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Sala-Heby Energi Elnät is a supplier of electrical power for the communities of Sala, Heby, Morgongåva and Björnarbo in Uppland, Sweden. The electrical power grid in this area is currently facing several challenges. Bottlenecks and power shortages are some of them. As an expansion of the Swedish power grid lies many years in the future, there is a need for other solutions to these problems. Because of this, Sala-Heby Energi Elnät is looking at the prospect of installing an energy storage system in the small community of Björnarbo. This report investigates a number of the most commonly used energy storage options available today and concludes that the most suitable choice for Sala-Heby Energi Elnät would be lithium-ion batteries implemented in a battery energy storage system, a BESS. This report also focuses on how a BESS can reduce power peaks by using a method called peak shaving. The financial implications of implementing a BESS of this kind for this purpose are taken into account as well. The study shows that by utilising a BESS with an energy capacity of 500kWh, the power peaks can be reduced by peak shaving. This not only provides a solution to the capacity problem in Sala-Heby Energi Elnät’s power grid, but a BESS could also allow for them to reduce their power subscription to Vattenfall, Sweden’s electricity provider. This would allow Sala-Heby Energi Elnät to make some financial savings. However, a BESS of this type would be very expensive. The conclusion is that a BESS could manage the energy consumption by using peak shaving but will only be financially profitable in the long run for Sala-Heby Energi Elnät.

Rechargeable lithium ion batteries (LIBs) have long been used to power not only portable devices, e.g., mobile phones and laptops, but also large scale systems, e.g., electrical grid and electric vehicles. To meet the ever increasing demand for renewable energy storage, tremendous efforts have been devoted to improving the energy/power density of LIBs. Known for its high theoretical capacity (4200 mAh/g), silicon has been considered as one of the most promising negative electrode materials for high-energy-density LIBs. However, diffusion-induced stresses can cause fracture and, consequently, rapid degradation in the electrochemical performance of Si-based negative electrodes. To mitigate the detrimental effects of the large volume change, several strategies have been proposed. This dissertation focuses on two promising approaches to make high performance and durable Si electrodes for high capacity LIBs. First, the effect of polymeric binders on the performance of Si-based electrodes is investigated. By studying two types of polymeric binders, polyvinylidene fluoride (PVDF) and sodium alginate (SA) using peel tests, SEM, XPS, and FTIR, I show that the high cohesive strength at the binder-silicon interface is responsible for the superior cell performance of the Si electrodes with SA as a binder. Hydrogen bonds formed between SA and Si is the main reason for the high cohesive strength since neither PVDF nor SA bonds covalently with Si. Second, the fabrication of high performance Si/polyacrylonitrile (PAN) composite electrode via oxidative pyrolysis is investigated. We show that high performance Si/polyacrylonitrile (PAN) composite negative electrodes can be fabricated by a robust heat treatment in air at a temperature between 250 and 400oC. Using Raman, SEM, XPS, TEM, TGA, and nanoindention, we established that oxidation, dehydration, aromatization, and intermolecular crosslinking take place in PAN during the heat treatment, resulting in a stable cyclized structure which functions as both a binder and a conductive agent in the Si/PAN composite electrodes. With a Si mass loading of 1 mg/cm2, a discharge capacity of ~1600 mAh/g at the 100th cycle is observed in the 400oC treated Si/PAN composite electrode when cycled at a rate of C/3. These studies on the structure-property-performance relations of Si based negative electrode may benefit the LIB community by providing (1) a guide for the design and optimization of binder materials for Si electrodes and (2) a facile method of synthesizing Si-based composite negative electrodes that can potentially be applied to other Si/polymer systems for further increasing the power/energy density and lower the cost of LIBs for electric vehicle applications and beyond.

Indiana University-Purdue University Indianapolis (IUPUI) / Electrospinning has gained immense interests in recent years due to its potential application in various fields, including energy storage application. The V2O5/GO as a layered crystal structure has been demonstrated to fabricate nanofibers with diameters within a range of ~300nm through electrospinning technique. The porous, hollow, and interconnected nanostructures were produced by electrospinning formed by polymers such as Polyvinylpyrrolidone (PVP) and Polyvinyl alcohol (PVA), separately, as solvent polymers with electrospinning technique. In this study, we investigated the synthesis of a graphene-modified nanostructured V2O5 through modified sol-gel method and electrospinning of V2O5/GO hybrid. Electrochemical characterization was performed by utilizing Arbin Battery cycler, Field Emission Scanning Electron Microscopy (FESEM), X-ray powder diffraction (XRD), Thermogravimetric analysis (TGA), Mercury Porosimetry, and BET surface area measurement. As compared to the other conventional fabrication methods, our optimized sol-gel method, followed by the electrospinning of the cathode material achieved a high initial capacity of 342 mAh/g at a high current density of 0.5C (171 mA/g) and the capacity retention of 80% after 20 cycles. Also, the prepared sol-gel method outperforms the pure V2O5 cathode material, by obtaining the capacity almost two times higher. The results of this study showed that post-synthesis treatment of cathode material plays a prominent role in electrochemical performance of the nanostructured vanadium oxides. By controlling the annealing and drying steps, and time, a small amount of pyrolysis carbon can be retained, which improves the conductivity of the V2O5 nanorods. Also, controlled post-synthesis helped us to prevent aggregation of electro-spun twisted nanostructured fibers which deteriorates the lithium diffusion process during charge/discharge of batteries.

京都大学 / 0048 / 新制・課程博士 / 博士(人間・環境学) / 甲第19072号 / 人博第725号 / 新制||人||174(附属図書館) / 26||人博||725(吉田南総合図書館) / 32023 / 京都大学大学院人間・環境学研究科相関環境学専攻 / (主査)教授 内本 喜晴, 教授 加藤 立久, 教授 吉田 寿雄 / 学位規則第4条第1項該当 / Doctor of Human and Environmental Studies / Kyoto University / DGAM

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第20580号 / 工博第4360号 / 新制||工||1678(附属図書館) / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 安部 武志, 教授 阿部 竜, 教授 作花 哲夫 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第21114号 / 工博第4478号 / 新制||工||1696(附属図書館) / 京都大学大学院工学研究科物質エネルギー化学専攻 / (主査)教授 安部 武志, 教授 作花 哲夫, 教授 陰山 洋 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DGAM

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Thesis (Ph.D.(Physics)) -- University of Limpopo, 2020 / We employ molecular dynamics simulations, using DL_POLY code, to study the structural behaviour of β-MnO2 cathode material during discharging through lithium-ion intercalation into the bulk, nanoparticle, nanorod, nanosheet, and nanoporous β-MnO2. It is shown that lithium-ions have an average coordination number of about 5.70 and prefer surface sites with high oxygen coordination. The average lattice parameter values at intercalation of 0.85 Li/Mn are found to be under 4% relative to the experimental values obtained at 0.92 Li/Mn. Moreover, all the lithiated β-MnO2 structures did not collapse at 0.85 Li/Mn as observed in the β-MnO2 mesoporous in experimental work. As lithium is limited, sodium is a good alternative charge carrier in lithium-ion batteries. As a result, we have also performed studies on sodium intercalation into bulk, nanoparticle, nanorod, nanosheet and nanoporous β-MnO2. The microstructures and radial distribution functions show that the β-MnO2 structures could be intercalated up to 0.24 Na/Mn without any obvious structural degradation. Beyond this sodium concentration, the microstructure collapses and become amorphous thus predicting a potentially lower capacity for Na-MnO2-β batteries. Also, as the voltage is an important factor in the energy density of lithium-ion batteries, we have studied the trends in the average intercalation potentials in relation to the various nano architectures. The trend, in increasing value of average intercalation potentials, were found to be bulk structure, nanorod, nanosheet, nanoporous and nanoparticle. This suggests that nanostructuring can enhance cell voltage. Mechanical properties studies on the pure and lithiated bulk and nanorod β-MnO2 were also performed through uniaxial compressive and tensile strain application. The results show that under compressive strain the bulk structure and nanorod mitigate stress through the contraction and collapse of the inherent tunnel structures, known to cause electrochemical inactivity, and also through the shifting of the MnO6 octahedral planes. The collapsing of tunnels was found to occur more on the bulk structure and less on the nanorod, while the MnO6 octahedral plane shifts were found to occur more on the nanorod and less on the bulk structure. Unoccupied 1x2 or conjoined 1x2 were found to result in structural collapse irrespective of the host nanoarchitecture. The X-ray diffraction pattern (v) plots suggest that lithium intercalation and compressive stress application have a similar impact on the underlying structure of the various nanostructures. The microstructure analysis for bulk β-MnO2 under tensile strain reveals that fracture occurred in the brookite region and along the dislocation/stacking fault. The nanorod β-MnO2 mitigated stress through a rutile-to-brookite phase transition which occurred in the unstrained Li0.73MnO2-β and under tensile strain in LixMnO2-β for x = 0.00, 0.03, 0.12, and 0.24. In both the bulk and nanorod β-MnO2 the brookite phase was succeeded by structural breakdown leading to fracture and served as an indicator for imminent structural failure upon more tensile strain application. / National Research Foundation (NRF)