic organophosphates in water and acetonitrile at room temperature over a period of 10h was investigated. In both solvents no decomposition of the investigated analytes was observed and therefore water as solvent for dilution of samples was proved as suitable.

Study of decomposition products by gas chromatography-mass spectrometry and ion chromatography-electrospray ionization-mass spectrometry in thermally decomposed lithium hexafluorophosphate-based lithium ion battery electrolytes

In this work, the thermal decomposition of a lithium ion battery electrolyte (1 M LiPF6 in ethylene carbonate/ethyl methyl carbonate, 50/50 wt%) with a focus on the formation of organophosphates was systematically studied. The quantification of non-ionic dimethyl fluorophosphate and diethyl fluorophosphate was performed with synthesized standards by gas chromatography-mass spectrometry. Due to absence of commercially available or synthesized standards for the monitoring of ionic methyl fluorophosphate, ethyl fluorophosphate and ethylene phosphate a method working with ion chromatography-electrospray ionization-mass spectrometry was developed, where dibutyl phosphate was used as an internal standard. In addition, an ion chromatography conductivity detection method with short analysis time for simultaneous determination and quantification of F−, PF6− and BF4− was developed. The formation and degradation of analytes was studied to show the dependence of different temperatures, electrolyte volumes and separator materials. The thermal aging experiments were carried out in gas-tight aluminum vials at 80 °C for three weeks. After the storage time, the samples were diluted with the appropriate analysis solvents and investigated with gas chromatography-mass spectrometry, ion chromatography and ion chromatography-electrospray ionization-mass spectrometry. Finally, the thermal degradation of the electrolyte at 85 °C after five days in aluminum and glass vials was studied.

Investigation of the Storage Behavior of Shredded Lithium‐Ion Batteries from Electric Vehicles for Recycling Purposes

Shredding of the cells is often the first step in lithium-ion battery (LIB) recycling. Thus, LiNi1/3 Mn1/3 Co1/3 O2 (NMC)/graphite lithium-ion cells from a field-tested electric vehicle were shredded and transferred to tinplate or plastic storage containers. The formation of hazardous compounds within, and being released from, these containers was monitored over 20 months. The tinplate cans underwent fast corrosion as a result of either residual charge in the active battery material, which could not fully be discharged because of contact loss to the current collector, or redox reactions between the tinplate surface and metal parts of the shredded material. The headspace compositions of the containers were investigated at room temperature and 150 °C using headspace-gas chromatography-mass spectrometry (HS-GC-MS). Samples of the waste material were also collected using microwave-assisted extraction and the extracts were analyzed over a period of 20 months using ion chromatography-electrospray ionization-mass spectrometry (IC-ESI-MS). LiPF6 was identified as a conducting salt, whereas dimethyl carbonate, ethyl methyl carbonate, and ethylene carbonate were the main solvent components. Cyclohexylbenzene was also detected, which is an additive for overcharge protection. Diethyl carbonate, fluoride, difluorophosphate and several ionic and non-ionic alkyl (fluoro)phosphates were also identified. Importantly, dimethyl fluorophosphate (DMFP) and diethyl fluorophosphate (DEFP) were quantified using HS-GC-MS through the use of an internal standard. DMFP, DEFP, and related compounds are known as chemical warfare agents, and the presence of these materials is of great interest. In the case of this study, these hazardous materials are present but in manageable low concentrations. Nonetheless, the presence of such compounds and their potential release during an accident that may occur during shredding or recycling of large amounts of LIB waste should be considered.

Structure determination of organic aging products in lithium-ion battery electrolytes with gas chromatography chemical ionization mass spectrometry (GC-CI-MS)

For Gas Chromatography Chemical Ionization Mass Spectrometry (GC-CI-MS) method development, a standard lithium-ion battery (LIB) electrolyte was thermally aged at 95 °C for a faster generation of decomposition products. Interestingly, phosphorous containing aging products were preferably formed in the first hours. Furthermore, the organic containing aging products without phosphorous are formed after longer times. Since, these compounds are very similar in structure, molecular mass and consequently in their fragmentation during electron ionization (EI) experiments, chemical ionization was applied to identify the structure of the LIB electrolyte aging products. Herein, the results of the structure determination of organic LIB electrolyte aging products with GC-CI-MS are presented. Furthermore, formation of the identified species and relative concentrations over a time period of 22 days were determined by using an internal standard.

Graphite Recycling from Spent Lithium-Ion Batteries.

The present work reports on challenges in utilization of spent lithium-ion batteries (LIBs)-an increasingly important aspect associated with a significantly rising demand for electric vehicles (EVs). In this context, the feasibility of anode recycling in combination with three different electrolyte extraction concepts is investigated. The first method is based on a thermal treatment of graphite without electrolyte recovery. The second method additionally utilizes a subcritical carbon-dioxide (subcritical CO2 )-assisted electrolyte extraction prior to thermal treatment. And the final investigated approach uses supercritical carbon dioxide (scCO2 ) as extractant, subsequently followed by the thermal treatment. It is demonstrated that the best performance of recycled graphite anodes can be achieved when electrolyte extraction is performed using subcritical CO2 . Comparative studies reveal that, in the best case, the electrochemical performance of recycled graphite exceeds the benchmark consisting of a newly synthesized graphite anode. As essential efforts towards electrolyte extraction and cathode recycling have been made in the past, the electrochemical behavior of recycled graphite, demonstrating the best performance, is investigated in combination with a recycled LiNi1/3 Co1/3 Mn1/3 O2 cathode.

Electrolyte Extraction—Sub and Supercritical CO 2

This chapter reports on experiments aimed at investigating the capability of pressurized carbon dioxide to extract the electrolyte from commercial available LIBs on a laboratory scale. Two different phase conditions of carbon dioxide (subcritical and supercritical) and two different extraction (static and dynamic) have been considered and analyzed for their strengths and weaknesses. Furthermore, the addition of co-solvents is examined with regard to their contribution to higher recovery rates. After reporting the optimized extraction method, the extracted electrolyte was analyzed by gas and ionic chromatography methods for potential de-composition products and their relative amount.

Potential Dangers During the Handling of Lithium-Ion Batteries

Due to their high voltage, high stored energy, and reactive components, lithium-ion batteries present a specific and significant hazard potential. This especially comes into play during recycling because nearly every safety precaution of a battery system and battery cell needs to be bypassed. Because the project partners of LithoRec II spared a thermal pre-treatment step to deactivate the batteries, the hazard potential and its handling played a major role. This chapter gives an overview of the hazards associated with lithium-ion batteries and describes their role in every process step.

Fast screening method to characterize lithium ion battery electrolytes by means of solid phase microextraction – gas chromatography – mass spectrometry

Several electrolytes of commercially available lithium ion batteries (LIBs) were analyzed by solid phase microextraction – gas chromatography – mass spectrometry (SPME-GC-MS). The uptake and subsequent injection of the conducting salt LiPF6 into the GC system was prevented by using a headspace SPME setup. Thus, a removal step prior to the GC-MS measurements was not necessary and it was possible to analyze the untreated electrolyte without injecting the hazardous LiPF6 into the GC system. Furthermore, all SPME experiments were carried out at room temperature to exclude further thermal alteration of the electrolyte during sampling. In LIB electrolytes, different linear and cyclic carbonate solvents and additives such as succinonitrile (SN) and fluoroethylene carbonate (FEC) could be identified using the SPME-GC-MS setup. Moreover, the aging products dimethyl-2,5-dioxahexane dicarboxylate (DMDOHC) and ethylmethyl-2,5-dioxahexane dicarboxylate (EMDOHC) were identified in the electrolyte of aged 18 650-type cells. In the case of the cells of one specific supplier, various additional hydrocarbons were detected via SPME-GC-MS. These compounds could not be obtained when a GC-MS setup with conventional liquid or headspace injection is used. Consecutive experiments were carried out by extracting the electrolyte components directly from the headspace above anode, separator and cathode of an aged 18 650-type cell, which confirmed the findings of the prior analysis of pure electrolytes. Within this work it was possible to develop a method for the investigation of LIB electrolytes and their decomposition products with high sensitivity and low GC column bleeding.