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Superior Reversible Hydrogen Storage of the LiBH4 + MgH2 System Enabled by High-Energy Ball Milling with In-Situ Aerosol Spraying
Title
Superior Reversible Hydrogen Storage of the LiBH4 + MgH2 System Enabled by High-Energy Ball Milling with In-Situ Aerosol Spraying
Creator
Ding, Zhao
Date
2019
Description
The prospect of LiBH4 + MgH2 mixture has been limited by its sluggish kinetics, despite its excellent hydrogen storage capacity theoretically....
Show moreThe prospect of LiBH4 + MgH2 mixture has been limited by its sluggish kinetics, despite its excellent hydrogen storage capacity theoretically. We have designed a novel process termed as high-energy ball milling of MgH2 at ambient temperature along with aerosol spraying of LiBH4 dissolved in tetrahydrofuran (THF) solution (BMAS) to improve the thermodynamic and kinetic performance of LiBH4 + MgH2 hydrogen storage materials. Through this BMAS process, we have demonstrated that, for the first time, the reaction between LiBH4 + MgH2 can take place near ambient temperature, and the in-situ formation of LiH and MgB2 during BMAS is achieved through a new reaction pathway in which nano-LiBH4 decomposes to Li2B12H12 first and the newly formed Li2B12H12 reacts with MgH2 to form LiH and MgB2.Using the newly designed automated BMAS apparatus, we have successfully produced a BMAS mixture containing 1 mole of MgH2 + 0.5 mole of LiBH4, i.e., with 25% LiBH4 in the mixture for the stoichiometric reaction. The BMAS powder with 25% LiBH4 can release and absorb ~5.7 wt.% H2 at 265 oC, which is the highest one ever reported for the LiBH4 + MgH2 system at temperature ≤ 265 oC. It is found that the unusually high reversible hydrogen storage is accomplished through two parallel reaction pathways. One is nano-LiBH4 decomposes to form Li2B12H12 and H2 first and then Li2B12H12 reacts with MgH2 to form MgB2, LiH and H2. The other is nano-MgH2 decomposes to form Mg and H2 first and then Mg reacts with LiBH4 to form MgB2, LiH and H2. These reaction pathways become possible because of the presence of nano-LiBH4 and nano-MgH2 and their intimate mixing, enabled by the BMAS process. We have also revealed that the solid-state dehydrogenation kinetics of the BMAS powder with 25% LiBH4 at 265 oC is nucleation-and-growth controlled. The rate-limiting step for dehydrogenation via the two parallel reaction pathways has been identified through examination of the elementary reactions as the nucleation and growth of reaction products LiH and MgB2. Given the significantly improved hydrogen storage capacity for the LiBH4 + MgH2 system obtained via BMAS, investigation on increasing the LiBH4 content in the BMAS powder from 25% to 50% is performed. It is shown that Mg(BH4)2 can be produced during the BMAS process and it contributes to H2 release at temperature ≤ 265 oC. Three parallel H2 release mechanisms have been identified from the BMAS powder. These include (i) nano-LiBH4 decomposes to form Li2B12H12 and H2 first and then Li2B12H12 reacts with MgH2 to form MgB2, LiH and H2, (ii) nano-Mg(BH4)2 decomposes to form MgH2, B and H2, and (iii) nano-MgH2 decomposes to Mg and H2. Together these three mechanisms result in 4.11 wt.% H2 release in the solid state at temperature ≤ 265 oC. Furthermore, the predicted property of Fe3B in absorbing more H2 than releasing it is confirmed experimentally for the first time in this study. Varied models have been identified to describe the kinetic of solid-state dehydrogenation of the BMAS powder with 50% LiBH4 at 265 oC with increasing cycles. Additionally, the geometries of the solid particles involving with the dehydrogenation have also been estimated.
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Effects of the Silicon Content on the Dimensional Changes of Electrodes for Lithium-ion Cells: An Electrochemical Dilatometry Study
Title
Effects of the Silicon Content on the Dimensional Changes of Electrodes for Lithium-ion Cells: An Electrochemical Dilatometry Study
Creator
Rodrigues Prado, Andressa Yasmim
Date
2021
Description
The continuous growth of the electric vehicle market has significantly increased the demand for Li-ion batteries (LIBs). However, state-of-the...
Show moreThe continuous growth of the electric vehicle market has significantly increased the demand for Li-ion batteries (LIBs). However, state-of-the-art LIBs are not yet able to meet the EV industry demand for high energy density and long cycle life rechargeable batteries, prompting efforts to improve the performance of Li-ion cells. In this context, silicon became the most promising next-generation active material for LIBs negative electrodes, especially because Si can significantly increase the lithium storage capacity of the commonly available anodes. Nonetheless, commercialization of Si-based electrodes has been hindered by the poor electrochemical performance of these electrodes, which is mainly attributed to the severe volumetric changes in the silicon particles related to the electrochemical reactions with Li. Since the electrodes are composites with a complex combination of various materials interspaced by pores, the electrode-level swelling may differ significantly from the particle-scale expansion. Furthermore, an increase in electrode thickness due to silicon expansion can have a direct effect on how Li-ion cells are designed, as the accommodation of electrode dilation requires additional cell space to prevent significant dynamic stresses. Thus, the actual volumetric energy density of a LIB cell depends on the electrode swelling, since the higher the magnitude of the electrode expansion, the lower the gains in energy density. Monitoring the electrode dilation is just as important as the electrochemical evaluation when designing cells with Si-based anodes.In this work, we use high-resolution operando electrochemical dilatometry to quantify the (de)lithiation-induced expansion/contraction of silicon, blended silicon-graphite and graphite electrodes, upon electrochemical cycling. We evaluate the relationship between electrode capacity and dilation and observe that while the lithiation capacity improved with increasing the silicon content, the electrode swelling is highly aggravated. For silicon-rich anodes, the electrode dilation can be higher than 300%, and the expansion profile consists of a combination of slow swelling at low levels of lithiation followed by an accelerated increase at higher lithium contents. This non-linear dilation allows for narrowing the swelling by limiting the electrode capacity. In addition, we investigate how electrode properties, such as porosity, affect the dilation profile, and quantify the irreversible expansion of the electrodes. Finally, we discuss some of the challenges associated with the dilatometry technique and suggest experimental approaches for obtaining consistent and reliable data.
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Synthesis and Processing of NaSICON Membranes with High Ionic Conductivity and Good Mechanical Strength
Title
Synthesis and Processing of NaSICON Membranes with High Ionic Conductivity and Good Mechanical Strength
Creator
Chiang, Shan-Ju
Date
2019
Description
Natrium super ion conductors (NaSICONs), Na1+xZr2SixP3-xO12 (0 ≤ x ≤ 3) are compounds that commonly used as solid electrolytes and membranes...
Show moreNatrium super ion conductors (NaSICONs), Na1+xZr2SixP3-xO12 (0 ≤ x ≤ 3) are compounds that commonly used as solid electrolytes and membranes of sodium based batteries, or in gas sensors and fuel cells due to their high sodium ion conductivity, low thermal expansion, and ability to accommodate ions in the lattice. However, NaSICON with high relative density (> 97%) and minimum impurity phases is found to be very difficult to obtain. Furthermore, the cost of the general synthesis methods is a serious drawback. Multi-high-temperature heating procedures is often employed to increase the density and to attain the single phase NaSICON because the particle size and free ZrO2 are better reduced. This research explores the possibility of densification and synthesis of NaSICON in one high-temperature reaction through a novel process termed Integrated Mechanical and Thermal Activation (IMTA) and the co-sintering behavior as well as the NaSICON composite membranes from tape casting. The sintering temperature of NaSICON was decreased by mechanical activation at room temperature using high-energy ball milling. Sintered NaSICON-based materials showed highest total ionic conductivity of 1.45 × 10-3 S cm-1 at room temperature and high density of 3.155 g cm-3 (96.5%). An alternative to obtaining full densification (99%) of NaSICON ceramics was developed utilizing traditional solid-state reaction. This sintered NaSICON without any sintering aid exhibited the total conductivity, 6.59 × 10-4 S cm-1 at 25 °C, and the highest density of 3.238 g cm-3, a better than 2.6% enhancement from the original samples.The second part of the work has comprised of successful fabrication of NaSICON/polymer composite membranes and bi-layered NaSICON/stainless steel membranes to enhance the mechanical flexibility of pure NaSICON films. The effect of different particle sizes of stainless steel on the sintering behavior and shrinkage rate were studied systematically. The effect of solid content in the slurry was also studied to control the density of both support layer and NaSICON body. The affect structural ratios have on co-sintered tapes along with ionic conductivity was investigated using Electrochemical Impedance Spectroscopy (EIS). The co-sintered membrane exhibited a total conductivity as high as 4.580 × 10-4 S/cm at room temperature. EIS results showed the high Na-ions conductivity strongly depends on the feature of grain boundary and the high densification of NaSICON layer.
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IN SITU X-RAY ABSORPTION SPECTROSCOPY STUDY OF TIN-BASED GRAPHITE COMPOSITE ANODES FOR LITHIUM-ION BATTERIES
Title
IN SITU X-RAY ABSORPTION SPECTROSCOPY STUDY OF TIN-BASED GRAPHITE COMPOSITE ANODES FOR LITHIUM-ION BATTERIES
Creator
Ding, Yujia
Date
2019
Description
Sn-based anode materials such as Sn, SnO2, Sn4P3, and SnS2 that exhibit large theoretical capacities are promising alternatives to traditional...
Show moreSn-based anode materials such as Sn, SnO2, Sn4P3, and SnS2 that exhibit large theoretical capacities are promising alternatives to traditional graphite anodes for Li-ion batteries. However, their capacities fade drastically in a few cycles due to substantial volume changes during the lithiation/delithiation process resulting in cracking and pulverization of the electrode. A graphite matrix is introduced by high-energy ball milling to obtain a graphite composite and enhance the electrochemical performance. Indeed, Sn4P3/graphite composite exhibits a reversible capacity of 651 mA h g-1 in the 100th cycle, and SnS2/graphite composite shows 591 mA h g-1 in the 50th cycle.To obtain a better understanding of the improved performance of the composite materials and the reason for the more gradual capacity fading, in situ EXAFS is used to investigate these mechanisms using in situ coin cells and in situ vacuum-sealed pouch cells. The collected EXAFS data were analyzed by modeling to extract detailed local environment changes during the lithiation/delithiation process.In the crystalline phases of Sn-based materials, the conversion reaction forming metallic Sn is partially reversible and partially irreversible, and the subsequent alloying/dealloying reaction forming LiSn alloys is reversible. Introducing the graphite matrix increases electrical conductivity and prevents aggregation of intermediate Sn clusters. The graphite matrix also plays a significant role in transforming composites into highly dispersed amorphous phases. These amorphous phases, formed in the first few cycles of Sn4P3/graphite and SnS2/graphite composites, exhibit excellent reversibility in both conversion and alloying/dealloying reactions, which is the main reason for the significant improvements in electrochemical performance. The slow growth of metallic Sn clusters and the slight reduction in amorphous phases result in gradual capacity loss over long-term cycling. Introducing the graphite matrix and creating highly dispersed composite samples are the successful strategies that can be scaled up to develop new battery materials in the future.
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Developing Advanced Materials for Carbon Dioxide Electroreduction to Value-Added Chemicals and Fuels
Title
Developing Advanced Materials for Carbon Dioxide Electroreduction to Value-Added Chemicals and Fuels
Creator
Esmaeilirad, Mohammadreza
Date
2023
Description
Developing highly efficient electrocatalysts for the carbon dioxide reductionreaction (CO2RR) to value-added fuels and chemicals offers a...
Show moreDeveloping highly efficient electrocatalysts for the carbon dioxide reductionreaction (CO2RR) to value-added fuels and chemicals offers a feasible pathway for renewable energy storage and could help mitigate the ever-increasing carbon dioxide (CO2) emissions from human activities. Different catalysts are known to catalyze CO2RR in aqueous solutions. Most known catalysts are only capable of transferring 2 electrons with needed protons to CO2 producing either carbon monoxide (CO) or formic acid (HCOOH). Copper (Cu) is the only electrocatalytic material that converts CO2 into different types of hydrocarbon products. Additionally, owing to Cu’s natural abundance and low cost, it has been intensively studied for CO2RR for decades. However, the required high input energy (overpotential), low product selectivity towards valuable fuel products, and the lack of long-term stability remain major challenges for Cu-based catalysts. This work aims to develop new materials that produce hydrocarbons at lower overpotentials with higher rates and greater selectivity than current copper catalysts. By implementing a process referred to as the electrocatalyst discovery cycle iterations between predications, catalyst testing, and active site characterization allow for the rational design and discovery of new and improved electrocatalysts for CO2RR. This methodology led to the discovery of different heteroatomic catalysts as low overpotential catalysts for electroreduction of CO2 high energy density hydrocarbon products.
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