Since the discovery of mechanically exfoliated graphene in 2004, research on ultrathin two-dimensional (2D) nanomaterials has grown exponentially in the fields of condensed matter physics, material science, chemistry, and nanotechnology. Highlighting their compelling physical, chemical, electronic, and optical properties, as well as their various potential applications, in this Review, we summarize the state-of-art progress on the ultrathin 2D nanomaterials with a particular emphasis on their recent advances. First, we introduce the unique advances on ultrathin 2D nanomaterials, followed by the description of their composition and crystal structures. The assortments of their synthetic methods are then summarized, including insights on their advantages and limitations, alongside some recommendations on suitable characterization techniques. We also discuss in detail the utilization of these ultrathin 2D nanomaterials for wide ranges of potential applications among the electronics/optoelectronics, electrocat...

Recent Advances in Ultrathin Two-Dimensional Nanomaterials

Gold nanoparticles have been used in biomedical applications since their first colloidal syntheses more than three centuries ago. However, over the past two decades, their beautiful colors and unique electronic properties have also attracted tremendous attention due to their historical applications in art and ancient medicine and current applications in enhanced optoelectronics and photovoltaics. In spite of their modest alchemical beginnings, gold nanoparticles exhibit physical properties that are truly different from both small molecules and bulk materials, as well as from other nanoscale particles. Their unique combination of properties is just beginning to be fully realized in range of medical diagnostic and therapeutic applications. This critical review will provide insights into the design, synthesis, functionalization, and applications of these artificial molecules in biomedicine and discuss their tailored interactions with biological systems to achieve improved patient health. Further, we provide a survey of the rapidly expanding body of literature on this topic and argue that gold nanotechnology-enabled biomedicine is not simply an act of ‘gilding the (nanomedicinal) lily’, but that a new ‘Golden Age’ of biomedical nanotechnology is truly upon us. Moving forward, the most challenging nanoscience ahead of us will be to find new chemical and physical methods of functionalizing gold nanoparticles with compounds that can promote efficient binding, clearance, and biocompatibility and to assess their safety to other biological systems and their long-term term effects on human health and reproduction (472 references).

The golden age: gold nanoparticles for biomedicine

The science and technology of ultracapacitors are reviewed for a number of electrode materials, including carbon, mixed metal oxides, and conducting polymers. More work has been done using microporous carbons than with the other materials and most of the commercially available devices use carbon electrodes and an organic electrolytes. The energy density of these devices is 3¯5 Wh/kg with a power density of 300¯500 W/kg for high efficiency (90¯95%) charge/discharges. Projections of future developments using carbon indicate that energy densities of 10 Wh/kg or higher are likely with power densities of 1¯2 kW/kg. A key problem in the fabrication of these advanced devices is the bonding of the thin electrodes to a current collector such the contact resistance is less than 0.1 cm2. Special attention is given in the paper to comparing the power density characteristics of ultracapacitors and batteries. The comparisons should be made at the same charge/discharge efficiency.

Ultracapacitors: Why, How, and Where is the Technology

In medicine, nanotechnology has sparked a rapidly growing interest as it promises to solve a number of issues associated with conventional therapeutic agents, including their poor water solubility (at least, for most anticancer drugs), lack of targeting capability, nonspecific distribution, systemic toxicity, and low therapeutic index. Over the past several decades, remarkable progress has been made in the development and application of engineered nanoparticles to treat cancer more effectively. For example, therapeutic agents have been integrated with nanoparticles engineered with optimal sizes, shapes, and surface properties to increase their solubility, prolong their circulation half-life, improve their biodistribution, and reduce their immunogenicity. Nanoparticles and their payloads have also been favorably delivered into tumors by taking advantage of the pathophysiological conditions, such as the enhanced permeability and retention effect, and the spatial variations in the pH value. Additionally, targeting ligands (e.g., small organic molecules, peptides, antibodies, and nucleic acids) have been added to the surface of nanoparticles to specifically target cancerous cells through selective binding to the receptors overexpressed on their surface. Furthermore, it has been demonstrated that multiple types of therapeutic drugs and/or diagnostic agents (e.g., contrast agents) could be delivered through the same carrier to enable combination therapy with a potential to overcome multidrug resistance, and real-time readout on the treatment efficacy. It is anticipated that precisely engineered nanoparticles will emerge as the next-generation platform for cancer therapy and many other biomedical applications.

Engineered Nanoparticles for Drug Delivery in Cancer Therapy

Lithium metal is an attractive anode material for rechargeable batteries, owing to its high theoretical specific capacity of 3,860 mAh g−1. Despite extensive research efforts, there are still many fundamental challenges in using lithium metal in lithium-ion batteries. Most notably, critical information such as its nucleation and growth behaviour remains elusive. Here we explore the nucleation pattern of lithium on various metal substrates and unravel a substrate-dependent growth phenomenon that enables selective deposition of lithium metal. With the aid of binary phase diagrams, we find that no nucleation barriers are present for metals exhibiting a definite solubility in lithium, whereas appreciable nucleation barriers exist for metals with negligible solubility. We thereafter design a nanocapsule structure for lithium metal anodes consisting of hollow carbon spheres with nanoparticle seeds inside. During deposition, the lithium metal is found to predominantly grow inside the hollow carbon spheres. Such selective deposition and stable encapsulation of lithium metal eliminate dendrite formation and enable improved cycling, even in corrosive alkyl carbonate electrolytes, with 98% coulombic efficiency for more than 300 cycles. Uncontrolled lithium deposition during cycling is a major concern in the development of lithium-based batteries. Here, the authors analyse the lithium nucleation pattern on various metal substrates and demonstrate that lithium can be selectively deposited in a nanoseed inside hollow carbon spheres.

https://web.stanford.edu/group/cui_group/papers/Kai_Cui_NATNRG_2016.pdf

Selective deposition and stable encapsulation of lithium through heterogeneous seeded growth

This communication reports a new theranostic system with a combination of capabilities to both enhance the contrast of photoacoustic (PA) imaging and control the release of a chemical or biological effector by high-intensity focused ultrasound (HIFU). The fabrication of this system simply involves filling the hollow interiors of gold nanocages with a phase-change material (PCM) such as 1-tetradecanol that has a melting point of 38−39 °C. The PCM can be premixed and thus loaded with a dye, as well as other chemical or biological effectors. When exposed to direct heating or HIFU, the PCM will melt and escape from the interiors of nanocages through small pores on the surface, concurrently releasing the encapsulated molecules into the surrounding medium. We can control the release profile by varying the power of HIFU, the duration of exposure to HIFU, or both.

/pdf/a-new-theranostic-system-based-on-gold-nanocages-and-phase-552qlufnco.pdf

A New Theranostic System Based on Gold Nanocages and Phase-Change Materials with Unique Features for Photoacoustic Imaging and Controlled Release

http://staff.ustc.edu.cn/~zengj/paper/31_Nano_Today_2011.pdf

Chemical transformations of nanostructured materials

TiO2 hollow shells with well-controlled crystallinity, phase, and porosity are desirable in many applications. In photocatalysis in particular, they can provide high active surface area, reduced diffusion resistance, and improved accessibility to reactants. Here, the results from studies of the causes for the failure of a prior etching and calcination scheme to make such shells and on a newly-developed simple yet robust process for producing uniform mesoporous TiO2 shells with precisely controllable crystallinity and phase are reported. The key finding is that base etching of the SiO2@TiO2 core-shell particles leads to the formation of sodium titanate species, which, if not removed, promote substantial crystal growth during calcination and destroy the structural integrity of the TiO2 shells. A simple acid treatment of the base-etched samples may convert the sodium titanates into protonated titanates, which not only prevent the formation of the impurity phases, but also help to maintain the structural integrity of the shell and allow precise control of the TiO2 phase and crystallinity. This new development affords convenient optimization of the structure of the hollow TiO2 shells toward efficient photocatalysts, which outperform the commercial P25-TiO2 in the photocatalytic decomposition of organic dye molecules.

Controllable Synthesis of Mesoporous TiO2 Hollow Shells: Toward an Efficient Photocatalyst

We have studied the chemical transformations in ultrathin chalcogenide nanowires with an aim to understand the parameters that control the morphology and crystal structure of the product. Ultrathin Te nanowires were transformed into Ag2Te nanowires with preservation of the single crystallinity. The Ag2Te nanowires were then converted into CdTe, ZnTe, and PbTe using cation-exchange reactions, and the CdTe nanowires were further transformed into PtTe2 nanotubes. On the basis of the solubility products of the ionic solids, the crystal structures of the involved solids, the reaction kinetics, and the reaction conditions for transformations, we were able to reach the following conclusions: (i) The solubility products of ionic solids can be used as a rough criterion to predict if the transformation is thermodynamically favorable or not. (ii) The morphological preservation of reactant nanowires is more sensitive to the change in length rather than the total volume in addition to the lattice matching between the ...

https://www.dstuns.iitm.ac.in/grouppresentations/2010/Chemical%20Transformations%20in%20Ultrathin.pdf

Chemical transformations in ultrathin chalcogenide nanowires.

A facile and quick approach to prepare self-assembled monolayers of water-dispersible particles on the water surface is presented. Particle suspensions in alcohols were dropped on a water reservoir to form long-range ordered monolayers of various particles, including spherical solid particles, soft hydrogel particles, metal nanoparticles, quantum dots, nanowires, single-wall carbon nanotubes (SWCNTs), nanoplates, and nanosheets. A systematic study was conducted on the variables affecting the monolayer assembly: the solubility parameter of spreading solvents, particle concentration, zeta potential of the particles in the suspension, surface tension of the water phase, hardness of the particles, and addition of a salt in the suspension. This method requires no hydrophobic surface treatment of the particles, which is useful to exploit these monolayer films without changing the native properties of the particles. The study highlights a quick 2D colloidal assembly without cracks in the wafer scale as well as t...

Geon Dae Moon

Papers

A New Theranostic System Based on Gold Nanocages and Phase-Change Materials with Unique Features for Photoacoustic Imaging and Controlled Release

Chemical transformations of nanostructured materials

Controllable Synthesis of Mesoporous TiO2 Hollow Shells: Toward an Efficient Photocatalyst

Chemical transformations in ultrathin chalcogenide nanowires.

Assembled monolayers of hydrophilic particles on water surfaces.