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Ferroelectric thin-film transistors (Fe-TFTs) have promising potential for flexible electronics, memory, and neuromorphic computing applications. Here, we report on a physics-based efficient device model for Fe-TFTs that effectively describes memory switching and device I–V characteristics. This model combines a stochastic multi-domain description of FE switching dynamics with a virtual source treatment of TFT device characteristics. It demonstrates that the memory window of Fe-TFTs depends on the amplitude and duration of the applied voltage pulses, thus suggesting quantitative means of programming and control. Additionally, we introduce a machine-learning-enabled method to automatically generate optimal voltage pulses for accurately programming multiple intermediate FE states, which is crucial for multi-bit memory and neuromorphic computing applications. To showcase the model's applications, we simulate a 4 × 4 crossbar array circuit based on Fe-TFTs, highlighting its utility in performing multiply-accumulate computing operations. This small array can achieve a high speed of ∼ 1.28 tera operations per second (OPS) and a power efficiency of ∼ 0.43 W/PetaOPS. The model developed here is valuable for exploring the capabilities of Fe-TFTs in future flexible memory and computing technologies. [ABSTRACT FROM AUTHOR]

Recently developed ductile inorganic semiconductors have opened a new avenue toward potential applications such as flexible electronics. Significant studies have been conducted based on different atomic models to understand the deformation mechanism using first-principle calculations; however, the comparative study on these atomic models remains unexplored. In this paper, taking Ag2S as an example, we simulated the slipping process using bulk, slab, and tilt-cell models. Systematic supercell tests were performed to investigate the convergence of the slip/cleavage energy based on the three atomic models. It was found that a reasonably large supercell is required to converge the slip/cleavage energy, and the ratio between minimum cleavage and maximum slip energy converges to a comparable value among different atomic models, where the tilt-cell and slab models show slightly higher energy ratio values compared with the bulk model. However, the comparison of different exchange-correlation functionals and van der Waals corrections indicates that the calculations of slip and cleavage energies are sensitive to the choice of calculation methods, highlighting the importance of using the same method for comparing slip and cleavage energies of different materials. This work provides insights into understanding different atomic models of ductility mechanisms in ductile inorganic semiconductors. [ABSTRACT FROM AUTHOR]

Cu2AgBiI6 films were prepared by a one-step spin coating method, and flexible memristors with an Ag/PMMA/Cu2AgBiI6/ITO structure were constructed. The devices showed a bipolar resistive switching behavior with low switching voltage, which is beneficial for reducing energy consumption. Furthermore, this study found that the device exhibits an endurance of about 900 cycles, a higher ON/OFF ratio of over 103, a long retention time (∼104 s), and high stabilities against mechanical stress. Remarkably, the present flexible memristor displayed extraordinary flexibility and stability, with no significant change for the resistive switching behavior even at various bending angles or after undergoing 900 bending cycles. This study establishes that the lead-free halide perovskite Cu2AgBiI6 can be used for the resistive random-access memory of flexible electronics. [ABSTRACT FROM AUTHOR]

It remains a challenge to produce soft robots that can mimic the responsive adaptability of living organisms. Rather than fabricating soft robots from bulk hydrogels,hydrogels are integrated into the interfacial assembly of aqueous two-phase systems to generate ultra-soft and elastic all-aqueous aquabots that exhibit responsive adaptability, that can shrink on demand and have electrically conductive functions. The adaptive functions of the aquabots provide a new platform to develop minimally invasive surgical devices, targeted drug delivery systems, and flexible electronic sensors and actuators.

Electronics today has evolved significantly, including its application in transparent and flexible devices. Flexible electronics offers new product concepts, including low production cost, low energy consumption, and sustainable and environmentally friendly materials. This concept leads to the development of novel materials that realize today's requirements. Incorporating optically transparent and flexible thin-film-based devices into the electronic circuitry helps in maintaining high conductivity along with achieving the similar electronic behavior of the conventional electronic gadgets. Thin-film diodes (TFDs) and thin-film transistors (TFTs) are the core materials to be incorporated as building blocks for flexible devices. Among them, oxide-based thin films have been marked to be significant because of their efficient electrical performance, low temperature processing, and device flexibility. The present article reviews the concepts and application of zinc oxide (ZnO) as the semiconducting material for flexible thin-film devices. We also review flexible and transparent TFDs and TFTs that are based prominently on ZnO as the semiconducting material. Furthermore, the present issues have also been addressed. [ABSTRACT FROM AUTHOR]

Carbon nanotube (CNT) based supercapacitors (SCs) were fabricated using magnesium phosphate (MgPO) as a redox material and recycled polypropylene (PP) as the mechanical support for the SC electrodes. Microscopy analysis indicated that the MgPO powder is composed of grains with sizes of 100–420 nm. Firstly, SCs were made with bare CNT electrodes, and these devices generated an energy density of 44.8 W h kg−1 and a maximum capacitance of 243.9 F g−1 (at 1 A g−1). Next, MgPO powder was added to the supercapacitor electrodes resulting in an increase of energy density and capacitance to 88.7 W h kg−1 and 443.8 F g−1, respectively. The CP increased even more (44%) after adding a mixture of MgPO/CuSO4 to the SC electrodes. Interestingly, the device made with MgPO/CuSO4 had the best electrochemical stability, with a capacitance retention of 92% after 500 cycles of charge–discharge. Spectroscopy analysis (XPS, UV-vis, and Raman) of the supercapacitor electrodes demonstrated the existence of the following redox species, which are useful to store charge: Mg2+/Mg0, oxygen vacancies, and P3+/P5+. The best device made with a mixture of redox powder MgPO/CuSO4 presented the highest capacitance (638.6 F g−1) because extra redox centers of Cu+/Cu2+ are found on its electrodes. Thus, combining magnesium phosphate materials and copper sulfate is a useful strategy not only to improve the electrochemical stability of carbon nanotube-based supercapacitors, but also to increase their capacitance/energy density, which are of interest for application in flexible electronics. [ABSTRACT FROM AUTHOR]

Ion‐conductive elastomers capable of damping can significantly mitigate the interference caused by mechanical noise during data acquisition in wearable and biomedical devices. However, currently available damping elastomers often lack robust mechanical properties and have a narrow temperature range for effective damping. Here, precise modulation of weak to strong ion‐dipole interactions plays a crucial role in bolstering network stability and tuning the relaxation behavior of supramolecular ion‐conductive elastomers (SICEs). The SICEs exhibit impressive mechanical properties, including a modulus of 13.2 MPa, a toughness of 65.6 MJ m−3, and a fracture energy of 74.9 kJ m−2. Additionally, they demonstrate remarkable damping capabilities, with a damping capacity of 91.2% and a peak tan δ of 1.11. Furthermore, the entropy‐driven rearrangement of ion‐dipole interactions ensures the damping properties of the SICE remain stable even at elevated temperatures (18–200 °C, with tan δ > 0.3), making it the most thermally resistant damping elastomer reported to date. Moreover, the SICE proves effective in filtering out various noises during physiological signal detection and strain sensing, highlighting its vast potential in flexible electronics. [ABSTRACT FROM AUTHOR]

Hydrogels hold great promise in the field of flexible electronics. Attempts in this area tend to the microstructure design of hydrogels, giving them specific adhesion and multi‐sensing functions. Here, a novel phase separation‐derived anisotropic adhesive structural color hydrogel film is presented for visually flexible electronics. The hydrogel film is generated by template replicating colloidal crystal by using phase separation emulsions of hydrophilic monomer (acrylic acid, AA), hydrophobic monomer (lauryl methacrylate, LMA), co‐monomer ([2‐(methacryloyloxy) ethyl] dimethyl‐(3‐sulfopropyl) ammonium hydroxide (SBMA)), surfactants (hexadecyl trimethyl ammonium bromide, CTAB) and initiator (ammonium persulphate (APS)). The appearance of phase separation results in asymmetric morphologies of hydrogel film, imparting them with anisotropic adhesive performance. Attributed to the formation of inverse opal scaffold structure, the hydrogel film is featured with vivid structural color, showing superior capability in self‐reporting mechanical behavior. Additionally, benefitting from the presence of abundant ions, the hydrogel film exhibits great conductivity. Thus, the resultant hydrogel film is demonstrated with stable dual‐signal sensing properties involving color‐changing and conductivity feedback ability to respond to human activities. These features make the proposed anisotropic adhesive structural color hydrogel film highly potential in the flexible electronic field. [ABSTRACT FROM AUTHOR]

Hydrogel‐based flexible solid‐state supercapacitors (SSCs) hold great promise for wearable electronics, yet significant challenges persist in simultaneously achieving excellent mechanical properties, high ionic conductivity, outstanding electrochemical properties, and wide operating temperature ranges. Here, this study presents a straightforward method for synthesizing dual crosslinked polyvinyl alcohol‐polyimide (PVA‐PI) organohydrogels via a simple one‐pot synthesis followed by a freezing‐thawing process. The controlled dual crosslinked networks with significanonetly different crosslinking densities and robust intermolecular hydrogen bonding interactions facilitated by the macromolecular crosslinker of PI, endow the organohydrogels with both high mechanical properties and ionic conductivity. Furthermore, SSCs based on PVA‐PI organohydrogels are fabricated, which can exhibit outstanding electrochemical performance at temperatures ranging from −40 to 80 °C. Specifically, the energy density reaches 16.7 µWh cm−2 even at −40 °C under a power density of 410.0 µW cm−2. These SSCs also show excellent performance stability under various deformations, such as bending and compression, alongside exceptional long‐term cycling stability (over 10 000 cycles) with high capacitance retention from −40 to 50 °C. The synthesis strategy, along with a robust mechanism for enhancing mechanical properties of hydrogels, demonstrated in this study offers insights for the development of strong hydrogels/organohydrogels with broad temperature adaptability for soft electronic applications. [ABSTRACT FROM AUTHOR]

Flexible lithium-ion batteries (LIBs) are receiving widespread attention, and how to obtain the high flexibility, safety, and energy density of LIBs at the same time are one of the main challenges in the field of flexible electronics. The multi-network structure formed by cellulose nanofiber (TOCNF) not only provided sufficient mechanical support and excellent flexibility for the electrode but also promoted uniform distribution of conductive agents and active materials. In this work, we prepared an eco-friendly TOCNF binder from wheat straw, using a method involving 2, 2, 6, 6-tetramethylpiperidinyl-1-oxyl oxidation and high-intensity ultrasonic treatment. Additionally, we enhanced the performance of TOCNF by introducing Li+ through ion exchange, resulting in lithium-functionalized cellulose nanofibers (TOCNF-Li), which were employed as a novel binder for LiFePO4 cathodes. The findings show that, when employing TOCNF-Li binder, batteries were able to obtain an initial discharge capacity of 163 mAh g–1 at 0.1 C rate and maintained 93.2% of the initial reversible capacity after 400 cycles at 2 C rate. Notably, at 5 C rate, the discharge capacity reached 133.7 mAh g−1, with a capacity decay of only 16.1%. TOCNF-Li played a role in increasing Li+ content, opening a new pathway for Li+ transport, consequently enhancing Li+ diffusion efficiency and charge–discharge performance. Overall, TOCNF-Li serves as a novel, environmentally friendly, and efficient binder for flexible LIBs. [ABSTRACT FROM AUTHOR]

With the development of nanotechnology, laser matter interaction has become intriguing for many applications, including the manufacturing of flexible electronics to improve interface behaviors. Employing high laser repetition rate nanojoining transfer patterning, this study ensures the robust and consistent stability of electrical properties of MWCNTs. This procedure meticulously eliminates contaminants from the interface between flexible PET substrates and carbon nanotube‐containing epoxy, significantly influencing the degree of alteration in composite material and interface behaviors. By increasing the laser repetition rate from the original sample to the sample irradiated by a laser with a repetition rate of 80 kHz, the defect concentration in carbon nanotubes decreases from 0.448 × 106/nm2 to 0.39376 × 106/nm2, respectively. The relationship between defect concentration and electrical conductivity in semiconductor carbon nanotubes under laser irradiation is multifaceted and context‐dependent. Optimizing the laser repetition rate is crucial in defining the kind and density of semiconductor carbon nanotubes. This study found an electrical conductivity of 3.6799 × 10−4 S/m at a laser repetition rate of 80 kHz. Laser ablation nanojoining with a high laser repetition rate is poised to become a key recycling method for plastic materials in future industries. When MWCNTs are used in processing new materials, this method not only enhances the electrical and mechanical properties of recycled plastics but also creates high‐performance composites with added value. Additionally, the quick nature of this process helps minimize toxicity in material processing by reducing exposure time and the need for harmful chemicals. These composites exhibit superior properties suitable for advanced applications such as flexible electronics, sensors, and nanocomposite materials, contributing to both sustainability and economic value in various industrial sectors. [ABSTRACT FROM AUTHOR]

Flexible and stretchable organic solar cells (FOSCs and SOSCs) hold immense potential due to their versatility and applicability in emerging areas such as wearable electronics, foldable devices, and biointegrated systems. Despite these promising applications, several challenges remain, primarily related to the mechanical durability, material performance, and scalability required for commercialization. This review comprehensively highlights recent advancements in the design and fabrication of FOSCs and SOSCs, with a particular emphasis on key functional layers, including transparent conductive electrodes, interfacial layers, photoactive materials, and top electrodes. Innovations in material design, such as active layers and transparent conductive electrodes with improved flexibility, are discussed alongside developments in device processes to achieve power conversion efficiencies exceeding 19%. Furthermore, the review addresses remaining challenges, including the need for scalable manufacturing techniques and enhanced mechanical robustness under strain. Finally, the prospects of FOSCs and SOSCs are analyzed, providing insights into how these technologies can contribute to the development of sustainable, high‐performance power sources for wearable electronic devices and other flexible electronics. This review offers valuable insights, bringing the commercialization of wearable, high‐performance FOSCs and SOSCs closer to reality. [ABSTRACT FROM AUTHOR]

Researchers and scientists have focused on the development and future opportunities of flexible sensors in food, environment and defense fields. In this study, we propose a flexible substrate material‐based nanofibril cellulose empty fruit bunch (NEFB)‐reinforced thermoplastic polyurethane (TPU) blend nanocomposite for flexible substrate materials. Untreated and treated nanofibril cellulose samples of empty fruit bunch (NEFB, 0, 1, 2, 3, 4 wt. %) were treated with 6 wt.% sodium hydroxide (NaOH) and subjected to internal Brabender mixer followed by a hot‐pressing machine. The density and tensile and dynamic mechanical properties of the nanocomposites were investigated for the treated and untreated samples. Tensile properties were characterized using a Universal Testing Machine, and the fracture mechanism after post‐tensile testing was determined by scanning electron microscopy (SEM). Increasing the content of untreated NEFB/TPU improved the tensile strength compared with 6% treated NEFB/TPU blend nanocomposites. Incorporating the nanofibril cellulose of empty fruit bunch at 2% into the TPU blend nanocomposites significantly increased E′, E" and Tg compared with other formulations. Highlights: Nanocellulose derived from plants is considered a promising material for flexible substrates in electronics due to its robust mechanical properties and eco‐friendliness.Malaysia's abundant empty fruit bunch (EFB) resources make it a possible source of nanocellulose, which improves the properties of polymers.The effect of sodium hydroxide (NaOH) treatment on the compatibility of EFB‐derived nanocellulose with polymer matrices was investigated.The addition of nanocellulose, particularly at a concentration of 1%, significantly increases the tensile strength of thermoplastic polyurethane nanocomposites, whereas 6% NaOH treatment has no effect.Dynamic mechanical analysis reveals high storage modulus at 2% nanofibril cellulose empty fruit bunch (NEFB) and energy dissipation at 4% NEFB as well as enhanced interfacial bonding at 1% NEFB. [ABSTRACT FROM AUTHOR]

Spintronics, micro/nanofabrication, and the semiconductor industry are undergoing significant transformations, highlighting the need for flexible technologie. This study examines the possibility of integrating topological insulators (TIs), specifically Bi2Te3 thin films (13–191 nm), into flexible spintronic applications through scalable magneto‐sputtering techniques, and investigates how structural organization influences electrical and topological properties through post‐thermal annealing. Films annealed above 250 °C display improved polycrystalline structure, larger crystallites, fewer local defects, and higher a room‐temperature Seebeck coefficient (S) and resistivity (ρ), suggesting decreased bulk electronic contributions. A metastable transport regime is identified in the temperature‐dependent resistivity of films annealed at 300 °C between 20–100 K; in this range, the thinnest film exhibits markedly metallic behavior, signaling the presence of topological surface states (TSS). Magnetoresistance measurements of as‐grown and annealed films, between 3–20 K, demonstrate weak antilocalization. Applying the Hikami‐Larkin‐Nagaoka model, α‐coefficients are found to scale with thickness from 0.5–1, indicating thickness‐controlled coupling of the TSS. Post‐annealing at 300 °C, the phase coherence length, Lϕ, of the thinner films increases, while the temperature dephasing rate shifts from ∼0.7 (as‐grown) to ∼0.5 (post‐annealing), aligning with expected values for 2D TSS. These are encouraging findings for large‐scale manufacturing flexible TI technologies, without sacrificing tunabilit. [ABSTRACT FROM AUTHOR]

As a type of bi-functional device, electrochromic supercapacitors (EC-SCs) have attracted extensive attention in diverse applications such as flexible electronics. However, despite recent encouraging progress, rational design and development of high-performance EC-SC materials with desirable stability remain challenging for practical applications. Here, we propose a fluorination strategy to develop high-performance EC-SC materials with tough hydrogen bonding cross-linked intermolecular polymer network by one-step electrosynthesis of 3-fluorothiophene. The electrosynthesized free-standing poly(3-fluorothiophene) (PFT) films simultaneously achieve high electrochromic performance (optical contrast 42% at 560 nm with reversible color changes between purple and blue), and good capacitance property (290 F·g−1, 1 A·g−1), as well as outstanding cyclic stability (<2% reduction after 20000 cycles). We further demonstrate the fabrication of PFT-based flexible electrochromic supercapacitor devices (FESDs), and the resultant devices can be used to visually monitor the energy storage state in real-time and maintain outstanding stability under mechanical distortion like bending. Such a tough fluorination hydrogen bonding cross-linking strategy may provide a new design concept for high-performance EC-SC materials and reliable FESDs toward practical applications. [ABSTRACT FROM AUTHOR]

The photovoltaic devices offer promising eco‐friendly solution for self‐powered flexible electronics. However, their fabrication on flexible substrate is not easy due to mismatches between the requirements of conventional microfabrication and the thermal, and mechanical features of the substrates. Herein, direct roll printed nanoscale photoactive electronic layers are presented, which are further processed to develop ≈315 µm2 sized miniaturized photovoltaic microcells. Using a set of 32 microcells, connected in parallel configuration, indoor light harvesting is shown at a maximum power density of ≈10 µW cm−2 under white LED illumination. Further, the dual functionality of developed microcells i.e., energy harvesting as well as wideband photodetection is demonstrated. As self‐powered photo sensors the developed photovoltaic microcells exhibit distinctive photo responses under white LED‐UV (365 nm)‐ NIR (850 nm) light illumination, with exceptionally high‐speed response (rise time τRise = 205 µs and fall time τFall = 2000 µs), and a peak responsivity of 2.48 A W−1 to UV light at zero bias voltage. The presented results show the potential usage of printed multifunctional photovoltaic microcells in a wide variety of applications such as self‐powered wearable and flexible electronic systems for health monitoring and indoor robotics. [ABSTRACT FROM AUTHOR]

At the forefront of technological advancement, the proliferation of portable and wearable electronics has necessitated the development of innovative power solutions. As these devices become increasingly indispensable in daily life, the demand for sustainable and adaptable power sources has intensified. This review focuses on integrated self‐charging power systems (SCPSs), which synergize energy storage systems, particularly through rechargeable batteries like lithium‐ion batteries, with energy harvesting from solar, mechanical, thermal, and chemical energy. These SCPSs extend operational times, reduce recharging frequency, and have the potential to develop self‐sufficient power systems. The study explores various approaches to optimize both individual components and the integrated power system for wearable and flexible electronics, covering SCPSs that combine multiple energy‐harvesting strategies. Special attention is given to design considerations, material advancements, and engineering challenges, alongside the latest research breakthroughs in energy harvesting and storage technology. The review concludes with an assessment of the prospects and challenges in the field of battery‐integrated energy harvesting systems, highlighting the need for advancements in energy density, power output, and safety to meet the demands of modern electronics. [ABSTRACT FROM AUTHOR]

There is a pressing need for flexible integrated systems owing to the swift progress of flexible electronics. Apart from flexibility, flexible supercapacitor (FSC) integrated systems exhibit certain characteristics like rapid charge–discharge rates, high power density, and excellent cycling stability, which makes them a promising candidate to serve as a vital component in flexible electronics. In this context, an in‐depth overview of recent progress in FSC‐integrated systems, including their design of structure, materials, fabrication techniques, and applications, is offered. On the basis of the current progress, the existing challenges and future prospects are also outlined and discussed. [ABSTRACT FROM AUTHOR]

As the development of flexible electronics continuously progresses, so does the demand for fabricated 3D electrodes via patterning technology. Electrochemical replication and transfer (ERT) has emerged as an efficient patterning technique, which deposits materials of interest on a predefined template via electroplating and subsequently transfers them onto target substrates. ERT can pattern large‐area 2D electrodes on nontraditional substrates whilst maintaining adequate flexibility, stretchability, and complex surface structures. This study extends the capability of ERT from 2D into 3D patterning. Via the rational design of a 3D SiO2/Si template, in which conductive Si trenches or holes are patterned with insulating SiO2 banks, electroplating of materials only occurs in the exposed Si surfaces so that both continuous and isolated 3D patterns with high aspect ratios up to 4:1 are realized. 3D‐ERT offers a high‐throughput and low‐cost approach to fabricating high Figure of Merit (>30 000) flexible transparent electrodes. Also, the application of 3D‐ERT in constructing highly sensitive, and self‐powered pressure sensors is showcased. [ABSTRACT FROM AUTHOR]

The hunt for sustainable and efficient energy harvesting and storage devices has driven significant interest in triboelectric nanogenerators (TENGs) as potential alternatives to traditional batteries for powering electronic devices. However, the development of biodegradable TENGs remains a formidable challenge. This study presents the preparation of a tribopositive material entirely composed of biodegradable poly(butylene adipate-co-terephthalate) (PBAT) polymer enhanced with CoFe2O4 (CF) nanoparticles. The CF nanoparticles, synthesized via the combustion method, were incorporated into the PBAT matrix through solvent casting to form films with varied filler content (0.2, 0.4, 0.6, 0.8, and 1 g). The CF nanoparticles structural, surface, and electrical properties were characterized using XRD and FTIR spectroscopy. At the same time, the morphology of the nanomaterials and their composites was analyzed by scanning electron microscopy. Specifically, the 0.8 g PBAT-CF TENG demonstrated superior performance, achieving an output voltage of 45.45 V and a current of 4.5 µA. Subsequent electrical studies, including charging commercial capacitors (1.0 to 47 μF) and powering LEDs and calculators, underscored the device's efficiency. The PBAT-CF TENG also effectively generated voltage and current signals from physical activities like walking and jumping. This innovative approach highlights the potential for biodegradable, high-performing, self-powered flexible electronics, and wearable devices, paving the way for sustainable technological advancements. [ABSTRACT FROM AUTHOR]

The development of flexible electronics technology has led to the creation of flexible energy storage devices (FESDs). In recent years, flexible self‐supporting cathodes have gained significant attention due to their high energy density, excellent mechanical performance, and strong structural plasticity among various cathode materials. Flexible self‐supporting cathodes enable larger active material loading capacity and conductive networks for electrodes, thereby perfectly meeting the mechanical and electrochemical performance requirements of FESDs. Currently, the focus of flexible self‐supporting cathodes lies in exploring flexible substrates or novel binders to enhance the flexibility of conventional cathode materials. However, the flexibility of cathode poses challenges as they are primarily composed of transition metal oxides, resulting in limited research on their flexibility. A comprehensive review and prospective analysis are of utmost importance to effectively advance the progress of flexible self‐supporting cathodes and propel their development forward. Herein, the present discourse delves into the latest advancements concerning flexible self‐supporting cathode, focusing on synthesis methodologies, structural design approaches, and characterization parameters. Examining the current progress, the inherent advantages, existing challenges, and potential prospects of these materials are comprehensively elucidated and emphasized. [ABSTRACT FROM AUTHOR]

Lightweight, flexible and highly conductive electromagnetic interference (EMI) shielding materials are of great importance for protecting flexible electronics and telecommunication devices under extremely high temperature conditions. A potential solution is to incorporate ceramic phases with highly conductive flexible carbon nanotube films to improve their thermal stability. However, the grain size of the ceramic phase generally increased significantly as the temperature increased which led to brittleness. In this work, a highly flexible carbon nanotube (CNT) film with controllable ceramic nanocrystals was prepared by precursor infiltration and pyrolysis. The silicon carbide (SiC) grain size in the nanocomposites was inhibited by the spatial confinement effects of CNT networks and a second amorphous SiBCN phase. The SiC grain size in the composite film decreased with the increase of the SiBCN content and the elongation at break of the nanocomposites improved significantly by 45 %. Moreover, the initial thermogravimetric temperature of the prepared films has been significantly improved to exceed 600 °C compared to the raw CNT film. Importantly, the nanocomposite film exhibited an average EMI shielding effectiveness of ∼40 dB from 8.2 to 12.4 GHz. Benefiting from the ultrafine grain size, the nanocomposite films could be folded and extended without micro-cracks over 1000 times. Combining the performance and mechanical properties of the nanocomposite film, this approach provides important guidance for designing high-performance CNT-based electromagnetic shielding materials with superior flexibility at elevated temperatures. [ABSTRACT FROM AUTHOR]

[Display omitted] Electrically conductive fiberfibre/fabric composites (ECFCs) are competitive candidates for use in wearable electronics. Therefore, it is essential to develop mechanically robust ECFC strain sensors with sensing performance. In this study, MXene assembly and hot-pressing were combined to prepare strong yet breathable ECFCs for strain and temperature sensing. Hydrogen bonding between MXene and polyurethane (PU) and ultrasonication-induced interfacial sintering were responsible for MXene nanosheets assembly on the PU nanofibers. MXene decoration made PU nanofibers electrically conductive, resulting in a conductive network. Hot-pressing improved interface adhesion among the conductive nanofibers. Thus, the mechanical properties of the nanofiber composites, including tensile strength, toughness and fracture energy, were enhanced. The nanofiber composites exhibited surface stability and durability. When the nanofiber composites were used as strain sensors, they showed breathability with a linear resistance response ranging from 1 % to 100 % and cycling stability. In addition, they produced stable sensing signals over 1000 cycles when a notch was present. They could also monitor temperature variations with a negative temperature coefficient (−0.146 %/°C). This study provides an interfacial regulation method for the preparation of multi-functional nanofiber composites with potential applications in flexible and wearable electronics. [ABSTRACT FROM AUTHOR]

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With the constant increase of electronic waste globally, society is demanding and governments are boosting the development of electronics with less pollutant materials and reduced environmental impact. One way to achieve this is to implement materials that are functional and structural at the same time, reducing material use and assembling parts. Further, printing techniques, such as screen printing, reduce considerably costs and time compared with conventional electronics; combined with methods to conform printed electronics to a 3D shape, such as thermoforming, allow to obtain nonplanar surface electronics simply and efficiently. Herein, screen‐printable inks made of styrene–ethylene/butylene–styrene and different aspect‐ratio carbon‐based materials for conformable electronics are reported. The inks are prepared with carbon black, carbon nanotubes, and reduced graphene oxide as conductive fillers, printed on a flexible substrate and thermoformed. Carbon black and carbon nanotube samples are functional after the process, with conductivities of 96 and 141 S m−1 for the best performing sample of each filler, respectively. Rheological, morphological, thermal, and electrical properties of the materials are also characterized. This study shows the influence of the filler's type and aspect ratio on the morphology and electrical conductivity of the printed materials before and after thermoforming. [ABSTRACT FROM AUTHOR]

Mica is a promising substrate for flexible photonic applications because it can be fabricated using wafer‐scale multiple exfoliations. However, the large lattice mismatch between mica and III‐nitrides hinders their application in III‐nitride semiconductor devices. In this study, two types of light‐emitting diode (LED) epilayers, blue and green, are epitaxially fabricated on 2‐inch exfoliated mica substrates using sputtered AlN as a buffer layer to address the lattice mismatch. The LED epilayers on mica substrate exhibit excellent single‐crystalline quality with a low threading dislocation density of 2.07 × 109 cm−2 in the GaN region and smooth surface morphology with a root mean square (RMS) roughness of 0.58 nm in a 5 × 5 µm2 scanned area, demonstrating that mica is an excellent platform for III‐nitride semiconductors. Moreover, the structures are reproduced stably on multiple exfoliated mica at the wafer scale, which verified the reusability and reproducibility of III‐nitride/mica in terms of crystallinity, surface morphology, and transparency. Strong electroluminescence of the LED epilayers confirmed the potential of mica in electrically driven flexible opto‐electronics. Therefore, this results demonstrated the potential of mica substrates in III‐nitride semiconductors and provide a novel pathway for revolutionizing the fabrication of III‐nitride‐based flexible devices. [ABSTRACT FROM AUTHOR]

Dielectrics are non‐conducting substances that are primarily utilized to hold electric charges. These materials are widely employed in the field of chemical mechanical, civil and structural engineering, because of their inherent insulating properties. Besides these domains, dielectric materials are also used in electrical and electronic applications. Dielectric materials have shown an ever‐increasing potential in recent years in the fabrication of antennas, sensors, and optical devices that are extensively utilized for on‐body, environmental, robotics, and biomedical applications. With inherent electrostatic shielding, insulation, and dielectric relaxations, these materials are used in intelligent electronic devices used for biomedical applications, smart devices, vehicles, and future IoT applications. Numerous applications necessitate multiple kinds of dielectric, classified based on their polarization, flexibility, thickness, dielectric constant, and specific application. In this extensive research review, the characteristics and various aspects of dielectric materials are discussed, followed by a thorough and detailed review of flexible dielectrics and their usage in flexible electronics. Additionally, the practicality and applications of these materials which come from a variety of publications in the literature are also discussed. Moreover, in‐depth study of dieletrics in sensors and RF applications are performed. [ABSTRACT FROM AUTHOR]

The article discusses the development of indoor solar cells to power the increasing number of IoT devices expected to be used indoors. Researchers are focusing on materials that can harvest indoor light efficiently, with organic photovoltaics, dye-sensitized solar cells, and perovskite solar cells being key technologies. Companies like Epishine, Saule Technologies, and Oxford PV are already showcasing products powered by indoor solar technologies, indicating a growing interest in integrating solar cells into electronics for sustainable energy solutions. [Extracted from the article]

The development of multifunctional supramolecular nanocomposite hydrogels remains challenging. Here, the dynamic host–guest interactions involving the host molecule CB[8] and guest units were utilized to prepare Fe3O4 hybrid supramolecular nanocomposite hydrogels. The results showed that the hydrogels obtained possessed a porous structure. The CB[8]‐modified Fe3O4 (Fe3O4@CB[8]) nanoparticles served as cross‐linkers in forming the network of hydrogels. By adjusting the Fe3O4@CB[8] content, the mechanical properties of the hydrogels could be controlled. The tensile stress was measured at 160 kPa with a fracture strain of 1380%, while the compression stress was 230 kPa at 70% compression strain. The self‐healing efficiency of the hydrogels at room temperature reached 95% after 24 h. The as‐obtained hydrogels show strain sensitivity and have the potential for applications in detecting elbow and finger movements. Our supramolecular nanocomposite hydrogels exhibit multiple functions, including self‐healing, injectability, photothermal responsiveness, and conductivity, making them suitable for integration into flexible electronics. Highlights: Fe3O4@CB[8] nanoparticles serve as cross‐linkers for the nanocomposite hydrogels.CB[8] based host–guest interactions enable hydrogels to self‐heal.Fe3O4@CB[8] endow hydrogels with stretchability and photothermal responsiveness.Hydrogels exhibit injectability, NIR responsiveness, and conductive ability. [ABSTRACT FROM AUTHOR]

Flexible electrochromic devices (FECDs) are promising candidates for the next generation of wearable electronics due to their low operating voltage and energy consumption. For the flexible electrochromic devices, the electrolyte is an important component. Typically, the electrolyte needs to be formulated according to the device structure and usage scenario. A high-performance electrolyte involves consideration of many factors, including choosing the right polymer, solvent, curing agent, and ion type to satisfy particular device specifications. In this work, a ultraviolet-curable solid–liquid host–guest (UV-SLHG) electrolyte is developed. Several aspects of performance are improved by introducing the solid–liquid coexisting microstructure without changing the electrolyte formulation, including excellent adhesion, a 30% increase in tensile characteristics, and a seven-fold increase in ionic conductivity when compared to a fully cured solid-state electrolyte. More importantly, the unique advantage of SLHG electrolytes lies that the thickness will not change significantly during bending. The FECD made by using the UV-SLHG-based electrolyte sustained 10,000 bending cycles at the bending radius of 2.5 mm while maintaining outstanding optical modulation. A wearable ring-type ECD and a battery-free FECD wine label were made as demonstrators. The UV-SLHG strategy is not only suitable for the FECDs but also universally applicable to other electrolyte-based of flexible electronics such as flexible capacitors and batteries. [ABSTRACT FROM AUTHOR]

Efficient electrical control of magnetic property is critical for the development of various spintronics. However, traditional magnetoelectric devices require adoption of piezoelectric component, resulting in complicated device architecture and complex conditioning circuit. More importantly, traditional strain-mediated magnetoelectric structures could not be developed in flexible form due to the existence of magnetostrictive component, which could be easily affected by mechanical deformation in flexible devices. Here we have systematically investigated pure current control of the magnetic properties of La0.7Sr0.3MnO3 thin films. Ferromagnetic to paramagnetic phase transition has been realized with a small current density of 5.2 × 103 A/cm2, which is three orders smaller than the working current density of spintronics based on spin-orbit torque and spin-transfer torque. The effective tuning of magnetic property has been attributed to the current induced Joule heating effect. For La0.7Sr0.3MnO3 film grown on flexible Mica with a smaller thermal conductivity, dramatic change of ferromagnetic resonance field of 1340 Oe and nonvolatile magnetization switching have been achieved with an ultra-small current density of 7.4 × 102 A/cm2. These results represent a crucial step towards effective electrical control of both static and dynamic magnetic properties in flexible magnetic thin films and open a new avenue for exploring electrical controlled flexible spintronics. [ABSTRACT FROM AUTHOR]

Stretchable electrodes are essential parts for flexible electronics which are widely applied in human health monitoring, wearable electronics, robotics etc. Conductive elastomer composites are good candidates for stretchable electrodes; however, it is a challenge to maintain the resistance of conductive elastomer composites during elongation due to the departure of filler networks. In this work, highly stretchable and conductive polydimethylsiloxane (PDMS)/nickel‐coated graphite (NCG) composites were fabricated based on the filler sedimentation method, in which NCG was modified by the coupling agent of the end alkyl group (dodecyltriethoxysilane, DTES) and end vinyl group (vinyltriethoxysilane, VTEO), considering the force between the filler networks and filler–matrix interface. The DTES modified NCG mainly improved the filler–matrix interface, which made the resistance of the composites clearly increase with strain, while the VTEO mainly heightened the NCG networks and made the resistance of the composites insensitive to a strain of 114% when the NCG content was 23.1 wt%. These quite interesting results are closely related to the force between the filler networks and filler–matrix interface during strain and they were proved in detail through the mechanical and electrical hysteresis performance. This work presents a facile method from the concept of stability of filler networks during strain to prepare highly stretchable and conductive composites. © 2024 Society of Chemical Industry. [ABSTRACT FROM AUTHOR]

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Researchers have created a modern infrared (IR) sensor that is both super-sensitive and highly flexible. This remarkable device possesses impressive properties of exceptional sensitivity (24,000%), high responsiveness (1.25 A/W), and fast response time (3 ms). This innovation stands out for its unique construction: an ultrathin layer of lead sulfide (PbS) deposited on a standard Whatman filter paper. This design achieves a photo-current 32 times greater than previous record-holding PbS thin films. The key advantage is its unmatched flexibility. This sensor can bend and flex without breaking, maintaining its IR detection capabilities even after enduring extreme bending cycles. This breakthrough paves the way for a new era of wearable IR photo sensors, flexible electronics, and medical applications. [ABSTRACT FROM AUTHOR]

The field of flexible electronics has experienced remarkable expansion in response to the escalating demand for lightweight, bendable, and multifunctional electronic devices. As the world increasingly integrates electronics seamlessly into everyday life, the importance of flexible electronics becomes more apparent. While existing reviews have examined materials used in flexible devices, they often overly focus on specific materials or provide broad generalizations about different material types. Thus, this review offers a concise yet comprehensive overview of critical inorganic film materials crucial to the advancement of flexible and wearable devices. Each material is introduced with a succinct overview of its structure and production processes. This review elucidates their unique characteristics and potential applications in flexible electronics by comparing their mechanical, electrical, and thermal properties. This review is a valuable resource for researchers entering this emerging field of flexible electronics, providing a concise yet comprehensive insight and property comparisons. Accompanied by figures illustrating material structures and applications, readers will gain access to summarized discussions. Comparative figures of material properties will enhance comprehension. Additionally, discussions on diverse applications will offer insight into their versatility across various fields of flexible electronics. [ABSTRACT FROM AUTHOR]

The solution-processed organic thin-film transistors (OTFTs) with a minimal device footprint and improved performance are desirable for flexible electronics and other circuit applications. It is demonstrated that the enhanced performance can be achieved for solution-processed OTFTs by adopting an improved Corbino structure. The bottom-gate bottom-contact OTFTs of W/L ratio of 500 are fabricated using the standard poly-3-hexylthiophene (P3HT) as a semiconductor with an improved interdigitated pseudo-Corbino (IPC) structure. The exhibited IPC structure is a combination of interdigitated structure in the enclosed-Corbino design to achieve infinite output resistance, suppressed parasitic leakage current, and high ON current by accommodating a high W/L ratio in a minimal device footprint. For the fabricated solution-processed OTFTs, infinite output resistance with an OFF-current of the order of 1 0 − 12 A and an ON/OFF ratio of drain current of the order of 1 0 7 is achieved. Incorporating an enhanced hexamethyldisilazane treatment of the Si O 2 gate dielectric improves the ON/OFF ratio to a record value of 1 0 8 and the mobility of the order of 1 0 − 2 cm 2 / Vs for P3HT. Implementation of IPC-TFT structure for intentionally chosen moderate-mobility, solution-processed P3HT semiconductor results in a consistent low OFF-current, high ON/OFF ratio, and infinite output resistance with excellent device-to-device uniformity. [ABSTRACT FROM AUTHOR]

Flexible resonant acoustic sensors exhibit enhanced sensitivity near their resonant frequencies and have attracted increasing interest as essential components for next‐generation human‐machine speech interactions. However, membrane‐based resonant acoustic sensors are bulky owing to the inherently high bending stiffness of the sensing membrane. Inspired by the tiny hair‐based sensitive acoustic receptors of spiders, this study reports a hair‐like piezoelectric resonant acoustic particle velocity sensor (HP‐APVS) that enables highly sensitive sound sensing with a significantly reduced size. The HP‐APVS device is essentially a polyimide cantilever array fabricated using Nb0.02‐Pb(Zr0.6Ti0.4)O3 (PZT) on polyimide and self‐bending processes. The experimental results demonstrate that the HP‐APVS shows a linear response to acoustic particle velocity instead of acoustic pressure, with enhanced sensitivity in the resonance mode. Additionally, the proposed HP‐APVS exhibits an outstanding speaker recognition rate of 95.3% with an error rate reduction of 75% compared with that of a reference commercial microphone, indicating many potential applications in the realms of biometric authentication, voice user interfaces, and other intelligent acoustic electronics. [ABSTRACT FROM AUTHOR]

The one-step direct laser writing process has been an efficient strategy for constructing flexible metal structures. However, the effect of laser wavelength on the structuring process remains unclear, thus restricting the universal manufacturing process development. In this work, the feasibility of one-step writing of flexible Cu structures with different wavelength continuous diode lasers has been verified. Here, photothermal reactions dominate in the decomposition of the reducing agent to form copper structures. Differences in the wavelength primarily affect the photothermal reaction amplitude for structuring, resulting in a variation in the formation of Cu structures. Under our processing conditions, the photothermal reaction induced by 532 nm laser is higher than 808 nm laser, a higher reduced-joining degree of the Cu structure can be achieved by 532 nm laser. This results in a superior conductivity, adhesion, and bendability of Cu structures fabricated by 532 nm laser than that of 808 nm laser. Furthermore, strain sensors that can detect different bending angles and bending frequencies have been fabricated by 532 nm laser-written structures to demonstrate their practical applications. [ABSTRACT FROM AUTHOR]

The rising flexible and intelligent electronics greatly facilitate the noninvasive and timely tracking of physiological information in telemedicine healthcare. Meticulously building bionic-sensitive moieties is vital for designing efficient electronic skin with advanced cognitive functionalities to pluralistically capture external stimuli. However, realistic mimesis, both in the skin's three-dimensional interlocked hierarchical structures and synchronous encoding multistimuli information capacities, remains a challenging yet vital need for simplifying the design of flexible logic circuits. Herein, we construct an artificial epidermal device by in situ growing Cu3(HHTP)2 particles onto the hollow spherical Ti3C2Tx surface, aiming to concurrently emulate the spinous and granular layers of the skin's epidermis. The bionic Ti3C2Tx@Cu3(HHTP)2 exhibits independent NO2 and pressure response, as well as novel functionalities such as acoustic signature perception and Morse code-encrypted message communication. Ultimately, a wearable alarming system with a mobile application terminal is self-developed by integrating the bimodular senor into flexible printed circuits. This system can assess risk factors related with asthmatic, such as stimulation of external NO2 gas, abnormal expiratory behavior and exertion degrees of fingers, achieving a recognition accuracy of 97.6% as assisted by a machine learning algorithm. Our work provides a feasible routine to develop intelligent multifunctional healthcare equipment for burgeoning transformative telemedicine diagnosis. Highlights: A smart wearable alarming system integrated artificial epidermal device for pluralistically identifying asthmatic attack risk factors, achieving a 97.6% classification accuracy as assisted by machine learning algorithm. A meticulous mimicry both in the advanced structural attributes and encoding information abilities of the skin was adopted to design a novel artificial epidermal device by integrating conductive Cu3(HHTP)2 coupled with spherical Ti3C2Tx. The bioinspired Ti3C2Tx@Cu3(HHTP)2 sensors can independently perceive NO2 gas and pressure-triggered stimuli. [ABSTRACT FROM AUTHOR]

An innovative approach has been adopted through the synthesis of a cost‐effective ferroelectric host polymer, which was integrated with Barium Titanate (BaTiO3) to develop an efficient electrospun Polyvinylidene Fluoride‐Hexafluoropropylene/BaTiO3 (PVdF‐HFP/BaTiO3) nanocomposite (PBT), designated for energy harvesting and piezocatalytic applications. FT‐IR affirmed the existence of the crystalline β‐phase within the nanofibers. SEM images showed that nanofiber diameter decreases as applied voltage is increased in electrospinning. The BaTiO3 nanoparticles were scattered evenly in PBT, but at lower voltages, they aggregate. PBT showed enhanced piezoelectric performance under higher voltage conditions, registering a maximum piezoelectric output of ~7.7 V and an output current of 0.77 μA. Moreover, the composite exhibited a power density of 14.15 mW/m2 at a load resistance of 20 MΩ. Fabricated piezoelectric nanogenerator (PENG) demonstrated practical utility in flexible electronics, notably in charging capacitors of 0.47 μF and 1 μF. Additionally, the piezocatalytic degradation of the antibiotic ciprofloxacin (CIP) was effectively achieved using the electrospun nanofibers, with an impressive degradation rate of up to 99.6 % within 30 minutes under acidic conditions, and the material displayed notable reusability, maintaining up to 95.5 % efficiency after five cycles. DFT calculations and COMSOL simulations alongside a comparative examination of the electronic properties of PBT. [ABSTRACT FROM AUTHOR]

Flexible electronics have revolutionized various industries by offering lightweight and conformable solutions for diverse applications. However, their vulnerability to environmental factors, particularly moisture, remains a critical challenge. Polymer composite coatings enriched with superhydrophobic properties have gained considerable attention as a promising solution to safeguard flexible electronics. The present research report is a comprehensive review of the recent advancements in the development and application of superhydrophobic polymer composite coatings in flexible electronics, highlighting its potential applications in sensors and EMI shielding. The improvement in superhydrophobic characteristics hinges upon the choice of materials, fabrication techniques, surface morphology, and topographical features. This review article elaborates on the selection criteria for various organic and inorganic fillers suitable for polymers possessing innate hydrophobic or conducting properties. The different materials used as fillers in polymer matrix for fabricating superhydrophobic coating, the factors affecting the superhydrophobic properties of surfaces, and the superhydrophobic properties of fabricated surfaces using different materials have been reported. [ABSTRACT FROM AUTHOR]

Lanthanum nickel oxide (LaNiO 3, LNO) films exhibit excellent electrical conductivity but poor mechanical properties, considerably limiting their further development in the field of flexible electronics. In this study, flexible LNO thin films of different thicknesses were fabricated on a unique two-dimensional (2D) mica platform using a simple metal organic deposition technique. The obtained LNO films exhibited a pseudocubic phase without impurities. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) characterisations proved that the films were well-crystallised, dense, and flat, with controllable thickness. In addition, the flexible LNO/mica element possesses low resistivity (5 × 10−4 Ω cm), translucency, and good bending resistance. The electrical resistivity can remain stable under various bending radii (r = 10∼2 mm), thousands of bending cycles, and a wide temperature range (28–200 °C), demonstrating good durability, mechanical stability and temperature resistance. Furthermore, a ferroelectric BiFeO 3 film was constructed based on the obtained conductive LNO electrode, which exhibited typical ferroelectric characteristics. This excellent performance suggests that the flexible LNO electrode is promising for flexible electronic applications. [ABSTRACT FROM AUTHOR]

Natural polymer substrates are gaining attention as substitutes for plastic substrates in electronics, aiming to combine high performance, intricate shape deformation, and environmental sustainability. Herein, natural wood veneer is converted into a transparent wood film (TWF) substrate. The combination of 3D printing and origami technique is established to create programmable wood-based origami electronics, which exhibit superior flexibility with high tensile strength (393 MPa) due to the highly aligned cellulose fibers and the formation of numerous intermolecular hydrogen bonds between them. Moreover, the flexible TWF electronics exhibit editable multiplexed configurations and maintain stable conductivity. This is attributed to the strong adhesion between the cellulose-based ink and TWF substrate by non-covalent bonds. Benefiting from its anisotropic structure, the programmability of TWF electronics is achieved through sequentially folding into predesigned shapes. This design not only promotes environmental sustainability but also introduces its customizable shapes with potential applications in sensors, microfluidics, and wearable electronics. Wood-based electronics are typically constrained in their ability to undergo complex shape deformation. Here, authors integrate transparent wood film and cellulose-based conductive ink for flexible electronic origami devices that have been demonstrated as a proof-of-concept for human motion sensors. [ABSTRACT FROM AUTHOR]

Flexible and biodegradable electronics have emerged as a promising solution for escalating electronic waste issue caused by the rapid development of skin patch electronics. Fully biodegradable displays are essential for visualizing biological/physical/chemical/electrochemical signals measured by a wide range of skin patch electronics. Here we propose fully biodegradable electrochromic display providing low operating voltage and low power consumption. The biodegradable transparent conductive electrode was fabricated by transferring free-standing tungsten nanomesh onto poly lactic-co-glycolic acid substrate using electrospinning templating, minimizing damage to the substrate. Electrochromic layer was tungsten oxide which is biodegradable, and a ferrocyanide/ferricyanide redox agent was utilized as a counter electrode reaction to enhance operational stability in an aqueous electrolyte by reducing operating voltage and side reactions. This display successfully visualized diverse signals from various biodegradable electronics such as UV sensors and electrochemical transistors, and finally underwent eco-friendly degradation in phosphate-buffered saline or soil under mild conditions. [ABSTRACT FROM AUTHOR]

The growing demand for wearable healthcare devices has led to an urgent need for cost-effective, wireless and portable breath monitoring systems. However, it is essential to explore novel nanomaterials that combine state-of-the-art flexible sensors with high performance and sensing capabilities along with scalability and industrially acceptable processing. In this study, we demonstrate a highly efficient NiS2-based flexible capacitive sensor fabricated via a solution-processible route using a novel single-source precursor [Ni{S2P(OPr)2}2]. The developed sensor could precisely detect the human respiration rate and exhibit rapid responsiveness, exceptional sensitivity and selectivity at ambient temperatures, with an ultra-fast response and recovery. The device effectively differentiates the exhaled breath patterns including slow, fast, oral and nasal breath, as well as post-exercise breath rates. Moreover, the sensor shows outstanding bending stability, repeatability, reliable and robust sensing performance and is capable of contactless sensing. The sensor was further employed with a user-friendly wireless interface to facilitate smartphone-enabled real-time breath monitoring systems. This work opens up numerous avenues for cost-effective, sustainable and versatile sensors with potential applications for Internet of Things-based flexible and wearable electronics. This article is part of the theme issue 'Celebrating the 15th anniversary of the Royal Society Newton International Fellowship'. [ABSTRACT FROM AUTHOR]

Reaping the benefits of the burgeoning investigation of gels in recent decades, flexible electronics based on conductive gels have been extensively explored. Gels consisting of polymer networks and solvents provide ideal platforms for fabricating flexible electronics due to their soft mechanical nature, excellent biocompatibility, water‐like environment, and ease of processing. The majority of investigations of flexible electronics primarily focus on functionalities such as sensing capability, energy density, luminance, fluctuating frequency, and so on, whereas the distinguishing feature of flexible electronics lies in its inherent deformable mechanics in comparison to metal‐ or semiconductor‐based stiff electronics. However, the comprehensive design and investigation of the mechanical properties of deformable conductive gels have not received sufficient attention to improve the overall performance of flexible electronics. A comprehensive summary is provided, listing six crucial mechanical parameters—stretchability, modulus, strength, elasticity, hysteresis, and fatigue—which exert significant influence on the functionalities of flexible electronics. This review aims to direct researchers’ attention toward the mechanical design of deformable conductive gels and presents representative strategies for their mechanical modulation. [ABSTRACT FROM AUTHOR]

Conjugated polymers (CPs) have emerged as pivotal functional materials in the realm of flexible electronics and optoelectronic devices due to their unique blend of mechanical flexibility, solution processability, and tunable optoelectronic properties. This review synthesizes the latest molecular simulation-driven insights obtained from various multiscale modeling techniques, including quantum mechanics (QM), all-atomistic (AA) molecular dynamics (MD), coarse-grained (CG) modeling, and machine learning (ML), to elucidate the optoelectronic, structural, and thermomechanical properties of CPs. By integrating findings from our recent computational work with key experimental studies, we highlight the molecular mechanisms influencing the multifunctional performance of CPs. This comprehensive understanding aims to guide future research directions and applications in the modeling assisted design of high-performance CP-based materials and devices. [ABSTRACT FROM AUTHOR]

Polydiacetylenes (PDAs) are renowned for their exceptional optical properties intricately linked to the polymer conformation, yet they exhibit poor conductivity in their undoped state. Despite this drawback, PDAs have garnered significant interest as sensing materials owing to their ability to undergo colorimetric shifts from blue to red in response to external stimuli. However, the irreversible nature of this transition has limited their utility in dynamic environments. In this study, we augment the sensing capabilities of PDA films beyond their irreversible optical response by inducing a reversible electronic response through conductivity modulation. We investigated polyamine‐substituted PDAs with enriched hydrogen‐bonding interaction sites for the concurrent changes in colorimetry and conductivity upon acetic acid (AA) vapor exposure. Coated on a flexible interdigitated electrode (IDE), we monitor the conductivity change throughout the blue‐to‐red phase transition. Remarkably, AA molecules act as dopants, significantly amplifying the system's conductivity. Although the PDA coating retains its red phase at postdopant removal, the electronic response reverts to its initial state, demonstrating reversibility. This reversible electronic response offers invaluable real‐time insights into the specific triggers within dynamic environments, underscores the adaptability of responsive conjugated polymers, and highlights a promising avenue for their utilization in various sensing and monitoring applications. [ABSTRACT FROM AUTHOR]