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In order to realize advanced flexible devices, it is critical to simultaneously ensure the flexibility and robustness of bonded joints in the electronic packages for the mechanical and electrical reliability. Flexible bonded joints of thin polymer substrates should be developed because the flexible substrates inevitably undergo extensive mechanical loads, including tension, bending, and twisting. While epoxy resins have been used to bind plastic substrates, they often exhibit inferior flexibility and poor fatigue resistance, which are caused by increased bonding thickness and inherent brittleness, respectively. To solve this problem, we adopted microwave heating of carbon nanotubes (CNTs) for bonding thin polymer substrates for flexible applications. Multiwalled carbon nanotubes are spray-coated onto flexible substrates with a thickness of less than 100 μm. Microwave irradiation was controlled to induce rapid thermal fusion bonding of a pair of thin polymer substrates, where glass plates were attached to prevent thermal distortion. To investigate the bonding mechanism, the polymer-CNT bonding interface was analyzed by using a scanning electron microscope. The mechanical robustness of the bonded joint was evaluated for different microwave power and irradiation times with a fixed frequency of 2.45 GHz. Flexibility of the bonded assembly was characterized by using a three-point bending test and a cross-sectional digital image correlation method with microscopic images. In addition, the bending endurance of a CNT electrode on a flexible substrate assembly was tested under static and dynamic bending. This work provides a concept for realizing flexible interconnections between electronic components, including flexible substrates and electrodes. [ABSTRACT FROM AUTHOR]

Surface-enhanced Raman spectroscopy (SERS), with high sensitivity to a broad range of molecules, can detect molecular "fingerprints" in a complex substance and thereby offers a promising solution for noninvasive medical diagnostics and personal healthcare monitoring. The eventual realization of such applications relies on SERS substrates with dense and uniform hot spots, good chemical stability, and high mechanical durability. With these criteria in mind, we developed a flexible nanoporous SERS substrate via the in situ synthesis of gold nanostars (AuNSs) on an ion-track-etched polycarbonate membrane. The nanoporous SERS substrate can realize analyte enrichment and exhibit excellent Raman performance by taking the advantage of hot spots on AuNSs. The SERS substrate yields highly repeatable and uniform signals for analytes (e.g., methylene blue) over a wide concentration range from 10–4 to 10–13 M. The flexible SERS substrate even can work well after 2000 times bending and exhibit excellent stability for long-term use. It can be prepared on a large scale with a low-cost and simple fabrication process and can be used repeatedly after cleaning to reduce the use-cost further. On-body experiments prove that the sweat SERS substrate allows effective identification of sweat contents, such as lactic acid and uric acid (UA), and the monitoring of diet-induced variation in sweat UA. The potential of the wearable nanoporous SERS substrates in sweat analysis thus has been demonstrated, opening possibilities for autonomous and noninvasive medical health monitoring. [ABSTRACT FROM AUTHOR]

Owing to the simplicity, scalability, and cost-efficiency, solution-processable two-dimensional (2D) semiconductors have attracted great interest in electronic applications, especially as the channel material for field-effect transistors (FETs). Inkjet printing is a lithography-free technique to achieve drop-on-demand patterning of solution-processable 2D ink. However, thus far, inkjet-printed 2D FETs exhibit limited performance due to the coffee-ring effect and consequent discontinuity of the printed 2D material films. Here, we report high-performance and flexible inkjet-printed MoS2 FETs with high mobilities and high on/off ratios and their gas sensing applications. By preparing high-quality MoS2 ink comprised of MoS2 nanoplates using electrochemical exfoliation and then applying a binary solvent comprised of 2-butanol and isopropanol, the obtained ink was printed to form a continuous and relatively uniform MoS2 film, and high-performance printed MoS2 FETs were demonstrated, with mobilities of 11 cm2 V–1 s–1 and on/off ratios of 106. Furthermore, low-voltage gate modulation was achieved by applying an ion gel gate, and robust electrical performance under tensile strain was observed for the ion gel-gated MoS2 FETs printed on flexible substrates. As the printed MoS2 film is abundant in edge sites and sulfur vacancies, we further demonstrated our MoS2 FETs as high-performance gas sensors with a limit of detection of 10 ppb for NO2 and 0.5 ppm for NH3, together with a fast recovery rate. [ABSTRACT FROM AUTHOR]

Graphene is considered an ideal material candidate in the design and manufacturing of flexible electronics and devices because of its ultrahigh out-of-plane mechanical flexibility along with high thermal conductivity. However, the associated thermal management is vulnerable to mechanical deformation and the thermal transport of graphene/substrate systems subjected to mechanical bending deformation remains fundamentally unclear. Here, we investigate the thermal transport of mechanically bent graphene on a flexible substrate using non-equilibrium molecular dynamics (NEMD) simulations. We find that the thermal conductivity shows an anomalous nonlinear decrease with the increase of bending curvature for a small-sized graphene/substrate and becomes nearly independent of bending curvature at a large-sized graphene/substrate. A two-phonon model is proposed to quantitatively correlate the thermal conductivity with bending curvature and graphene size, and the predictions are in great agreement with simulations. We further elucidate the underlying mechanism of phonon transport coupled with graphene size and bending curvature by systematically studying the phonon population difference, phonon spectral energy density, and spectral decomposed thermal conductance of graphene/substrate systems. This work uncovers a fundamental mechanism of mechanical and thermal coupling and correlation in graphene/substrate systems for their enabled applications in flexible electronics and also offers guidance in the thermal management of graphene-based flexible devices undergoing severe mechanical deformation. [ABSTRACT FROM AUTHOR]

Electrospun nanofibers have become an important component in fabricating flexible electronic devices because of their permeability, flexibility, stretchability, and conformability to three-dimensional curved surfaces. This review delves into the advancements in adaptable and flexible electronic devices using electrospun nanofibers as the substrates and explores their diverse and innovative applications. The primary development of key substrates for flexible devices is summarized. After briefly discussing the principle of electrospinning, process parameters that affect electrospinning, and two major electrospinning techniques (i.e., single-fluid electrospinning and multifluid electrospinning), the review shines a spotlight on the recent breakthroughs in multifunctional and stretchable electronic devices that are based on electrospun substrates. These advancements include flexible sensors, flexible energy harvesting and storage devices, flexible accessories for electronic devices, and flexible environmental monitoring devices. In particular, the review outlines the challenges and potential solutions of developing electrospun nanofibers for flexible electronic devices, including overcoming the incompatibility of multiple interfaces, developing 3D microstructure sensor arrays with gradient geometry for various imperceptible on-skin devices, etc. This review may provide a comprehensive understanding of the rational design of application-oriented flexible electronic devices based on electrospun nanofibers.

Spintronic THz emitters have been widely studied due to their advantages of broadband frequency, high efficiency, and easy fabrication. The spintronic THz signal is proportional to the magnetization of the ferromagnetic (FM) layer and requires an external magnetic field to maximize the THz signal intensity. Recently, a field-free emitter was designed based on a CoFeB/IrMn 3 heterostructure via the exchange bias between two films. However, field-free spintronic THz emitters based on a common FM/nonmagnetic metal structure are rare. Here, we fabricate a tunable and field-free THz emitter with giant THz emission modulation ability based on a polyimide/CoFeB/Pt heterostructure. The THz emission can be modulated by changing the curvature radius of the polyimide substrate. After the emitter is forward bent, the THz radiation without an external magnetic field is stronger than in the flat state with a field, which we attribute to in-plane magnetic anisotropy on the FM layer induced by the tensile strain. When we curve the emitter backward, the THz intensity decreases sharply. Moreover, the modulation (Δ S / S max ) of the THz wave from the forward-curved and backward-curved emitter is over 95%, and the device shows good cyclic repeatability. We provide a novel way to design field-free spintronic THz sources, and flexible devices are promising for application in THz devices.

We present a new approach to achieve nanoscale transistors on ultrathin flexible substrates with conventional electron-beam lithography. Full devices are first fabricated on a gold sacrificial layer covering a rigid silicon substrate, and then coated with a polyimide film and released from the rigid substrate. This approach bypasses nanofabrication constraints on flexible substrates: (i) electron-beam surface charging, (ii) alignment inaccuracy due to the wavy substrate, and (iii) restricted thermal budgets. As a proof-of-concept, we demonstrate ∼100 nm long indium tin oxide (ITO) transistors on ∼6 μm thin polyimide. This is achieved with sub-20 nm misalignment or overlap between source (or drain) and gate contacts on flexible substrates for the first time. The estimated transit frequency of our well-aligned devices can be up to 3.3 GHz, which can be further improved by optimizing the device structure and performance.

In order to obtain a flexible aerogel substrate for conductive materials used in the electrode, polydopamine-anchored cellulose nanofiber (PDA@CNF) was introduced into a polyethylene imine-poly(vinyl alcohol) (PEI-PVA) cross-linking network which used 4-formylphenylboronic acid (4FPBA) as bridge. The incorporation of rigid CNF as a structural scaffold effectively improved the pore architecture of the aerogel, potentially providing substantial advantages for the infiltration and deposition of conductive materials. Additionally, the outstanding stability and flexibility exhibited by the aerogel in aqueous solutions suggest its significant potential for applications in flexible electrodes. Furthermore, electrochemical experiments showed that the rapid pathway formed between PDA and PEI could enhance the charge-transfer rate within the aerogel substrate. It is anticipated that such an enhancement would significantly benefit the electrochemical attributes of the electrode. Inspired by mussels, our introduced PDA-anchored rigid CNF into flexible polymer networks to fabricate aerogel substrates for electrode materials. This study would contribute to the development and utilization of flexible electrodes while reducing carbon footprint in energy production and conversion processes.

This study presents the development of gas sensors based on the PEDOT:PSS@ZnO hybrid active layer slot-die printing aqueous ink. Two different zinc oxide (ZnO) nanoparticles were studied to form the nanocomposites, as well as the use of glass and PET substrates to manufacture the devices. Despite the influence of the morphology of the active layer, all device variations studied here exhibited high response values for methanol gas at room temperature, in addition to presenting good repeatability, reversibility, and the possibility of technology transfer to flexible substrates. Furthermore, PEDOT:PSS@ZnO showed good selectivity to methanol compared to ethanol, ammonia, and CO 2 . The best devices showed responses greater than 700% in detecting methanol.

The metallization of flexible polymer surface is a necessary process to realize the electrical interconnection of insulating substrates, which is of great significance for the fabrication of flexible wearable electronics. Herein, a method for the fabrication of a metal/polymer composite is presented on the basis of a silver nanowire (AgNW) conductive composite by direct copper electroplating. A precoating was first coated on the polyethylene terephthalate (PET) substrate to form the interspace structures on the surface. AgNWs could just be embedded into these interspace structures by the means of coating to obtain excellent adhesion. Furthermore, these interspace structures were filled with deposited copper atoms, thus contributing to a strong interlock between the plated copper layer and the substrate. The obtained Cu/PET composites were subjected to morphological and mechanical characterizations to analyze the peeling strength, crystalline structure, and surface morphology of the plated copper layer. Experimental results show that the plated copper layer is dense and consistent with a maximum peel strength of 11 N cm–1. In addition, large scale of the Cu/PET (20 cm × 30 cm) composite with a thickness of 21 μm was fabricated by this method, and copper patterns were further fabricated using a conventional etching process. The fabricated copper patterns exhibit an outstanding electrical stability after 3000 times of a bending fatigue test, proving the excellent flexibility of the Cu/PET composite. In conclusion, this approach provides an insight into the design of metal/polymer composites addressing a significant potential application in flexible printed circuit, electrode, and antenna for wearable electronics. [ABSTRACT FROM AUTHOR]

Flexible electronics for harsh and hazardous environments could offer a broad range of technological applications from conformal structural health monitoring, hypersonics, to telecommunication systems. However, advanced materials with the capability of additive manufacturing and the tolerance to extreme operating conditions are imperative. Here, we report high-temperature radiofrequency electronics with thermal management by printing copper hybrid conductors onto flexible thin alumina ribbon ceramic and ceramic fiber/silica aerogel composite. Regulating thermal stability, tuning resonance frequency, and increasing current-carrying ability of printed electronics are synergistically achieved using a flexible thermal-insulation ceramic fiber/silica aerogel composite or thermally conductive alumina ribbon ceramic substrates and high-temperature copper–graphene conductors. The printed copper conductor coatings exhibit tunable antenna resonance and electromagnetic interference effectiveness of 70 dB at a thickness of 5 μm, opening a pathway toward flexible hybrid radiofrequency electronics with thermal management. [ABSTRACT FROM AUTHOR]

Flexible pressure sensors (FPSs) based on biomass materials have gained considerable attention for their potential in wearable electronics, human-machine interaction, and environmental protection. Herein, flexible silver nanowire-dual-cellulose paper (SNdCP) containing common cellulose fibers, cellulose nanofibers (CNFs), and silver nanowires (AgNWs) for FPSs was assembled by a facile papermaking strategy. Compared with bacterial cellulose (BC) and cellulose nanocrystals (CNCs), CNFs possess better dimensions and reinforcement, which enables the composite paper to exhibit better mechanical properties (tensile stress of 164.65 MPa) and electrical conductivity (11600 S·m -1 ), providing more possibilities for FPSs. Benefiting from these advantages, we construct an easily processable and sensitive human-interactive FPS based on a composite paper with high sensitivity (0.050 kPa -1 ), fast response/recovery time (158/95 ms), and exceptional stability (>1000 bending cycles), capable of responding to finger motions, voice recognition, and human pulses; through further employment as the array unit and a control circuit, the observed highly adaptive mechano-electric transformability and functions are well maintained. Overall, a facile and versatile strategy with the potential to provide clues for the fabrication of cellulose-based FPSs with outstanding performance was introduced.

This study investigates the influence of surface nitridation of Ta metal foil substrates on the growth of GaN nanorods using the laser molecular beam epitaxy (LMBE) technique and the field emission characteristics of the grown GaN nanorod ensemble. Surface morphology examinations underscore the pivotal role of Ta foil nitridation in shaping the dimensions and densities of GaN nanorods. Bare Ta foil fosters the formation of high-density, vertically self-aligned GaN nanorods at a growth temperature of 700 °C. Furthermore, the density of these nanorods is directly related to the duration of Ta foil nitridation, with increased duration leading to a reduced nanorod density. X-ray Photoelectron Spectroscopy (XPS) studies reveal that the transition of the Ta foil surface from tantalum oxide to tantalum nitride during nitridation emerges as a crucial factor influencing GaN nanorod growth. Photoluminescence (PL) spectroscopy at ambient temperature reveals a strong near-band-edge (NBE) emission peak with negligible defect-related peaks, displaying the high optical quality of the GaN nanorods. The highly dense vertically aligned GaN nanorod ensemble growth without Ta prenitridation exhibits the most favorable field emission performance, featuring a turn-on field of 2.1 V/μm, a field enhancement factor of 2480, and a stable long-term operation at the emission current density of 2.26 mA/cm 2 . This study advances the understanding of the role of the surface chemistry of metal foil in determining GaN nanorod growth and opens up exciting possibilities for tailoring advanced optoelectronic devices for specific application requirements.

This work reports the growth of stable TiO2 nanotube arrays on flexible Kapton substrates by electrochemical anodization of a sputtered Ti (titanium) film. Although such nanotubes are conventionally fabricated on Ti foils, obtaining these on polymer-based flexible substrates remained a challenge because of higher annealing temperature not compatible with thermal stability of the substrates. Here, we demonstrate the fabrication of TiO2 nanotubes (1.5 μm long and 80 nm diameter) by anodization of the Ti film deposited using the RF sputtering technique at two different substrate temperatures (room temperature and 300 °C). Nanoindentation and nanoscratch techniques reveal better adhesion of the Ti film with an underlying Kapton substrate for 300 °C deposition temperature. Such investigations reveal a more than twofold enhancement of the "rear pileup" for the Ti film deposited at elevated temperature compared to that at room temperature. The amorphous TiO2 nanotubes are crystallized at 220 °C for 3 h using a solvothermal technique that allows crystallization at temperatures much lower than the annealing temperature. Application of these nanotubes for photo-electrochemical water splitting reveals a photocurrent density of 18 μA/cm2 under AM 1.5 G conditions. Furthermore, the charge density and flat band potential (VFB) are calculated from Mott–Schottky analysis, showing features comparable to the TiO2 nanotubes on the Ti foil crystallized through thermal annealing. The present work establishes a scalable approach for developing TiO2 nanotube arrays on the flexible substrate and its use for photo-electrochemical solar energy conversion. [ABSTRACT FROM AUTHOR]

Printing graphene-based nanomaterials on flexible substrates has become a burgeoning platform for next-generation technologies. Combining graphene and nanoparticles to create hybrid nanomaterials has been proven to boost device performance, thanks to their complementary physical and chemical properties. However, high growth temperatures and long processing times are often required to produce high-quality graphene-based nanocomposites. For the first time, we report a novel scalable approach for additive manufacturing of Sn patterns on polymer foil and their selective conversion into nanocomposite films under atmospheric conditions. A combination of inkjet printing and intense flashlight irradiation techniques is studied. Light pulses that are selectively absorbed by the printed Sn patterns cause a temperature of over 1000 °C to be reached locally in a split second without damaging the underlying polymer foil. The top surface of the polymer foil at the interface with printed Sn becomes locally graphitized and acts as a carbon source, transforming printed Sn into Sn@graphene (Sn@G) core-shell patterns. Our results revealed a decrease in electrical sheet resistance, with an optimal value ( R s were applied. These graphene-protected Sn nanoparticle patterns exhibit excellent resistance against air oxidation for months. Finally, we demonstrate the implementation of Sn@G patterns as electrodes for Li-ion microbatteries (LIBs) and triboelectric nanogenerators (TENGs), showing remarkable performance. This work offers new insight into the development of a versatile, eco-friendly, and cost-effective technique for producing well-defined patterns of graphene-based nanomaterials directly on a flexible substrate using different light-absorbing nanoparticles and carbon sources.2 were applied. These graphene-protected Sn nanoparticle patterns exhibit excellent resistance against air oxidation for months. Finally, we demonstrate the implementation of Sn@G patterns as electrodes for Li-ion microbatteries (LIBs) and triboelectric nanogenerators (TENGs), showing remarkable performance. This work offers new insight into the development of a versatile, eco-friendly, and cost-effective technique for producing well-defined patterns of graphene-based nanomaterials directly on a flexible substrate using different light-absorbing nanoparticles and carbon sources.

Strong and ultrastrong coupling between intersubband transitions in quantum wells and cavity photons have been realized in mid-infrared and terahertz spectral regions. However, most previous works employed a large number of quantum wells on rigid substrates to achieve coupling strengths reaching the strong or ultrastrong coupling regime. In this work, we experimentally demonstrate ultrastrong coupling between the intersubband transition in a single quantum well and the resonant mode of photonic nanocavity at room temperature. We also observe strong coupling between the nanocavity resonance and the second-order intersubband transition in a single quantum well. Furthermore, we implement for the first time such intersubband cavity polariton systems on soft and flexible substrates and demonstrate that bending of the single quantum well does not significantly affect the characteristics of the cavity polaritons. This work paves the way to broaden the range of potential applications of intersubband cavity polaritons including soft and wearable photonics.

Looking for high-performance substrates is an important goal of current surface enhanced Raman scattering (SERS) research. Herein, ultrathin multilayer rhenium (Re) nanosheets as a rare-earth metal substrate are found to have extraordinary SERS performance. These Re nanosheets are prepared through a convenient low-temperature molten salt strategy, and their total thickness is ∼5 nm, including 3-4 layers of ultrathin nanosheets with a thickness of only ∼1 nm. The viscosity of molten salt plays a key role in the formation of these ultrathin layered nanosheets. These nanosheets exhibit a strong and well-defined localized surface plasmon resonance (SPR) effect in the visible light region. The plasmonic Re nanosheets show excellent SERS performance with high sensitivity, chemical stability, and signal repeatability. The lowest detection limit for toxic compounds is 10 -12 mol, and the corresponding Raman enhancement factor is 9.1 × 10 8 . A composite enhancement mechanism caused by localized-SPR and charge transport has played an important role in the rare-earth-SERS. High-throughput multiassay analysis is performed on the flexible membrane assembled from the Re nanosheets, which highlights that our system is capable of rapid separation and identification of the samples containing various analytes.

Solar-driven interfacial steam generation (SDISG), as an emerging green and renewable approach to overcome water shortage, is very suitable for remote locations, developing countries, and disaster zones because it does not require an additional energy supply. However, the traditional metal-based and carbon-based absorbers always suffered from fragility (or rigidity) and the complex preparation process, which dramatically inhibited their transportation and installation in areas with poor infrastructure. Therefore, there is an urgent need to develop a universal method to fabricate flexible solar evaporators. Herein, a novel solar evaporator that integrates a flexible matrix (Cu mesh or textile) and a hierarchical Fe-MOF-74 photothermal absorber component is perfectly prepared for the rapid and efficient SDISG. Notably, the results show that Fe-MOF-74-based flexible textile matrix composites exhibit outstanding light absorption (83.81%), low thermal conductivity (0.1730 W/m K), super hydrophilic properties (within 50 ms, the contact angle is close to 0°), excellent salt resistance, high evaporation rate (1.35 kg/m 2 h), and photothermal conversion efficiency (η is 81.5% under one sun, stable for 30 days). Owing to the flexibility, recyclability, and above-mentioned excellent performance, the prepared hierarchical Fe-MOF-74-based flexible composite systems are more practical for transportation, large-scale production, and stable and efficient applications. As a result, this work offers new insight into the future development of the combination of a MOF-based photothermal absorber and flexible substrates, as well as for the application of interfacial solar seawater desalination, and provides a new reference for other applications.

The design and high-throughput manufacturing of thin renewable energy devices with high structural and atomic configurational stability are crucial for the fabrication of green electronics. Yet, this concept is still in its infancy. In this work, we report the extraordinary durability of thin molecular interlayered organic flexible energy devices based on chemically tuned cellulose nanofiber transparent films that outperform glass by decreasing the substrate weight by 50%. The nanofabricated flexible thin film has an exceptionally low thermal coefficient of expansion of 1.8 ppm/K and a stable atomic configuration under a harsh fabrication condition (over 190 °C for an extended period of 5 h). A flexible optoelectronic device using the same renewable cellulose nanofiber film substrate was found to be functionally operational over a life span of 5 years under an intermittent operating condition. The success of this device's stability opens up an entirely new frontier of applications of flexible electronics.

We report a chemiresistive cyclohexanone sensor on a flexible substrate based on single-walled carbon nanotubes (SWCNTs) functionalized with thiourea (TU) derivatives. A wrapper polymer containing both 4-vinylpyridine (4VP) groups and azide groups (P(4VP-VBAz)) was employed to obtain a homogeneous SWCNT dispersion via noncovalent functionalization of SWCNTs. The P(4VP-VBAz)-SWCNT composite dispersion was then spray-coated onto an organosilanized flexible poly(ethylene terephthalate) (PET) film to achieve immobilizing quaternization between the pyridyl groups from the polymer and the functional PET substrate, thereby surface anchoring SWCNTs. Subsequent surface functionalization was performed to incorporate a TU selector into the composites, resulting in P(Q4VP-VBTU)-SWCNT, for the detection of cyclohexanone via hydrogen bonding interactions. An increase in conductance was observed as a result of the hydrogen-bonded complex with cyclohexanone resulting in a higher hole density and/or mobility in SWCNTs. As a result, a sensor device fabricated with P(Q4VP-VBTU)-SWCNT composites exhibited chemiresistive responses (Δ G / G 0 ) of 7.9 ± 0.6% in N 2 (RH 0.1%) and 4.7 ± 0.4% in air (RH 5%), respectively, upon exposure to 200 ppm cyclohexanone. Selective cyclohexanone detection was achieved with minor responses (Δ G / G 0 < 1.4% at 500 ppm) toward interfering volatile organic compounds (VOC). analytes. We demonstrate a robust sensing platform using the polymer-SWCNT composites on a flexible PET substrate for potential application in wearable sensors.

Current-induced magnetization switching by spin-orbit torque generated in heavy metals offers an enticing realm for energy-efficient memory and logic devices. The spin Hall efficiency is a key parameter in describing the generation of spin current. Recent findings have reported enhancement of spin Hall efficiency by mechanical strain, but its origin remains elusive. Here, we demonstrate a 45% increase in spin Hall efficiency in the platinum/cobalt (Pt/Co) bilayer, of which 78% of the enhancement was preserved even after the strain was removed. Spin transparency and X-ray magnetic circular dichroism revealed that the enhancement was attributed to a bulk effect in the Pt layer. This was further confirmed by the linear relationship between the spin Hall efficiency and resistivity, which indicates an increase in skew-scattering. These findings shed light on the origin of enhancement and are promising in shaping future utilization of mechanical strain for energy-efficient devices.

Graphene exhibits both high electrical conductivity and large elastic modulus, which makes it an ideal material candidate for many electronic devices. At present not much work has been conducted on using graphene to construct thermoelectric devices, particularly due to its high thermal conductivity and lack of bulk fabrication. Films of graphene-based materials, however, and their nanocomposites have been shown to be promising candidates for thermoelectric energy generation. Exploring methods to enhance the thermoelectric performance of graphene and produce bulk samples can significantly widen its application in thermoelectrics. Realization of bulk organic materials in the thermoelectric community is highly desired to develop cheap, Earth-abundant, light, and nontoxic thermoelectric generators. In this context, this work reports a new approach using pressed pellets bars of few-layered graphene (FLG) nanoflakes employed in thermoelectric generators (TEGs). First, FLG nanoflakes were produced by a novel dry physical grinding technique followed by graphene nanoflake liberation using plasma treatment. The resultant material is highly pure with very low defects, possessing 3 to 5-layer stacks as proved by Raman spectroscopy, X-ray diffraction measurement, and scanning electron microscopy. The thermal and electronic properties confirm the anisotropy of the material and hence the varied performance characteristics parallel to and perpendicular to the pressing direction of the pellets. The full thermoelectric properties were characterized both parallel and perpendicular to the pressing direction, and the proof-of-concept thermoelectric generators were fabricated with variable amounts of legs.

Single-walled carbon nanotubes (SWCNTs) have attracted significant attention due to their outstanding properties. For their wide applications in electronics and optoelectronics, pure semiconducting SWCNTs (s-SWCNTs) and their precise placement are preconditions. Recent advances have focused on developing effective strategies to separate s-SWCNTs from raw SWCNTs, a mixture of metallic and semiconducting nanotubes, and deposit s-SWCNTs on target substrates. Herein, a polyfluorene-based alternative copolymer (PFBP) containing the benzophenone group was employed. PFBP achieved higher yield for s-SWCNTs than the well-studied poly(9,9-dioctylfluorene) through solution process. Subsequently, the dispersed s-SWCNTs were immobilized on a flexible polyethylene terephthalate in a facile manner by the photoreactive benzophenone group upon exposure to UV irradiation, and chemically robust patterns were fabricated from micro to macro scales through photomasks. Our method accomplished by utilizing photoimmobilization is a simple cleaning procedure and an important step forward in pitch scaling for further applications of conjugated polymer wrapped s-SWCNTs.

Flexible electronic technology has attracted great attention due to its wide range of potential applications in the fields of healthcare, robotics, and artificial intelligence, etc . In this work, we have successfully fabricated flexible AlGaN/GaN high-electron-mobility transistors (HEMTs) arrays through a low-damage and wafer-scale substrate transfer technology from a rigid Si substrate. The flexible AlGaN/GaN HEMTs have excellent electrical performances with the I d,max achieving 290 mA/mm at V gs = +2 V and the g m,max reaching to 40 mS/mm. The piezotronic effect provides a different freedom to optimize device performances, and flexible HEMTs can endure the larger mechanical distortions. Based on the piezotronic effect, we applied an external stress to significantly modulate the electrical performances of flexible HEMTs. The piezotronic effect modulated flexible AlGaN/GaN HEMTs exhibit great potential in human-machine interface, intelligent microinductor systems, and active sensors, etc , and introduce an opportunity to sensing or feedback external mechanical stimuli and so on.

We investigated the effect of inductively coupled plasma (ICP) on multilayer electrodes for flexible capacitive touch sensors. We found that using ICP during Ag deposition generally increased the conductivity and transmittance of multilayer electrodes. As a result, in the case of the multilayer electrode with an ICP power of 150 W during Ag deposition, 5.7 Ω/sq of sheet resistance and 89.6% of transmittance (550 nm) have been achieved. We demonstrate that the crystallization of the ICP supplied Ag layer in multilayer electrodes leads to the smooth surface roughness of the multilayer film; the smooth surface roughness provided low light scattering. As a result, the crystallized Ag thin film by ICP improved the sheet resistance and transmittance of multilayer electrodes. Finally, we fabricated a 221 × 130 mm (active layer)-sized single-layer touch screen panel (TSP) using multilayer electrodes with ICP on a corning glass and polyethylene terephthalate flexible substrate. The single-layer TSPs show high linearity and sensitivity with multitouches.

The use of flexible and highly conducting molybdenum (Mo) foil as a substrate offers several advantages such as a high thermal stability, smooth surface, and chemical inertness for the fabrication of high-efficiency thin film solar cells (TFSCs) by lowering the manufacturing costs. Here, we report a record preliminary efficiency of ∼8% for sputtered-grown Cu 2 ZnSn(S,Se) 4 (CZTSSe) TFSCs on flexible and lightweight Mo foils. Careful studies were focused on identifying the role of preparative parameters such as annealing temperature, absorber composition, and post-preparative optimization to bridge the obtained record efficiency of ∼8% to a previous record efficiency of 7.04% for Na-incorporated CZTSSe sputter-based TFSCs. Interestingly, the preliminary record efficiency of ∼8% for our CZTSSe device grown via a scalable sputtering method was achieved by optimizing the absorber quality and post-preparative device optimization. While our preliminary results with a record efficiency demonstrate the potential of sputtering method, there is much scope for further improvement in the device efficiency by thoroughly understanding alkali element doping in the absorber layer.

Disorder is emerging as a strategy for fabricating random laser sources with very promising materials, such as perovskites, for which standard laser cavities are not effective or too expensive. We need, however, different fabrication protocols and technologies for reducing the laser threshold and controlling its emission. Here, we demonstrate an effectively solvent-engineered method for high-quality perovskite thin films on a flexible polyimide substrate. The fractal perovskite thin films exhibit excellent optical properties at room temperature and easily achieve lasing action without any laser cavity above room temperature with a low pumping threshold. The lasing action is also observed in curved perovskite thin films on flexible substrates. The lasing threshold can be further reduced by increasing the local curvature, which modifies the scattering strengths of the bent thin film. We also show that the curved perovskite lasers are extremely robust with respect to repeated deformations. Because of the low spatial coherence, these curved random laser devices are efficient and durable speckle-free light sources for applications in spectroscopy, bioimaging, and illumination.

Water collection has been extensively researched due to its potential for mitigating the water scarcity in arid and semiarid regions. Numerous structures mimicking the fog-harvesting strategy of organisms have been fabricated for improving water-collecting efficiency. In this contribution, we demonstrate four-level wedge-shaped tracks inspired by leaf vein for enhancing directional water collection. Superhydrophilic Cu(OH) 2 nanowires are introduced and prepared on flexible hydrophobic polyethylene terephthalate (PET) substrates by alkali-assisted surface oxidation at room temperature. They provide abundant capillary paths for promoting droplet absorption and forming water film tracks. Then, the hierarchical wedge-shaped tracks enable the water to be transported to a certain accumulation region spontaneously owing to the continuous Young-Laplace pressure difference. As a result, the four-level wedge-shaped tracks on PET substrate achieve the highest water-collecting efficiency, increasing by nearly 1150 and 510% compared to the bare PET and Cu(OH) 2 nanowires on PET, respectively. After being bent for 10 5 cycles at a radius of 10 mm, the samples can still preserve high efficiency, indicating that the synthetic structures possess outstanding durability. Our approach provides a novel strategy for water collection and paves ways for directional liquid transportation and microfluidic devices.

Selenium (Se) is one of the potential candidates as photodetector because of its outstanding properties such as high photoconductivity (∼8 × 10 4 S cm -1 ), piezoelectricity, thermoelectricity, and nonlinear optical responses. Solution phase synthesis becomes an efficient way to produce Se, but a contamination issue that could deteriorate the electric characteristic of Se should be taken into account. In this work, a facile, controllable approach of synthesizing Se nanowires (NWs)/films via a plasma-assisted growth process was demonstrated at the low substrate temperature of 100 °C. The detailed formation mechanisms of nanowires arrays to thin films at different plasma powers were investigated. Moreover, indium (In) layer was used to enhance the adhesive strength with 50% improvement on a SiO 2 /Si substrate by mechanical interlocking and surface alloying between Se and In layers, indicating great tolerance for mechanical stress for future wearable devices applications. Furthermore, the direct growth of Se NWs/films on a poly(ethylene terephthalate) substrate was demonstrated, exhibiting a visible to broad infrared detection ranges from 405 to 1555 nm with a high on/off ratio of ∼700 as well as the fast response time less than 25 ms. In addition, the devices exhibited fascinating stability in the atmosphere over one month.

In this study, we report on an automated method based on a handwritten technique for the fabrication of low-cost gas sensors based on carbon nanotube (CNT) networks. Taking advantage of the inherent low-cost, flexible, and uncomplicated characteristics of pen-based techniques and combining them with an automated robotic system allows for high-resolution patterns, high reproducibility, and relatively high throughput considering the limitations of parallel processing. To showcase this, gas sensors capable of sensing NH 3 , CO 2 , CO, and ethanol, as well as temperature and relative humidity, are fabricated and characterized displaying competitive performance in relation to previously reported devices. The presented process is compatible with a variety of solutions and inks and, as such, allows for an easy integration into existing printing and coating frameworks with the greatest advantage being the ease of creating prototypes because of the nonstringent material requirements.

We develop an "acceptor dimerization" strategy by a bis-diketopyrrolopyrrole (2DPP) for an ambipolar organic semiconductor. Copolymers of 2DPP and benzothiadiazole (BTz) derivatives, P2DPP-BTz and P2DPP-2FBTz, are designed and synthesized. Both of the polymers exhibit narrow optical bandgaps of ca. 1.30 eV. The strong electron-withdrawing property of 2DPP results in low-lying lowest unoccupied molecular orbital (LUMO) energy levels of the polymers, improving the electron mobilities. 2D grazing incident X-ray diffraction and atomic force microscopy indicate that the P2DPP-BTz exhibits a small π-π stacking distance of 3.59 Å and a smooth interface, thus promoting high mobility. To take full advantage of the flexibility of organic semiconductors, flexible field-effect transistors (FETs) were fabricated on poly(ethylene terephthalate) (PET) substrates. The FETs based on P2DPP-BTz show high performance with hole and electron mobilities of 1.73 and 2.58 cm 2 V -1 s -1 , respectively. Our results demonstrate that the 2DPP acceptor is a promising building block for high-mobility ambipolar polymers.

Direct graphene synthesis on substrates via chemical vapor deposition (CVD) is an attractive approach for manufacturing flexible electronic devices. The temperature for graphene synthesis must be below ∼200 °C to prevent substrate deformation while fabricating flexible devices on plastic substrates. Herein, we report a process whereby defect-free graphene is directly synthesized on a variety of substrates via the introduction of an ultrathin Ti catalytic layer, due to the strong affinity of Ti to carbon. Ti with a thickness of 10 nm was naturally oxidized by exposure to air before and after the graphene synthesis, and the various functions of neither the substrates nor the graphene were influenced. This report offers experimental evidence of high-quality graphene synthesis on Ti-coated substrates at 150 °C via CVD. The proposed methodology was applied to the fabrication of flexible and transparent thin-film capacitors with top electrodes of high-quality graphene.

We report a light, flexible, and low-power poly(ionic liquid)/alumina composite CO 2 sensor. We monitor the direct-current resistance changes as a function of CO 2 concentration and relative humidity and demonstrate fast and reversible sensing kinetics. Moreover, on the basis of the alternating-current impedance measurements we propose a sensing mechanism related to proton conduction and gas diffusion. The findings presented herein will promote the development of organic/inorganic composite CO 2 gas sensors. In the future, such sensors will be useful for numerous practical applications ranging from indoor air quality control to the monitoring of manufacturing processes.

We report the instantaneous pulsed-light cross-linking of polymer gate dielectrics on a flexible substrate by using intensely pulsed white light (IPWL) irradiation. Irradiation with IPWL for only 1.8 s of a poly(4-vinylphenol) (PVP) thin film with the cross-linking agent poly(melamine-co-formaldehyde) (PMF) deposited on a plastic substrate was found to yield fully cross-linked PVP films. It was confirmed that the IPWL-cross-linked PVP films have smooth pinhole-free surfaces and exhibit a low leakage current density, organic solvent resistance, and good compatibility with organic semiconductor, and that they can be used as replacements for typical PVP dielectrics that are cross-linked with time and energy intensive thermal heating processes. The synchronization of the IPWL irradiation with substrate transfer was found to enable the preparation of cross-linked PVP films on large area substrates with a highly uniform capacitance. Flexible OTFT based on IPWL-cross-linked PVP dielectrics were found to exhibit good electrical performance that is comparable to that of devices with thermally cross-linked PVP dielectric, as well as excellent deformation stability even at a bending radius of 3 mm.

Due to their superior physical properties, titanium dioxide (TiO 2 ) nanotube arrays are one of the most investigated nanostructure systems in materials science until now. However, it is still a great challenge to achieve damage-free techniques to realize controllable, cost-effective, and high-performance TiO 2 nanotube arrays on both rigid and flexible substrates for different technological applications. In this work, we demonstrate a unique strategy to achieve self-assemble crystalline, large-area, and regular TiO 2 nanotube arrays on various substrates via hybrid combination of conventional semiconductor processes. Besides the usual applications of TiO 2 as carrier transport layers in thin-film electronic devices, we demonstrate that the periodic TiO 2 nanotube arrays can show the effect of optical grating with large-area uniformity. Specifically, the fabricated nanotube geometries, such as the tube height, pitch, diameter, and wall thickness, as well as the crystallinity can be reliably controlled by varying the processing conditions. More importantly, utilizing these nanotube arrays in perovskite solar cells can further enhance the optical absorption, leading to improved power conversion efficiency. In contrast to other typical template-assisted fabrication approaches, we employ a soft template here, which would enable the construction of nanotube arrays without any significant damage associated with template removal. Furthermore, without the thermal restriction of underlying substrates, these crystalline nanotube arrays can be transferred to mechanically flexible substrates by a simple one-step method, which can expedite these nanotubes for potential utilization in other application domains.

Ultrasensitive flexible strain sensors were developed through the combination of shear alignment of a high concentration graphene oxide (GO) dispersion with fast and precise patterning of multiple rectangular features on a flexible substrate. Resistive changes in the reduced GO films were investigated under various uniaxial strain cycles ranging from 0.025 to 2%, controlled with a motorized nanopositioning stage. The devices uniquely combine a very small detection limit (0.025%) and a high gauge factor with a rapid fabrication process conducive to batch production.

Copper nanomaterials suffer from severe oxidation problem despite the huge cost effectiveness. The effect of two different processes for conventional tube furnace heating and selective laser sintering on copper nanoparticle paste is compared in the aspects of chemical, electrical and surface morphology. The thermal behavior of the copper thin films by furnace and laser is compared by SEM, XRD, FT-IR, and XPS analysis. The selective laser sintering process ensures low annealing temperature, fast processing speed with remarkable oxidation suppression even in air environment while conventional tube furnace heating experiences moderate oxidation even in Ar environment. Moreover, the laser-sintered copper nanoparticle thin film shows good electrical property and reduced oxidation than conventional thermal heating process. Consequently, the proposed selective laser sintering process can be compatible with plastic substrate for copper based flexible electronics applications.

Using electrical characteristics from three-terminal field-effect transistors (FETs), we demonstrate substantial strain induced band gap tunability in transition metal dichalcogenides (TMDs) in line with theoretical predictions and optical experiments. Devices were fabricated on flexible substrates, and a cantilever sample holder was used to apply uniaxial tensile strain to the various multilayer TMD FETs. Analyzing in particular transfer characteristics, we argue that the modified device characteristics under strain are clear evidence of a band gap reduction of 100 meV in WSe2 under 1.35% uniaxial tensile strain at room temperature. Furthermore, the obtained device characteristics imply that the band gap does not shrink uniformly under strain relative to a reference potential defined by the source/drain contacts. Instead, the band gap change is only related to a change of the conduction band edge of WSe2, resulting in a decrease in the Schottky barrier (SB) for electrons without any change for hole injection into the valence band. Simulations of SB device characteristics are employed to explain this point and to quantify our findings. Last, our experimental results are compared with DFT calculations under strain showing excellent agreement between theoretical predictions and the experimental data presented here.

Recent progress in the field of microsystems on flexible substrates raises the need for alternatives to the stiffness of classical actuation technologies. This paper reports a top-down process to microfabricate soft conducting polymer actuators on substrates on which they ultimately operate. The bending microactuators were fabricated by sequentially stacking layers using a layer polymerization by layer polymerization of conducting polymer electrodes and a solid polymer electrolyte. Standalone microbeams thinner than 10 μm were fabricated on SU-8 substrates associated with a bottom gold electrical contact. The operation of microactuators was demonstrated in air and at low voltage (±4 V).

Metal thin film electrodes on flexible polymer substrates are inherently unstable against humidity and mechanical stresses because of their poor adhesion properties. We introduce a novel approach for improving the adhesion characteristics of metal-polymer interface based on the nanostructuring of the polymer substrate by using nanoimprint lithography. The adhesion characteristics of metal-polymer interface were measured by accelerated test, cyclic bending test and double cantilever beam (DCB) test. The interface of Au/Ti dual layer thin film and nanoimprinted PMMA substrate shows over 2.03 and 1.95 times higher adhesion energy (G(c)) than that of Au/Ti dual layer thin film and plane PMMA substrate in air and wet environments, respectively. The adhesion energy between metal thin film and polymer substrate was dramatically improved by the increased surface roughness and mechanical interlocking effect of numerous nanoscale anchors at the edges of nanoimprinted surface, which was verified by both experiment and numerical analysis.

Composite films consisting of poly(3,4-ethylenedioxythiophene) (PEDOT) and graphene oxide (GO) were electrochemically polymerized by electrooxidation of EDOT in ionic liquid (BMIMBF4) onto flexible electrode substrates. Two polymerization approaches were compared, and the cyclic voltammetry (CV) method was found to be superior to potentiostatic polymerization for the growth of PEDOT/GO films. After deposition, incorporated GO was reduced to rGO by a rapid electrochemical method of repetitive cathodic potential cycling, without using any reducing reagents. The films were characterized in 3-electrode configuration in BMIMBF4. Symmetric supercapacitors with aqueous electrolyte were assembled from the composite films and characterized through cyclic voltammetry and galvanostatic discharge tests. It was shown that PEDOT/rGO composites have better capacitive properties than pure PEDOT or the unreduced composite film. The cycling stability of the supercapacitors was also tested, and the results indicate that the specific capacitance still retains well over 90% of the initial value after 2000 consecutive charging/discharging cycles. The supercapacitors were demonstrated as energy storages in a room light energy harvester with a printed organic solar cell and printed electrochromic display. The results are promising for the development of energy-autonomous, low-power, and disposable electronics.

Highly transparent mesoporous titanium dioxide (TiO2; anatase) thin films were prepared at room temperature via ultraviolet (UV) irradiation of hybrid polymer-TiO2 nanoparticle thin films. This approach utilized a UV-curable polymer in conjunction with the photocatalytic activity of TiO2 to form and degrade the organic component of the composite films in one step, producing films with well-controlled porosity and refractive index. By adjustment of the loading of TiO2 nanoparticles in the host polymer, the refractive index was tuned between 1.53 and 1.73. Facile control of these properties and mild processing conditions was leveraged to fabricate robust one-dimensional photonic crystals (Bragg mirrors) consisting entirely of TiO2 on silicon and flexible poly(ethylene terephthalate) substrates. The mesoporous Bragg mirrors were shown to be effective chemical vapor sensors with strong optical responses.

Recent development of laser-induced hydrothermal growth enabled direct digital growth of ZnO nanowire array at an arbitrary position even on 3D structures by creating a localized temperature field through a photothermal reaction in liquid environment. However, its spatial size was generally limited by the size of the focused laser spot and the thermal diffusion, and the target material has been limited to ZnO. In this paper, we demonstrated a next generation laser-induced hydrothermal growth method to grow nanowire on a selected area that is even smaller than the laser focus size by designing laser absorption layer. The control of laser-induced temperature field was achieved through adjusting the physical properties of the substrate (dimension and thermal conductivity), and it enabled a successful synthesis of smaller nanowire array without changing any complex optics. Through precise localized temperature control with laser, this approach could be extended to various nanowires including ZnO and TiO2 nanowires even on heat sensitive polymer substrate.

A graphene (Gr) on a polyimide (PI) polymer film (Gr-PI film), obtained by a direct peel-off technique, is proposed and investigated. Thanks to its high transparency, electrical conductivity, mechanical strength, and chemical durability, the Gr-PI film is an ideal substrate for flexible electronic and optoelectronic devices, including transistors, light-emitting diodes, and plasmonic antennas. It is obtained using a straightforward method. After spin coating and curing a PI film on Gr previously grown on Cu, one can separate the Gr-PI film from the Cu foil thanks to the difference in the adhesive energy between the Gr-Cu and Gr-PI interfaces. The resulting Gr-PI film shows an average electrical sheet resistance ranging from 520 to 860 Ω/sq and a very high optical transmission (>90%), which have allowed the demonstration of a transparent heater. The surface morphology of the Gr-PI film follows that of the Cu foil, with the latter maintaining its surface properties and allowing in this way its reuse in subsequent chemical vapor deposition growth. The method can also be applied to patterned Gr, as is demonstrated for nanosize ribbons with a width of a few tens of nanometers.

Flexible thin film solar cells are an alternative to both utility-scale and building integrated photovoltaic installations. The fabrication of these devices over electrically conducting low-cost foils requires the deposition of dielectric barrier layers to flatten the substrate surface, provide electrical isolation between the substrate and the device, and avoid the diffusion of metal impurities during the relatively high temperatures required to deposit the rest of the solar cell device layers. The typical roughness of low-cost stainless-steel foils is in the hundred-nanometer range, which is comparable or larger than the thin film layers comprising the device and this may result in electrical shunts that decrease solar cell performance. This manuscript assesses the properties of different single-layer and bilayer structures containing ceramics inks formulations based on Al2O3, AlN, or Si3N4 nanoparticles and deposited over stainless-steel foils using a rotogravure printing process. The best control of the substrate roughness was achieved for bilayers of Al2O3 or AlN with mixed particle size, which reduced the roughness and prevented the diffusion of metals impurities but AlN bilayers exhibited as well the best electrical insulation properties.

We report a flexible high-performance conducting film using an embedded copper nanowire transparent conducting electrode; this material can be used as a transparent electrode platform for typical flexible optoelectronic devices. The monolithic composite structure of our transparent conducting film enables simultaneously an outstanding oxidation stability of the copper nanowire network (14 d at 80 °C), an exceptionally smooth surface topography (R(rms) < 2 nm), and an excellent opto-electrical performances (Rsh = 25 Ω sq(-1) and T = 82%). A flexible organic light emitting diode device is fabricated on the transparent conducting film to demonstrate its potential as a flexible copper nanowire electrode platform.