Sodium-ion batteries (SIBs) are considered as a promising alternative to lithium-ion batteries (LIBs) for large-scale renewable energy storage units due to the abundance of sodium resource and its low cost. However, the development of anode materials for SIBs to date has been mainly limited to some traditional anodes for LIBs, such as carbonaceous materials. SnSe2 is a member of two dimensional layered transition metal dichalcogenide (TMD) family, which has been predicted to have high theoretical capacity as anode material for sodium ion batteries (756 mAh g-1), thanks to its layered crystal structure. Yet, there have been no studies on using SnSe2 as Na ion battery anode. In this thesis, we developed a simple synthesis method to prepare pure SnSe2 nanosheets, employing N2 saturated NaHSe solution as a new selenium source. The SnSe2 2D sheets achieve theoretical capacity during the first cycle, and a stable and reversible specific capacity of 515 mAh g-1 at 0.1 A g-1 after 100 cycles, with excellent rate performance. Among all of the reported transition metal selenides, our SnSe2 sample has the highest reversible capacity and the best rate performances. A combination of ex-situ high resolution transmission electron microscopy (HRTEM) and X-ray diffraction was used to study the mechanism of sodiation and desodiation process in this SnSe2, and to understand the reason for the excellent results that we have obtained. The analysis indicate that a combination of conversion and alloying reactions take place with SnSe2 anodes during battery operation, which helps to explain the high capacity of SnSe2 anodes for SIBs compared to other binary selenides. Density functional theory was used to elucidate the volume changes taking place in this important 2D material.

Cell wall is the major barrier in the delivery of biomolecules such as nucleic acids into the plant cell. Biological (bacteria or viruses) and biolistic (particle-based) methods are used to deliver nucleic acids into the plant cell. However, these methods have significant limitations when it comes to species range, scalability, and field assays. In this work, we report the use of layered double hydroxide (LDH) topically applied to deliver RNA molecules into the plant cell. LDH were assembled by methanol-based co-precipitation of magnesium and aluminum nitrate solution with sodium hydroxide and finally dispersed in deionized water. The assembled LDH were physically characterized by AFM, zeta-sizer and their binding to RNA was confirmed by gel electrophoresis. LDH complexed with double stranded RNA (dsRNA) was topically applied to Nicotiana benthamiana leaves. As a model system, virus specific dsRNA-LDH complexes were used to activate cellular RNAi machinery against Tomato Yellow leaf Curl Virus (TYLCV) in N. benthamiana plants. Our results demonstrated that topical application of the TYLCV specific dsRNA-LDH complexes reduce viral genome accumulation and viral symptoms development. Similarly, dsRNA-LDH protected plants produce typical leaves, flowers, and seeds, confirming efficient virus resistance compared unprotected TYLCV infected plants. Topical application and noninvasive delivery of nucleic acid has several advantages, as these methods are specie independent, easy to scale up, applied with low-pressure spray, requires no tissue culture and no sophisticated equipment. The LDH based noninvasive delivery of nucleic acids has the capability to overcome the cell wall barrier limitations and will open new opportunities to exploit the full potential of cellular machinery to produce resilient plants and insure sustainable food production.

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Thin nanoporous films are attractive for many potential uses for example gas separation, catalysis, filtration of viruses, ore flotation, or as low-dielectric-constant materials. Zeolite and mesoporous materials are the two important nanoporous material classes. In this thesis, we synthesized and characterized two different thin nanoporous films; (i) mesostructured films at the mica-solution interface; (ii) mechanical exfoliated zeolites. The mesoporous materials are well-defined pore shoe and size, and exhibit various morphologies, such as thin films, etc. In contrast, zeolites are a kind of perfect crystal and the morphologies are strongly related to their structures and are difficult to control. Therefore, first we synthesis mesostructured films at mica-solution interface in acidic solution. In-situ Atomic Force Microscopy (AFM) has been used to reveal the formation process of organic and inorganic mesophase films at the molecular level. Then, we synthesized two-dimensional zeolite structures via mechanical exfoliation process that does not involve any chemical intervention and can be applicable to a wide variety of structures with different chemical makeup. Three different zeolite structure nanosheets related to the structure code MWW, UTL, and MFI have been prepared. AFM and TEM have been used to characterized the exfoliated single nanosheet. In order to broaden the application of the single zeolite nanosheet, platinum nano-clusters are encapsulated within mechanical exfoliated zeolite MFI nanosheets by ion exchange from aqueous solution of [Pt(NH3)4](NO3)2. High-angle annular dark field scanning transmission electron microscopy has been used to indicate the Pt clusters in the zeolite MFI structures. Because of the property of the mechanically as-synthesised exfoliated MFI nanosheets that is the long hydrocarbon chains are essentially intact on both sides of the inorganic layer, and can prevent thickening of the zeolite MFI nanosheets along b-axis, we use the mechanically exfoliated MFI as seeds for further growth to form large scale MFI membrane with uniform nano-thickness. Encapsulating noble metals within the channels or cavities of zeolites has already drawn numerous attentions because the well-defined zeolite structure is able to constrain the metal nanoparticle (NPs) aggregation size and enhance the diversity and activity for catalysis. We use the organic surfactant (C22-6-6Br2) and [Pt(NH3)4](NO3)2 as the structure and metal precursor to form Pt-containing nanowires; and use F- to inhibit the premature precipitation of Pt precursors. After involving F-, the Pt-containing nanowire structures were generated.

In the last decades several new nanostructures of carbon have been discovered, including carbon nanotubes (CNTs), and the recently discovered 2-dimensional graphene. These new materials exhibit extraordinary and unique properties—making them extremely interesting both for fundamental science and for future applications. It is, however, of crucial importance to develop new and improved fabrication and processing methods for these carbon nanomaterials. In this thesis the concept of applying solution chemistry and solution-based techniques to fabricate and to deposit graphene and other carbon nanomaterials is explored. An area-selective deposition method was developed for CNT and carbon-coated iron nanoparticles. By utilizing organic functionalization the properties of the nanomaterials were tuned, with the purpose to make them soluble in a liquid solvent and also enable them to selectively adsorb to non-polar surfaces. The first step of the functionalization process was an acid treatment, to introduce defects in the materials. This method was also used to create defects in so-called carbon nanosheets (CNS). The effect of the defect formation on the electric properties of the graphene-like CNS was studied; it was found that the resistance of the CNS could be reduced to 1/50 by acid treating of the sample. Also, the effect of the created defects on gas adsorption to the surface of the CNS has been investigated. This was done using atomic layer deposition (ALD) of TiO2 on the CNS, and a clear change in nucleation be-havior was seen due to the acid-treatment. Furthermore, a solution-based new method for fabrication of graphene was developed; this method combines intercalation of bromine into graphite with ultrasonic treatment to exfoliate flakes into a solvent. From the solvent the flakes can be deposited onto an arbitrary substrate. Several important parameters in the method were investigated in order to optimize the process. One important parameter proved to be the choice of solvent in all steps of the procedure; it was shown to influence sonication yield, flake size, and deposition results. Toluene was identified as a suitable solvent. A mild heat-treatment of the starting material was also identified as a way to increase the exfoliation yield. Using this method, fabrication of few-layer graphene sheets was achieved and areas down to 3 layers in thickness were identified—this is in the very forefront of current solution-based graphene fabrication techniques.

Doctor of Philosophy / Physics / Christopher M. Sorensen / We demonstrated that gram quantities of pristine graphene nanosheets (GNs) can be produced via detonation of a hydrocarbon. This one-step and catalyst-free method is eco-friendly and economical for the production of GNs. The hydrocarbons detonated were C₂H₂, C₂H₄, C₃H₈ and CH₄ in the presence of O₂. The carbon products obtained from the detonation were analyzed by XRD, TEM, XPS and Raman spectroscopy. Depending upon the ratio of O₂ to C₂H₂, the GNs of size up to ~ 250 nm, SSA up to ~ 200 m²/g and yield up to 70% with 2-3 layers' stack have been obtained so far. N₂O was determined as a good alternative to O₂ as an oxidizer to produce GNs by detonating C₂H₂ with it. A two-color pyrometer was designed and calibrated to measure the temperature of the detonation of hydrocarbons. The measured detonation temperatures were in between 2700 K and 4300 K. Along with the high detonation temperature, the composition of precursor hydrocarbon was observed to be crucial as well to determine its suitability to detonate with oxidizer to produce GNs. The hydrocarbons C₂H₂ and C₂H₄ were determined as the suitable precursors to produce GNs whereas detonation of C₃H₈ yields mere amorphous carbon soot and CH₄ gives no solid carbon while detonated with O₂. It has been proposed that the hydrocarbons with C/H≥0.5 are suitable for GNs production by detonation method. Highly oxidized graphene nanosheets (OGNs) were produced by solution-based oxidation of GNs prepared via a controlled detonation of acetylene at O₂/C₂H₂=0.8. The produced OGNs were about 250 nm in size and hydrophilic in nature. The C/O ratio was dramatically reduced from 49:1 in the pristine GNs to about 1:1 in OGNs, as determined by X-ray photoelectron spectroscopy. This C/O in OGNs is the least ever found in all oxidized graphitic materials that have been reported. Thus, the OGNs produced from the detonated GNs with such high degree of oxidation herein yields a novel and promising material for future applications.

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No / Here we report a hierarchical composite structure composed of few-layers molybdenum disulfide nanosheets supported by vertical graphene on conductive carbon cloth (MDNS/VG/CC) for high-performance electrochemical hydrogen evolution reaction (HER). In the fabrication, 3D vertical graphene is first prepared on carbon cloth by a micro-wave plasma enhanced chemical vapor deposition (MPCVD) and then few-layers MoS2 nanosheets are in-situ synthesized on the surface of the vertical graphene through a simple hydrothermal reaction. This integrated catalyst exhibits an excellent HER electrocatalytic activity including an onset potential of 50 mV, an overpotential at 10 mA cm(-2) (eta(10)) of 78 mV, a Tafel slop of 53 mV dec(-1), and an excellent cycling stability in acid solution. The excellent catalytic performance can be ascribed to the abundant active edges provided by the vertical MoS2 nanosheets, as well as the effective electron transport route provided by the graphene arrays on the conductive substrate. Moreover, the vertical graphene offers robust anchor sites for MoS2 nanosheets and appropriate intervals for electrolyte infiltration. This not only benefits hydrogen convection and release but also avoids the damaging or restacking of catalyst in electrochemical processes. / This work was financially supported by the National Natural Science Foundation of China (Grant nos. 61176007, 51372213, and 51402343).