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[Display omitted] Application of metal organic frameworks (MOFs) on sensors is of great interest for researchers. Film forming ability of the sensing material is very important for both the preparation process and sensing properties of the devices. Humidity sensors based on UIO-66 derived polyelectrolyte films were well prepared by in situ thiol-ene click cross-linking polymerization in this work. The hydrophilicity of the sensing film could be controlled by the feed ratios. The optimized humidity sensor shows a fast response to RHs change (Res/Rec time is 3.1 s/1.5 s, respectively) with ∼1.2% RH of humidity hysteresis. The water molecules adsorption behavior of the film and the sensing mechanism were also be investigated. The humidity sensor with good water and thermal stability and repeatability was applied in breath monitoring, which can well distinguish different breath states. [ABSTRACT FROM AUTHOR]

Low humidity detection has been a great challenge in the field of humidity sensing. In recent years, polyelectrolytes have been proven to be promising materials for highly sensitive humidity sensors. In this work, cross-linked poly(ionic liquid)s (PILs) were prepared for low humidity detection. The strong hydrophilicity of PILs contributes to humidity sensing while the cross-linked structure guarantees the stability of the sensing film. The optimized sensor shows high response (48.0) in 5–35% RH, with short response/recovery time (1 s/10 s) and a small humidity hysteresis (0.2% RH). The possible sensing mechanism of the sensors was discussed. • Cross-linked poly(ionic liquid)s were used as low humidity sensitive materials. • The optimized sensor shows high response in 5–35% RH. • The optimized sensor has short recovery time and small humidity hysteresis. • The introduction of glycerol could reduce the impedance of the sensor. [ABSTRACT FROM AUTHOR]

Owing to the outstanding dielectric properties derived from the conjugated π-electron systems, conjugated polymers have been explored and developed in capacitive humidity sensors for a few decades. In this work, a series of composites – mesoporous silica and semiconducting polymers – MCM-41 (MCM, Mesoporous Crystalline Material)/PEDOT (poly(3,4-ethylenedioxythiophene)) were chemically obtained by in-situ polymerization at 0 °C, while the amounts of PEDOT were adjusted by different evaporation times of EDOT (3,4-ethylenedioxythiophene) in the porous MCM-41 film. Additionally, it was able to modulate both the dielectricity and porosity of the composites via this convenient approach. The obtained capacitive humidity sensors based on MCM-41/PEDOT composites exhibit much better sensing performance than their bulk counterparts, with wider humidity sensing range, higher sensitivity and much faster response speed. [ABSTRACT FROM AUTHOR]

Highlights • A novel MCM-41/PPy (Polypyrrole) based humidity sensor was prepared. • An in-situ way of loading PPy into the channels of MCM-41 framework was used for quantity control. • The MCM-41/PPy (90) sensor shows a high sensitivity and wider humidity sensing range than MCM-41sensor or PPy sensor. • A proper mechanism about dielectric constant change was discussed to explain the sensing phenomenon. Abstract Inorganic zeolites, such as MCM (Mesoporous Crystalline Material), are widely used as skeleton to load humidity sensitive materials for constructing high-performance humidity sensor. In this work, an in-situ preparation method was developed to prepare MCM-41/polypyrrole (PPy) humidity sensors, by inducing the polymerization of pyrrole vapor inside MCM-41 film that was coated on the ceramics substrate with carbon interdigital electrodes. MCM-41/PPy sensors with different polymerization times were fabricated, and their capacitance humidity sensing properties demonstrate much better performance than individual MCM-41 sensor or PPy sensor, with high sensitivity and a wide humidity sensing range. The sensing properties of MCM-41/PPy sensors were further optimized by controlling the polymerization time. In addition, a humidity sensing mechanism explanation is discussed at the end of this paper. [ABSTRACT FROM AUTHOR]

Composites fabricated by mesoporous silica loading hydrophilic elements have been widely investigated as humidity sensitive materials. The physical mixing process for loading hydrophilic elements is difficult to guarantee the uniformity and structural stability of the composites. Furthermore, the poor dispersibility of the silica skeleton restricts its solution processability. Herein, solution processible organic-inorganic hybrid materials were synthesized via a thiol-ene click reaction between sulfhydryl functionalized microporous silica nanoparticles (MSNs) and hydrophilic alkenyl monomer. The optimal hybrid material could disperse in water stably with a concentration of 50 mg/mL owing to the small particle size (about 105 nm) and the hydrophilic characteristic. Humidity sensors were fabricated by solution process and the humidity sensing properties were investigated. The sensor exhibits high sensitivity (about three orders impedance modulus change), small hysteresis (∼2% RH) and rapid response (the response and recovery time are 5 and 40 s, respectively) in the humidity range of 11%–95% RH. [ABSTRACT FROM AUTHOR]

A novel organic-inorganic hybrid material with the core-shell framework was prepared by modifying the poly(vinylsulfonic acid, sodium salt) (PSS) on vinyl functionalized silica nanoparticles (VSNs) via the free radical polymerization. SNs with different contents of PSS were prepared and the structures were carefully characterized. The hybrid material could enhance the durability of PSS under high humidity environment. Meanwhile, the SNs skeleton provides interstitial channels in the PSS@SNs films, which are available for water molecules transport. The PSS coated SNs (PSS@SNs) films were formed by drop-coating and their sensing properties were investigated. The impedance of the optimal humidity sensor changed more than four orders of magnitude over the relative humidity range of 33–95%, with good linearity under semi-logarithm scale (R 2 = 0.950) and a small humidity hysteresis of 2% RH. The obtained sensor also showed rapid response to humidity change (the response and recovery time were 2 and 65 s, respectively). Finally, the resultant sensor was explored for respiratory rate monitoring. [ABSTRACT FROM AUTHOR]

Mesoporous silicas loading hydrophilic materials composites were widely used in humidity sensors during the last decade. However, the physical mixing process used for loading the hydrophilic materials in the channel of mesoporous silicas is hard to guarantee their uniform dispersion, and there is no strong force to bind the host and guest materials together. To solve above problems, novel vinyl functionalized mesoporous silicas (SBA-15-vinyl) were chemically modified with hydrophilic sodium p -styrenesulfonate (SSS) with free radical polymerization. The chemical and porous structures of the obtained hybrid materials (SBA-15-PSSx) were characterized by fourier transform infrared spectroscopy (FT-IR), elemental analyses (EA), X-ray diffraction (XRD), high resolution transmission electron microscopy (HRTEM) and N 2 adsorption-desorption. The humidity sensing properties of the sensors based on SBA-15-vinyl and SBA-15-PSS indicate the introduction of PSS could effectively enhance the sensing properties of SBA-15-vinyl. The impedance of the optimized sensor changed by more than three orders of magnitude over the relative humidity (RH) range of 11%–95%, with rapid response to RH change. [ABSTRACT FROM AUTHOR]

Self-supported polymer films were fabricated by the thiol-ene click cross-linking reaction in this work. The cross-linked frameworks were used to guarantee the stability the films. The hydrophilic monomer with different contents were introduced into the self-supported thick films and uniformly dispersed in the polymer frameworks. The interdigitated electrodes were screen printed with silver paste on the self-supported films to obtain humidity sensors. Herein, the self-supported film acts as both the sensor substrate and the humidity-sensing material. The humidity sensing performances of the obtained sensors were systematically researched. By optimizing the ratio of hydrophilic monomer in the polymer films, the sensitivities of the sensors were enhanced from 1.58 to 103.75 (in the humidity from 11% RH to 95% RH), the response under low RH environment was significantly improved with good linearity. The response/recovery times of the sensor within the humidity range are measured to be 12.5 s and hundreds of seconds. The prepared flexible sensors possess certain mechanical properties, and exhibit good stability under bending and long-term tests up to 60 days. The applications of the as-prepared sensor in the detection of non-contact human skin humidity, human respiration and relative humidity of green plant were explored. The sensor shows excellent sensing performance in various applications and indicates the potential application in wearable and multifunctional devices. [Display omitted] • Self-supported polymer films were fabricated by the thiol-ene click cross-linking reaction. • Flexible and stable humidity sensors were fabricated by screen printing electrodes on the self-supported films. • The roles of the self-supported film are the substrate of the sensor, as both the humidity-sensing material. • The humidity sensing properties and the multifunctional applications of the obtained sensors were systematically researched. [ABSTRACT FROM AUTHOR]

Low humidity detection has always been a challenge in the field of humidity detection. Humidity sensors base on ionic liquid modified metal organic frameworks (MOFs) derived polymer films were prepared in this work. The ionic liquid ligand was uniformly introduced in the frameworks of UIO-66 to enhance the hydrophilicity of sensing materials, the caused defects sites are beneficial for adsorption and desorption, and the MOFs based functional films were easily obtained by in situ photoinduced thiol-ene click reaction. The obtained humidity sensor exhibits a linear response in low relative humidity (RH) range (5% RH - 30% RH) with a tiny humidity hysteresis (~0.2% RH) and short response time to humidity change (response/recovery time is 0.6 s/1.7 s, respectively). ● Humidity sensors based on ionic liquid modified UIO-66 derived polyelectrolyte films were prepared. ● The sensors were prepared facilely in situ on the electrodes by thiol-ene click polymerization in batches. ● The sensor presents linear response under low humidity (5% RH - 30% RH) with a small hysteresis and fast response speed. ● The introduction of ILs and the resulting defect sites are the reasons for effective low humidity detection. [ABSTRACT FROM AUTHOR]

[Display omitted] • Humidity sensors based on glycidyl trimethyl ammonium chloride (EPTAC) modified cellulose paper via a facile solution method were fabricated. • The paper is used for the purpose of the humidity sensing material and the sensor substrate. • The as-fabricated paper-based humidity sensor is provided with outstanding humidity sensing properties and good stability. • The humidity sensor was applied to multifunctional applications including human breath rate, non-contact switch and skin humidity. It is of great significance to exploit a simple, cost-effective and environmentally friendly preparation method of multifunctional humidity sensors. However, most humidity sensors need complex manufacturing processes, high cost and narrow usage range. Herein, humidity sensors based on glycidyl trimethyl ammonium chloride (EPTAC) modified cellulose paper via a facile solution method were fabricated, among which the paper is used for the purpose of the humidity sensing material and the sensor substrate. The sensitivity of the obtained sensor was improved by the modification of EPTAC, the response time was decreased to 25 s, which is equivalent to the first-rate paper-based humidity sensors. In addition, the paper-based humidity sensor is provided with well flexibility and biocompatibility, and it exhibits multifunctional applications in respiratory monitoring, non-contact switch and skin humidity monitoring. The low cost and facile preparation technique in this work could provide a useful strategy for developing multifunctional humidity sensor. [ABSTRACT FROM AUTHOR]

• The porous ionogel humidity sensitive material was successfully fabricated with the aid of PAA as the template and humidity sensing component. • The humidity sensor based on the porous ionogel shows rapid response (1.2/0.6 s) to humidity change. • Various molecular weights PAA were applied to investigate PAA's function in pore construction and humidity sensing. • The ultrafast-response humidity sensor can accurately record the human breath in real time, which is benefit for respiration data calculation. Electronic devices that can accurately record and monitor human respiration in real-time are of great interest for researchers. Ultrafast-response ionogel humidity sensors that can follow the human respiration were realized by an in-situ vinyl-thiol click reaction in this work. Polyacrylic acid (PAA) was utilized both as the template to construct porous films and for preparing humidity sensing component. The obtained optimal sensor owns a rapid response to humidity change (response and recovery time is 1.2 s and 0.6 s, respectively) and a small humidity hysteresis (∼2.2% RH). The water adsorption capability and sensing mechanism were investigated systematically. The ionogel humidity sensor with good stability and repeatability was applied in breath monitoring, which has a great potential application in diagnostic breath analysis. [ABSTRACT FROM AUTHOR]