A Shape Memory High‐Voltage Supercapacitor with Asymmetric Organic Electrolytes for Driving an Integrated NO2 Gas Sensor

A high‐voltage supercapacitor with shape memory for driving an integrated NO₂ gas sensor is fabricated using a Norland Optical Adhesive 63 polymer substrate, which can recover the original shape after deformation by short‐time heating. The supercapacitor consists of multiwalled carbon nanotube electrodes and organic electrolyte. By using organic electrolyte consisting of adiponitrile, acetonitrile, and dimethyl carbonate in an optimized volume ratio of 1:1:1, a high operation voltage of 2 V is obtained. Furthermore, asymmetric electrolytes with different redox additives of hydroquinone and 1,4‐dihydroxyanthraquinone to the anode and cathode, respectively, enhance both capacitance and energy density by ≈40 times compared to those of supercapacitor without redox additives. The fabricated supercapacitor on the Norland Optical Adhesive 63 polymer substrate retains 95.8% of its initial capacitance after 1000 repetitive bending cycles at a bending radius of 3.8 mm. Furthermore, the folded supercapacitor recovers its shape upon heating at 70 °C for 20 s. In addition, 90% of the initial capacitance is retained even after the 20th shape recovery from folding. The fabricated supercapacitor is used to drive integrated NO₂ gas sensor on the same Norland Optical Adhesive 63 substrate attached onto skin to detect NO₂ gas, regardless of deformation due to elbow movement.     

High Areal Capacitance of N‐Doped Graphene Synthesized by Arc Discharge

The lack of cost effective, industrial‐scale production methods hinders the widespread applications of graphene materials. In spite of its applicability in the mass production of graphene flakes, arc discharge has not received considerable attention because of its inability to control the synthesis and heteroatom doping. In this study, a facile approach is proposed for improving doping efficiency in N‐doped graphene synthesis through arc discharge by utilizing anodic carbon fillers. Compared to the N‐doped graphene (1–1.5% N) synthesized via the arc process according to previous literature, the resulting graphene flakes show a remarkably increased doping level (≈3.5% N) with noticeable graphitic N enrichment, which is rarely achieved by the conventional process, while simultaneously retaining high turbostratic crystallinity. The electrolyte ion storage of synthesized materials is examined in which synthesized N‐doped graphene material exhibits a remarkable area normalized capacitance of 63 µF cm^?2. The surprisingly high areal capacitance, which is superior to that of most carbon materials, is attributed to the synergistic effect of extrinsic pseudocapacitance, high crystallinity, and abundance of exposed graphene edges. These results highlight the great potentials of N‐doped graphene flakes produced by arc discharge in graphene‐based supercapacitors, along with well‐studied active exfoliated graphene and reduced graphene oxide.     

Microparticle‐Based Soft Electronic Devices: Toward One‐Particle/One‐Pixel

While microparticle (MP) assemblies have long attracted academic interest, few practical applications of assembled MPs have been achieved because of technological difficulties related to MP synthesis, MP position registration, and the absence of device concepts. The precise positioning of functional MPs in a proper stencil can produce flexible/stretchable electronic devices, even when the MPs themselves are rigid. In recent years, remarkable progress has been made in the programmable position registration of MPs, production of functional MPs, and concepts for MP‐based, pixel‐type electronic devices. This progress report reviews the recent technological advances in MP assembly and discusses the technological challenges preventing the realization of the one‐particle/one‐pixel concept.     

Toward Artificial Cells: Novel Advances in Energy Conversion and Cellular Motility

The demand to discover every single cellular component has been continuously increasing along with the development of biological techniques. The bottom‐up approach to construct a cell‐mimicking system from well‐defined and tunable compositions is accelerating, with the ultimate goal of comprehending a biological cell. From among the available techniques, the artificial cell has been increasingly recognized as one of the most powerful tools for building a cell‐like system from scratch. This review summarizes the development of artificial cells, from a pure giant unilamellar vesicle (GUV) to a controllable, self‐fueled proteoliposome, both of which are highly compartmentalized. The basic components of an artificial cell, as well as the optimal conditions required for successful, reproducible GUV formation and protein reconstitution, are discussed. Most importantly, progress in studying the metabolic reactions in and the motility of a reconstituted artificial cell are the main focus of the review. The ability to perform a complicated reaction cascade in a controllable manner is highlighted as a promising perspective to obtaining an autonomous and movable GUV.     

Plasmon‐Induced Hot Carrier Separation across Dual Interface in Gold–Nickel Phosphide Heterojunction for Photocatalytic Water Splitting

Precise control of the topology of metal nanocrystals and appropriate modulation of the metal–semiconductor heterostructure is an important way to understand the relationship between structure and material properties for plasmon‐induced solar‐to‐chemical energy conversion. Here, a bottom‐up wet chemical approach to synthesize Au/Ni₂P heterostructures via Pt‐catalyzed quasi‐epitaxial overgrowth of Ni on Au nanorods (NR) is presented. The structural motif of the Ni₂P is controlled using the aspect ratio of the Au NR and the effective micelle concentration of the C₁₆TAB capping agent. Highly ordered Au/Pt/Ni₂P nanostructures are employed as the photoelectrocatalytic anode system for water splitting. Electrochemical and ultrafast absorption spectroscopy characterization indicates that the structural motif of the Ni₂P (controlled by the outer‐shell deposition of Ni) helps to manipulate hot electron transfer during surface plasmon decay. With optimized Ni₂P thickness, Pt‐tipped Au NR with an aspect ratio of 5.2 exhibits a geometric current density of 10 mA cm^?2 with an overpotential of 140 mV. The photoanode displays unprecedented long‐term stability with continuous chronoamperometric performance of 50 h at an input potential of 1.5 V with over 30 days. This work provides definitive guidance for designing plasmonic–catalytic nanomaterials for enhanced solar‐to‐chemical energy conversion.     

An On‐Chip Break Junction System for Combined Single‐Molecule Conductance and Raman Spectroscopies

Systems that are capable of robustly reproducing single‐molecule junctions are an essential prerequisite for enabling the wide‐spread testing of molecular electronic properties, the eventual application of molecular electronic devices, and the development of single‐molecule based electrical and optical diagnostics. Here, a new approach is proposed for achieving a reliable single‐molecule break junction system by using a microelectromechanical system device on a chip. It is demonstrated that the platform can (i) provide subnanometer mechanical resolution over a wide temperature range (≈77–300 K), (ii) provide mechanical stability on par with scanning tunneling microscopy and mechanically controllable break junction systems, and (iii) operate in a variety of environmental conditions. Given these fundamental device performance properties, the electrical characteristics of two standard molecules (hexane‐dithiol and biphenyl‐dithiol) at the single‐molecule level, and their stability in the junction at both room and cryogenic temperatures (≈77 K) are studied. One of the possible distinctive applications of the system is demonstrated, i.e., observing real‐time Raman scattering in a single‐molecule junction. This approach may pave a way to achieving high‐throughput electrical characterization of single‐molecule devices and provide a reliable platform for the convenient characterization and practical application of single‐molecule electronic systems in the future.     

Wearable Energy Generating and Storing Textile Based on Carbon Nanotube Yarns

The challenges of textiles that can generate and store energy simultaneously for wearable devices are to fabricate yarns that generate electrical energy when stretched, yarns that store this electrical energy, and textile geometries that facilitate these functions. To address these challenges, this research incorporates highly stretchable electrochemical yarn harvesters, where available mechanical strains are large and electrochemical energy storing yarns are achieved by weaving. The solid‐state yarn harvester provides a peak power of 5.3 W kg^?1 for carbon nanotubes. The solid‐state yarn supercapacitor provides stable performance when dynamically deformed by bending and stretching, for example. A textile configuration that consists of harvesters, supercapacitors, and a Schottky diode is produced and stores as much electrical energy as is needed by a serial or parallel connection of the harvesters or supercapacitors. This textile can be applied as a power source for health care devices or other wearable devices and be self‐powered sensors for detecting human motion.     

Covalent 0D–2D Heterostructuring of Co9S8–MoS2 for Enhanced Hydrogen Evolution in All pH Electrolytes

Ultrasmall Co₉S₈ nanoparticles are introduced on the basal plane of MoS₂ to fabricate a covalent 0D–2D heterostructure that enhances the hydrogen evolution reaction (HER) activity of electrochemical water splitting. In the heterostructure, separate phases of Co₉S₈ and MoS₂ are formed, but they are connected by Co–S–Mo type covalent bonds. The charge redistribution from Co to Mo occurring at the interface enhances the electron‐doped characteristics of MoS₂ to generate electron‐rich Mo atoms. Besides, reductive annealing during the synthesis forms S defects that activates adjacent Mo atoms for further enhanced HER activity as elucidated by the density functional theory (DFT) calculation. Eventually, the covalent Co₉S₈–MoS₂ heterostructure shows amplified HER activity as well as stability in all pH electrolytes. The synergistic effect is pronounced when the heterostructure is coupled with a porous Ni foam (NF) support to form Co₉S₈–MoS₂/NF that displays superior performance to those of the state‐of‐the‐art non‐noble metal electrocatalysts, and even outperforms a commercial Pt/C catalyst in a practically meaningful, high current density region in alkaline (>170 mA cm^?2) and neutral (>60 mA cm^?2) media. The high HER performance and stability of Co₉S₈–MoS₂ heterostructure make it a promising pH universal alternative to expensive Pt‐based electrocatalysts for practical water electrolyzers.     

Surface modified solution‐derived nickel oxide film via ion‐beam irradiation as a liquid crystal alignment layer

In this article, we demonstrate the liquid crystal (LC) alignment characteristics of solution‐derived nickel oxide (NiO) film modified with ion‐beam (IB) irradiation. Cross‐polarized optical microscopy and pretilt angle measurements verified that uniform LC alignment was achieved using the NiO film as an alignment layer regardless of IB incidence angle. Contact angle measurements revealed that all of the NiO films had a deionized water contact angle below 90°, which indicates that they had hydrophilic surfaces that had an effect on the homogeneous LC alignment. Atomic force microscopy was conducted to determine the physical surface modification due to the IB irradiation, which showed that it reduced the size of the surface grains with agglomerations depending on the surface tilt from the IB incidence angle. Furthermore, microgroove structures strongly related to uniform LC alignment were observed after IB irradiation. Chemical surface modification was investigated via an X‐ray photoelectron spectroscopy analysis which revealed that IB irradiation modified the chemical bonds in the NiO film, and this affected the LC alignment state. Thus, these results indicate that using NiO film exposed to IB irradiation as an alignment layer is a suitable method for LC applications.