Towards high performance and durable soft tactile actuators.

Soft actuators are gaining significant attention due to their ability to provide realistic tactile sensations in various applications. However, their soft nature makes them vulnerable to damage from external factors, limiting actuation stability and device lifespan. The susceptibility to damage becomes higher with these actuators often in direct contact with their surroundings to generate tactile feedback. Upon onset of damage, the stability or repeatability of the device will be undermined. Eventually, when complete failure occurs, these actuators are disposed of, accumulating waste and driving the consumption of natural resources. This emphasizes the need to enhance the durability of soft tactile actuators for continued operation. This review presents the principles of tactile feedback of actuators, followed by a discussion of the mechanisms, advancements, and challenges faced by soft tactile actuators to realize high actuation performance, categorized by their driving stimuli. Diverse approaches to achieve durability are evaluated, including self-healing, damage resistance, self-cleaning, and temperature stability for soft actuators. In these sections, current challenges and potential material designs are identified, paving the way for developing durable soft tactile actuators.

Size-Selective Ionic Crosslinking Provides Stretchable Mixed Ionic-Electronic Conductors.

Mechanically compliant conductors are of utmost importance for the emerging fields of soft electronics and robotics. However, the development of intrinsically deformable organic conductors remains a challenge due to the trade-off between mechanical performance and charge mobility. In this study, we report a solution to this issue based on size-selective ionic crosslinking. This rationally designed crosslinking mediated by length-regulated oligo(ethylene glycol) pendant groups and metal ions simultaneously improved the softness and toughness and ensured excellent mixed ionic-electronic conductivity in poly(3,4-ethylenedioxythiophene):polystyrene sulfonate composite materials. Moreover, the added ions remarkably promoted accumulation of charge carriers in response to temperature gradient, thus offering a viable approach to stretchable thermoelectric generators with enhanced stability against humidity.

Ferroelastic-switching-driven large shear strain and piezoelectricity in a hybrid ferroelectric.

Materials that can produce large controllable strains are widely used in shape memory devices, actuators and sensors1,2, and great efforts have been made to improve the strain output3-6. Among them, ferroelastic transitions underpin giant reversible strains in electrically driven ferroelectrics or piezoelectrics and thermally or magnetically driven shape memory alloys7,8. However, large-strain ferroelastic switching in conventional ferroelectrics is very challenging, while magnetic and thermal controls are not desirable for practical applications. Here we demonstrate a large shear strain of up to 21.5% in a hybrid ferroelectric, C6H5N(CH3)3CdCl3, which is two orders of magnitude greater than that in conventional ferroelectric polymers and oxides. It is achieved by inorganic bond switching and facilitated by structural confinement of the large organic moieties, which prevents undesired 180° polarization switching. Furthermore, Br substitution can soften the bonds, allowing a sizable shear piezoelectric coefficient (d35 ≈ 4,830 pm V-1) at the Br-rich end of the solid solution, C6H5N(CH3)3CdBr3xCl3(1-x). The electromechanical properties of these compounds suggest their potential in lightweight and high-energy-density devices, and the strategy described here could inspire the development of next-generation piezoelectrics and electroactive materials based on hybrid ferroelectrics.

Synergistic Effect of PVDF-Coated PCL-TCP Scaffolds and Pulsed Electromagnetic Field on Osteogenesis.

Bone exhibits piezoelectric properties. Thus, electrical stimulations such as pulsed electromagnetic fields (PEMFs) and stimuli-responsive piezoelectric properties of scaffolds have been investigated separately to evaluate their efficacy in supporting osteogenesis. However, current understanding of cells responding under the combined influence of PEMF and piezoelectric properties in scaffolds is still lacking. Therefore, in this study, we fabricated piezoelectric scaffolds by functionalization of polycaprolactone-tricalcium phosphate (PCL-TCP) films with a polyvinylidene fluoride (PVDF) coating that is self-polarized by a modified breath-figure technique. The osteoinductive properties of these PVDF-coated PCL-TCP films on MC3T3-E1 cells were studied under the stimulation of PEMF. Piezoelectric and ferroelectric characterization demonstrated that scaffolds with piezoelectric coefficient d33 = -1.2 pC/N were obtained at a powder dissolution temperature of 100 °C and coating relative humidity (RH) of 56%. DNA quantification showed that cell proliferation was significantly enhanced by PEMF as low as 0.6 mT and 50 Hz. Hydroxyapatite staining showed that cell mineralization was significantly enhanced by incorporation of PVDF coating. Gene expression study showed that the combination of PEMF and PVDF coating promoted late osteogenic gene expression marker most significantly. Collectively, our results suggest that the synergistic effects of PEMF and piezoelectric scaffolds on osteogenesis provide a promising alternative strategy for electrically augmented osteoinduction. The piezoelectric response of PVDF by PEMF, which could provide mechanical strain, is particularly interesting as it could deliver local mechanical stimulation to osteogenic cells using PEMF.

All 3D Printed Stretchable Piezoelectric Nanogenerator for Self-Powered Sensor Application.

With the rapid development of wearable electronic systems, the need for stretchable nanogenerators becomes increasingly important for autonomous applications such as the Internet-of-Things. Piezoelectric nanogenerators are of interest for their ability to harvest mechanical energy from the environment with its inherent polarization arising from crystal structures or molecular arrangements of the piezoelectric materials. In this work, 3D printing is used to fabricate a stretchable piezoelectric nanogenerator which can serve as a self-powered sensor based on synthesized oxide-polymer composites.

Ti3 C2 MXene Paper for the Effective Adsorption and Controllable Release of Aroma Molecules.

Olfactory sensing and perception play an important role in people's daily lives and greatly affects senses, emotions, and behavior. In particular, the development of the controlled release of aroma enhances human's well-being and strengthens interactions with surroundings through olfactory display, especial when combined with visual and audial cues. Here, Ti3 C2 MXene plays a dual-function role as the adsorption site of aroma molecules and the heating source for the controlled release of aroma molecules. Due to abundant termination groups on the surface and the metallic nature, Ti3 C2 MXene provides abundant active sites for the interaction with aroma molecules; simultaneously, MXene can be electrically heated to thermally desorb the aroma molecules from the interaction sites. This approach eliminates the interface incompatibility issues between the heating source and the molecular encapsulation layer in conventional olfactory display system. This work presents the controlled release of the aroma molecule phenethyl alcohol (PA) using Ti3 C2 MXene paper. Ti3 C2 MXene paper serves as the adsorption material and a heating source that achieves 100 °C within 1 s. The relative amount of PA released reaches nearly 100% after 1 min of heating.

Progress on wearable triboelectric nanogenerators in shapes of fiber, yarn, and textile.

Textile has been known for thousands of years for its ease of use, comfort, and wear resistance, which resulted in a wide range of applications in garments and industry. More recently, textile emerges as a promising substrate for self-powered wearable power sources that are desired in wearable electronics. Important progress has been attained in the exploitation of wearable triboelectric nanogenerators (TENGs) in shapes of fiber, yarn, and textile. Along with the effective integration of other devices such as supercapacitor, lithium battery, and solar cell, their feasibility for realizing self-charging wearable systems has been proven. In this review, according to the manufacturing process of traditional textiles starting from fibers, twisting into yarns, and weaving into textiles, we summarize the progress on wearable TENGs in shapes of fiber, yarn, and textile. We explicitly discuss the design strategies, configurations, working mechanism, performances, and compare the merits of each type of TENGs. Finally, we present the perspectives, existing challenges and possible routes for future design and development of triboelectric textiles.

A Nonpresodiate Sodium-Ion Capacitor with High Performance.

Sodium-ion capacitors (SICs) have received intensive attention due to their high energy density, high power density, long cycle life, and low cost of sodium. However, the lack of high-performance anode materials and the tedious presodiation process hinders the practical applications of SICs. A simple and effective strategy is reported to fabricate a high-performance SIC using Fe1- x S as the anode material and an ether-based electrolyte. The Fe1- x S electrode is found to undergo a reversible intercalation reaction after the first cycle, resulting in fast kinetics and excellent reversibility. The Fe1- x S electrode delivers a high capacity of 340 mAh g-1 at 0.05 A g-1 , 179 mAh g-1 at high current of 5 A g-1 and an ultralong cycling performance with 95% capacity retention after 7000 cycles. Coupled with a carbon-based cathode, a high-performance SIC without the presodiation process is successfully fabricated. The hybrid device demonstrates an excellent energy density of 88 Wh kg-1 and superior power density of 11 500 W kg-1 , as well as an ultralong lifetime of 9000 cycles with over 93% capacity retention. An innovative and efficient way to fabricate SICs with both high energy and power density utilizing ether-based electrolytes can be realized to eliminate the presodiation process.

Rational Design of Amphiphilic Peptides and Its Effect on Antifouling Performance.

Biofouling, the unwanted adhesion of organisms to surfaces, has a negative impact on energy, food, water, and health resources. One possible strategy to fight biofouling is to modify the surface using a peptide-based coating that will change the surface properties. We reveal the importance of rational design and positioning of individual amino acids in an amphiphilic peptide sequence. By just manipulating the position of the amino acids within the peptide chain having the same chemical composition, we improved the antifouling performance of an amphiphilic peptide-based coating, Phe(4-F)-Lys-DOPA, by 30%. We have judiciously tailored the peptide configurations to achieve the best antifouling performance by (i) positioning the amino acid lysine adjacent to the DOPA moiety in the linear peptide chain for better adhesion, (ii) having a linear fluorinated N-terminal to improve the packing density of the film by straightening the peptide chain, and (iii) placing DOPA at the C-terminal. We have also compared the antifouling performances of amphiphilic, hydrophobic, hydrophilic, and alternately arranged peptides. Our results show a reduction of ∼80% in bacterial adhesion for an amphiphilic peptide-coated surface when compared to a bare titanium surface. This work provides important strategic design guidelines for future peptide-related materials that have effective antifouling properties.

A High-Performance Lithium-Ion Capacitor Based on 2D Nanosheet Materials.

Lithium-ion capacitors (LICs) are promising electrical energy storage systems for mid-to-large-scale applications due to the high energy and large power output without sacrificing long cycle stability. However, due to the different energy storage mechanisms between anode and cathode, the energy densities of LICs often degrade noticeably at high power density, because of the sluggish kinetics limitation at the battery-type anode side. Herein, a high-performance LIC by well-defined ZnMn2 O4 -graphene hybrid nanosheets anode and N-doped carbon nanosheets cathode is presented. The 2D nanomaterials offer high specific surface areas in favor of a fast ion transport and storage with shortened ion diffusion length, enabling fast charge and discharge. The fabricated LIC delivers a high specific energy of 202.8 Wh kg-1 at specific power of 180 W kg-1 , and the specific energy remains 98 Wh kg-1 even when the specific power achieves as high as 21 kW kg-1 .

Next-Generation Multifunctional Electrochromic Devices.

The rational design and exploration of electrochromic devices will find a wide range of applications in smart windows for energy-efficient buildings, low-power displays, self-dimming rear mirrors for automobiles, electrochromic e-skins, and so on. Electrochromic devices generally consist of multilayer structures with transparent conductors, electrochromic films, ion conductors, and ion storage films. Synthetic strategies and new materials for electrochromic films and transparent conductors, comprehensive electrochemical kinetic analysis, and novel device design are areas of active study worldwide. These are believed to be the key factors that will help to significantly improve the electrochromic performance and extend their application areas. In this Account, we present our strategies to design and fabricate electrochromic devices with high performance and multifunctionality. We first describe the synthetic strategies, in which a porous tungsten oxide (WO3) film with nearly ideal optical modulation and fast switching was prepared by a pulsed electrochemical deposition method. Multiple strategies, such as sol-gel/inkjet printing methods, hydrothermal/inkjet printing methods, and a novel hybrid transparent conductor/electrochromic layer have been developed to prepare high-performance electrochromic films. We then summarize the recent advances in transparent conductors and ion conductor layers, which play critial roles in electrochromic devices. Benefiting from the developments of soft transparent conductive substrates, highly deformable electrochromic devices that are flexible, foldable, stretchable, and wearable have been achieved. These emerging devices have great potential in applications such as soft displays, electrochromic e-skins, deformable electrochromic films, and so on. We finally present a concept of multifunctional smart glass, which can change its color to dynamically adjust the daylight and solar heat input of the building or protect the users' privacy during the daytime. Energy can also be stored in the smart windows during the daytime simultaneously and be discharged for use in the evening. These results reveal that the electrochromic devices have potential applications in a wide range of areas. We hope that this Account will promote further efforts toward fundamental research on electrochromic materials and the development of new multifunctional electrochromic devices to meet the growing demands for next-generation electronic systems.

Development and applications of transparent conductive nanocellulose paper.

Increasing attention has been paid to the next generation of 'green' electronic devices based on renewable nanocellulose, owing to its low roughness, good thermal stability and excellent optical properties. Various proof-of-concept transparent nanopaper-based electronic devices have been fabricated; these devices exhibit excellent flexibility, bendability and even foldability. In this review, we summarize the recent progress of transparent nanopaper that uses different types of nanocellulose, including pure nanocellulose paper and composite nanocellulose paper. The latest development of transparent and flexible nanopaper electronic devices are illustrated, such as electrochromic devices, touch sensors, solar cells and transistors. Finally, we discuss the advantages of transparent nanopaper compared to conventional flexible plastic substrate and the existing challenges to be tackled in order to realize this promising potential.

Highly Transparent Conducting Nanopaper for Solid State Foldable Electrochromic Devices.

It is of great challenge to develop a transparent solid state electrochromic device which is foldable at the device level. Such devices require delicate designs of every component to meet the stringent requirements for transparency, foldability, and deformation stability. Meanwhile, nanocellulose, a ubiquitous natural resource, is attracting escalating attention recently for foldable electronics due to its extreme flexibility, excellent mechanical strength, and outstanding transparency. In this article, transparent conductive nanopaper delivering the state-of-the-art electro-optical performance is achieved with a versatile nanopaper transfer method that facilitates junction fusing for high-quality electrodes. The highly compliant nanopaper electrode with excellent electrode quality, foldability, and mechanical robustness suits well for the solid state electrochromic device that maintains good performance through repeated folding, which is impossible for conventional flexible electrodes. A concept of camouflage wearables is demonstrated using gloves with embedded electrochromics. The discussed strategies here for foldable electrochromics serve as a platform technology for futuristic deformable electronics.

Oxidative intercalation for monometallic Ni(2+) -Ni(3+) layered double hydroxide and enhanced capacitance in exfoliated nanosheets.

Monometallic Ni(2+) -Ni(3+) layered double hydroxide (LDH) is prepared using a simple oxidative intercalation process and may be further exfoliated into positively charged Ni(OH)2 unilamellar sheets. The superior capacitive behavior of the unilamellar sheets stranded in carbon nanotubes (CNTs) networks is achieved because of the complete interfacial charge storage arising from the confined Faradaic reactions at the interfacial region. 3D nanosheet/CNT composites are prepared using an in situ electrostatic assembly of positive charged sheets with CNTs bearing negative charges. The restacking of active nanosheets during electrochemical cycling is effectively prohibited. Consequently, the outstanding specific capacitance and remarkable rate capability of the nanosheet/CNT hybrid electrodes are demonstrated, making them promising candidates for high performance supercapacitors, combining high-energy storage densities with high levels of power delivery.

Stretchable energy storage and conversion devices.

Stretchable electronics are a type of mechanically robust electronics which can be bended, folded, crumpled and stretched and represent the emerging direction towards next-generation wearable and implantable devices. Unlike existing electronics based on rigid Si technologies, stretchable devices can conform to the complex non-coplanar surfaces and provide unique functionalities which are unreachable with simple extension of conventional technologies. Stretchable energy storage and conversion devices are the key components for the fabrication of complete and independent stretchable systems. In this review, we present the recent progresses in the developments of stretchable power sources including supercapacitors, batteries and solar cells. Representative structural and material designs to impart stretchability to the originally rigid devices are discussed. Advantages and drawbacks associated with the fabrication methods are also analysed. Summaries of the research progresses along with future development directions for this exciting field are also presented.

Insights on the fundamental capacitive behavior: a case study of MnO2.

In this work, an insightful study on the fundamental capacitive behavior of MnO2 based electrodes is carried out using MnO2 hierarchical spheres (MHSs) and MnO2 nanoneedles (MNs) as examples. An overall understanding of the relationship between the capacitive performance and the electrode configuration as well as the morphology of active material, loading density, porosity of electrode, and electrolyte concentration is investigated comprehensively. Our analyses show that MnO2 with thin structure is of advantage to increase the utility of active material and to deliver higher specific capacitance, as the faradic reaction happens at/near the surface. Creation of an efficient path for the transport of electrons and ions is crucial to achieve high rate capabilities. Cycling stability could be improved by suppressing the side reaction. It is also important to shed light on the charge contribution from a graphite paper (GP) substrate since it may cause a misinterpretation of the capacitive behavior. This study provides a comprehensive understanding on the fundamental capacitive behavior of MnO2 based electrodes and gives useful clues for designing high performance supercapacitors.

Hollow LiMn(2)O(4) nanocones as superior cathode materials for lithium-ion batteries with enhanced power and cycle performances.

Single-crystalline LiMn(2)O(4) hollow nanocones are synthesized via a template-engaged low-temperature lithiation reaction. When applied as cathode materials for lithium-ion batteries, they can deliver a high specific capacity of 127.1 mAh g(-1) at 0.1 C and the capacity still maintains 100 mAh g(-1) even at 50°C. After over 1000 cycles at 5°C, 94.8% of the initial capacity is retained.

Plasma modified MoS(2) nanoflakes for surface enhanced raman scattering.

Though the SERS effect based on pristine MoS2 is hardly observed, however, the plasma treated MoS2 nanoflakes can be used as an ideal substrate for surface enhanced Raman scattering. It is proved that the structural disorder induced generation of local dipoles and adsorption of oxygen on the plasma treated MoS2 nanosheets are the two basic and important driven forces for the enhancement of Raman signals of surface adsorbed R6G molecules.

Open-circuit voltage improvement in tantalum-doped TiO2 nanocrystals.

Enhanced electron concentration derived from Ta(5+) doping is responsible for the open-circuit voltage improvement due to the upward shift of the Fermi level, but the oxygen defects generated retard the negative shift of the Fermi level. By mediating the trap states, highly efficient DSSC devices could be achieved.