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Bacterial infections and multiple encrustations are life-threatening complications in patients implanted with urological devices. Limited by time-consuming procedures and substrate dependence, it is difficult to simultaneously prevent the aforementioned complications. Herein, is reported the design of a salt-triggered chondroitin sulfate complex (CS/Si-N+ ) coating with adaptive dissociation, which realizes the dual functions of antibacterial and anti-multiple encrustations in urological devices with arbitrary shapes. The existence of covalent interactions between the complex and the interface ensures the formation of a robust coating, especially in harsh environments. Benefiting from the adaptive dissociation of the ion pairs in the CS/Si-N+ coating in urine electrolytes, the exposed ion groups and enhanced hydrophilicity are more conducive to the inhibition of bacterial infection and multiple encrustations simultaneously. The coating exhibits broad-spectrum bactericidal effects. As a proof of concept, in a simulated metabolic encrustation model, the coating exhibits significant advantages in resisting calcium oxalate encrustation, with a reduction in the calcium content by over 90%. In addition, this non-leachable all-in-one coating shows good biocompatibility in a pig in vivo model. Such a coating strategy is expected to be a practical approach for preventing urological medical device-related complications. This work is supported by National Natural Science Foundation of China (Grant Nos. 51973221, 52173237, 22107099, and 52293384), Youth Innovation Promotion Association of CAS (Grant No. Y2021066), National Key Research and Development Program of China (Grant Nos.2020YFC1106900 and 2021YFC2101700), Scientific and Technological Development Program of Jilin Province (Grant No. 20210101385JC), and High-Tech Research & Development Program of CAS-WEGO Group.

Humans rely increasingly on sensors to address grand challenges and to improve quality of life in the era of digitalization and big data. For ubiquitous sensing, flexible sensors are developed to overcome the limitations of conventional rigid counterparts. Despite rapid advancement in bench-side research over the last decade, the market adoption of flexible sensors remains limited. To ease and to expedite their deployment, here, we identify bottlenecks hindering the maturation of flexible sensors and propose promising solutions. We first analyze challenges in achieving satisfactory sensing performance for real-world applications and then summarize issues in compatible sensor-biology interfaces, followed by brief discussions on powering and connecting sensor networks. Issues en route to commercialization and for sustainable growth of the sector are also analyzed, highlighting environmental concerns and emphasizing nontechnical issues such as business, regulatory, and ethical considerations. Additionally, we look at future intelligent flexible sensors. In proposing a comprehensive roadmap, we hope to steer research efforts towards common goals and to guide coordinated development strategies from disparate communities. Through such collaborative efforts, scientific breakthroughs can be made sooner and capitalized for the betterment of humanity. Agency for Science, Technology and Research (A*STAR) National Research Foundation (NRF) Submitted/Accepted version Y.L., Z.L., M.Z., and X.C. acknowledge the National Research Foundation, Singapore (NRF) under NRF’s Medium Sized Centre: Singapore Hybrid-Integrated Next-Generation μElectronics (SHINE) Centre funding programme, and AME programming funding scheme of Cyber Physiochemical Interface (CPI) project (no. A18A1b0045). Y.L. acknowledges National Natural Science Foundation of China (62201243). C.J. acknowledges funding support from the National Key R&D Program of China (no. 2019YFA0706100), the National Natural Science Foundation of China (82151305), Lingang Laboratory (LG-QS-202202-09). T.Q.T. and N.E.L. acknowledge support by the Basic Science Research Program (no. 2020R1A2C3013480) through the National Research Foundation of Korea (NRF) funded by the Ministry of Science and ICT. A.F. acknowledges the AFOSR (grant FA9550-22-1-0423). Y.L. and Y.Z. would like to acknowledge the NSF (award no. 2134664) and NIH (award no. R01HD108473) for financial support. X.F. acknowledges the support from the National Natural Science Foundation of China (grant no. U20A6001). L.Y. would like to thank the A*STAR Central Research Fund (CRF) and the AME Programmatic A18A1b0045 (Cyber Physiochemical Interfaces) for funding support. C.F.G. acknowledges the National Natural Science Foundation of China (no. T2225017). T.Q.T. acknowledges the Brain Pool Program (No. 2020H1D3A2A02111068) through the National Research Foundation (NRF) funded by the Ministry of Science. Z.L. acknowledges the support from RIE2020 AME Programmatic Grant funded by A*STAR-SERC, Singapore (Grant No. A18A1b0045). X.G. acknowledges funding support through the Shanghai Science and Technology Commission (grant no. 19JC1412400), the National Science Fund for Excellent Young Scholars (grant no. 61922057). C.D. acknowledges National Science Foundation CAREER: Conformable Piezoelectrics for Soft Tissue Imaging (grant no. 2044688) and MIT Media Lab Consortium funding. D.K. and O.G.S. acknowledge Leibniz Association and the German Research Foundation DFG (Gottfried Wilhelm Leibniz Program SCHM 1298/22-1, KA5051/1-1 and KA 5051/3-1), as well as the Leibniz association (Leibniz Transfer Program T62/2019). C.W. acknowledges the National Key Research and Development Program of China (grant no. 2021YFA1202600), National Natural Science Foundation of China (grant no. 62174082). A.V.-Y.T., E.Z., Y.Z., X.Z., and J.P. acknowledge the National Research Foundation, Singapore (NRF) under NRF’s Medium Sized Centre: Singapore Hybrid-Integrated Next-Generation μElectronics (SHINE) Centre funding programme, and AME programming funding scheme of Cyber Physiochemical Interface (CPI) project (no. A18A1b0045). R.Z. acknowledges National Natural Science Foundation of China (grant no. 51735007) and Beijing Natural Science Foundation (grant no. 3191001). N.M. acknowledges the support by JST PRESTO Grant Number JPMJPR20B7 and JST Adaptable and Seamless Technology transfer Program through Target-driven R&D (ASTEP) grant number JPMJTM22BK. C.P. acknowledges the Korean government (Ministry of Science and ICT, MSIT) (2022R1A4A3032923). M.W. acknowledges the National Key R&D Program of China under Grant (2021YFB3601200). X.Z. acknowledges National Natural Science Foundation of China (no. 62074029). S.X. acknowledges the 3M nontenured faculty award. T.-W.L. and D.-G.S. acknowledge the Pioneer Research Center Program through the National Research Foundation of Korea funded by the Ministry of Science, ICT & Future Planning (grant no. NRF-2022M3C1A3081211). C.T.L. would like to acknowledge support from the Institute for Health Innovation and Technology (iHealthtech), the MechanoBioEngineering Laboratory at the Department of Biomedical Engineering and the Institute for Functional Intelligent Materials (I-FIM) at the National University of Singapore (NUS). C.T.L. also acknowledges support from the National Research Foundation and A*STAR, under its RIE2020 Industry Alignment Fund − Industry Collaboration Projects (IAF-ICP) (grant no. I2001E0059) − SIA-NUS Digital Aviation Corp Lab and the NUS ARTIC Research (grant no. HFM-RP1). X.Y. acknowledges funding support by City University of Hong Kong (grant no. 9667221). T.X. and X.Z. acknowledge National Natural Science Foundation of China (22234006). B.C.K.T. acknowledges Cyber-Physiochemical Interfaces CPI, A*STAR A18A1b0045. H.G. acknowledges a research start-up grant (002479-00001) from Nanyang Technological University and the Agency for Science, Technology and Research (A*STAR) in Singapore. W.G. acknowledges National Science Foundation grant 2145802. D.J.L. acknowledges support from the US National Science Foundation grant number CBET-2223566. G.Y. acknowledges support from The Welch Foundation award F-1861, and Camille Dreyfus Teacher-Scholar Award. M.D.D. acknowledges funding support from NSF (grant no. EEC1160483). J.-H.A acknowledges the National Research Foundation of Korea (NRF-2015R1A3A2066337). J.C. acknowledges the Henry Samueli School of Engineering & Applied Science and the Department of Bioengineering at the University of California, Los Angeles for startup support and a Brain & Behavior Research Foundation Young Investigator Grant. K.T. acknowledges JST AIP Accelerated Program (no. JPMJCR21U1) and JSPS KAKENHI (grant no. JP22H00594). P.S.W. acknowledges the National Science Foundation (CMMI1636136) for support. A.M.A., M.C.H., and P.S.W. thank the National Institute on Drug Abuse (DA045550) for support. S.M. and X.C. appreciated the support from the Smart Grippers for Soft Robotics (SGSR) Programme under the National Research Foundation, Prime Minister’s Office, Singapore under its Campus of Research Excellence and Technological Enterprise (CREATE) programme.

The drift or fall of stretchable neural microelectrodes from the surface of wet and dynamic tissues severely hampers the adoption of microelectrodes for electrophysiological signal monitoring. Endowing the stretchable electrodes with adhesive ability is an effective way to overcome these problems. Current adhesives form tough adhesion to tissues by covalent interaction, which decreases the biocompatibility of the adhesives. Here, we fabricate a strong electrostatic adhesive (noncovalent interaction), highly conformal, stretchable microelectrode arrays (MEAs) for the electrophysiological interface. This MEA was composed of polypyrrole (PPy) as the electrode material and hydrogel as the stretchable substrate [the cross-linked and copolymerized hydrogel of 2-acrylamido-2-methylpropane sulfonic acid (AMPS), gelatin, chitosan, 2-methoxyethyl acrylate, and acrylic acid is named PAGMA]. Strong and stable electrostatic adhesion (85 kPa) and high stretchability (100%) allow for the integration of PPy MEAs based on the PAGMA hydrogel substrate (PPy-PAGMA MEAs) on diverse wet dynamic tissues. Additionally, by adjusting the concentration of AMPS in PAGMA, the hydrogel (PAGMA-1) can produce tough adhesion to many inorganic and elastomer materials. Finally, the PPy-PAGMA MEAs were toughly and conformally adhered on the rat's subcutaneous muscle and beating heart, and the rat's electrophysiological signals were successfully recorded. The development of these adhesive MEAs offers a promising strategy to establish stable and compliant electrode-tissue interfaces.

Liquid metal (especially eutectic gallium indium, EGaIn) nanoparticle inks overcome the poor wettability of high surface tension EGaIn to elastomer substrates and show great potential in soft electronics. Normally, a sintering strategy is required to break the oxide shells of the EGaIn nanoparticles (EGaIn NPs) to achieve conductive paths. Herein, for the first time, we prepared the thermal-sinterable EGaIn NP inks by introducing thermal expansion microspheres (TEMs) into EGaIn NP solution. Through the mechanical pressure induced by the expansion of the heated TEMs, the printed EGaIn NPs can be sintered into electrically conductive paths to achieve highly stretchable bioelectrode arrays, which exhibit giant electromechanical performance (up to 680% strain), good cyclic stability (over 2 × 10

Solar-driven interfacial evaporation (SIE) is emerging as an energy-efficient technology to alleviate the global water shortages. However, there is a fatal disadvantage in using SIE, that is, the volatile organic compounds (VOCs) widely present in feedwater would concurrently evaporate and transport in distilled water, which threatens the water safety. Photocatalysis is a sustainable technology for pollution control, and after years of development, it has become a mature method. Considering the restriction by the insufficient reaction of the permeating VOCs on the two-dimensional (2D) light-available interface of conventional materials, a 3D photocatalytic approach can be established to boost VOC rejection for photothermal evaporation. In the present work, a light-permeable solar evaporator with 3D photocatalytic sites is constructed by a porous sponge decorated with BiOBrI nanosheets with oxygen-rich vacancies. The 3D microchannels in the evaporator provide a light-permeable path with the deepest irradiation depth of about 580 μm, and the reactive interface is increased by tens of times compared with the traditional 2D membrane, resulting in suppression of VOC remnants in distilled water by around four orders of magnitude. When evaporating river water containing 5 mg L

Neural electrodes, as a bridge for bidirectional communication between the body and external devices, are crucial means for detecting and controlling nerve activity. The electrodes play a vital role in monitoring the state of neural systems or influencing it to treat disease or restore functions. To achieve high-resolution, safe and long-term stable nerve recording and stimulation, a neural electrode with excellent electrochemical performance (

Solar distillation is emerging as a robust and energy-effective tool for water purification and freshwater production. However, many water sources contain harmful volatile organic compounds (VOCs), which can evaporate through the photothermal evaporators and be collected together with distilled water, or even be enriched in the distilled water. In view of the penetration of volatile organic compounds, herein, we rationally demonstrate a dual-scale porous, photothermal/photocatalytic, flexible membrane for intercepting volatile organic compounds during solar distillation, which is based on a mesoporous oxygen-vacancy-rich TiO2-x nanofibrous membrane (m-TiO2-x NFM). The dual-scale porous structure was constructed by micrometer-sized interconnected tortuous pores formed by the accumulation of m-TiO2-x nanofibers and nanometer-sized pores in the m-TiO2-x individual nanofibers. Consequently, the membrane can sustainably in situ intercept VOCs by providing more photocatalytic reactive sites for collision (mainly by mesopores) and longer tortuous channels for prolonging VOC retention (mainly by micrometer-sized pores); thus, it results in less than 5% of phenol residual in distilled water. As a proof of concept, when the m-TiO2-x NFM is employed to purify practical river water in an evaporation prototype under real solar irradiation, complex volatile natural organic contaminants can be effectively intercepted and the produced distilled water meets the drinking water standards of China. This development will promote the application prospects of solar distillation.

Non-invasive on-skin electrodes record the electrical potential changes from human skin, which reflect body condition and are applied for healthcare, sports management, and modern lifestyle. However, current on-skin electrodes have poor conformal properties under sweaty condition in real-life due to decreased electrode-skin adhesion with sweat film at the interface. Here, we fabricated bio-composite electrodes based on silk fibroin (SF) through interfacial polymerization which is applicable on sweaty skin. Interfacial polymerized conductive polypyrrole (PPy) and SF are structurally interlocked and endow the whole electrode with uniform stretchability. Existence of water results in similar Young’s modulus of SF to the skin and enhanced interfacial adhesion. It keeps the electrodes conformal to skin under sweaty condition and allows reliable collection of ambulatory electrophysiological signals during sports and sweating. Wearable devices with these electrodes were used to acquire continuous and stable real-time electrocardiography (ECG) signals during running for 2 hours. The collected signals can provide information for sports management and are also analyzed by artificial intelligence to show their potential for intelligent human emotion monitoring. Our strategy provides opportunities to record long-term continuous electrophysiological signals in real-life conditions for various smart monitoring systems. NRF (Natl Research Foundation, S’pore) ASTAR (Agency for Sci., Tech. and Research, S’pore) Accepted version

Solar distillation through photothermal evaporators has approached solar light energy (E1) limit under no solar concentration but still suffers from modest vapor and clean water production. Herein, a nature-inspired low-tortuosity three-dimensional (3D) evaporator is demonstrated to significantly improve water production. The solar evaporator, prepared from polypyrrole-modified maize straw (PMS), had upright vascular structures enabling high water lifting and horizontal microgaps facilitating broad water distribution to the out-surface. Consequently, this novel PMS evaporator dramatically enhanced the utilization of the solar heat energy stored in the environment (E2) for promoting evaporation. The maximum vapor generation rate of a single PMS respectively increases 2.5 and 6 times compared with the conventional 3D evaporators and the planar evaporators of an identical occupied area. Consequently, a scaled-up PMS array achieved a state-of-the-art vapor generation rate of 3.0 L m-2 h-1 (LMH) under a simulated condition and a record-high clean water production of 2.2 LMH for actual seawater desalination under natural conditions (1 sun intensity). This breakthrough reveals great potentials for cost-effective freshwater production as well as the rational design of high-performance photothermal evaporators for solar distillation.

Newer efficient photo-thermal materials and structural engineering have been developed to combine solar energy with seawater to produce water for human consumption or irrigation. However, the water production rate still needs to be increased. Herein, we report a simple approach for developing an integrated photo-electro-thermal evaporation system that provides a high evaporation rate in the day and produces water continually using the electro-thermal effect in the dark. Solar energy is not only absorbed and directly converted to heat in an evaporator, electric power from solar cells is also converted into heat to produce even more vapor. Such a photo-electro-thermal evaporation system reached a record high water-generation rate of 4.73 kg m−2 h−1 under 1 sun illumination. The evaporation system capable of continuous day and night operation provides a water generation of 79.39 kg m−2 under the conditions of a simulated day, near 100% salt rejection, and excellent bactericidal performance.

Polymer doping is a significant approach to precisely control nucleation and crystal growth of perovskites and enhance electronic quality in perovskite solar cells (PSC) prepared in air. Here, a brand-new self-healing polysiloxane (SHP) with dynamic 2,6-pyridinedicarboxamide (PDCA) coordination units and plenty of hydrogen bonds was designed and incorporated into perovskite films. PDCA units, showing strong intermolecular Pb 2+ -N amido , I - -N pyridyl , and Pb 2+ -O amido coordination interactions, were expected to enhance crystallinity and passivate the grain boundary. In addition, abundant hydrogen bonds in SHP afforded the self-healing of cracks at grain boundaries for fatigue PSCs. Significantly, the doped device demonstrated a champion efficiency of 19.50% with inconspicuous hysteresis, almost rivaling those achieved in control atmosphere. This strategy of heterocyclic-based macromolecular doping in PSCs will pave a way for realizing efficient and durable crystalline semiconductors.

Although a solar–thermal conversion technique shows great potential for seawater desalination, there remains a grand challenge in exploring low-cost and high-efficiency photothermal materials. We report here a molten salt assisted galvanic replacement method for preparing a hollow black TiAlOx composite, which features a high solar absorptivity with up to 90.2% and has a high efficiency of 71.1% in a high salinity solution containing 15.3 wt% NaCl (∼5 times more concentrated than seawater). We exemplify the practical application of such hollow black TiAlOx composites as photothermal composites by setting up the automatic and manual tracking of solar desalination devices with a photic area of ∼1.0 m2, which can produce purified water with a rate of above 4.0 L m−2 day−1 in high-salinity water under natural light irradiation, and maintains good stability upon 5 days of continuous running. The advantages of the as-developed hollow black TiAlOx composites, including scalability, low cost, and high photothermal conversion efficiency, may open up a promising avenue practical application in seawater desalination. We would like to thank the support of the NSFC (51702284, 21875253), the Fundamental Research Funds for the Central Universities (112109*172210171) and the Startup Foundation for Hundred-Talent Program of Zhejiang University (112100- 193820101/001/022).

The high thickness of the wearable device restricts its conformal adhesion to the human skin, which results in low sensitive and unstable detection to the physiological signals. Here, an ultrathin wearable sensor with conformal skin adhesion was developed. It showed high sensitivity and good stability in physiological signal monitoring (e. g., human pulse).

Solar evaporation through a photothermal porous material provides a feasible and sustainable method for water remediation. Several photothermal materials have been developed to enhance solar evaporation efficiency. However, a critical limitation of current photothermal materials is their inability to separate water from the volatile organic compounds (VOCs) present in wastewater. Here, a microstructured ultrathin polymeric membrane that enables freshwater separation from VOC pollutants by solar evaporation with a VOC removal rate of 90%, is reported. The different solution-diffusion behaviors of water and VOCs with polymeric membranes facilitate their separation. Moreover, owing to increased light absorption, enlarged liquid–air interface, and shortened mass transfer distance, the microstructured and ultrathin configuration of the membrane helps to balance the tradeoff between permeation selectivity and water production capacity. The membrane is not only effective for evaporation of simulated volatile pollutants in a prototype, but can also intercept complex volatile organic contaminants in natural water sources and produce water that meets drinking-water standards. With practical demonstration and satisfactory purification performance, this work paves the way for practical application of solar evaporation for effective water remediation. National Research Foundation (NRF) Accepted version The authors thank the financial support from the National Natural Science Foundation of China (Grant Nos. 52070052, 51903068, and 51761145031), Singapore National Research Foundation (NRF2017NRFNSFC001-048) and Natural Science Foundation of Heilongjiang Province, China (YQ2020E011).

Herein, we report a de novo chemical design of supramolecular polymer materials (SPMs-1–3) by condensation polymerization, consisting of (i) soft polymeric chains (polytetramethylene glycol and tetraethylene glycol) and (ii) strong and reversible quadruple H-bonding cross-linkers (from 0 to 30 mol %). The former contributes to the formation of the soft domain of the SPMs, and the latter furnishes the SPMs with desirable mechanical properties, thereby producing soft, stretchable, yet tough elastomers. The resulting SPM-2 was observed to be highly stretchable (up to 17 000% strain), tough (fracture energy ∼30 000 J/m2), and self-healing, which are highly desirable properties and are superior to previously reported elastomers and tough hydrogels. Furthermore, a gold, thin film electrode deposited on this SPM substrate retains its conductivity and combines high stretchability (∼400%), fracture/notch insensitivity, self-healing, and good interfacial adhesion with the gold film. Again, these properties are all highly complementary to commonly used polydimethylsiloxane-based thin film metal electrodes. Last, we proceed to demonstrate the practical utility of our fabricated electrode via both in vivo and in vitro measurements of electromyography signals. This fundamental understanding obtained from the investigation of these SPMs will facilitate the progress of intelligent soft materials and flexible electronics. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Accepted version

Two-dimensional titanium carbide as a novel electrode material has been widely researched in the field of energy storage in recent years. However, the restacking of Ti3C2Tx nanosheets is still a challenge, which largely restricts their development. Here, we employ the 3D architecture of a Ti3C2Tx aerogel to restrict the restacking of 2D Ti3C2Tx nanosheets. This special structure can not only effectively reduce the restacking of 2D materials, but also accelerate the transport of electrolyte ions in the electrode. The as-prepared Ti3C2Tx aerogel possessed a large special surface area of 108 m2 g−1 and achieved a special capacitance of 349 F g−1 which is retained even at a high scan rate of 2000 mV s−1 in the 3 M H2SO4 electrolyte, indicating an ultrahigh rate capability. Moreover, at a higher current density of 20 A g−1, 90% of the initial capacitance is also retained after 20 000 charging–discharging cycles, revealing an excellent cycling stability. Furthermore, the mechanism of charge storage was investigated.

Stretchable devices, with the capability of retaining their functionalities under stretching, are drawing much attention as a promising solution to address the mechanical mismatch between traditional stiff electronics and soft curvilinear biological systems. Intensive efforts have been made toward the advancement of stretchable devices, such as the development of novel mechanically durable materials, deformable conductors and circuits, novel processing methods, and elastic matrixes for stretchable substrates and system integration. Among these, the elastic substrate constitutes the component that bears the applied strain and thus endows the device with stretchability, rendering its properties crucial to the overall performance of stretchable devices. This article provides a summary of the elastic materials commonly employed as stretchable substrates, as well as reveals fundamental insights into the properties requirements in the selection of stretchable substrates. Important challenges and strategies in the development of elastic matrices for stretchable devices are also discussed. Published version

The oxygen-reduction reaction (ORR) draws an extensive attention in many applications, and there is a growing interest to develop effective ORR electrocatalysts. Iron carbide (Fe3C) is a promising alternative to noble metals (e.g., platinum), but its performances need further improvement, and the real role of the Fe3C phase remains unclear. In this study, we synthesize Fe3C/tungsten carbide/graphitic carbon (Fe3C/WC/GC) nanocomposites, with waste biomass (i.e., pomelo peel) serving as carbon source, using a facile, one-step carbon thermal-reduction method. The nanocomposite is characterized by a porous structure consisting of uniform Fe3C nanoparticles encased by graphitic carbon (GC) layers with highly dispersed nanosized WC. The Fe3C provides the active sites for ORR, while the graphitic layers and WC nanoparticles can stibilize the Fe3C surface, preventing it from dissociation in the electrolyte. The Fe3C/WC/GC nanocomposite is highly active, selective, and stable toward four-electron ORR in pH-neutral...

The emulation of human sensation, perception, and action processes has become a major challenge for bioinspired intelligent robotics, interactive human-machine interfacing, and advanced prosthetics. Reflex actions, enabled through reflex arcs, are important for human and higher animals to respond to stimuli from environment without the brain processing and survive the risks of nature. An artificial reflex arc system that emulates the functions of the reflex arc simplifies the complex circuit design needed for "central-control-only" processes and becomes a basic electronic component in an intelligent soft robotics system. An artificial somatic reflex arc that enables the actuation of electrochemical actuators in response to the stimulation of tactile pressures is reported. Only if the detected pressure by the pressure sensor is above the stimulus threshold, the metal-organic-framework-based threshold controlling unit (TCU) can be activated and triggers the electrochemical actuators to complete the motion. Such responding mechanism mimics the all-or-none law in the human nervous system. As a proof of concept, the artificial somatic reflex arc is successfully integrated into a robot to mimic the infant grasp reflex. This work provides a unique and simplifying strategy for developing intelligent soft robotics, next-generation human-machine interfaces, and neuroprosthetics. NRF (Natl Research Foundation, S’pore) ASTAR (Agency for Sci., Tech. and Research, S’pore) MOE (Min. of Education, S’pore) Accepted version

Although a solar-thermal conversion technique shows great potential for seawater desalination, there remains a grand challenge in exploring low-cost and high-efficiency photothermal materials. We report here a molten salt assisted galvanic replacement method for preparing a hollow black TiAlO

Two-dimensional titanium carbide as a novel electrode material has been widely researched in the field of energy storage in recent years. However, the restacking of Ti3C2Tx nanosheets is still a challenge, which largely restricts their development. Here, we employ the 3D architecture of a Ti3C2Tx aerogel to restrict the restacking of 2D Ti3C2Tx nanosheets. This special structure can not only effectively reduce the restacking of 2D materials, but also accelerate the transport of electrolyte ions in the electrode. The as-prepared Ti3C2Tx aerogel possessed a large special surface area of 108 m2 g-1 and achieved a special capacitance of 349 F g-1 which is retained even at a high scan rate of 2000 mV s-1 in the 3 M H2SO4 electrolyte, indicating an ultrahigh rate capability. Moreover, at a higher current density of 20 A g-1, 90% of the initial capacitance is also retained after 20 000 charging-discharging cycles, revealing an excellent cycling stability. Furthermore, the mechanism of charge storage was investigated.

To enhance the intensity of Raman signal from a novel perspective in bio-inspiration, a SERS substrate similar to the insects' compound eyes was designed. The interface assembly and interface transfer of PS spheres were used to fabricate continuous Ag nano-bowls on the Si micro-cones, which avoids the limitation that the traditional method cannot realize the assembly of Ag nano-bowls on the substrate with obviously undulated structure. This bio-inspired structure is an excellent absorber of light, which greatly enhances the SERS signal intensity. The enhancement factor of 3D Ag nano-bowls is 5.5 times than that of 2D Ag nano-bowls on the flat substrate. At the same time, this bio-inspired SERS substrate was applied to the quantitative and qualitative detection of Hg2+, and its detection limit for Hg2+ can reach to 10−11 M. Adding the bio-inspired concept to the design of the SERS substrate will provide a new insight to realize the highly sensitive Raman detection.

A soft thermal sensor with mechanical adaptability is fabricated by the combination of single-wall carbon nanotubes with carboxyl groups and self-healing polymers. This study demonstrates that this soft sensor has excellent thermal response and mechanical adaptability. It shows tremendous promise for improving the service life of soft artificial-intelligence robots and protecting thermally sensitive electronics from the risk of damage by high temperature.

Flexible thin-film organic semiconductor devices have received wide attention due to favorable properties such as light-weight, flexibility, reproducible semiconductor resources, easy tuning of functional properties via molecular tailoring, and low cost large-area solution-procession. Among them, ultraflexible electronics, usually with minimum bending radius of less than 1 mm, are essential for the development of epidermal and bio-implanted electronics, wearable electronics, collapsible and portable electronics, three dimensional (3D) surface compliable electronics, and bionics. This review firstly gives a brief introduction of development from flexible to ultraflexible organic semiconductor electronics, and design of ultraflexible devices, then summarizes the recent advances in ultraflexible thin-film organic semiconductor devices, focusing on organic field effect transistors, organic light-emitting diodes, organic solar cells and organic memory devices.

Skin-inspired haptic-memory devices, which can retain pressure information after the removel of external pressure by virtue of the nonvolatile nature of the memory devices, are achieved. The rise of haptic-memory devices will allow for mimicry of human sensory memory, opening new avenues for the design of next-generation high-performance sensing devices and systems.

A bioinspired active anode with a suction effect is demonstrated for microbial fuel cells by constructing polypyrrole (PPy) nanotubular arrays on carbon textiles. The oxygen in the inner space of the nanosucker can be depleted by micro-organisms with the capability of facul-tative respiration, forming a vacuum, which then activates the electrode to draw the microorganism by suction and thus improve the bioelectricity generation.

Stretchable electronics, which can retain their functions under stretching, have attracted great interest in recent decades. Elastic substrates, which bear the applied strain and regulate the strain distribution in circuits, are indispensable components in stretchable electronics. Moreover, the self-healing property of the substrate is a premise to endow stretchable electronics with the same characteristics, so the device may recover from failure resulting from large and frequent deformations. Therefore, the properties of the elastic substrate are crucial to the overall performance of stretchable devices. Poly(dimethylsiloxane) (PDMS) is widely used as the substrate material for stretchable electronics, not only because of its advantages, which include stable chemical properties, good thermal stability, transparency, and biological compatibility, but also because of its capability of attaining designer functionalities via surface modification and bulk property tailoring. Herein, the strategies for fabricating stretchable electronics on PDMS substrates are summarized, and the influence of the physical and chemical properties of PDMS, including surface chemical status, physical modulus, geometric structures, and self-healing properties, on the performance of stretchable electronics is discussed. Finally, the challenges and future opportunities of stretchable electronics based on PDMS substrates are considered.

Solar-driven distillation is now considered as a rising technology for the supply of fresh water in the rare areas. As the crucial part of solar distillation, photothermal materials have been flourished investigated. Herein, we report a universal and facile method to construct a photothermal layer on various substrates to enhance the interfacial water evaporation via polypyrrole (PPy) polymerization and silver nanoparticles (Ag NPs) deposition. The photothermal Ag/PPy layer was firmly coated on six different substrates with an average solar absorption of 95.4% and Ag loading of 94.3 mg/L. One of the optimized resultant membranes (substrate is cellulose fibers) presents the ultrahigh solar evaporation rate of 1.55 kg m−2h−1 and a corresponding light-to-vapor efficiency of 92.6% with a silver loading of 74 μg cm−2. Bacterial diffusion inhibition zone experiments revealed clear antibacterial effects of the Ag/PPy membrane on bacteria. Furthermore, the Ag NPs deposited membrane had a rechargeability for multiple times upon their depletion, indicating sustainable anti-bacteria potential. Hence, our facial fabricated photothermal Ag/PPy layer can apply to substrates with different types for enhanced photothermal and anti-biocorrosion capacity, and may pave a new way to the long-term practical sustainable technique for the clean water production application.

Biological wastewater treatment (BWT), which is used to manage global wastewater, suffers from a sharp decrease in microbial activity at low temperature (

Fouling of polymeric membranes remains a major challenge for long‐term operation of oily‐water remediation. The common reclamation methods to recycle fouled membranes have the issues of either incomplete degradation of organic pollutants or damage to filter membranes. Here, a calcinable polymer membrane with effective reclamation after fouling is reported, which shows full recovery of the original oil/water separation efficiency. The membrane is made of polysulfonamide/polyacrylonitrile fibers by emulsion electrospinning, followed by hydrothermal decoration of TiO2 nanoparticles. The bonding structured fibrous membrane displays outstanding thermal stability in air (400 °C), strong acid/alkali resistance (at the pH range from 1 to 13), and robust tensile strength. As a result, the chemically fouled polymeric membrane can be easily reclaimed without decreasing in separation performance and mechanical properties by annealing treatment. As a proof‐of‐concept, the as‐prepared membrane is integrated into a wastewater separation tank, which achieves a high water flux over 3000 L m−2 h−1 and oil rejection efficiency of 99.6% for various oil‐in‐water emulsions. The presented strategy on membrane fabrication is believed to be an effective remedy for membrane fouling, and should apply in a wider field of filtration industry. NRF (Natl Research Foundation, S’pore) Accepted version

Tactile sensors capable of perceiving biophysical signals such as force, pressure, or strain have attracted extensive interest for versatile applications in electronic skin, noninvasive healthcare, and biomimetic prostheses. Despite these great achievements, they are still incapable of detecting bio/chemical signals that provide even more meaningful and precise health information due to the lack of efficient transduction principles. Herein, a tactile chemomechanical transduction strategy that enables the tactile sensor to perceive bio/chemical signals is proposed. In this methodology, pyramidal tactile sensors are linked with biomarker‐induced gas‐producing reactions, which transduce biomarker signals to electrical signals in real time. The method is advantageous as it enhances electrical signals by more than tenfold based on a triple‐step signal amplification strategy, as compared to traditional electrical biosensors. It also constitutes a portable and general platform capable of quantifying a wide spectrum of targets including carcinoembryonic antigen, interferon‐γ, and adenosine. Such tactile chemomechanical transduction would greatly broaden the application of tactile sensors toward bio/chemical signals perception which can be used in ultrasensitive portable biosensors and chemical‐responsive chemomechanical systems. NRF (Natl Research Foundation, S’pore) MOE (Min. of Education, S’pore) Accepted version

Soft and stretchable electronic devices are important in wearable and implantable applications because of the high skin conformability. Due to the natural biocompatibility and biodegradability, silk protein is one of the ideal platforms for wearable electronic devices. However, the realization of skin-conformable electronic devices based on silk has been limited by the mechanical mismatch with skin, and the difficulty in integrating stretchable electronics. Here, silk protein is used as the substrate for soft and stretchable on-skin electronics. The original high Young's modulus (5-12 GPa) and low stretchability ( 400%, respectively. This plasticization is realized by the addition of CaCl2 and ambient hydration, whose mechanism is further investigated by molecular dynamics simulations. Moreover, highly stretchable (>100%) electrodes are obtained by the thin-film metallization and the formation of wrinkled structures after ambient hydration. Finally, the plasticized silk electrodes, with the high electrical performance and skin conformability, achieve on-skin electrophysiological recording comparable to that by commercial gel electrodes. The proposed skin-conformable electronics based on biomaterials will pave the way for the harmonized integration of electronics into human. NRF (Natl Research Foundation, S’pore) ASTAR (Agency for Sci., Tech. and Research, S’pore) MOE (Min. of Education, S’pore) Accepted version

Stretchability plays an important role in wearable devices. Repeated stretching often causes the conductivity dramatically decreasing due to the damage of the inner conductive layer, which is a fatal and undesirable issue in this field. Herein, a convenient rolling strategy to prepare conductive fibers with high stretchability based on a spiral structure is proposed. With the simple rolling design, low resistance change can be obtained due to confined elongation nof the gold thin-film cracks, which is caused by the encapsulated effect in such a structure. When the fiber is under 50% strain, the resistance change (R/R0) is about 1.5, which is much lower than a thin film at the same strain (R/R0 ≈ 10). The fiber can even afford a high load strain (up to 100%), but still retain good conductivity. Such a design further demonstrates its capability when it is used as a conductor to confirm signal transfer with low attenuation, which can also be woven into textile to fabricate wearable electronics. MOE (Min. of Education, S’pore)

Wearable healthcare presents exciting opportunities for continuous, real-time, and noninvasive monitoring of health status. Even though electrochemical and optical sensing have already made great advances, there is still an urgent demand for alternative signal transformation in terms of miniaturization, wearability, conformability, and stretchability. Mechano-based transductive sensing, referred to the efficient transformation of biosignals into measureable mechanical signals, is claimed to exhibit the aforementioned desirable properties, and ultrasensitivity. In this Concept, a focus on pressure, strain, deflection, and swelling transductive principles based on micro-/nanostructures for wearable healthcare is presented. Special attention is paid to biophysical sensors based on pressure/strain, and biochemical sensors based on microfluidic pressure, microcantilever, and photonic crystals. There are still many challenges to be confronted in terms of sample collection, miniaturization, and wireless data readout. With continuing efforts toward solving those problems, it is anticipated that mechano-based transduction will provide an accessible route for multimode wearable healthcare systems integrated with physical, electrophysiological, and biochemical sensors. NRF (Natl Research Foundation, S’pore)

Highly stretchable microsupercapacitors with stable electrochemical performance are fabricated. Their excellent stretchable and electrochemical performance relies on the suspended wavy structures of graphene microribbons. This avoids the detachment and cracks of the electrode materials. In addition, it ensures the electrode fingers keep a relatively constant distance so the stability of the microsupercapacitors can be enhanced.

La(OH)3 nanorods immobilized in polyacrylonitrile (PAN) nanofibers (PLNFs) were fabricated for the first time by electrospinning and a subsequent in situ surfactant-free precipitation method and then applied as a highly efficient phosphate scavenger to realize nutrient-starvation antibacteria for drinking water security. The immobilization by PAN nanofibers effectively facilitated the in situ formation of the aeolotropic and well-dispersed La(OH)3 nanostructures and, thus, rendered higher phosphate removal efficiency due to more exposed active sites for binding phosphate. The maximum phosphate capture capacity of La(OH)3 nanorods in PAN nanofibers was around 8 times that of the La(OH)3 nanocrystal fabricated by precipitation without PAN protection. Moreover, remarkably fast adsorption kinetics and high removal rate were observed toward low concentration phosphate due to the high activity of our materials, which can result in a stringent phosphate-deficient condition to kill microorganisms in water effectively. The present material is also capable of preventing sanitized water from recontamination by bacteria and keeping water biologically stable for drinking. Impressively, stabilized by PAN nanofibers, the La(OH)3 nanorods can be easily separated out after reactions and avoid leaking into water. The present development has great potential as a promising antimicrobial solution for practical drinking water security and treatment with a negligible environmental footprint.