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Abstract Moisture-driven electricity generators (MEGs) have been extensively researched; however, high-performance flexible variants have seldom been demonstrated. Here we present a novel complex coacervation with built-in potential strategy for developing a high-performance uniaxial MEG, featuring a core of poly(3,4-ethylenedioxythiophene) (PEDOT) with a built-in charge potential and a gel shell composed of poly(diallyldimethylammonium chloride) (PDDA) and sodium alginate (NaAlg) coacervate. The complex coacervation of two oppositely charged polyelectrolytes produces extra mobile carriers and free volume in the device; meanwhile, the PEDOT core’s surface charge significantly accelerates carrier diffusion. Consequently, the uniaxial fiber-based MEG demonstrates breakthrough performance, achieving an output voltage of up to 0.8 V, a maximum current density of 1.05 mA/cm2, and a power density of 184 μW/cm2 at 20% relative humidity. Moreover, the mechanical robustness is ensured for the PEDOT nanoribbon substrate without performance degradation even after 100,000 folding cycles, making it suitable for self-powered human interactive sensor and synapse. Notably, we have constructed the inaugural MEG-synapse self-powered device, with a fiber-based MEG successfully operating a synaptic memristor, thereby emulating autonomous human synapses linked with fibrous neurons. Overall, this work pioneers innovative design strategies and application scenarios for high-performance MEGs.

Abstract Optical encryption technologies based on room-temperature light-emitting materials are of considerable interest. Herein, we present three-dimensional (3D) printable dual-light-emitting materials for high-performance optical pattern encryption. These are based on fluorescent perovskite nanocrystals (NCs) embedded in metal-organic frameworks (MOFs) designed for phosphorescent host-guest interactions. Notably, perovskite-containing MOFs emit a highly efficient blue phosphorescence, and perovskite NCs embedded in the MOFs emit characteristic green or red fluorescence under ultraviolet (UV) irradiation. Such dual-light-emitting MOFs with independent fluorescence and phosphorescence emissions are employed in pochoir pattern encryption, wherein actual information with transient phosphorescence is efficiently concealed behind fake information with fluorescence under UV exposure. Moreover, a 3D cubic skeleton is developed with the dual-light-emitting MOF powder dispersed in 3D-printable polymer filaments for 3D dual-pattern encryption. This article outlines a universal principle for developing MOF-based room-temperature multi-light-emitting materials and a strategy for multidimensional information encryption with enhanced capacity and security.

Soft actuators that can operate at high temperatures are of great interest in emerging research fields such as microfluidics, soft robotics, automotive, aircraft, and bioelectronics. However, most polymer-based flexible actuators suffer from performance degradation at elevated temperatures above 60 °C. In this paper, we present the high-temperature electromechanical actuation of relaxor ferroelectric polymers solution-blended with normal ferroelectric polymers. We conduct a systematic analysis of the electromechanical properties of three unimorph actuators with relaxor ferroelectric poly(vinylidene fluoride-trifluoroethylene-chlorofluoroethylene)s [P(VDF-TrFE-CFE)s] containing different amounts of chlorofluoroethylene (CFE) moieties (approximately 1, 3.5, and 9 wt%). In this study, we propose the film stress, given as Young's modulus times strain, as the measure of the electromechanical performance of soft bending actuators under loading, rather than strain or strain energy density. We demonstrate that a relaxor ferroelectric actuator with 1-wt% CFE, which mixes high-modulus ferroelectric crystal domains with an optimized electrostrictive relaxor phase, develops a high film stress of ∼3.5 MPa. When blended with the normal ferroelectric P(VDF-TrFE), the actuator exhibits excellent film stress of approximately 3.1 MPa at an elevated temperature of 60 °C comparable with that at 25 °C. The high-modulus ferroelectric crystals in P(VDF-TrFE) reinforce the mechanical properties of the actuator at elevated temperatures, generating high-temperature electromechanical actuation with a large strain and strain energy density of approximately 1.6% and 23 mJ/cm², respectively. We also demonstrate successful microfluidic pump operation at 60°C with our actuator using a relaxor ferroelectric polymer blended with an intrinsic ferroelectric polymer.

Abstract In this study, we present a promising and facile approach toward the fabrication of non-toxic, water-stable, and eco-friendly luminescent fiber paper composed of polycaprolactone (PCL) polymer and CsPbBr3@SiO2 core–shell perovskite nanocrystals. PCL-perovskite fiber paper was fabricated using a conventional electrospinning process. Transmission electron microscopy (TEM) clearly revealed incorporation of CsPbBr3@SiO2 nanocrystals in the fibers, while scanning electron microscopy (SEM) demonstrated that incorporation of CsPbBr3@SiO2 nanocrystals did not affect the surface and diameter of the PCL-perovskite fibers. In addition, thermogravimetric analysis (TGA) and contact angle measurements have demonstrated that the PCL-perovskite fibers exhibit excellent thermal and water stability. The fabricated PCL-perovskite fiber paper exhibited a bright green emission centered at 520 nm upon excitation by ultra-violet (UV) light (374 nm). We have demonstrated that fluorescent PCL-perovskite fiber paper is a promising candidate for anti-counterfeiting applications because various patterns can be printed on the paper, which only become visible after exposure to UV light at 365 nm. Cell proliferation tests revealed that the PCL-perovskite fibers are cytocompatibility. Consequently, they may be suitable for biocompatible anti-counterfeiting. The present study reveals that PCL-perovskite fibers may pave way toward next generation biomedical probe and anti-counterfeiting applications. Graphical Abstract

ABSTRACT For changing environmental circumstances, interactive structural color (SC) observation is a promising strategy to store and express external information. SCs based on self-assembled block copolymer (BCP) photonic crystals have been a research focus due to their facile and diverse nanostructures relying on the volume ratio of blocks. Their unique nano-architectonics can reflect incident light due to constructive interference of the two different dielectric constituents. Their excellent ability to change nano-architectonics in response to external stimuli (i.e. humidity, temperature, pH, and mechanical force) allows for a programmable and stimuli-interactive BCP SC display. In this review, recent advances in programmable and stimuli-interactive SC displays with the 1-dimensional self-assembled BCP nano-architectonics are comprehensively discussed. First, this review focuses on the development of programmable BCP SCs that can store various information. Second, stimuli-interactive BCP SCs capable of responding reversibly to external stimuli are also addressed. Particularly, reversible BCP SC changes are suitable for rewritable displays and emerging human-interactive BCP SC displays that detect various human information through changes in electric signals with the simultaneous alteration of the BCP SCs. Based on previously reported literature, the current challenges in this research field are further discussed, and the perspective for future development is presented in terms of material, nano-architectonics, and process.

Abstract Overcoming the thermal sensitivity of the van‐der Waals layered material, an inevitable high defect concentration in a large area (2 × 2 cm2) vapor phase grown few‐layer MoS2 (2.3 nm thick) is uniformly repaired over the entire area through thermal process. The defect concentration of the healed sample decreased by 3.8 times, and both the PL intensity and field‐effect mobility over the entire area increased by more than two times. Through observing in situ photoluminescence (PL) spectra with raising temperature, it is confirmed that the oxygen‐substitutional healing proceeds radically from the starting point at which trion dissociation energy is zero, inducing e–h plasma. At this time, for achieving successful healing of the entire area, immediate cooling is required to prevent accelerated oxidation when reaching the critical temperature. Considering the laboratory‐dependent crystalline quality of vapor‐phase grown transition metal dichalcogenides (TMDs), the methodology to find the optimal thermal healing temperature through in situ PL monitoring will be quite useful.

Abstract An additive, 1,4‐butadiene sulfone (BDS), which generates H2SO3 by in situ thermal retro‐Diels‐Alder decompositions, is used for preparing high β‐phase polyvinylidene fluoride (PVDF) films. Because of preferential multiple non‐covalent interactions of H2SO3 with all‐trans configuration of PVDF, β‐phase PVDF is spontaneously induced without mechanical drawing and/or extensive thermal annealing process. PVDF films cast from PVDF/BDS/water solutions exhibit high β‐phase content (fβ = 95%) when the BDS concentration is only cBDS = 1.0 wt%, which is confirmed by polarized optical microscopy (POM), SEM, Fourier transform infrared spectroscopy (FT‐IR), differential scan calorimetry (DSC), and 2D grazing incidence wide‐angle X‐ray scattering (GIWAXS). Because of the high β‐phase content, PVDF films prepared by using BDS exhibit excellent ferroelectric and piezoelectric properties (Ec = 50 MV/m, Pr = 5 µC/cm2, and d33 = ≈‐25 pm/V). Furthermore, a triboelectric nanogenerator (TENG) developed with high β‐phase PVDF film exhibits enhanced performance as 2.5 times higher than neat PVDF film in output charge density, allowing reliable operation of conventional electronic devices.

Designing human-interactive displays enabling the simultaneous sensing, visualization, and memorization of a magnetic field remains a challenge. Here, the authors present a skin-patchable magneto-interactive electroluminescent display by employing a magnetic field-dependent conductive gate, thereby enabling 3D motion tracking.

Though liquid sensing platforms are highly sought after for emerging biomedical applications, current technology is limited in its capacity to directly sense and store information. Here, the authors report a sensing memory platform that senses, monitors, and stores information on various liquids.

Abstract Lightweight and flexible tactile learning machines can simultaneously detect, synaptically memorize, and subsequently learn from external stimuli acquired from the skin. This type of technology holds great interest due to its potential applications in emerging wearable and human‐interactive artificially intelligent neuromorphic electronics. In this study, an integrated artificially intelligent tactile learning electronic skin (e‐skin) based on arrays of ferroelectric‐gate field‐effect transistors with dome‐shape tactile top‐gates, which can simultaneously sense and learn from a variety of tactile information, is introduced. To test the e‐skin, tactile pressure is applied to a dome‐shaped top‐gate that measures ferroelectric remnant polarization in a gate insulator. This results in analog conductance modulation that is dependent upon both the number and magnitude of input pressure‐spikes, thus mimicking diverse tactile and essential synaptic functions. Specifically, the device exhibits excellent cycling stability between long‐term potentiation and depression over the course of 10 000 continuous input pulses. Additionally, it has a low variability of only 3.18%, resulting in high‐performance and robust tactile perception learning. The 4 × 4 device array is also able to recognize different handwritten patterns using 2‐dimensional spatial learning and recognition, and this is successfully demonstrated with a high degree accuracy of 99.66%, even after considering 10% noise.

Abstract Graphene oxide (GO) doping and reduction allow for physicochemical property modification to suit practical application needs. Herein, the challenge of simultaneous low‐thermal‐budget heteroatom doping of GO and its reduction in ambient air is addressed through the synthesis of B‐doped reduced GO (B@rGO) by flash irradiation of boric acid loaded onto a GO support with intense pulsed light (IPL). The effects of light power and number of shots on the in‐depth sequential doping and reduction mechanisms are investigated by ex situ X‐ray photoelectron spectroscopy and direct millisecond‐scale temperature measurements (temperature >1600 °C, < 10‐millisecond duration, ramping rate of 5.3 × 105 °C s−1). Single‐flash IPL allows the large‐scale synthesis of substantially doped B@rGO (≈3.60 at% B) to be realized with a thermal budget 106‐fold lower than that of conventional thermal methods, and the prepared material with abundant B active sites is employed for highly sensitive and selective room‐temperature NO2 sensing. Thus, this work showcases the great potential of optical annealing for millisecond‐scale ultrafast reduction and heteroatom doping of GO in ambient air, which allows the tuning of multiple physicochemical GO properties.

Self-assembled systems are normally composed of incompressible building blocks, which constrain their space filling efficiency. Yu et al. show programmable, densely packed clusters using thermally expandable soft microparticles, whereby the self-assembling process is realized via a jamming transition.

Kimet al. report a polymeric-based electroluminescent interactive display that actively detects and visualizes an external conductive object under an alternating current. Fingerprint visualization and dynamic monitoring of metallic liquid flow are demonstrated.

Abstract In addition to the demand for stimuli‐responsive sensors that can detect various vital signals in epidermal skin, the development of electronic skin displays that quantitatively detect and visualize various epidermal stimuli such as the temperature, sweat gland activity, and conductance simultaneously are of significant interest for emerging human‐interactive electronics used in health monitoring. Herein, a novel interactive skin display with epidermal stimuli electrode (ISDEE) allowing for the simultaneous sensing and display of multiple epidermal stimuli on a single device is presented. It is based on a simple two‐layer architecture on a topographically patterned elastomeric polymer composite with light‐emitting inorganic phosphors, upon which two electrodes are placed with a certain parallel gap. The ISDEE is directly mounted on human skin, which by itself serves as a field‐responsive floating electrode of the display operating under an alternating current (AC). The AC field exerted on the epidermal skin layer depends on the conductance of the skin, which can be modulated based on a variety of physiological skin factors, such as the temperature, sweat gland activity, and pressure. Conductance‐dependent field‐induced electroluminescence is achieved, giving rise to an on‐hand sensing display platform where a variety of human information can be directly sensed and visualized.

In this study, the contact mechanism between Ag–Al and Si and the change in contact resistance (Rc) were analyzed by varying the firing profile. The front electrode of an n-type c-Si solar cell was formed through a screen-printing process using Ag–Al paste. Rc was measured by varying the belt speed and peak temperature of the fast-firing furnace. Rc value of 6.98 mΩ-cm−2 was obtained for an optimal fast-firing profile with 865 °C peak temperature and 110 inches per min belt speed. The contact phenomenon and the influence of impurities between the front-electrode–Si interface and firing conditions were analyzed through scanning electron microscopy (SEM) and energy-dispersive X-ray spectroscopy (EDS). The EDS analysis revealed that the peak firing temperature at 865 °C exhibited a low atomic weight percentage of Al (0.72 and 0.36%) because Al was involved in the formation of alloy of Si with the front electrode. Based on the optimal results, a solar cell with a conversion efficiency of 19.46% was obtained.

In this paper, the relationship between coordination complexes and electrical properties according to the bonding structure of boron and silicon was analyzed to optimize the p–n junction quality for high-efficiency n-type crystalline solar cells. The p+ emitter layer was formed using boron tribromide (BBr3). The etch-back process was carried out with HF-HNO3-CH3COOH solution to vary the sheet resistance (Rsheet). The correlation between boron–silicon bonding in coordination complexes and electrical properties according to the Rsheet was analyzed. Changes in the boron coordination complex and boron–oxygen (B–O) bonding in the p+ diffused layer were measured through X-ray photoelectron spectroscopy (XPS). The correlation between electrical properties, such as minority carrier lifetime (τeff), implied open-circuit voltage (iVoc) and saturation current density (J0), according to the change in element bonding, was analyzed. For the interstitial defect, the boron ratio was over 1.8 and the iVoc exceeded 660 mV. Additional gains of 670 and 680 mV were obtained for the passivation layer AlOx/SiNx stack and SiO2/SiNx stack, respectively. The blue response of the optimized p+ was analyzed through spectral response measurements. The optimized solar cell parameters were incorporated into the TCAD tool, and the loss analysis was studied by varying the key parameters to improve the conversion efficiency over 23%.

This paper presents a power-generating sensor array in a flexible and stretchable form. The proposed device is composed of resistive strain sensors, capacitive tactile sensors, and a triboelectric energy harvester in a single platform. The device is implemented in a woven textile structure by using proposed functional threads. A single functional thread is composed of a flexible hollow tube coated with silver nanowires on the outer surface and a conductive silver thread inside the tube. The total size of the device is 60 × 60 mm2 having a 5 × 5 array of sensor cell. The touch force in the vertical direction can be sensed by measuring the capacitance between the warp and weft functional threads. In addition, because silver nanowire layers provide piezoresistivity, the strain applied in the lateral direction can be detected by measuring the resistance of each thread. Last, with regard to the energy harvester, the maximum power and power density were measured as 201 μW and 0.48 W/m2, respectively, when the device was pushed in the vertical direction.