Search

High-sensitivity strain sensing elements with a wide strain range, fast response, high stability, and small sensing areas are desirable for constructing strain sensor arrays with high temporospatial resolution. However, current strain sensors rely on crack-based conductive materials having an inherent tradeoff between their sensing area and performance. Here, we present a molecular-level crack modulation strategy in which we use layer-by-layer assembly to introduce strong, dynamic, and reversible coordination bonds in an MXene and silver nanowire-matrixed conductive film. We use this approach to fabricate a crack-based stretchable strain sensor with a very small sensing area (0.25 mm2). It also exhibits an ultrawide working strain range (0.001–37%), high sensitivity (gauge factor ~500 at 0.001% and >150,000 at 35%), fast response time, low hysteresis, and excellent long-term stability. Based on this high-performance sensing element and facile assembly process, a stretchable strain sensor array with a device density of 100 sensors per cm2 is realized. We demonstrate the practical use of the high-density strain sensor array as a multichannel pulse sensing system for monitoring pulses in terms of their spatiotemporal resolution. This work proposes a cracking control strategy using MXene and silver nanowire composite films to achieve a stretchable strain sensor system with high resolution, range, sensitivity, speed, and stability [ABSTRACT FROM AUTHOR]

Designing autonomously oscillating materials is highly desirable for emerging smart material fields but challenging. Herein, a type of hypercrosslinked metal–organic polyhedra (HCMOPs) membranes formed by covalent crosslinking of boronic acid‐modified Zr‐based MOPs with polyvinyl alcohol (PVA) are rationally designed. In these membranes, MOPs serve as high‐connectivity nodes and provide dynamic borate bonds with PVA in hypercrosslinked networks, which can be broken/formed reversibly upon the stimulus of water vapor. The humidity response characteristic of HCMOPs promotes their self‐oscillating and self‐healing properties. HCMOP membranes can realize a self‐oscillating property above the water surface even after loading a cargo that is 1.5 times the weight of the membrane due to the fast adsorption and desorption kinetics. Finally, the HCMOP actuator can realize energy conversion from mechanical energy into electricity when coupled with a piezoelectric membrane. This work not only paves a new avenue to construct MOP‐polymer hybrid materials but also expands the application scopes of MOPs for smart actuation devices. [ABSTRACT FROM AUTHOR]

We show with simplified numerical models, that for the kind of RBMK operated in Chernobyl: The core was unstable due to its large size and to its weak power counter-reaction coefficient, so that the power of the reactor was not easy to control even with an automatic system. Xenon oscillations could easily be activated. When there was xenon poisoning in the upper half of the core, the safety rods were designed in such a way that, at least initially, they were increasing (and not decreasing) the core reactivity. This reactivity increase has been sufficient to lead to a very high pressure increase in a significant amount of liquid water in the fuel channels thus inducing a strong propagating shock wave leading to a failure of half the pressure tubes at their junction with the drum separators. The depressurization phase (flash evaporation) following this failure has produced, after one second, a significant decrease of the water density in half the pressure tubes and then a strong reactivity accident due to the positive void effect reactivity coefficient. We evaluate the fission energy released by the accident

Carbon nanotubes (CNTs) have established their promising application as infrared photodetector and the photothermoelectric (PTE) effect is demonstrated to play a critical role. While extensive studies are focused on the optoelectronic behaviors, the thermoelectric conversion involved in the PTE has been pursued to less extent probably due to the overall low thermopower under infrared (IR) illumination. Herein, to trigger a stronger PTE response, Au/CNT heterojunctions are formed by Au nanoparticles (NPs) decoration of CNT films to facilitate both light absorption and carrier transportation, so that thermoelectric property is enhanced simultaneously. Significant boost on infrared radiation energy conversion capability is therefore enabled in Au NPs decorated CNT film, delivering maximum output voltage of 26.1 mV and power of 27.3 µW, outperforming the state‐of‐the art photodetectors based on PTE effect. The transport mechanism is revealed via combining in situ Kelvin Probe Force Microscope mapping of the surface potential and macroscopic transport and output performances under IR illumination. Finally, the IR detection function is validated via an 8‐channel IR detector prototype, presenting sensitive responsivity and long‐term cyclic stability. The study thus demonstrates the PTE effect as a promising platform toward high‐performance optoelectronic applications such as IR detection and solar energy harvesting. [ABSTRACT FROM AUTHOR]

Highlights: A strategy that combines multi-mode scanning probe microscopy-based electrical characterization and nano-infrared spectroscopy is developed. A series of samples with different coupling agents and nanoparticles are characterized to unveil the local structure-property correlation of the interface in ferroelectric polymer nanocomposites. The formation of hydrogen bond between the surface modifiers and the ferroelectric polymer enhances the β-phase content and reduces the domain size of the interface, and hence promotes the local piezoelectric effect and breakdown strength. Ferroelectric polymer nanocomposites possess exceptional electric properties with respect to the two otherwise uniform phases, which is commonly attributed to the critical role of the matrix–particle interfacial region. However, the structure–property correlation of the interface remains unestablished, and thus, the design of ferroelectric polymer nanocomposite has largely relied on the trial-and-error method. Here, a strategy that combines multi-mode scanning probe microscopy-based electrical characterization and nano-infrared spectroscopy is developed to unveil the local structure–property correlation of the interface in ferroelectric polymer nanocomposites. The results show that the type of surface modifiers decorated on the nanoparticles can significantly influence the local polar-phase content and the piezoelectric effect of the polymer matrix surrounding the nanoparticles. The strongly coupled polar-phase content and piezoelectric effect measured directly in the interfacial region as well as the computed bonding energy suggest that the property enhancement originates from the formation of hydrogen bond between the surface modifiers and the ferroelectric polymer. It is also directly detected that the local domain size of the ferroelectric polymer can impact the energy level and distribution of charge traps in the interfacial region and eventually influence the local dielectric strength. [ABSTRACT FROM AUTHOR]

Mechanically robust polymers are broadly applied engineering materials, in which internal, hidden defects resulting from mechanical, electrical and thermal fatigues are one of the major factors threatening their long-term stability. Self-healing of these defects requires the ability of spontaneous crack closure without manually holding the broken parts together, which is not accessible in mechanically robust polymers with previous approaches. Here, we report a self-healing polymer that can be reversibly switched between the glassy state and the high-elastic state, as enabled by the coexistence of reversible and permanent crosslinking sites in the synthesized dynamic crosslinker. This design allows for complete repair of internal defects for multiple times while maintaining the dimensional stability of mechanically robust polymers during the healing process. In addition, this self-healing material is readily prepared by curing the commercially available epoxy monomer with the synthesized dynamic crosslinker, which endows this approach with great potential for industrial applications. [ABSTRACT FROM AUTHOR]

Compact solid‐state refrigeration systems that offer a high specific cooling power and a high coefficient of performance (COP) are desirable in a wide range of applications where efficient and localized heat transfer is required. Here, a double‐unit electrocaloric (EC) polymer‐based refrigeration device with high intrinsic thermodynamic efficiency is demonstrated using a flexible EC polymer film with improved performance by doping plasticizer and an electrostatic actuation mechanism. The double‐unit refrigeration device achieves a large temperature span of 4.8 K, which is 71% higher than that of the single‐unit device. A specific cooling power of 3.6 W g−1 and a maximum COP of 8.3 for the cooling device are produced. The surface temperature of a central processing unit (CPU) cooled by an active EC device is 22.4 K lower than that of the CPU cooled in air. The highly efficient and compact EC cooling device demonstrated here not only leapfrogs the performance of existing solid‐state cooling technologies, but also brings solid state cooling closer to reality for a variety of practical applications that require compact or mechanically flexible refrigeration. [ABSTRACT FROM AUTHOR]

The applications of lithium metal anode are limited by uncontrollable lithium dendrite growth and infinite volume changes during cycling. These fundamental issues are exacerbated at high cycling current densities and capacities. Herein, a mechanically stable and resilient lithium metal host is fabricated by covalently cross‐linking a highly‐conductive and lithiophilic MXene/silver nanowire scaffold through a silylation reaction between MXene nanosheets and polysiloxane. Compared with the control sample (an MXene scaffold assembled by weak van der Waals forces), the covalently cross‐linked MXene scaffold displays excellent mechanical strength and resilience, which is conducive to buffer the large internal stress fluctuations generated during rapid and deep lithium plating‐stripping and guaranteed that the integrated framework structure is maintained during long‐term charging‐discharging cycles. When used in a symmetric cell, the lithium composite anode based on the covalently cross‐linked MXene host affords an unprecedented cyclic lithium plating‐stripping stability of a record‐high 3000 h lifespan at an ultrahigh current density (20 mA cm−2) and areal capacity (10 mAh cm−2). When this composite anode is coupled with a LiNi0.5Co0.2Mn0.3O2 cathode, the full cell delivers an ultrahigh rate of 10 C for up to 1000 cycles, with an average capacity decay of 0.043% per cycle and a stable Coulombic efficiency of 98.7%. [ABSTRACT FROM AUTHOR]

A solar‐thermal water evaporation structure that can continuously generate clean water with high efficiency and good salt rejection ability under sunlight is highly desirable for water desalination, but its realization remains challenging. Here, a hierarchical solar‐absorbing architecture is designed and fabricated, which comprises a 3D MXene microporous skeleton with vertically aligned MXene nanosheets, decorated with vertical arrays of metal–organic framework‐derived 2D carbon nanoplates embedded with cobalt nanoparticles. The rational integration of three categories of photothermal materials enables broadband light absorption, efficient light to heat conversion, low heat loss, rapid water transportation behavior, and much‐improved corrosion and oxidation resistance. Moreover, when assembling with a hydrophobic insulating layer with hydrophilic channel, the MXene‐based solar absorber can exhibit effective inhibition of salt crystallization due to the ability to advect and diffuse concentrated salt back into the water. As a result, when irradiating under one sun, the solar‐vapor conversion efficiency of the MXene‐based hierarchical design can achieve up to ≈93.4%, and can remain over 91% over 100 h to generate clean vapor for stable and continuous water desalination. This strategy opens an avenue for the development of MXene‐based solar absorbers for sustainable solar‐driven desalination. [ABSTRACT FROM AUTHOR]

While stretchable micro‐supercapacitors (MSCs) have been realized, they have suffered from limited areal electrochemical performance, thus greatly restricting their practical electronic application. Herein, a facile strategy of 3D printing and unidirectional freezing of a pseudoplastic nanocomposite gel composed of Ti3C2Tx MXene nanosheets, manganese dioxide nanowire, silver nanowires, and fullerene to construct intrinsically stretchable MSCs with thick and honeycomb‐like porous interdigitated electrodes is introduced. The unique architecture utilizes thick electrodes and a 3D porous conductive scaffold in conjunction with interacting material properties to achieve higher loading of active materials, larger interfacial area, and faster ion transport for significantly improved areal energy and power density. Moreover, the oriented cellular scaffold with fullerene‐induced slippage cell wall structure prompts the printed electrode to withstand large deformations without breaking or exhibiting obvious performance degradation. When imbued with a polymer gel electrolyte, the 3D‐printed MSC achieves an unprecedented areal capacitance of 216.2 mF cm−2 at a scan rate of 10 mV s−1, and remains stable when stretched up to 50% and after 1000 stretch/release cycles. This intrinsically stretchable MSC also exhibits high rate capability and outstanding areal energy density of 19.2 µWh cm−2 and power density of 58.3 mW cm−2, outperforming all reported stretchable MSCs. [ABSTRACT FROM AUTHOR]