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Ion-molecular engineered negative-thermovoltage cellulose ionogel overcoming the trade-off mechanical strength and conductivity.

In recent years, the development of multi-functional supercapacitors with high flexibility and strong environmental adaptability has gradually become a focus of attention.

Although single-atom catalysts (SACs) have been largely explored in lithium-sulfur (Li-S) batteries, the commonly reported nonpolar transition metal-N

A raindrop solar cell can work either on rainy days to collect mechanical energy of the raindrops or on sunny days to harvest solar energy, which achieves high energy conversion efficiency in various energy environments. However, the low efficiency of raindrop energy harvesting is a dominating barrier to the raindrop solar cells in practical applications. In this work, a MoO

A PbSe colloidal quantum dot (QD) is typically a solution-processed semiconductor for near-infrared (NIR) optoelectronic applications. However, the wide application of PbSe QDs has been restricted due to their instability, which requires tedious synthesis and complicated treatments before being applied in devices. Here, we demonstrate efficient NIR photodetectors based on the room-temperature, direct synthesis of semiconducting PbSe QD inks. The in-situ passivation and the avoidance of ligand exchange endow PbSe QD photodetectors with high efficiency and low cost. By further constructing the PbSe QDs/ZnO heterostructure, the photodetectors exhibit the NIR responsivity up to 970 mA/W and a detectivity of 1.86 × 1011 Jones at 808 nm. The obtained performance is comparable to that of the state-of-the-art PbSe QD photodetectors using a complex ligand exchange strategy. Our work may pave a new way for fabricating efficient and low-cost colloidal QD photodetectors.

A flexible and stable power supply is essential to the rapid development of wearable electronic devices. In this work, a transparent, flexible, temperature-stable and ionogel electrode-based self-healing triboelectric nanogenerator (IS-TENG) was developed. The ionogel with excellent stretchability (1,012%), high ionic conductivity (0.3 S·m−1) and high-temperature stability (temperature range of −77 to 250 °C) was used as the electrode of the IS-TENG. The IS-TENG exhibited excellent transparency (92.1%) and stability. The output performance did not decrease when placed in a 60 °C oven for 48 h. In addition, the IS-TENG behaved like a stable output in the range of −20 to 60 °C. More importantly, the IS-TENG could also achieve self-healing of electrical performance at temperatures between −20 and 60 °C and its output can be restored to its original state after healing. When the single-electrode IS-TENG with an area of 3 cm × 3 cm was conducted under the working frequency of 1.5 Hz, the output values for open-circuit voltage, short-circuit current, short-circuit transferred charge, and maximum peak power density were 189 V, 6.2 µA, 57 nC, and 2.17 W·m−2, respectively. The IS-TENG enables to harvest biomechanical energy, and drive electronic devices. Furthermore, the application of IS-TENGs as self-driven sensors for detecting human behavior was also demonstrated, showing good application prospects in the field of wearable power technology and self-driven sensing.

Triboelectric sensors provide an effective approach to solving the power supply problem for distributed sensing nodes. However, the poor stability and repeatability of the output signal limit its further development due to structural deficiencies and intrinsic working mechanisms. This work proposes a contact-separation mode laminated triboelectric nanogenerator (L-TENG) by introducing multifunctional layers to regulate triboelectric charges. A liquid metal Galinstan and PDMS mixture with a dense microstructure array is fabricated as the dielectric layer. Liquid squalene is filled in the space between two triboelectric layers to eliminate the influence of moisture in the air. A Cu shield film is sputtered on the surface to screen the electrostatic interference and enhance the repeatability. Owing to the effective design, the sensitivity of the L-TENG could reach 6.66 kPa

Solid-state electrolytes (SSEs) have attracted considerable attention as an alternative for liquid electrolytes to improve safety and durability. Sodium Super Ionic CONductor (NASICON)-type SSEs, typically Na3Zr2Si2PO12, have shown great promise because of their high ionic conductivity and low thermal expansivity. Doping La into the NASICON structure can further elevate the ionic conductivity by an order of magnitude to several mS/cm. However, the underlying mechanism of ionic transportation enhancement has not yet been fully disclosed. Herein, we fabricate a series of Na3+xLaxZr2-xSi2PO12 (0 ≤ x ≤ 0.5) SSEs. The electronic and local structures of constituent elements are studied via synchrotron-based X-ray absorption spectroscopy, and the ionic dynamics and Na-ion conduction mechanism are investigated by solid-state nuclear magnetic resonance spectroscopy. The results prove that La3+ ions exist in the form of phosphate impurities such as Na3La(PO4)2 instead of occupying the Zr4+ site. As a result, the increased Si/P ratio in the NASICON phase, accompanied by an increase in the sodium ion occupancy, makes a major contribution to the enhancement of ionic conductivity. The spin-lattice relaxation time study confirms the accelerated Na+ motions in the altered NASICON phase. Modifications on the Si/P composition can be a promising strategy to enhance the ionic conductivity of NASICON.

Pressure sensors have attracted much attention for their potential applications in health monitoring, wearable devices, electronic skins, smart robots, etc. With the rapid development of the Internet of Things, considering the large number and small scale of sensors, power consumption has become a key factor in large-scale applications. A new generation of self-powered pressure sensors based on a triboelectric nanogenerator has been developed in terms of its incomparable advantages in power consumption and potential performance. Based on the coupling effects of triboelectrification and electrostatic induction, it enables obtaining information on the mechanical input, e.g., magnitude and frequency, by analyzing the electrical output signals. Intensive efforts have been devoted to improving the sensing performance of triboelectric pressure sensors to meet the demands of practicality. In this review, the key advancements in materials, structures and applications of self-powered triboelectric pressure sensors are systematically reviewed. Then, the theoretical basis, impact mechanism and approaches to optimize the pressure sensing performance have been comprehensively analyzed. Finally, the future perspectives of self-powered triboelectric pressure sensors have also been discussed.

Bone repair in real time is a challenging medical issue for elderly patients; this is mainly because aged bone marrow mesenchymal stem cells (BMSCs) possess limited osteogenesis potential and repair capacity. In this study, triboelectric stimulation technology is used to achieve bone repair via mechanosensation of Piezo1 by fabricating a wearable pulsed triboelectric nanogenerator (WP-TENG) driven by human body movement. A peak value of 30 µA has the optimal effects to rejuvenate aged BMSCs, enhance their osteogenic differentiation, and promote human umbilical vein endothelial cell tube formation. Further, previous studies demonstrate that triboelectric stimulation of a WP-TENG can reinforce osteogenesis of BMSCs and promote the angiogenesis of human umbilical vein endothelial cells (HUVECs). Mechanistically, aged BMSCs are rejuvenated by triboelectric stimulation via the mechanosensitive ion channel Piezo1. Thus, the osteogenesis potential of BMSCs is enhanced and the tube formation capacity of HUVECs is improved, which is further confirmed by augmented bone repair and regeneration in in vivo investigations. This study provides a potential signal transduction mechanism for rejuvenating aged BMSCs and a theoretical basis for bone regeneration using triboelectric stimulation generated by a WP-TENG.

Metal-nitrogen-carbon materials are promising catalysts for CO2 electroreduction to CO. Herein, by taking the unique hierarchical carbon nanocages as the support, an advanced nickel-nitrogen-carbon single-site catalyst is conveniently prepared by pyrolyzing the mixture of NiCl2 and phenanthroline, which exhibits a Faradaic efficiency plateau of > 87% in a wide potential window of −0.6–−1.0 V. Further S-doping by adding KSCN into the precursor much enhances the CO specific current density by 68%, up to 37.5 A·g−1 at −0.8 V, along with an improved CO Faradaic efficiency plateau of > 90%. Such an enhancement can be ascribed to the facilitated CO pathway and suppressed hydrogen evolution from thermodynamic viewpoint as well as the increased electroactive surface area and improved charge transfer fromkinetic viewpoint due to the S-doping. This study demonstrates a simple and effective approach to advanced electrocatalysts by synergetic modification of the porous carbon-based support and electronic structure of the active sites.

The electrochemical reduction of CO2 to ethylene provides a carbon-neutral avenue for the conversion of CO2 to value-added fuels and feedstocks, so contributing to the storage of intermittent renewable electricity. The exploration of efficient electrocatalysts with high ethylene selectivity and productivity is highly desirable but remains challenging. Here, we present a Cu-based catalyst derived from a metal–organic framework (Cu-MOF) which shows enhanced performance due to its porous morphology, complex oxidation states and strong lattice strain. X-ray diffraction, X-ray photoelectron spectroscopy, and X-ray absorption spectroscopy are utilized to track the evolution of the crystal structure and oxidation states during the reaction, and the results reveal that Cu2+ ions are rapidly reduced to Cu+ and then slowly to Cu0, resulting in a Cu@CuxO core@shell structure. The tensile strain caused by the distorted grain is beneficial for the activation of CO2. Cu+/Cu0 interfaces formed through stabilized Cu+ facilitate *CO–CO dimerization, promoting conversion to C2+ products and suppressing conversion to C1 products. The optimized catalyst exhibits a 51% Faraday efficiency (FE) for ethylene and a 70% FE for C2+ products, with 20 h operational stability in an H-cell configuration, and a partial ethylene current density of 150 mA cm−2 in a flow-cell configuration.

Stretchable triboelectric nanogenerators (TENGs) have been made available for a large amplitude of human body movement as an effective wearable power source. However, the elasticity and performance of such a kind of device seriously decline in a harsh environment, especially below sub-zero temperature. In this work, an anti-freezing hydrogel was synthesized by one-step radical polymerization of acrylamide monomer in hydroxyethyl cellulose aqueous solution. After adding LiCl into the hydrogel, it can be cooled to temperatures as low as −69 °C without freezing. The hydroxyethyl cellulose not only enhances the mechanical properties as a physical crosslinking agent but also provides water retention properties. With a constant elongation of ∼150%, the anti-freezing hydrogel based TENG (AH-TENG) has been successfully demonstrated to harvest human biomechanical energy to drive wearable electronic devices, even in a harsh ice and snow environment. At a fixed frequency of 2.5 Hz, an AH-TENG with a 3 × 3 cm2 area achieved an output of 285 V, 15.5 μA, 90 nC and an instantaneous peak power density of 626 mW m−2, respectively. This work is anticipated to provide a promising approach for the advancement of flexible energy sources under harsh conditions.

As accurate step counting is a critical indicator for exercise evaluation in daily life, pedometers give a quantitative prediction of steps and analyze the amount of exercise to regulate the exercise plan. However, the merchandized pedometers still suffer from limited battery life and low accuracy. In this work, an integrated self-powered real-time pedometer system has been demonstrated. The highly integrated system contains a porous triboelectric nanogenerator (P-TENG), a data acquisition and processing (DAQP) module, and a mobile phone APP. The P-TENG works as a pressure sensor that generates electrical signals synchronized with users' footsteps, and combining it with the analogue front-end (AFE) circuit yields an ultrafast response time of 8 ms. Moreover, the combination of a mini press-to-spin-type electromagnetic generator (EMG) and a supercapacitor enables a self-powered and self-sustained operation of the entire pedometer system. This work implements the regulation of TENG signals by electronic circuit design and proposes a highly integrated system. The improved reliability and practicality provide more possibilities for wearable self-powered electronic devices.

The components in traditional human–machine interaction (HMI) systems are relatively independent, distributed and low-integrated, and the wearing experience is poor when the system adopts wearable electronics for intelligent control. The continuous and stable operation of every part always poses challenges for energy supply. In this work, a triboelectric technology-based all-in-one self-powered HMI system for wireless remote telemetry and the control of intelligent cars is proposed. The dual-network crosslinking hydrogel was synthesized and wrapped with functional layers to fabricate a stretchable fibrous triboelectric nanogenerator (SF-TENG) and a supercapacitor (SF-SC), respectively. A self-charging power unit containing woven SF-TENGs, SF-SCs, and a power management circuit was exploited to harvest mechanical energy from the human body and provided power for the whole system. A smart glove designed with five SF-TENGs on the dorsum of five fingers acts as a gesture sensor to generate signal permutations. The signals were processed by the microcontroller and then wirelessly transmitted to the intelligent car for remote telemetry and control. This work is of paramount potential for the application of various terminal devices in self-powered HMI systems with high integration for wearable electronics.

Ion concentration in water is a key criterion for evaluating water quality. In this work, we developed a self-powered on-line ion concentration monitor in water transportation based on impedance matching effect of triboelectric nanogenerator (TENG). A rotary disc-shaped TENG (RD-TENG) and an ion concentration sensor were fabricated based on the industrial printed circuit board (PCB) technology. Flowing water in the pipeline acts as the energy source to drive the RD-TENG and generate an open-circuit (Voc) of 210 V. The ion concentration sensor exhibits a nearly pure resistance characteristic under the alternating current (AC) signal with the frequency below 500 Hz, corresponding to the rotation speed of 250 rpm for the RD-TENG. The impedance matching relationship between the RD-TENG and the ion concentration sensor was experimentally studied and applied to elucidate the sensing mechanism. Finally, a self-powered sensing system integrated with an alarm circuit was assembled which exhibits excellent responsibility and high sensitivity. The change of ion concentration with only 1 × 10−5 mol/L can light up an alarm LED.

Constructing electronic systems without an external power source is urgently required toward self-powered photodetection. In this work, we proposed a self-driven photodetection system with a MoS2 nanosheets photodetector as light intensity sensor, a vertical contact-separate mode triboelectric nanogenerator (CS-TENG) as power source, and several LEDs as alarm. The MoS2 based planar photodetector was fabricated by conventional photolithography technique and lift-off process. It is highly sensitive for visible light illumination with high current on-off ratio and excellent reproducibility characteristics under light on-off switching. When conjuncting these functional devices, the induced output voltage of the CS-TENG is tuned by the load resistance of the photodetector, which is responded to the light intensity. The mechanism can be ascribed to the impedance matching effect between specific output characteristics of TENG and working status of photodetector. By adding a Zener diode acts as a voltage regulator, the self-driven renders the voltage and current varying from 1.58 to 20.60 V and 0.06–4.78 μA in a range of light intensity from 0 to 3.19 W/m2, respectively. Finally, it is demonstrated that the output of CS-TENG varies with the variable working states of the MoS2 photodetector and then accurately reflects on the lighted number of LEDs.

Cell stimulation by electric signal is an important approach for the advancement of biomedicine. Triboelectric nanogenerators (TENG), capable of converting mechanical energies to electricity, provides an alternative strategy to stimulate cells in a desired fashion. In this work, a TENG driven electric stimulation system has been designed for biosafety evaluation and exploration of the fibroblast cell behaviors. A rotatory disc-shaped TENG (RD-TENG) was fabricated to obtain an adjustable range of alternating current outputs. The peak current generated in a range of 10–50 μA is suitable for promoting cellular proliferation behavior of L929 cells. At the optimum value of 50 μA, the promotion rate reached 53.8 ± 2.66% after two-day of intermittent stimulation. Also, the migration rate was increased by about 67% than that of the cells in the control group. In addition, under stimulation, the proliferation-related gene of L929 cells - proliferating cell nuclear antigen (Pcna) and the two migration-related genes - fibroblast growth factor 2 (Fgf2) and delta like non-canonical notch ligand 1 (Dlk1) were also found up-regulated, suggesting that TENG stimulation regulates cell proliferation and migration at the level of gene expression. The present study demonstrates the effectiveness of TENG and its safe operation conditions in biomedical stimulation, which paves a way for practical application of TENG on tissue formation, reepithelialization and tissue remodeling.

Triboelectric nanogenerator (TENG) is a new emerging and cost-effective technology for harvesting water wave energy because of its unmatchable performance in low frequency and randomly directed motions. Here, we report an approach that significantly increased the output power of spherical TENGs by optimizing both materials and structural design. Fabricated with an acrylic hollow sphere as its shell and a rolling flexible liquid/silicone as the soft core, the soft-contact spherical triboelectric nanogenerator (SS-TENG) presents up to 10-fold enhancement to the maximum output charge compared to that of a conventional Polytetrafluoroethylene (PTFE) based hard-contact one, which is resulted from the significantly increased contact area. Besides, the output is tunable through controlling the softness of the liquid/silicone core. Our finding provides a new optimization methodology for TENGs and enable its more promising usage in harvesting large-scale blue energy from water wave in oceans as well as feeble but ubiquitous wind energy.

Self-healable soft conductors, which can withstand certain degrees of deformation and can recover from damage spontaneously, are essential for wearable applications. In this work, a soft hydrogel based self-healing triboelectric nanogenerator (HS-TENG), which is highly deformable, and both mechanically and electrically self-healable, has been successfully fabricated from a poly(vinyl alcohol)/agarose hydrogel. The incorporation of photothermally active polydopamine particles and multiwalled carbon nanotubes (MWCNTs) allows the HS-TENG to be physically self-healed in ∼1 min upon exposure to near-infrared (NIR) light. At the same time, the chemical self-healing of the HS-TENG can be triggered by water spraying at 25 °C when introducing water-active dynamic borate bonds into the hydrogel. The applicability of the HS-TENG as a soft energy device to harvest human motion energies has been demonstrated. By tapping the HS-TENG with various deformations, the rectified electricity can charge commercial LEDs with sustainable energy. Working in single-electrode mode, the electrical outputs of the HS-TENG in terms of short-circuit transferred charge (Qsc), open circuit voltage (Voc) and short-circuit current (Isc) reach ∼32 nC, ∼95 V and ∼1.5 μA, respectively, and remain stable even with 200% strain since the MWCNTs disperse evenly in the matrix and play the role of conductive fillers in the HS-TENG.

Colloidal quantum dots (QDs) are semiconductor nanocrystals which exhibit discrete energy levels. They are promising building blocks for optoelectronic devices, thanks to their tunable band structure. Here, we explore a nanoengineering approach to highlight the influence of an alloyed interface on the optical and electronic properties of CdSe/(CdS)6 “giant” core/shell (CS) QDs by introducing CdSexS1-x interfacial layers between core and shell. By incorporating of CdSexS1-x interfacial layers, CdSe/(CdSexS1-x)4/(CdS)2 (x = 0.5) core/shell (CSA1) QDs exhibit a broader absorption response towards longer wavelength and higher electron-hole transfer rate due to favorable electronic band alignment with respect to CS QDs, as confirmed by optical absorption, photoluminescence (PL) and transient fluorescence spectroscopic measurements. In addition, simulations of spatial probability distributions show that the interface layer enhances electron-hole spatial overlap. As a result, CSA1 QDs sensitized solar cells (QDSCs) yield a maximum photoconversion efficiency (PCE) of 5.52%, which is 79% higher than QDSCs based on reference CS QDs. To fully demonstrate the structural interface engineering approach, the CdSexS1-x interfacial layers were further engineered by tailoring the selenium (Se) and sulfur (S) molar ratios during in situ growth of each interfacial layer. This graded alloyed CdSe/(CdSexS1-x)5/(CdS)1 (x = 0.9–0.1) core/shell (CSA2) QDs show a further broadening of the absorption spectrum, higher carrier transport rate and modified confinement potential with respect to CSA1 QDs as well as reference CS QDs, yielding a PCE of 7.14%. Our findings define a promising approach to improve the performance of QDSCs and other optoelectronic devices based on CS QDs.

Mesoporous TiO2 sensitized with colloidal quantum dots (QDs) is considered as a promising system for photoelectrochemical (PEC) hydrogen generation, in view of its low cost and high solar energy to fuel conversion efficiency. On the other hand, the limited long term stability and low current density of this system still hinder its commercialization. Here, we report a CdSe/CdSeS alloy/CdS core/shell/shell QD sensitized mesoporous TiO2 photoanode, which exhibits high performance and long-term stability for solar-driven hydrogen generation. A gradient CdSe/alloy-shell/CdS core/shell/shell structure is designed to accelerate exciton separation through the band engineering approach. Compared with the common CdSe/CdS core/shell structure, light absorption of QDs containing an intermediate alloyed layer is extended to longer wavelengths and more importantly, the photocurrent density is improved up to 17.5 mA cm−2 under one sun illumination (AM 1.5 G, 100 mW cm−2), a record value for PEC cells based on colloidal QDs for hydrogen generation. In addition, the as-fabricated PEC cell shows an unprecedented long-term stability, maintaining 50% of its initial value after continuous operation for over 39 hours, indicating that the gradient core/shell/shell QD based photoanode is a promising candidate for solar-driven hydrogen generation.

Lithium nitrate (LiNO3) has been the most studied electrolyte additive in lithium-sulfur (Li-S) cells, due to its known function of suppressing the shuttle effect in Li-S cells, which provides a significant increase in the cell's coulombic efficiency and cycling stability. Previous studies indicated that LiNO3 participated in the formation of a passive layer on the lithium electrode and thus suppressed the redox shuttle of the dissolved polysulfides. However, the effects of the LiNO3 on the positive electrode materials have rarely been investigated. By combining scanning electron microscopy, element-selective X-ray absorption spectroscopy, and electrochemical characterizations, we performed a comprehensive study of how the LiNO3 altered the properties of the sulfur electrode/electrolyte interface in Li-S cells and thus influenced the cell performance. We found that LiNO3 is a double-edged sword in the Li-S cell: on one hand, it increased the consumption of the active sulfur; on the other hand, it promoted the survival of the carbon matrix constituent in the sulfur electrode. These two competitive effects indicated that a proper moderate concentration of LiNO3 is required to achieve an optimized cell performance.

The exploration of advanced functional materials from natural resources is significantly important to green and sustainable development. Herein, we design an ultrafast humidity-driven bending response system using asymmetrically patterned cellulose nanofiber (CNF)/graphene oxide (GO) composite films. The CNF/GO composite films are fabricated by vacuum-assisted filtration, followed by a surface imprinting technique. The results reveal that the composite films possess excellent linear response to humidity change and cycle stability in the relative humidity (RH) range from 25 to 85%. The curvature of the film varies from 0.012 to 0.260 cm-1 as the RH changes from 25 to 85%, and the response time is only 3-5 s. The outstanding humidity response is attributed to the addition of GO that actively interacts with water, enhancing the flexibility and humidity sensitivity of the composite films. In addition, asymmetrical patterning improves the water transfer rate by confinement and renders an easy deformation of composite films under the same stress. Molecular dynamics simulation and finite element analysis are used to further elucidate the mechanism therein. Furthermore, this CNF/GO composite film is also an effective hygroelectric generator, with an output voltage as high as 286 mV. This smart CNF/GO film with responsive humidity-driven deformation shows potential applications as a biomimetic leaf, a proximity sensor, and a moisture-driven electricity generator. This work inspires a new approach of smart material design with nanocellulose and GO and promotes their further applications.

Silicene as a novel and unique two-dimensional nanomaterial attracts considerable research interest; however, obtaining free-standing silicene still poses challenges due to its instability in air. In this work, we report the synthesis of protected silicene through chemical vapor deposition (CVD), in which silicene is sandwiched by graphene (G@S@G) covered on a Cu substrate. Graphene plays the role of both a substrate and protector, which can help silicene stabilize in air. These findings were verified by means of advanced microscopic and spectroscopic investigations accompanied by density functional theory (DFT) simulations. A large area of G@S@G can be obtained and tailored in any type of shape based on the Cu film. G@S@G shows n-type semiconductor character confirmed by a field-effect transistor (FET) device.

The portable UV photodetector is used to timely remind humans of overexposure to UV radiation. However, the traditional UV photodetector cannot meet the practical demands, and the power supply problem hinders its further development. In this work, we demonstrated a flexible, transparent, and self-powered UV photodetector by coupling of triboelectric and photoelectric effects. The device integrates a flexible ZnO nanoparticle (NP) UV photodetector, a transparent- and flexible-film-based TENG (TFF-TENG), commercial chip resistors, and LEDs on the PET thin film. The TFF-TENG could harvest mechanical energy from finger tapping and sliding motion and power the ZnO NP UV photodetector to realize self-powered detection. The voltage of the constant resistors connected with the UV photodetector in series changes from 0.5 to 19 V under the UV light with power intensities increasing from 0.46 to 21.8 mW/cm2, and the voltage variation is reflected by the number of LEDs directly. The excellent flexibility and transparency of the device could extend its application scenarios; for example, such a portable device could be applied to real-time monitoring of the UV radiation to remind humans of intense UV light.

Exosomes are membrane-enclosed extracellular vesicles carrying multiple biomolecules for intercellular communications. Accurate detection of exosomes could provide critical clinical information and show great significance for early diagnosis and personalized therapy of cancer. In this work, we propose a triboelectric sensing strategy for direct quantification of exosomes based on the contact-electrification effect. The target exosomes can be selectively captured on the three-dimensional tetrahedral DNA (TDNA) monolayer. The electrons transfer between abundant amino groups from exosomes and the tribo-materials contribute to the measured signal. Due to the specific output characteristic, it is able to directly discriminate 3 exosomes /μL with a linear range from 20 to 1000 exosomes/μL, even without any signal amplification. The challenges for distinguishing different cell line-derived exosomes and anti-interference in complicated biological serum systems show good performances. The presence of target exosomes can also be easily determined by visual observation of LED lighted by the generated electric energy. The proposed method can be used as a powerful tool for ultrasensitive analysis of exosomes, which is expected to have broad biological and analytical applications.

Potassium ion hybrid capacitors (PIHCs) have attracted considerable interest due to their low cost, competitive power/energy densities, and ultra-long lifespan. However, the more sluggish insertion kinetics of battery-type anodes than capacitor-type cathodes in PIHCs seriously limits their practical application. Therefore, developing advanced anodes with high capacitor and suitable K

Self-powered sensors, as the essential information notes in low power consumption of Internet of healthcare, exhibit a great potential to monitor the state of human health in real time. In this work, a bamboo-inspired self-powered triboelectric sensor (BSTS) using 3D-printing and freeze-drying fabrication processes is presented. The designed triboelectric layer with hollow and bamboo-joint microstructures has a low equivalent stiffness coefficient and a great deformation limit, contributing significantly to the high sensitivity and wide detection range of BSTS. An electromechanical model was proposed to better understand the influence mechanism of inner structures in the dielectric layer on the sensing performance. The sensitivity of the BSTS can reach 3.627 kPa-1 in the pressure range of 0-8 kPa and still keep 1.264 kPa-1 in the range of 8-80 kPa. Moreover, the BSTS is able to detect tiny pressure as low as 5 Pa and possesses ultra-fast response time of 40 ms. A touch-controlled lighting system and a sitting posture monitoring system based on the BSTS for healthcare application are demonstrated. This strategy paves a way to fabricate the self-powered triboelectric pressure sensor with high sensitivity in all working ranges.

Triboelectric nanogenerators (TENGs), as a new emerging and cost-effective approach, shows a promising prospective for harvesting blue energy. However, several challenges still exist limiting output performance, such as the package and low frequency of water wave. Here, we proposed an atmospheric pressure difference driven energy harvesting methodology for harvesting low-frequency ocean wave energy, especially for near-shore ocean waves. Through the methodology, it enables to transform intermittent and low frequency water wave movement into stored-energy and then release the energy in form of airflow and trigger continuous and high frequency movement, which greatly improves working efficiency of TENGs. With the smart design of a soft membrane, this methodology can well achieve waterproof effect by outer framework and be well matched different frequency ocean waves. To demonstrate the feasibility, two specific TENG structures have been demonstrated as examples: a flutter-driven TENG (FD-TENG) driven by lower speed airflow and a disc-shaped TENG (DS-TENG) triggered by stronger airflow. This methodology demonstrates perspectives toward blue energy dream and further expands the practical application of TENGs for large-scale blue energy from water wave in oceans.

Although there has been rapid advancement in wearable electronics, challenges still remain in developing wearable and sustainable power sources with simple fabrication and low cost. In this work, we demonstrate a flexible coaxial fiber by fabricating a one-dimensional triboelectric nanogenerator (TENG) outside and a supercapacitor (SC) inside, which can not only harvest mechanical energy but also store energy in the all-in-one fiber. In such a coaxial fiber, carbon fiber bundles are utilized as the electrode material for the TENG as well as the active and electrode material for the SC. Meanwhile, silicone rubber serves as the separator between the SC and TENG, as the triboelectric material for the TENG, and as the encapsulation material for the whole fiber as well. Moreover, both SC and TENG exhibit good performance and stability, which ensures their long-term use in daily life. Because of the flexibility and durability of the carbon fiber and silicone rubber, the proposed coaxial fibers show great flexibility, which could be further knitted as cloth for sustainably powering wearable electronic devices. This work presents a promising platform for wearable electronics as well as smart textiles.

Two-dimensional (2D) nonlayered nanomaterials have attracted extensive attention for electronic and optoelectronic applications recently because of their distinct properties. In this work, we first employed a facile one-step method to synthesize 2D nonlayered cadmium sulfide selenide (CdS xSe1- x, x = 0.33) nanosheets with a highly crystalline structure and then we introduced a generic spin-coating approach to fabricate hybrid nanomaterials composed of PbS quantum dots (QDs) and 2D CdS xSe1- x nanosheets and demonstrated their potential for high-performance broadband photodetectors. Compared with pure 2D CdS xSe1- x nanosheet photodetectors, the photoelectric performance of the PbS/CdS xSe1- x hybrid nanostructure is enhanced by 3 orders of magnitude under near-infrared (NIR) light illumination and maintains its performance in the visible (Vis) range. The photodetector exhibits a broadband response range from Vis to NIR with an ultrahigh light-to-dark current ratio (3.45 × 106), a high spectral responsivity (1.45 × 103 A/W), and high detectivity (1.05 × 1015 Jones). The proposed QDs/2D nonlayered hybrid nanostructure-based photodetector paves a promising way for next-generation high-performance broadband optoelectronic devices.

The development of Pt-based core/shell nanoparticles represents an emerging class of electrocatalysts for fuel cells, such as methanol oxidation reaction (MOR) and ethanol oxidation reaction (EOR). Here, we present a one-pot synthesis approach to prepare hexagonal PtBi/Pt core/shell nanostructure composed of an intermetallic Pt1Bi1 core and an ultrathin Pt shell with well-defined shape, size, and composition. The structure and the synergistic effect among different components enhanced their MOR and EOR performance. The optimized Pt2Bi nanoplates exhibit excellent mass activities in both MOR (4,820 mA·mgPt –1) and EOR (5,950 mA·mgPt–1) conducted in alkaline media, which are 6.15 times and 8.63 times higher than those of commercial Pt/C, respectively. Pt2Bi nanoplates also show superior operation durability to commercial Pt/C. This work may inspire the rational design and synthesis of Pt-based nanoparticles with improved performance for fuel cells and other applications.

The observation of a spontaneous electron enrichment at the apexes of bismuth vanadate (BiVO4) nanopyramidal arrays is achieved by performing synchrotron-based angular dependent X-ray absorption spectroscopy. In accordance with density function theory calculations, the formation of (112) facets enriched apexes is proposed. Such intrinsically electron-enriched (112) facets at the apexes produce a potential facilitating the diffusion of photoexcited holes, which not only mitigates the recombination with the photoexcited electrons, but also provide an active reaction site for the photoassisted selective growth of cobalt phosphate (CoPi), a well known and highly active co-catalyst for water oxidation at the apex of BiVO4 nanopyramids. Benefiting from the element-resolved properties of synchrotron-based X-ray spectroscopy, 3d electrons on the vanadium site are directly resolved by resonant inelastic X-ray scattering measurements. Due to this unique morphology, the charge at the apex is expected to induce a strong interaction with CoPi, as a result of the metal-to-ligand charge transfer spectroscopy feature observed from the cobalt site. Substantial evidences are collected by means of comprehensive soft X-ray spectroscopy techniques with high spectral resolution revealing the atomic-scale origin and the nature of the synergy as well as the strong correlation between its unique structural properties and the electronic structure of this novel highly-ordered hybrid photocatalyst and its significantly improved photoelectrochemical performance.

High-energy and high-power-density lithium-ion batteries are promising energy storage systems for future portable electronics and electric vehicles. Here, three-dimensional (3D) patterned electrodes are created through the paste-extrusion-based 3D printing technique realizing a trade-off between high energy density and power density. The 3D electrodes possess several distinct merits over traditional flat thick electrodes, such as higher surface area, shorter ion transport path, and improved mechanical strength. Benefiting from these advantages, the 3D-printed thick electrodes present the higher specific capacity and improved cycling stability compared with those of the conventional thick electrodes. Upon comparison to the previous studies on 3D-printed electrodes, this study investigates the influence and optimization of 3D-printed LiFePO4 (LFP) electrodes with three different geometric shapes to achieve a high rate performance and long-term cycling stability. Accordingly, a series of 3D electrodes with d...

Loading metal guests within metal–organic frameworks (MOFs) via secondary functional groups is a promising route for introducing or enhancing MOF performance in various applications. In this work, 14 metal ions (Li+, Na+, K+, Mg2+, Ca2+, Ba2+, Zn2+, Co2+, Mn2+, Ag+, Cd2+, La3+, In3+, and Pb2+) have been successfully introduced within the MIL-121 MOF using a cost-efficient route involving free carboxylic groups on the linker. The local and long-range structure of the metal-loaded MOFs is characterized using multinuclear solid-state NMR and X-ray diffraction methods. Li/Mg/Ca-loaded MIL-121 and Ag nanoparticle-loaded MIL-121 exhibit enhanced H2 and CO2 adsorption; Ag nanoparticle-loaded MIL-121 also demonstrates remarkable catalytic activity in the reduction of 4-nitrophenol.

Hematite is one of the most promising photoanodes for photoelectrochemical (PEC) solar water splitting. However, due to the low conduction band position for water reduction, an external bias is necessarily required with the consumption of extra power. In this work, a titanium modified hematite (Ti-Fe2O3) photoanode-based self-powered PEC water splitting system in tandem with a rotatory disc-shaped triboelectric nanogenerator (RD-TENG) has been developed. It is a fantastic strategy to effectively drive the hematite-based PEC water splitting by using the environmental mechanical energy through a TENG. When the rotation speed is 65 rpm (water flowing rate ∼0.61 m/s), the peak current reaches to 0.12 mA under illumination contrast to that in the dark with almost zero. As for 80 rpm, the peak currents are 0.17 and 0.33 mA in the dark or under illumination, respectively, indicating the simultaneous occurrence of electrolysis and PEC water splitting. When higher than 120 rpm, the peak current in the dark is near...

Flexible and broadband photodetectors have drawn extensive attention due to their potential application in foldable displays, optical communications, environmental monitoring, etc. In this work, a flexible photodetector based on the crystalline PbS quantum dots (QDs)/ZnO nanoparticles (NPs) heterostructure was proposed. The photodetector exhibits a broadband response from ultraviolet-visible (UV-Vis) to near infrared detector (NIR) range with a remarkable current on/off ratio of 7.08×103 under 375 nm light illumination. Compared with pure ZnO NPs, the heterostructure photodetector shows the three orders of magnitude higher responsivity in Vis and NIR range, and maintains its performance in the UV range simultaneously. The photodetector demonstrates a high responsivity and detectivity of 4.54 A W−1 and 3.98×1012 Jones. In addition, the flexible photodetectors exhibit excellent durability and stability even after hundreds of times bending. This work paves a promising way for constructing next-generation high-performance flexible and broadband optoelectronic devices.

The urgent demand for portable electronics has promoted the development of high-efficiency, sustainable, and even stretchable self-charging power sources. In this work, we propose a flexible self-charging power unit based on folded carbon (FC) paper for harvesting mechanical energy from human motion and power portable electronics. The present unit mainly consists of a triboelectric nanogenerator (FC-TENG) and a supercapacitor (FC-SC), both based on folded carbon paper, as energy harvester and storage device, respectively. This favorable geometric design provides the high Young’s modulus carbon paper with excellent stretchability and enables the power unit to work even under severe deformations, such as bending, twisting, and rolling. In addition, the tensile strain can be maximized by tuning the folding angle of the triangle-folded carbon paper. Moreover, the waterproof property of the packaged device make it washable, protect it from human sweat, and enable it to work in harsh environments. Finally, the as-prepared self-charging power unit was tested by placing it on the human body to harvest mechanical energy from hand tapping, foot treading, and arm touching, successfully powering an electronic watch. This work demonstrates the impressive potential of stretchable self-charging power units, which will further promote the development of high Young’s modulus materials for wearable/portable electronics.