Explore the vast range of titles available.

Interests in evaluating lifecycle energy use in urban transport have been growing as a research topic. Various studies have evaluated the relationship between the intracity transport energy use and population density and commonly identified its negative correlation. However, a diachronic transition in an individual city has yet to be fully analyzed. As such, this study employed transport energy intensity widely used for evaluating transport energy efficiency and obtained the transport energy intensity for each transportation means including walk, bicycle, automobile (conventional vehicles, electric vehicles, hybrid vehicles, and fuel cell vehicles), bus and electric train by considering the lifecycle energy consumption. Then, the intracity lifecycle transport energy intensity of 38 cities in Japan in 1987–2015 was computed, assuming that the cause of diachronic transition of intracity transport energy efficiency is the modal shifting and electricity mix change. As a result, the greater level of population density was associated with the lower intracity transport energy intensity in Japanese cities. The negative slope of its regression line increased over time since the intracity lifecycle transport energy intensity in cities with low population density continuously increased without any significant change of population density. Finally, this study discussed the strategic implications particularly in regional areas to improve the intracity lifecycle transport energy efficiency.

A shining example of doping Many technological materials are intentionally 'doped' by the introduction of trace amounts of foreign elements to impart new and useful properties — a classic example is the doping of semiconductors. Feng Wang et al . describe a system in which lanthanide doping can be used to control the growth of NaYF 4 nanocrystals, making it possible to simultaneously tune the size, crystallographic phase and optical properties of the resulting materials. These findings increase our understanding of doping-induced structural transformations, and provide a straightforward route for the controlled synthesis of luminescent nanocrystals for many applications. Many technological materials are intentionally 'doped' with foreign elements to impart new and desirable properties, a classic example being the doping of semiconductors to tune their electronic behaviour. Here lanthanide doping is used to control the growth of nanocrystals, allowing for simultaneous tuning of the size, crystallographic phase and optical properties of the hybrid material. Doping is a widely applied technological process in materials science that involves incorporating atoms or ions of appropriate elements into host lattices to yield hybrid materials with desirable properties and functions. For nanocrystalline materials, doping is of fundamental importance in stabilizing a specific crystallographic phase 1 , modifying electronic properties 2 , 3 , 4 , modulating magnetism 5 as well as tuning emission properties 6 , 7 , 8 , 9 . Here we describe a material system in which doping influences the growth process to give simultaneous control over the crystallographic phase, size and optical emission properties of the resulting nanocrystals. We show that NaYF 4 nanocrystals can be rationally tuned in size (down to ten nanometres), phase (cubic or hexagonal) and upconversion 10 , 11 , 12 emission colour (green to blue) through use of trivalent lanthanide dopant ions introduced at precisely defined concentrations. We use first-principles calculations to confirm that the influence of lanthanide doping on crystal phase and size arises from a strong dependence on the size and dipole polarizability of the substitutional dopant ion. Our results suggest that the doping-induced structural and size transition, demonstrated here in NaYF 4 upconversion nanocrystals, could be extended to other lanthanide-doped nanocrystal systems for applications ranging from luminescent biological labels 12 to volumetric three-dimensional displays 13 .

Broader applications of carbon nanotubes to real-world problems have largely gone unfulfilled because of difficult material synthesis and laborious processing. We report high-performance multifunctional carbon nanotube (CNT) fibers that combine the specific strength, stiffness, and thermal conductivity of carbon fibers with the specific electrical conductivity of metals. These fibers consist of bulk-grown CNTs and are produced by high-throughput wet spinning, the same process used to produce high-performance industrial fibers. These scalable CNT fibers are positioned for high-value applications, such as aerospace electronics and field emission, and can evolve into engineered materials with broad long-term impact, from consumer electronics to long-range power transmission.

The complex structure of wood, one of the most abundant biomaterials on Earth, has been optimized over 270 million years of tree evolution. This optimization has led to the highly efficient water and nutrient transport, mechanical stability and durability of wood. The unique material structure and pronounced anisotropy of wood endows it with an array of remarkable properties, yielding opportunities for the design of functional materials. In this Review, we provide a materials and structural perspective on how wood can be redesigned via structural engineering, chemical and/or thermal modification to alter its mechanical, fluidic, ionic, optical and thermal properties. These modifications enable a diverse range of applications, including the development of high-performance structural materials, energy storage and conversion, environmental remediation, nanoionics, nanofluidics, and light and thermal management. We also highlight advanced characterization and computational-simulation approaches for understanding the structure–property–function relationships of natural and modified wood, as well as informing bio-inspired synthetic designs. In addition, we provide our perspective on the future directions of wood research and the challenges and opportunities for industrialization. The porous hierarchical structure and anisotropy of wood make it a strong candidate for the design of materials with various functions, including load bearing, multiscale mass transport, and optical and thermal management. In this Review, the composition, structure, characterization methods, modification strategies, properties and applications of natural and modified wood are discussed.

Localized surface plasmon resonances of an individual silver nanocube are reconstructed in three dimensions using electron energy-loss spectrum imaging, resulting in a better understanding of the optical response of noble-metal nanoparticles. Observing surface excitations for nano-optics Metal nanoparticles exhibit a range of striking and useful optical properties thanks to the excitation of localized surface plasmon resonances (LSPRs). But the precise relationship between the three-dimensional structure of the nanoparticles and the resulting LSPRs can be hard to determine. Paul Midgley and colleagues have developed a spectrally sensitive imaging technique, based on electron energy-loss spectroscopy, that permits three-dimensional visualization of many of the key features associated with these LSPRs. With this technique, the interplay between the LSPRs, nanoparticle structure and substrate–nanoparticle interactions can be directly probed. This study focuses on silver nanocubes, but the method demonstrated is applicable to similar plasmonic phenomena across all metal nanoparticles. The remarkable optical properties of metal nanoparticles are governed by the excitation of localized surface plasmon resonances (LSPRs). The sensitivity of each LSPR mode, whose spatial distribution and resonant energy depend on the nanoparticle structure, composition and environment, has given rise to many potential photonic, optoelectronic, catalytic, photovoltaic, and gas- and bio-sensing applications 1 , 2 , 3 . However, the precise interplay between the three-dimensional (3D) nanoparticle structure and the LSPRs is not always fully understood and a spectrally sensitive 3D imaging technique is needed to visualize the excitation on the nanometre scale. Here we show that 3D images related to LSPRs of an individual silver nanocube can be reconstructed through the application of electron energy-loss spectrum imaging 4 , mapping the excitation across a range of orientations, with a novel combination of non-negative matrix factorization 5 , 6 , compressed sensing 7 , 8 and electron tomography 9 . Our results extend the idea of substrate-mediated hybridization of dipolar and quadrupolar modes predicted by theory, simulations, and electron and optical spectroscopy 10 , 11 , 12 , and provide experimental evidence of higher-energy mode hybridization. This work represents an advance both in the understanding of the optical response of noble-metal nanoparticles and in the probing, analysis and visualization of LSPRs.

Key insights into the behavior of materials can be gained by observing their structure as they undergo lattice distortion. Laser pulses on the femtosecond time scale can be used to induce disorder in a \"pump-probe\" experiment with the ensuing transients being probed stroboscopically with femtosecond pulses of visible light, x-rays, or electrons. Here we report three-dimensional imaging of the generation and subsequent evolution of coherent acoustic phonons on the picosecond time scale within a single gold nanocrystal by means of an x-ray free-electron laser, providing insights into the physics of this phenomenon. Our results allow comparison and confirmation of predictive models based on continuum elasticity theory and molecular dynamics simulations.

Silver (Ag) has been under development for use as interconnect material for power electronics packaging since the late 1980s. Despite its long development history, high thermal and electrical conductivities, and lead-free composition, sintered Ag technology has limited market penetration. This review sets out to explore what is required to make this technology more viable. This review also covers the origin of sintered Ag, the different types and application methods of sintered Ag pastes and laminates, and the long-term reliability of sintered Ag joints. Sintered Ag pastes are classified according to whether pressure is required for sintering and further classified according to their filler sizes. This review discusses the main methods of applying Ag pastes/laminates as die-attach materials and the related processing conditions. The long-term reliability of sintered Ag joints depends on the density of the sintered joint, selection of metallization or plating schemes, types of substrates, substrate roughness, formulation of Ag pastes/laminates, joint configurations (i.e., joint thicknesses and die sizes), and testing conditions. This paper identifies four challenges that must be overcome for the proliferation of sintered Ag technology: changes in materials formulation, the successful navigation of the complex patent landscape, the availability of production and inspection equipment, and the health concerns of Ag nanoparticles. This paper is expected to be useful to materials suppliers and semiconductor companies that are considering this technology for their future packages.

Graphene nanoribbons: a slice of the action Graphene, made up of graphite sheets a single atom thick, is an electronic conductor. However thin strips of the material, called graphite nanoribbons or GNRs, can express different electronic properties depending on their width. This tunability could lead them to overtake nanotubes for some applications. Producing bulk quantities of ribbons in a scalable manner has been a challenge until now, but it is required for using them in electronics applications. A team from Stanford University team now report an approach to reliably produce sub-10-nm graphene nanoribbons by partial encapsulation of carbon nanotubes in a polymer. A longitudinal strip of the nanotube remains exposed and can be cut by plasma etching, resulting in the unzipping of the nanotube when the polymer is removed, and formation of a thin strip of graphene. The potential of the material was demonstrated by using it to produce effective field-effect transistors. Unlike graphene itself, or carbon nanotubes, very narrow nanoribbons of graphene are completely semiconducting. Dai and colleagues reliably produce bulk quantities of sub-10 nm graphene nanoribbons by partial encapsulation of carbon nanotubes in a polymer. The exposed part of the nanotube can be cut by plasma etching, so that the nanotube unzips when the polymer is removed, leaving a very thin strip of graphene. Graphene nanoribbons (GNRs) are materials with properties distinct from those of other carbon allotropes 1 , 2 , 3 , 4 , 5 . The all-semiconducting nature of sub-10-nm GNRs could bypass the problem of the extreme chirality dependence of the metal or semiconductor nature of carbon nanotubes (CNTs) in future electronics 1 , 2 . Currently, making GNRs using lithographic 3 , 4 , 6 , chemical 7 , 8 , 9 or sonochemical 1 methods is challenging. It is difficult to obtain GNRs with smooth edges and controllable widths at high yields. Here we show an approach to making GNRs by unzipping multiwalled carbon nanotubes by plasma etching of nanotubes partly embedded in a polymer film. The GNRs have smooth edges and a narrow width distribution (10–20 nm). Raman spectroscopy and electrical transport measurements reveal the high quality of the GNRs. Unzipping CNTs with well-defined structures in an array will allow the production of GNRs with controlled widths, edge structures, placement and alignment in a scalable fashion for device integration.

Single-walled carbon nanotubes can be classified as either metallic or semiconducting, depending on their conductivity, which is determined by their chirality. Existing synthesis methods cannot controllably grow nanotubes with a specific type of conductivity. By varying the noble gas ambient during thermal annealing of the catalyst, and in combination with oxidative and reductive species, we altered the fraction of tubes with metallic conductivity from one-third of the population to a maximum of 91%. In situ transmission electron microscopy studies reveal that this variation leads to differences in both morphology and coarsening behavior of the nanoparticles that we used to nucleate nanotubes. These catalyst rearrangements demonstrate that there are correlations between catalyst morphology and resulting nanotube electronic structure and indicate that chiral-selective growth may be possible.

The capabilities of additive manufacturing technologies to fabricate multi-material structures have been investigated in many studies. However, only a few of the technologies have been used to fabricate products for direct application. The full development of the capability will enable the fabrication of innovative engineering structures consisting of function-specific material members that cannot be realized using conventional methods. In this work, a methodology for fabricating dual-material engineering structures using ultrasonic additive manufacturing (UAM) was developed. An example structure consisting of members designed to carry tension and compression loads were fabricated using composite materials and Al 3003 matrix material respectively. MetPreg®/Al 3003 and Ti/Al 3003 composite materials were respectively used as tension members in two different structure samples. Single-material copies of the dual-material structures were fabricated using Al 3003 for load-carrying capability comparison. The results of the load tests carried out shows that the dual-material structures could withstand much higher loads than similar structures entirely made of the matrix Al 3003 material. This is an indication that UAM can be effectively used to fabricate multi-material engineering structures.