High-power fiber lasers have experienced a dramatic development over the last decade. Further increasing the output power needs an upscaling of the fiber mode area, while maintaining a single-mode output. Here, we propose an all-solid anti-resonant fiber (ARF) structure, which ensures single-mode operation in broadband by resonantly coupling higher-order modes into the cladding. A series of fibers with core sizes ranging from 40 to 100 μm are proposed exhibiting maximum mode area exceeding 5000 μm2. Numerical simulations show this resonant coupling scheme provides a higher-order mode (mainly TE01, TM01, and HE21) suppression ratio of more than 20 dB, while keeping the fundamental mode loss lower than 1 dB/m. The proposed structure also exhibits high tolerance for core index depression.

Faraday effect measurements of holmium oxide (Ho2O3) ceramics-based magneto-optical materials, highly potential material candidates for high-energy laser Faraday isolators, are presented in this paper. Temperature dependence of the Verdet constant of nondoped Ho2O3 ceramics was measured for temperatures 15–305 K at $1.064~\unicode[STIX]{x03BC}\text{m}$ wavelength. The Verdet constant dispersion for wavelengths 0.5–$1~\unicode[STIX]{x03BC}\text{m}$ and $1.064~\unicode[STIX]{x03BC}\text{m}$ was measured for both nondoped Ho2O3 ceramics and Ho2O3 ceramics doped with terbium Tb3+ (0.2 at. %) and cerium Ce3+ (0.1 at. %) ions. The results suggest that the relatively low level of doping of Ho2O3 with these ions has no significant boosting impact on the Faraday effect. Therefore, other compositions of Ho2O3 ceramics-based magneto-optical materials, as well as various doping concentrations, should be further examined.

Phases of general formula (RE, A)2M3O7 (RE=lanthanide, A=Ca, Sr, Ba; M=Ga, Al) are of interest for their nonlinear optical properties and have potential as solid state lasers. Their structures have been refined using X-ray and neutron diffraction data and are related to gehlenite, Ca2Al2SiO7, with M cations occupying Al and Si sites and RE and A cations sharing the Ca site with no evidence for ordering, although they occur in the ratio 1:1 because of stoichiometry; the M cations are tetrahedrally coordinated. (RE, Ba)2M3O7 compounds cannot be synthesized for M=Al or for RE cations smaller than Sm; this limitation is believed to be due to size mismatch between cations within the structure.

Self-assembly—the spontaneous generation of order in systems of components—is ubiquitous in chemistry; in biology, it generates much of the functionality of the living cell. Self-assembly is relatively unused in microfabrication, although it offers opportunities to simplify processes, lower costs, develop new processes, use components too small to be manipulated robotically, integrate components made using incompatible technologies, and generate structures in three dimensions and on curved surfaces. The major limitations to the self-assembly of micrometer- to millimeter-sized components (mesoscale self-assembly) do not seem to be intrinsic, but rather operational: selfassembly can, in fact, be reliable and insensitive to small process variations, but fabricating the small, complex, functional components that future applications may require will necessitate the development of new methodologies. Proof-of-concept experiments in mesoscale self-assembly demonstrate that this technique poses fascinating scientific and technical challenges and offers the potential to provide access to hard-to-fabricate structures.

A new approach to general sensors for odors and volatile organic compounds (VOCs) using thin films of chemically responsive dyes as a colorimetric sensor array is described. This optoelectronic “nose,” by using an array of multiple dyes whose colors change based on the full range of intermolecular interactions, provides enormous discriminatory power among odorants in a simple device that can be easily digitally imaged. High sensitivities (ppb) have been demonstrated for the detection of biologically important analytes such as amines, carboxylic acids, and thiols. By the proper choice of dyes and substrate, the array can be made essentially nonresponsive to changes in humidity.

An effective way to build ordered materials with micrometer- or submicrometer-sized features is to pack together monodisperse (equal-sized) colloidal particles. But most monodisperse particles in this size range are spheres, and thus one problem in building new micrometer-scale ordered materials is controlling how spheres pack. In this article, we discuss how this problem can be approached by constructing and studying packings in the few-sphere limit. Confinement of particles within containers such as micropatterned holes or spherical droplets can lead to some unexpected and diverse types of polyhedra that may become building blocks for more complex materials. The packing processes that form these polyhedra may also be a source of disorder in dense bulk suspensions.

The primary aim of this issue of MRS Bulletin is to present an overview of the deployment of optical-fiber sensors in a selected range of applications. The topics covered include a general introduction to optical fibers; a review of the sensing mechanisms that are available to monitor strain, temperature, pressure, chemical species, damage, and acoustic emission; and the use of optical-fiber sensors in medical applications. This introductory article presents a brief discussion of the advantages and disadvantages of optical-fiber sensors.

Combinatorial methods are high-efficiency methods to create large composition “libraries” of materials, for example, continuous composition variations, and test those compositions systematically in parallel for specific properties of interest, in contrast to the time-consuming one-composition-at-a-time approach. These methods have captured the attention of the materials industry with the promise of providing new discoveries “faster, better, and cheaper.” However, in the academic community, combinatorial methods often meet with less enthusiasm, perhaps due to the perception of combinatorial methodology as an Edisonian approach to science. The facts are quite to the contrary. In addition to impressive successes arising from the application of combinatorial methods to materials discovery, results coming out of systematic high-throughput investigations of complex materials phenomena (which would be too time-consuming or expensive to undertake) provide data leading to improvement in theories and models of materials chemistry and physics. Indeed, combinatorial methods provide a new paradigm for advancing a central scientific goal—the fundamental understanding of structure–property relationships of materials behavior.

The rapid development of modern photonic technologies—for example, mercury-free lamps, flat-panel displays, and solid-state lamps—demands the timely discovery of advanced phosphors. A combinatorial process has been developed to dramatically accelerate the experimental search for such phosphors. High-density phosphor “libraries” containing from 100 to over 1000 discrete chemical compositions on a 1 in. × 1 in. substrate have been made in thin-film or powder form using selective vapor deposition and liquid-dispensing techniques, respectively. In this article, the existing methods of combinatorial synthesis and screening of phosphors will be reviewed with examples. These methods may also be used to screen organic-based solid-state materials and optimize their device properties. In this regard, combinatorial and spreading techniques have been utilized to study and rapidly optimize organic light-emitting devices (OLEDs).