High‐Performance Dopamine Sensors Based on Whole‐Graphene Solution‐Gated Transistors

Solution‐gated graphene transistors with graphene as both channel and gate electrodes are fabricated for the first time and used as dopamine sensors with the detection limit down to 1 nM, which is three orders of magnitude better than that of conventional electrochemical measurements. The sensing mechanism is attributed to the change of effective gate voltage applied on the transistors induced by the electro‐oxidation of dopamine at the graphene gate electrodes. The interference from glucose, uric acid, and ascorbic acid on the dopamine sensor is characterized. The selectivity of the dopamine sensor is dramatically improved by modifying the gate electrode with a thin Nafion film by solution process. This work paves the way for developing many other biosensors based on the solution‐gated graphene transistors by specifically functionalizing the gate electrodes. Because the devices are mainly made of graphene, they are potentially low cost and ideal for high‐density integration as multifunctional sensor arrays.     

A Photoresponsive Red‐Hair‐Inspired Polydopamine‐Based Copolymer for Hybrid Photocapacitive Sensors

Inspired by the powerful photosensitizing properties of the red hair pigments pheomelanins, a photoresponsive cysteine‐containing variant of the adhesive biopolymer polydopamine (pDA) is developed via oxidative copolymerization of dopamine (DA) and 5‐S‐cysteinyldopamine (CDA) in variable ratios. Chemical and spectral analysis indicate the presence of benzothiazole/benzothiazine units akin to those of pheomelanins. p(DA/CDA) copolymers display ­impedance properties similar to those of biological materials and a marked photoimpedance response to light stimuli. The use of the p(DA/CDA) copolymer to implement a solution‐processed hybrid photocapacitive/resistive metal‐insulator‐semiconductor (MIS) device disclosed herein is the first example of technological exploitation of photoactive, red‐hair‐inspired biomaterials as soft enhancement layer for silicon in an optoelectronic device. The bio‐inspired materials described herein may provide the active component of new hybrid photocapacitive sensors with a chemically tunable response to visible light.     

Evaluation of Encoded Layer‐By‐Layer Coated Microparticles As Protease Sensors

Proteases are important pharmaceutical targets for new drugs because of their involvement in numerous disease processes. This study evaluates whether photophysically encoded microparticles carrying fluorescently labeled protease substrates (peptides) at their surface show potential for detecting proteases in a sample. Layer‐by‐layer (LbL) polyelectrolyte coatings, containing a red‐labeled peptidic trypsin substrate, are carefully designed and applied at the surface of the encoded microparticles. The peptide‐loaded LbL coatings lose their red fluorescence upon incubation in a trypsin solution, indicating that LbL‐coated microparticles show potential to screen for the presence of active proteases in biological samples.     

Bioinspired Geometry‐Switchable Janus Nanofibers for Eye‐Readable H2 Sensors

Nanoscale architectures found in nature have unique functionalities and their discovery has led to significant advancements in various fields including optics, wetting, and adhesion. The sensilla of arthropods, comprised of unique hierarchical structures, are a representative example which inspired the development of various bioinspired systems, owing to their hypersensitive and ultrafast responsivity to mechanical and chemical stimuli. This report presents a geometry‐switchable and highly H₂‐reactive Janus nanofiber (H‐NF) array inspired by the structural features of the arthropod sensilla. The H‐NF array (400 nm diameter, 4 µm height, 1.2 µm spacing distance, and hexagonal array) exhibits reversible structural deformation when exposed to a flammable concentration of hydrogen gas (4 vol% H₂ in N₂) with fast response times (5.1 s). The structural change can be detected with the bare eye, which is a result of change in the optical transmittance due to the structural deformation of the H‐NF array. Based on these results, an eye‐readable H₂‐sensor that requires no additional electrical apparatus is demonstrated, including wetting‐controllable H₂‐selective smart surfaces and H₂‐responsive fasteners.     

Self‐Powered Sensors Enabled by Wide‐Bandgap Perovskite Indoor Photovoltaic Cells

A new approach to ubiquitous sensing for indoor applications is presented, using low‐cost indoor perovskite photovoltaic cells as external power sources for backscatter sensors. Wide‐bandgap perovskite photovoltaic cells for indoor light energy harvesting are presented with the 1.63 and 1.84 eV devices that demonstrate efficiencies of 21% and 18.5%, respectively, under indoor compact fluorescent lighting, with a champion open‐circuit voltage of 0.95 V in a 1.84 eV cell under a light intensity of 0.16 mW cm^?2. Subsequently, a wireless temperature sensor self‐powered by a perovskite indoor light‐harvesting module is demonstrated. Three perovskite photovoltaic cells are connected in series to create a module that produces 14.5 µW output power under 0.16 mW cm^?2 of compact fluorescent illumination with an efficiency of 13.2%. This module is used as an external power source for a battery‐assisted radio‐frequency identification temperature sensor and demonstrates a read range by of 5.1 m while maintaining very high frequency measurements every 1.24 s. The combined indoor perovskite photovoltaic modules and backscatter radio‐frequency sensors are further discussed as a route to ubiquitous sensing in buildings given their potential to be manufactured in an integrated manner at very low cost, their lack of a need for battery replacement, and the high frequency data collection possible.     

Self‐Healable and Recyclable Tactile Force Sensors with Post‐Tunable Sensitivity

It is challenging to post‐tune the sensitivity of a tactile force sensor. Herein, a facile method is reported to tailor the sensing properties of conductive polymer composites by utilizing the liquid‐like property of dynamic polymer matrix at low strain rates. The idea is demonstrated using dynamic polymer composites (CB/dPDMS) made via evaporation‐induced gelation of the suspending toluene solution of carbon black (CB) and acid‐catalyzed dynamic polydimethylsiloxane (dPDMS). The dPDMS matrices allow CB to redistribute to change the sensitivity of materials at the liquid‐like state, but exhibit typical solid‐like behavior and thus can be used as strain sensors at normal strain rates. It is shown that the gauge factor of the polymer composites can be easily post‐tuned from 1.4 to 51.5. In addition, the dynamic polymer matrices also endow the composites with interesting self‐healing ability and recyclability. Therefore, it is envisioned that this method can be useful in the design of various novel tactile sensing materials for many applications.     

Pixel‐Structured Scintillator with Polymeric Microstructures for X‐Ray Image Sensors

We introduce a pixel‐structured scintillator realized on a flexible polymeric substrate and demonstrate its feasibility as an X‐ray converter when it is coupled to photosensitive elements. The sample was prepared by filling Gd₂O₂S:Tb scintillation material into a square‐pore‐shape cavity array fabricated with polyethylene. For comparison, a sample with the conventional continuous geometry was also prepared. Although the pixelated geometry showed X‐ray sensitivity of about 58% compared with the conventional geometry, the resolving power was improved by about 70% above a spatial frequency of 3 mm^?1. The spatial frequency at 10% of the modulation‐transfer function was about 6 mm^?1.     

Bubble‐Decorated Honeycomb‐Like Graphene Film as Ultrahigh Sensitivity Pressure Sensors

Recently, macroporous graphene monoliths (MGMs), with ultralow density and good electrical conductivity, have been considered as excellent pressure sensors due to their excellent elasticity with a rapid rate of recovery. However, MGMs can only exhibit good sensitivity when the strain is higher than 20%, which is undesirable for touch‐type pressure sensors, such as artificial skin. Here, an innovative method for the fabrication of freestanding flexible graphene film with bubbles decorated on honeycomb‐like network is demonstrated. Due to the switching effect depended on “point‐to‐point” and “point‐to‐face” contact modes, the graphene pressure sensor has an ultrahigh sensitivity of 161.6 kPa^?1 at a strain less than 4%, several hundred times higher than most previously reported pressure sensors. Moreover, the graphene pressure sensor can monitor human motions such as finger bending and pulse with a very low operating voltage of 10 mV, which is sufficiently low to allow for powering by energy‐harvesting devices, such as triboelectric generators. Therefore, the high sensitivity, low operating voltage, long cycling life, and large‐scale fabrication of the pressure sensors make it a promising candidate for manufacturing low‐cost artificial skin.     

Low‐Dimensional Transition Metal Dichalcogenide Nanostructures Based Sensors

Two‐dimensional (2D) transition metal dichalcogenides (TMDs) nanostructures have been widely applied in environmental and biological analysis, biomedicine, electronic devices, and hydrogen evolution catalysis. Meanwhile, this excitement in 2D TMDs has spilled over to their counterparts of different dimensionalities like one‐dimensional (1D) and zero‐dimensional (0D) TMDs nanostructures. Eventual physical and chemical properties of TMDs nanostructures still remain to be highly dependent on their dimensionalities and size scale, and recently creatively exploring these physical and chemical properties is extremely impactful for the sensing field of TMD nanomaterials. Herein, we review a wide range of sensing applications based on not only graphene‐like 2D TMDs nanostructures but also the rapidly emerging subclasses of 1D, and 0D TMDs nanostructures. Their unique and interesting structures, excellent properties, and valid preparation methods are also included and the analytical objectives, ranging from heavy metal ions to small molecules, from DNA to proteins, from liquids to even vapors, can be met with extremely high selectivity and sensitivity. We have also analyzed our current understanding of 0D and 1D TMDs nanostructures and learning from graphene with the goal of contributing fresh ideas to the overall development of more advanced future TMDs based sensors.     

Self‐Recovering Triboelectric Nanogenerator as Active Multifunctional Sensors

A novel self‐recovering triboelectric nanogenerator (STENG) driven by airflow is designed as active multifunctional sensors. A spring is assembled into the STENG and enables the nanogenerator to have self‐recovering characteristic. The maximum output voltage and current of the STENG is about 251 V and 56 μA, respectively, corresponding to an output power of 3.1 mW. The STENG can act as an active multifunctional sensors that includes a humidity sensor, airflow rate sensor, and motion sensor. The STENG‐based humidity sensor has a wide detection range of 20%–100%, rapid response time of 18 ms, and recovery time of 80 ms. Besides, the STENG could be utilized in the application of security monitoring. This work expands practical applications of triboelectric nanogenerators as active sensors with advantages of simple fabrication and low cost.     

Stretchable‐Rubber‐Based Triboelectric Nanogenerator and Its Application as Self‐Powered Body Motion Sensors

A stretchable‐rubber‐based (SR‐based) triboelectric nanogenerator (TENG) is developed that can not only harvest energy but also serve as self‐powered multifunctional sensors. It consists of a layer of elastic rubber and a layer of aluminum film that acts as the electrode. By stretching and releasing the rubber, the changes of triboelectric charge distribution/density on the rubber surface relative to the aluminum surface induce alterations to the electrical potential of the aluminum electrode, leading to an alternating charge flow between the aluminum electrode and the ground. The unique working principle of the SR‐based TENG is verified by the coupling of numerical calculations and experimental measurements. A comprehensive study is carried out to investigate the factors that may influence the output performance of the SR‐based TENG. By integrating the devices into a sensor system, it is capable of detecting movements in different directions. Moreover, the SR‐based TENG can be attached to a human body to detect diaphragm breathing and joint motion. This work largely expands the applications of TENG not only as effective power sources but also as active sensors; and opens up a new prospect in future electronics.     

Ultralight and Binder‐Free All‐Solid‐State Flexible Supercapacitors for Powering Wearable Strain Sensors

Flexible energy storage devices play a pivotal role in realizing the full potential of flexible electronics. This work presents high‐performance, all‐solid‐state, flexible supercapacitors by employing an innovative multilevel porous graphite foam (MPG). MPGs exhibit superior properties, such as large specific surface area, high electric conductivity, low mass density, high loading efficiency of pseudocapacitive materials, and controlled corrugations for accommodating mechanical strains. When loaded with pseudocapacitive manganese oxide (Mn₃O₄), the MPG/Mn₃O₄ (MPGM) composites achieve a specific capacitance of 538 F g^?1 (1 mV s^?1) and 260 F g^?1 (1 mV s^?1) based on the mass of pure Mn₃O₄ and entire electrode composite, respectively. Both are among the best of Mn₃O₄‐based supercapacitors. The MPGM is mechanically robust and can go through 1000 mechanical bending cycles with only 1.5% change in electric resistance. When integrated as all‐solid‐state symmetric supercapacitors, they offer a full cell specific capacitance as high as 53 F g^?1 based on the entire electrode and retain 80% of capacitance after 1000 continuous mechanical bending cycles. Furthermore, the all‐solid‐state flexible supercapacitors are incorporated with strain sensors into self‐powered flexible devices for detection of both coarse and fine motions on human skins, i.e., those from finger bending and heart beating.