Highly Elastic, Robust, and Efficient Hydrogel Solar Absorber against Harsh Environmental Impacts.

Solar distillation is a promising approach for addressing water scarcity, but relentless stress/strain perturbations induced by wind and waves would inevitably cause structural damage to solar absorbers. Despite notable advances in efficient solar absorbers, there have been no reports of compliant and robust solar absorbers withstanding practical mechanical impacts. Herein, an elastic and robust hydrogel absorber that exhibited a high level of evaporation performance was fabricated by introducing ion-coordinated MXene nanosheets as photothermal conversion units and mechanically enhanced fillers. The ion-coordinated MXene nanosheets acting as strong cross-linking points provided excellent elasticity and robustness to the hydrogel absorber. As a result, the evaporation rate of hydrogel absorber, with a high initial value of 2.61 kg m-2 h-1 under one sun irradiation, remained at 2.15 kg m-2 h-1 under a 100% tensile strain state and 2.40 kg m-2 h-1 after 10 000 stretching-releasing cycles. This continuous and stable water desalination approach provides a promising device for actual seawater distillation.

Temperature Sensors Integrated with an Electrochromic Readout toward Visual Detection.

Temperature sensors have attracted great attention for personal health care and disease diagnosis in recent years. However, it is still a great challenge to fabricate reliable and highly sensitive temperature sensors that can convert physiological signals into easily readable signals in a convenient way. Herein, an integrated smart temperature sensor system based on a traditional temperature sensor and electrochromic display is proposed for real-time visual detection of temperature. Significantly, a voltage-regulated electrochromic device (ECD) based on tungsten oxide (WO3) and polyaniline (PANI) as the real-time visualization window was integrated into the platform to provide feedback on the temperature change. The ECD would change its color from green to blue based on the electrical signal of the temperature sensor, resulting in a visualized readout that can be monitored through our naked eye. Additionally, the smart temperature sensor system possesses an extremely durable property and cycle stability, remaining around 90% of the initial value even after 15,000 s continuous cycle. Thus, the novel design and low power consumption advantages make it a good candidate to pave the way for developing interactive wearable electronics and intelligent robots as real-time temperature feedback systems.

The Influence of Fiber on the Mechanical Properties of Geopolymer Concrete: A Review.

Geopolymer is widely used as a supplement to cementitious composites because of its advantages of low carbon and environmental protection, and geopolymer concrete is also broadly used in practical engineering. In recent years, geopolymer concrete has attracted increasing interest owing to its superior mechanical properties, and a series of research results have been obtained. In this paper, from the preparation of geopolymer concrete, based on the characteristics that geopolymer concrete is brittle and easy to crack, the types and basic properties of fibers to enhance the toughness of concrete are analyzed, the advantages and disadvantages of different fibers used as a material to enhance the toughness of concrete are summarized, and we review the effects of type, shape, volume rate, aspect ratio, and hybrid fiber combinations on the static mechanical properties. The results indicate that fibers have significant potential to enhance the compressive strength, splitting tensile strength, flexural strength, and fracture toughness of geopolymer concrete, and the optimal fiber volume rate seems to be related to the fiber type. Whereas the effect of aspect ratio and hybrid fiber combinations on the properties of geopolymer concrete seems to be obvious. This paper reviews the influence of fiber on the basic mechanical properties of geopolymer concrete, which provides a solid foundation to promote the further development and application of the research on the toughness of fiber-reinforced geopolymer concrete and provides recommendations for future research.

Extremely Robust and Multifunctional Nanocomposite Fibers for Strain-Unperturbed Textile Electronics.

Textile electronics are needed that can achieve strain-unaltered performance when they undergo irregular and repeated strain deformation. Such strain-unaltered textile electronics require advanced fibers that simultaneously have high functionalities and extreme robustness as fabric materials. Current synthetic nanocomposite fibers based on inorganic matrix have remarkable functionalities but often suffer from low robustness and poor tolerance against crack formation. Here, we present a design for a high-performance multifunctional nanocomposite fiber that is mechanically and electrically robust, which was realized by crosslinking titanium carbide (MXene) nanosheets with a slide-ring polyrotaxane to form an internal mechanically-interlocked network. This inorganic matrix nanocomposite fiber featured distinct strain-hardening mechanical behavior and exceptional load-bearing capability (toughness approaching 60 MJ m-3 and ductility over 27%). It retained 100% of its ductility after cyclic strain loading. Moreover, the high electrical conductivity (>1.1 × 105 S m-1 ) and electrochemical performance (>360 F cm-3 ) of the nanocomposite fiber can be well retained after subjecting the fiber to extensive (>25% strain) and long-term repeated (10 000 cycles) dimensional changes. Such superior robustness allowed for the fabrication of the nanocomposite fibers into various robust wearable devices, such as textile-based electromechanical sensors with strain-unalterable sensing performance and fiber-shaped supercapacitors with invariant electrochemical performance for 10 000 strain loading cycles.

Self-Healing and Shape Memory Hypercrosslinked Metal-Organic Polyhedra Polymers via Coordination Post-Assembly.

Coordination-driven crosslinking networks with reversible and dynamic characteristics are gaining increasing interest in diverse application fields. Herein, we use a coordination crosslinking approach using metal-organic polyhedra (MOPs) as high-connectivity building blocks to post-assemble a class of coordination hypercrosslinked MOP (CHMOP) polymers. The introduction of 12-connected MOP nodes to the polymeric networks is critical to producing membranes that overcome the trade-off between mechanical properties and dynamic healing, and meanwhile possess multifunctionalities including shape memory, solution processability, and 3D printing. The CHMOPs can also be used for anticorrosion coating and achieve function couplings, e.g., shape memory-assisted self-healing (SMASH), which have not been achieved in the MOP-based hybrid materials yet. This work not only offers a feasible strategy to construct new multifunctional materials but also greatly expands the application scopes of MOPs.

Coordination Chemistry Engineered Polymeric Carbon Nitride Photoanode with Ultralow Onset Potential for Water Splitting.

Construction of an intimate film/substrate interface is of great importance for a photoelectrode to achieve efficient photoelectrochemical performance. Inspired by coordination chemistry, a polymeric carbon nitride (PCN) film is intimately grown on a Ti-coated substrate by an in situ thermal condensation process. The as-prepared PCN photoanode exhibits a record low onset potential (Eonset ) of -0.38 V versus the reversible hydrogen electrode (RHE) and a decent photocurrent density of 242 µA cm-2 at 1.23 VRHE for water splitting. Detailed characterization confirms that the origin of the ultralow onset potential is mainly attributed to the substantially reduced interfacial resistance between the Ti-coated substrate and the PCN film benefitting from the constructed interfacial sp2 N→Ti coordination bonds. For the first time, the ultralow onset potential enables the PCN photoanode to drive water splitting without external bias with a stable photocurrent density of ≈9 µA cm-2 up to 1 hour.

Highly Sensitive Temperature-Pressure Bimodal Aerogel with Stimulus Discriminability for Human Physiological Monitoring.

Multimodal sensor with high sensitivity, accurate sensing resolution, and stimuli discriminability is very desirable for human physiological state monitoring. A dual-sensing aerogel is fabricated with independent pyro-piezoresistive behavior by leveraging MXene and semicrystalline polymer to assemble shrinkable nanochannel structures inside multilevel cellular walls of aerogel for discriminable temperature and pressure sensing. The shrinkable nanochannels, controlled by the melt flow-triggered volume change of semicrystalline polymer, act as thermoresponsive conductive channels to endow the pyroresistive aerogel with negative temperature coefficient of resistance of -10.0% °C-1 and high accuracy within 0.2 °C in human physiological temperature range of 30-40 °C. The flexible cellular walls, working as pressure-responsive conductive channels, enable the piezoresistive aerogel to exhibit a pressure sensitivity up to 777 kPa-1 with a detectable pressure limit of 0.05 Pa. The pyro-piezoresistive aerogel can detect the temperature-dependent characteristics of pulse pressure waveforms from artery vessels under different human body temperature states.

Pushing detectability and sensitivity for subtle force to new limits with shrinkable nanochannel structured aerogel.

There is an urgent need for developing electromechanical sensor with both ultralow detection limits and ultrahigh sensitivity to promote the progress of intelligent technology. Here we propose a strategy for fabricating a soft polysiloxane crosslinked MXene aerogel with multilevel nanochannels inside its cellular walls for ultrasensitive pressure detection. The easily shrinkable nanochannels and optimized material synergism endow the piezoresistive aerogel with an ultralow Young's modulus (140 Pa), numerous variable conductive pathways, and mechanical robustness. This aerogel can detect extremely subtle pressure signals of 0.0063 Pa, deliver a high pressure sensitivity over 1900 kPa-1, and exhibit extraordinarily sensing robustness. These sensing properties make the MXene aerogel feasible for monitoring ultra-weak force signals arising from a human's deep-lying internal jugular venous pulses in a non-invasive manner, detecting the dynamic impacts associated with the landing and take-off of a mosquito, and performing static pressure mapping of a hair.

An in situ and rapid self-healing strategy enabling a stretchable nanocomposite with extremely durable and highly sensitive sensing features.

Progress toward the development of wearable electromechanical sensors with durable and reliable sensing performance is critical for emerging wearable integrated electronic applications. However, it remains a long-standing challenge to realize mechanically stretchable sensing materials with extremely durable and high-performing sensing ability due to the fundamental dilemma lying in the sensing mechanism. In this work, we proposed an in situ and rapid self-healing strategy through nano-confining a dynamic host-guest supramolecular polymer network in a graphene-based multilevel nanocomposite matrix to fabricate a mechanically stretchable and structurally healable sensing nanocomposite which is provided with intriguing sensing durability and sensitivity simultaneously. When repeatedly stretching and releasing the nanocomposite sensing film, the fast association kinetics of cyclodextrin and adamantane host-guest inclusion complexes and good polymer chain dynamics in the supramolecular polymer network endowed by the nanoconfinement effect enable autonomous and rapid repair of the micro-cracks in situ generated in the sensing material. As a result, our strain sensing devices can achieve an extremely high durability and retain stable sensing performance even after over 100 000 stretching-releasing cycles at large strain of 50%. Moreover, the brittle nature originated from the inorganically dominated structure in conjunction with the thermodynamically stable host-guest interactions and dynamic hydrogen bonds inside the multilevel nanocomposite allow the sensing material to exhibit an ultrahigh gauge factor over 1500 with a large working strain of 58%. This work presents a reliable approach for the construction of ultradurable and high-performing wearable electronics.

Highly Stretchable Shape Memory Self-Soldering Conductive Tape with Reversible Adhesion Switched by Temperature.

HIGHLIGHTS: Shape memory self-soldering tape used as conductive interconnecting material. Perfect shape and conductivity memory performance and anti-fatigue performance. Reversible strong-to-weak adhesion switched by temperature. With practical interest in the future applications of next-generation electronic devices, it is imperative to develop new conductive interconnecting materials appropriate for modern electronic devices to replace traditional rigid solder tin and silver paste of high melting temperature or corrosive solvent requirements. Herein, we design highly stretchable shape memory self-soldering conductive (SMSC) tape with reversible adhesion switched by temperature, which is composed of silver particles encapsulated by shape memory polymer. SMSC tape has perfect shape and conductivity memory property and anti-fatigue ability even under the strain of 90%. It also exhibits an initial conductivity of 2772 S cm-1 and a maximum tensile strain of ~ 100%. The maximum conductivity could be increased to 5446 S cm-1 by decreasing the strain to 17%. Meanwhile, SMSC tape can easily realize a heating induced reversible strong-to-weak adhesion transition for self-soldering circuit. The combination of stable conductivity, excellent shape memory performance, and temperature-switching reversible adhesion enables SMSC tape to serve two functions of electrode and solder simultaneously. This provides a new way for conductive interconnecting materials to meet requirements of modern electronic devices in the future.

Highly Stretchable Carbon Nanotubes/Polymer Thermoelectric Fibers.

Thermoelectric (TE) technology provides a new way to directly harvest and convert the heat continuously released from the human body. The greatest challenge for TE materials applied in wearable TE generators is compatible with the constantly changing morphology of the human body while offering a continuous and stable power output. Here, a stretchable carboxylic single-walled carbon nanotube (SWNT)-based TE fiber is prepared by an improved wet-spinning method. The stable Seebeck coefficient of the annealed carboxylic SWNT-based TE fiber is 44 µV/K even under the tensile strain of ∼30%. Experimental results show that the fiber can continue to generate constant TE potential when it is changed to various shapes. The new stretchable TE fiber has a larger Seebeck coefficient and more stretchability than existing TE fibers based on the Seebeck effect, opening a path to using the technology for a variety of practical applications.

Plasmonic Ti3C2Tx MXene Enables Highly Efficient Photothermal Conversion for Healable and Transparent Wearable Device.

Skin-mountable and transparent devices are highly desired for next-generation electronic applications but are susceptible to unexpected ruptures or undesired scratches, which can drastically reduce the device lifetime. Developing wearable and transparent materials with healable function that can recover their original functionality after mechanical damage under mild and noninvasive repairing operation is thus imperative. Herein, we demonstrate that the incorporation of ultrasmall quantities of plasmonic silver nanoparticle (AgNP)@MXene nanosheet hybrids to serve as photothermal fillers in waterborne elastic polyurethane enables high transparency as well as effective light-triggered healing capabilities for wearable composite coatings. The AgNP@MXene hybrid functions as a highly effective photon captor, energy transformer, and molecular heater due to the amalgamation of (1) ultrahigh photothermal conversion efficiency, high thermal conductivity, and structural properties of MXene, (2) the outstanding plasmonic effect of AgNPs, and (3) the synergistic effects from their hybrids. The resulting wearable composite coating with ultralow loading of plasmonic AgNP@MXene hybrids (0.08 wt % or 0.024 vol %) can produce a significant temperature increase of ∼111 ± 2.6 °C after the application of 600 mW cm-2 light irradiation for 5 min, while maintaining a high optical transmittance of ∼83% at a thickness of ∼60 µm. This local temperature increase can rapidly heal the mechanical damage to the composite coating, with a healing efficiency above 97%.

Probing the role of O-containing groups in CO2 adsorption of N-doped porous activated carbon.

Porous activated carbons (PACs) are promising candidates to capture CO2 through physical adsorption because of their chemical stability, easy-synthesis, cost-effectiveness and good recyclability. However, their low CO2 adsorption capacity, especially low CO2/N2 selectivity, has limited their practical applications. In this work, an optimized PAC with a large specific surface area, a small micropore size, and a large micropore volume has been synthesized by one-step carbonization/activation of casein using K2CO3 as a mild activation agent. It showed a remarkably enhanced CO2 adsorption capacity as high as 5.78 mmol g-1 and an excellent CO2/N2 selectivity of 144 (25 °C, 1 bar). Based on DFT calculations and experimental results, the coexistence of adjacent pyridinic N and -OH/-NH2 species was proposed for the first time to make an important contribution to the ultra-high CO2 adsorption performance, especially CO2/N2 selectivity. This work provides effective guidance to design PAC adsorbents with high CO2 adsorption performance. The content of pyridine N combined with -OH/-NH2 was further elevated by additional nitrogen introduction, resulting in a further enhanced CO2 adsorption capacity up to 5.96 mmol g-1 (25 °C, 1 bar). All these results suggest that, in addition to the well-defined pore structure, pyridinic N with neighboring OH or NH2 species played an important role in enhancing the CO2 adsorption performance of PACs, thus providing effective guidance for the rational design of CO2 adsorbents.

Amorphous Fe²âº-rich FeOx loaded in mesoporous silica as a highly efficient heterogeneous Fenton catalyst.

A simple physical-vapor-infiltration (PVI) method using ferrocene as the iron source, has been developed to load FeOx into the pore channels of mesoporous silica SBA-15. The obtained FeOx/SBA-15 composite has a high loading amount of FeOx (e.g. 26.64 wt% Fe content obtained at PVI duration 17 h and calcination temperature 450 °C) but unblocked pore channels thanks to the unique preparation strategy. The FeOx species are amorphous, rich of Fe(2+) and have been highly dispersed as a nanocoating onto the pore channel surface. The FeOx/SBA-15 composite was used as a heterogeneous Fenton catalyst to degrade Acid orange 7 (AO7). It showed a high catalytic activity and degradation efficiency, which was attributed to the high proportion of Fe(2+) in the amorphous FeOx and their favorable adsorption capability for the dye. The influences of the PVI duration, the calcination temperature and the Fenton reaction conditions (FeOx/SBA-15 dosages, H2O2 dosages and initial pH value) on the catalytic activity were investigated in detail.