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.

Self-assembly, a process in which molecules, polymers, and particles are driven by local interactions to organize into patterns and functional structures, is being exploited in advancing silicon electronics and in emerging, unconventional electronics. Silicon electronics has relied on lithographic patterning of polymer resists at progressively smaller lengths to scale down device dimensions. Yet, this has become increasingly difficult and costly. Assembly of block copolymers and colloidal nanoparticles allows resolution enhancement and the definition of essential shapes to pattern circuits and memory devices. As we look to a future in which electronics are integrated at large numbers and in new forms for the Internet of Things and wearable and implantable technologies, we also explore a broader material set. Semiconductor nanoparticles and biomolecules are prized for their size-, shape-, and composition-dependent properties and for their solution-based assembly and integration into devices that are enabling unconventional manufacturing and new device functions.

The effects of the Mg/Si ratio and aging treatment on the strength and electrical conductivity of Al–Mg–Si 6201 conductor alloys were investigated. Four experimental alloys with different Mg/Si ratios of 2, 1.5, 1, and 0.86 and with a constant Mg level of 0.65 wt% were prepared. It was revealed that excessive Si (a low Mg/Si ratio) increased the peak strength, while the corresponding electrical conductivity decreased. To fulfill the minimum required electrical conductivity (52.5% IACS), the alloys with low Mg/Si ratios required a longer aging time after peak aging to improve electrical conductivity. The alloy with an Mg/Si ratio of ~1 was the best candidate, exhibiting the highest strength up to 54% IACS. On the high end of electrical conductivity (54–56% IACS), the alloy with an Mg/Si ratio of ~1.5 provides a better compromise between strength and electrical conductivity. Furthermore, the strengthening mechanisms and the factors influencing electrical conductivity were discussed for further optimization.