This work investigated the photophysical pathways for light absorption, charge generation, and charge separation in donor–acceptor nanoparticle blends of poly(3-hexylthiophene) and indene-C60-bisadduct. Optical modeling combined with steady-state and time-resolved optoelectronic characterization revealed that the nanoparticle blends experience a photocurrent limited to 60% of a bulk solution mixture. This discrepancy resulted from imperfect free charge generation inside the nanoparticles. High-resolution transmission electron microscopy and chemically resolved X-ray mapping showed that enhanced miscibility of materials did improve the donor–acceptor blending at the center of the nanoparticles; however, a residual shell of almost pure donor still restricted energy generation from these nanoparticles.

Potassium and cerium co-doped Bi4Ti2.86W0.14O12 ceramics with a formula of (K0.5Ce0.5)xBi4−xTi2.86W0.14O12 (abbreviated as KC100x-BITW, x = 0, 0.02, 0.04, 0.06, 0.08, 0.1) were prepared by a conventional solid-state reaction method. The effect of (K0.5Ce0.5) complex doping amount on the structure, dielectric, and piezoelectric properties of the KC100x-BITW ceramics was investigated. X-ray diffraction results indicated that the KC100x-BITW ceramics are Aurivillius-type phase with the bismuth layer structure. (K0.5Ce0.5) complex addition first increases and then decreases the grain size which can be observed by scanning electron microscopy. With the increase of (K0.5Ce0.5) complex doping amount, the Curie temperature (TC) was slightly decreased from 632 to 608 oC. The dielectric and piezoelectric properties were optimized in KC100x-BITW ceramics with x = 0.08 as follows: d33 = 24 pC/N, kp = 8.2%, Qm = 6766, εr = 135 (@100 kHz), tanδ = 0.28% (@100 kHz), Tc = 611 oC, and resistivity ρ = 2.9 × 106 Ω cm at 500 oC, indicating that the KC100x-BITW ceramics are suitable for high-temperature piezoelectric sensing applications.

Nickel-coated carbon nanotubes (Ni-CNTs) were achieved by electroless plating. Laser cladded IN718 and IN718 with 10, 30, and 50 wt% additions of Ni-CNTs were fabricated. The structural evolution of CNTs in the laser-deposited layers was studied; the microstructure, tensile, and wear properties of the laser-cladded alloys were characterized. The results show that CNTs in the laser-deposited layers are mostly transformed to carbon nanoproducts (CNPs) in the forms of graphene nanosheets, graphene fragments, carbon nanoribbons, and diamond-like nanoparticles by unzipping, interbonding, collapsing, and curvature of CNTs. The interdendritic Laves phase formation is dramatically depressed due to the addition of Ni-CNTs, but the excess addition of the Ni-CNTs can undesirably increase the formation of NbC. The addition of Ni-CNTs effectively improves the tensile and wear properties. The most superior tensile and wear properties are achieved in the layers with 30 and 50 wt% additions of Ni-CNTs, respectively. The generation of intermetallic phase and CNPs are revealed to be two dominant effects both on the tensile and wear properties of the laser-cladded alloys.

Tracing the flow of solid matter during an explosion requires a rugged tag that can be measured by a unique identifiable signature. Silica-covered semiconductor quantum dots (QDs) provide a unique and tunable photoluminescent signature that emits from within a sacrificial outer layer. Five types of silica-covered zinc sulfide QDs were synthesized and covalently bound to commercial luminescent powders. The combination of five dots and five powders enables a matrix of 25 unique tags. The tracers are shown to be tolerant of environments associated with chemical explosives and provides a unique tag to evaluate debris fields.

The field of self-assembly has moved far beyond early work, where the focus was primarily the resultant beautiful two- and three-dimensional structures, to a focus on forming materials and devices with important properties either otherwise not available, or only available at great cost. Over the last few years, materials with unprecedented electronic, photonic, energy-storage, and chemical separation functionalities were created with self-assembly, while at the same time, the ability to form even more complex structures in two and three dimensions has only continued to advance. Self-assembly crosscuts all areas of materials. Functional structures have now been realized in polymer, ceramic, metallic, and semiconducting systems, as well as composites containing multiple classes of materials. As the field of self-assembly continues to advance, the number of highly functional systems will only continue to grow and make increasingly greater impacts in both the consumer and industrial space.

Electrochemical energy-storage systems such as supercapacitors and lithium-ion batteries require complex intertwined networks that provide fast transport pathways for ions and electrons without interfering with their energy density. Self-assembly of nanomaterials into hierarchical structures offers exciting possibilities to create such pathways. This article summarizes recent research achievements in self-assembled zero-dimensional, one-dimensional, and two-dimensional nanomaterials, ordered pore structure materials, and the interfaces between these. We analyze how self-assembly strategies can create storage architectures that improve device performance toward higher energy densities, longevity, rate capability, and device safety. At the end, the remaining challenges of scalable low-cost manufacturing and future opportunities such as self-healing are discussed.

One of the leading challenges in chemical sciences is the separation of complex mixtures. This is of vital importance for areas such as commodity chemical generation, where there is a need for the generation of high-purity chemical streams. Due to this, there has been a strong push toward the investigation of new materials capable of achieving chemoselective separation, with self-assembled materials having shown a great deal of promise for such separations. Many self-assembled materials are desirable candidates due to their low-cost synthesis, structural self-regulation, tunable properties, and an overall ease of composite material preparation. In this article, we aim to introduce examples of novel self-assembled materials and their practical usage in chemical separations. The specific approaches to fabricate these materials, as well as the strengths and shortcomings associated with their structures, will also be described. The strategies presented here will emphasize the production and employment of nonconventional self-assembled materials that exhibit a high potential for the advancement of the science of chemical separations.

Waterproof bioelectrodes enable long-term biological monitoring and the assessment of performances of athletes in water. Existing gel electrodes change their electrical properties even when covered with a waterproof film. Here, the authors present the poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS)/poly(styrene-butadiene-styrene) (SBS) bi-layer nanosheet and waterproof film for a comfortable waterproof bioelectrode. PEDOT:PSS/SBS is fully foldable with a conductivity loss of only 5%. This foldable nanosheet electrode provides a reliable electrical connection between the skin and the wire. The waterproof film-covered bioelectrode enables continuous monitoring of electrocardiograms in water, showing a signal-to-noise ratio of 21.5 dB for the R wave and 17.5 dB for the T wave, comparable to atmospheric measurements, and sensing a change in heart rate from 79 to 131 bpm during bathing.

Colloidal synthesis methods and ultrahigh-vacuum molecular beam epitaxy can tailor semiconductor-based nanoscale single emitters—quantum dots—as the building blocks for classical optoelectronic devices, such as lasers, light-emitting devices, and display technologies. These novel light sources have a basic resemblance of luminescent organic molecules, individually and in the aggregated forms. Highly ordered superstructures of quantum dots, obtained via scalable bottom-up self-assembly, exhibit diverse collective phenomena, such as band-like charge transport or superradiant emission. Superradiance emerges from coherent coupling of several emitters via a common radiation field resulting in a single giant dipole leading to short (sub-nanosecond) and intense (proportional to the squared number of coupled emitters) bursts of light. In this article, we review the basic principles and progress in the development of superradiant emitters with organic molecules and inorganic quantum dots, in view of their integration into classical and novel quantum light sources.

Self-assembly enables hierarchical organization and compartmentalization of matter previously observed only in natural materials. Simple chemical motifs can be used to fabricate structures with diverse range of architectures and properties. The design principles, originally found in nature, are being implemented in self-assembled materials. The examples include high mechanical strength of bones and nacre achieved through hierarchical organic–inorganic organization, and DNA nanotechnology enabled by complementary bonding of DNA molecules. Building materials with controlled architectures from the nanoscale to the macroscale will lead to a combination of properties that will have significant impacts on fields ranging from tissue regeneration to optoelectronics.

MXenes are a large family of two-dimensional (2D) transition-metal carbides, nitrides, and carbonitrides. The MXene family has expanded since their original discovery in 2011, and has grown larger with the discovery of ordered double transition-metal (DTM) MXenes. These DTM MXenes differ from their counterpart mono-transition-metal (mono-M) MXenes, where two transition metals can occupy the metal sites. Ordered DTM MXenes are comprised of transition metals in either an in-plane or out-of-plane ordered structure. Additionally, some DTM MXenes are in the form of random solid solutions, which are defined by two randomly distributed transition metals throughout the 2D structure. Their different structures and array of transition-metal pairs provide the ability to tune DTM MXenes for specific optical, magnetic, electrochemical, thermoelectric, catalytic, or mechanical behavior. This degree of control over their composition and structure is unique in the field of 2D materials and offers a new avenue for application-driven design of functional nanomaterials. In this article, we review the synthesis, structure, and properties of DTM MXenes and provide an outlook for future research in this field.