1 |
Mitigating Polysulfide Shuttling in Li-S BatteryLi, Mengliu 16 November 2019 (has links)
The energy source shortage has become a severe issue, and solving the problem with renewable and sustainable energy is the primary trend. Among the new generation energy storage, lithium-sulfur (Li-S) battery stands out for its low cost, high theoretical capacity (1,675 mAh g-1), and environmentally friendly properties. Intensive researches have been focusing on this system and significant improvement has been achieved. However, several problems still need to be resolved for its practical application, especially for the “shuttle effect” issue coming from the dissolved intermediate polysulfides, which could cause rapid capacity decay and low Coulombic efficiency (CE). Several methods are proposed to eliminate this issue, including using interlayers, modifying separators, and protecting the lithium anode.
A carbon interlayer is first introduced to compare the function of the graphene and carbon nanotubes (CNTs), while the CNTs performs better with its higher conductivity and 3D network structure. The following study is conducted based on this finding.
A more efficient method is to modify the separator with functional materials. 1) The dissolved polysulfide (Sn2-) could be repelled by electrostatic forces. With the Poly (styrene sulfonate) (PSS), the separator could function as an anion barrier to the intermediate polysulfides. 2D ultra-thin zinc benzimidazolate coordination polymer has the OH- functional groups and works with the same mechanism. 2) A novel covalent organic framework (COF) has a relatively small pore size, which can block the polysulfide and restrain them at the cathode side. 3) Metal-organic framework (MOF) materials have the adjustable pore size and structure, which can absorb and trap polysulfides within their cavities. Moreover, the dense stacking of the MOF particles creates a physical blocking for the polysulfides, which efficiently suppresses the diffusion process.
Protection of the lithium surface directly with an artificial layer or a solid electrolyte interphase (SEI) can inhibit the polysulfide deposition and suppress the lithium dendrite. A polyvinylidene difluoride (PVDF) membrane is used as an artificial film on lithium anode, which could greatly enhance the battery cyclability and CE. Future work will be conducted based on this concept, especially building an artificial SEI.
|
2 |
Rechargeable Potassium-Oxygen Battery for Low-Cost High-Efficiency Energy StorageRen, Xiaodi, Ren 20 December 2016 (has links)
No description available.
|
3 |
Aqueous Zinc-ion Batteries: Applications and Zinc Anode ProtectionLiu, Yi 04 November 2022 (has links)
With the rapid growth of the world population and the process of industrialization of modern society, the demand for energy continues to rise sharply. There is a pessimistic prediction that a peak of consumption primarily fossil fuels will happen in the 2020s to 2030s, hence it is urgent to develop alternative renewable clean energy sources before this coming energy crisis. But the availability of renewable clean energy always is discontinuous, uncontrollable, and unstable. Besides, the generated renewable energy cannot be used directly. Therefore, an energy storage system is urgently needed as the medium to harvest and store the energy generated from the intermittent renewable resource, and also to regulate the electricity output, and improve the tolerance ability of the power grid to renewable energy.
Rechargeable aqueous zinc-ion battery, especially those that use mild electrolytes, is drawing more and more attention in the past decades and is regarded as the most promising candidate for large-scale energy storage systems. Compared with the widely used lithium-ion battery which dominated the commercial energy market now, the aqueous zinc-ion battery holds the merits of high theoretical capacity (820 mAh/g gravimetric capacity and 5855 mAh/m3 volumetric capacity), low electrochemical potential (-0.763 V vs. SHE) and high energy density due to the two-electron redox reaction, high abundance in the earth crust and high mass production, low toxicity, and environmental benignity, and the most valuable advantage intrinsic safety in aqueous electrolyte.
In this dissertation, the first part focuses on the preliminary application of an aqueous zinc-ion battery. One kind of planar on-chip aqueous zinc-ion micro-battery with high-rate performance was designed and fabricated. The PEDOT and MnO2 cathode can suppress the dissolution of electrode material which can highly improve the cycling performance of the micro-battery. The as-prepared micro-battery displays a high specific capacity of 25.8 μAh/cm2 after 25 activation cycles at a current density of 1 mA/cm2. A reversible specific capacity of 6.2 μAh/cm2 is achieved after 200 cycles, with 55.4 % of the initial discharge capacity retention. To improve the cycling performance of the aqueous zinc-ion battery, the second part of this thesis is preparing a highly enhanced reversibility Zn anode by in-situ texturing. The crystal plane (002)-textured Zn anode with an ultrathin passivation layer suppressed the Zn corrosion and enhanced the full battery performance. Based on these merits, the cycling stability of the Zn anode is enhanced from 791 hours to more than 1500 hours. The coulombic efficiency (CE) of a Zn||Ti asymmetric cell is greater than 90% over 500-hour cycles. For the Zn||MnO2 full cell, the addition of H3PO4 into the electrolyte improves both the rate capability and cycling stability of Zn||MnO2 cells. More importantly, a highly reversible Zn||O2 full cell is demonstrated at a large depth of discharge of Zn (DODZn > 10%), projecting the lower bounds of the cell-level specific energy of lithium-ion batteries.:Abstract I
Kurzfassung III
List of Abbreviations IX
Chapter 1 Background and motivation 1
1.1 Research motivation 1
1.2 Aim of this dissertation 2
1.3 Dissertation structure 3
Chapter 2 Introduction of aqueous zinc-ion battery and anode protection strategies 5
2.1 Introduction of aqueous zinc-ion battery 5
2.2 The challenges of zinc anode 8
2.2.1 Dendrites and protrusion 9
2.2.2 Hydrogen evolution reaction 10
2.2.3 Passivation layer 10
2.3 The strategies of zinc anode protection 11
2.3.1 Surface engineering 11
2.3.2 Electrolyte modification 15
2.3.3 3D structural skeleton and alloy strategies 22
Chapter 3 Experiment characterizations and calculations 25
3.1 Electrochemical methods 25
3.1.1 Chronoamperometry 25
3.1.2 Chronopotentiometry 26
3.1.3 Cyclic voltammetry 27
3.1.4 Galvanostatic charge/discharge 28
3.1.5 Electrochemical impedance spectroscopy 29
3.1.6 Tafel measurement 30
3.2 Characterization methods 31
3.2.1 X-ray diffraction 31
3.2.2 Scanning electron microscope 32
3.2.3 X-ray photoelectron spectroscopy 32
3.2.4 Raman spectroscopy 33
3.3 Experimental calculations 34
3.3.1 b value calculation 34
3.3.2 CE calculation 34
3.3.3 RTC calculation 35
3.3.4 DFT calculation 36
3.3.5 DOD calculation 37
3.3.6 Corrosion rate calculation 38
Chapter 4 A planar on-chip aqueous zinc-ion micro-battery with high-rate performance 41
4.1 Introduction 41
4.2 Experimental section 43
4.2.1 Interdigitated electrodes 43
4.2.2 Preparation of micro-battery 44
4.2.3 Microstructural properties characterization 45
4.2.4 Electrochemical characterization 45
4.3 Results and discussion 46
4.3.1 Characterization of micro-battery 46
4.3.2 Electrochemical performance measurement 49
4.4 Conclusions 56
Chapter 5 Highly enhanced reversibility of a Zn anode by in-situ texturing 57
5.1 Introduction 57
5.2 Experimental section 63
5.2.1 Preparation of the textured Zn anode 63
5.2.2 Synthesis of cathode materials 63
5.2.3 Electrochemical and material characterizations 64
5.3 Results and discussions 64
5.3.1 Nonuniform Zn deposition on an epitaxial substrate 65
5.3.2 In-situ texturing and SEI formation during the cycling 72
5.3.3 Full-cell performance 77
5.4 Conclusions 81
Chapter 6 Summary and outlook 83
6.1 Summary 83
6.2 Outlook 84
References: 87
Acknowledgment 99
Publications 101
Curriculum Vitae 103
Selbstständigkeitserklärung 105
|
Page generated in 0.0781 seconds