Jingjing Qiu

Carbon nanotube integrated multifunctional multiscale composites

Carbon nanotubes (CNTs) demonstrate extraordinary properties and show great promise in enhancing out-of-plane properties of traditional polymer composites and enabling functionality, but current manufacturing challenges hinder the realization of their potential. This paper presents a method to fabricate multifunctional multiscale composites through an effective infiltration-based vacuum-assisted resin transfer moulding (VARTM) process. Multi-walled carbon nanotubes (MWNTs) were infused through and between glass-fibre tows along the through-thickness direction. Both pristine and functionalized MWNTs were used in fabricating multiscale glass-fibre-reinforced epoxy composites. It was demonstrated that the mechanical properties of multiscale composites were remarkably enhanced, especially in the functionalized MWNT multiscale composites. With only 1?wt% loading of functionalized MWNTs, tensile strength was increased by 14% and Youngs modulus by 20%, in comparison with conventional fibre-reinforced composites. Moreover, the shear strength and short-beam modulus were increased by 5% and 8%, respectively, indicating the improved inter-laminar properties. The strain?stress tests also suggested noticeable enhancement in toughness. Scanning electron microscopy (SEM) characterization confirmed an enhanced interfacial bonding when functionalized MWNTs were integrated into epoxy/glass-fibre composites. The coefficient thermal expansion (CTE) of functionalized nanocomposites indicated a reduction of 25.2% compared with epoxy/glass-fibre composites. The desired improvement of electrical conductivities was also achieved. The multiscale composites indicated a way to leverage the benefits of CNTs and opened up new opportunities for high-performance multifunctional multiscale composites.

Surface Plasmon-Driven Water Reduction: Gold Nanoparticle Size Matters

Water reduction under two different visible-light ranges (λ > 400 nm and λ > 435 nm) was investigated in gold-loaded titanium dioxide (Au-TiO2) heterostructures with different sizes of Au nanoparticles (NPs). Our study clearly demonstrates the essential role played by Au NP size in plasmon-driven H2O reduction and reveals two distinct mechanisms to clarify visible-light photocatalytic activity under different excitation conditions. The size of the Au NP governs the efficiency of plasmon-mediated electron transfer and plays a critical role in determining the reduction potentials of the electrons transferred to the TiO2 conduction band. Our discovery provides a facile method of manipulating photocatalytic activity simply by varying the Au NP size and is expected to greatly facilitate the design of suitable plasmonic photocatalysts for solar-to-fuel energy conversion.

Polyvinylpyrrolidone-induced anisotropic growth of gold nanoprisms in plasmon-driven synthesis.

After more than a decade, it is still unknown whether the plasmon-mediated growth of silver nanostructures can be extended to the synthesis of other noble metals, as the molecular mechanisms governing the growth process remain elusive. Herein, we demonstrate the plasmon-driven synthesis of gold nanoprisms and elucidate the details of the photochemical growth mechanism at the single-nanoparticle level. Our investigation reveals that the surfactant polyvinylpyrrolidone preferentially adsorbs along the nanoprism perimeter and serves as a photochemical relay to direct the anisotropic growth of gold nanoprisms. This discovery confers a unique function to polyvinylpyrrolidone that is fundamentally different from its widely accepted role as a crystal-face-blocking ligand. Additionally, we find that nanocrystal twinning exerts a profound influence on the kinetics of this photochemical process by controlling the transport of plasmon-generated hot electrons to polyvinylpyrrolidone. These insights establish a molecular-level description of the underlying mechanisms regulating the plasmon-driven synthesis of gold nanoprisms.

Surface Plasmon Mediated Chemical Solution Deposition of Gold Nanoparticles on a Nanostructured Silver Surface at Room Temperature

Sub-15 nm Au nanoparticles have been fabricated on a nanostructured Ag surface at room temperature via a liquid-phase chemical deposition upon excitation of the localized surface plasmon resonance (SPR). Measurement of the SPR-mediated photothermal local heating of the substrate surface by a molecular thermometry strategy indicated the temperature to be above 230 °C, which led to an efficient decomposition of CH(3)AuPPh(3) to form Au nanoparticles on the Ag surface. Particle sizes were tunable between 3 and 10 nm by adjusting the deposition time. A surface-limited growth model for Au nanoparticles on Ag is consistent with the deposition kinetics.

A Facile Solvothermal Synthesis of Octahedral Fe3O4 Nanoparticles

Anisotropic Fe3 O4 octahedrons are obtained via a simple solvothermal synthesis with appropriate sizes for various technological applications. A complete suite of materials characterization methods confirms the magnetite phase for these structures, which exhibit substantial saturation magnetization and intriguing morphologies for a wide range of applications.

Metallic Nanostructures for Catalytic Applications

The discovery of substantial catalytic activity over metallic nanostructures has established a modern industrialized society, largely sustained by heterogeneous catalysts for supplying a wide variety of consumer and industrial goods. Heterogeneous catalysts allow for highly efficient and selective chemical processes, while simultaneously reducing the energy costs associated with chemical manufacturing by lowering the activation energy of the desired product pathway. The remarkable catalytic activity of metallic nanostructures is intimately linked to their unique physical and electronic properties. Unfortunately, the catalytic efficiency of modern heterogeneous catalysts is often hindered by poor control over active catalytic sites and a substantial thermal energy requirement for reaction, which leads to a significant reduction in catalyst lifetime and imposes a growing strain on the environment. Recent breakthroughs involving the precise control over the size, shape, and electronic structure of metallic nanostructures as well as the optimization of metal-support interactions have paved the way for highly efficient catalytic materials poised to ease these environmental burdens. The continued optimization and development of photoresponsive metallic nanostructures using Earth-abundant materials is expected to further reduce both the energetic and financial requirements for obtaining highly efficient and selective heterogeneous catalysts. Deeper fundamental understanding of the physical and electronic properties governing the catalytic properties of these metallic nanostructures promises to provide a means of engineering highly efficient catalysts capable of meeting the pressing material needs of the growing industrial world while achieving a sustainable economic landscape.

Solvent Control of Surface Plasmon-Mediated Chemical Deposition of Au Nanoparticles from Alkylgold Phosphine Complexes.

Bottom-up approaches to nanofabrication are of great interest because they can enable structural control while minimizing material waste and fabrication time. One new bottom-up nanofabrication method involves excitation of the surface plasmon resonance (SPR) of a Ag surface to drive deposition of sub-15 nm Au nanoparticles from MeAuPPh3. In this work we used density functional theory to investigate the role of the PPh3 ligands of the Au precursor and the effect of adsorbed solvent on the deposition process, and to elucidate the mechanism of Au nanoparticle deposition. In the absence of solvent, the calculated barrier to MeAuPPh3 dissociation on the bare surface is <20 kcal/mol, making it facile at room temperature. Once adsorbed on the surface, neighboring MeAu fragments undergo ethane elimination to produce Au adatoms that cluster into Au nanoparticles. However, if the sample is immersed in benzene, we predict that the monolayer of adsorbed solvent blocks the adsorption of MeAuPPh3 onto the Ag surface because the PPh3 ligand is large compared to the size of the exposed surface between adsorbed benzenes. Instead, the Au-P bond of MeAuPPh3 dissociates in solution (Ea = 38.5 kcal/mol) in the plasmon heated near-surface region followed by the adsorption of the MeAu fragment on Ag in the interstitial space of the benzene monolayer. The adsorbed benzene forces the Au precursor to react through the higher energy path of dissociation in solution rather than dissociatively adsorbing onto the bare surface. This requires a higher temperature if the reaction is to proceed at a reasonable rate and enables the control of deposition by the light induced SPR heating of the surface and nearby solution.