The increasing number of IoT devices has led to more electronic waste production, which harms the environment and human health. Self-powered sensor systems are a solution, but they often use toxic materials. We propose using biocompatible peanut skin as the active material for a self-powered humidity sensor (PSP-SPHS) through integration with a peanut-skin-based triboelectric nanogenerator (PSP-TENG). The PSP-TENG was characterized electrically and showed promising results, including an open circuit voltage (162 V), short circuit current (0.2 µA), and instantaneous power (2.2 mW) at a loading resistance of 20 MΩ. Peanut skin is a great choice for the sensor due to its porous surface, large surface area, eco-friendliness, and affordability. PSP-TENG was further used as a power source for the PSP-humidity sensor. PSP-SPHS worked as a humidity-dependent resistor, whose resistance decreased with increasing relative humidity (%RH), which further resulted in decreasing voltage across the humidity sensor. This proposed PSP-SPHS exhibited a good sensitivity (0.8 V/RH%), fast response/recovery time (4/10 s), along with excellent stability and repeatability, making it a potential candidate for self-powered humidity sensor technology.

Metal–organic frameworks (MOFs) are known for their high porosity and stability, making them ideal for various applications, including energy harvesting. A simple synthesis method was used to synthesize zinc‐based metal–organic frameworks (Zn‐MOFs) and introduce them into an ultra‐stretchable Ecoflex polymer as functional fillers. We developed triboelectric nano generator (TENG) devices using Ecoflex, both pristine and modified with different Zn‐MOF concentrations, to evaluate their performance. The output voltage, current, and instantaneous power of Zn‐MOF‐modified Ecoflex TENG devices were 3, 4, and 5 times higher than pristine Ecoflex TENGs. This improvement is due to Zn‐MOF's large surface area, porous structure, charge trapping sites, improved surface roughness, and electron cloud conduction. The improved TENG device achieved 36 mW of maximum power and 40 mW m⁻² power density. The Flexible TENG device powered LEDs and stored energy in capacitors by converting mechanical energy into electrical energy. We integrated flexible TENG device into cardiac patients' shoes to monitor running speeds and identify dangerous velocities using wireless IoT cloud monitoring. Real‐time notifications and wireless data transmission to families and emergency personnel allowed immediate assistance.

In-situ iodine (I₂)-doped atmospheric pressure (AP) plasma polymerization is proposed, based on a newly designed AP plasma reactor with a single wire electrode that enables low-voltage-driven plasma polymerization. The proposed AP plasma reactor can proceed plasma polymerization at low voltage levels, thereby enabling an effective in-situ I₂ doping process by maintaining a stable glow discharge state even if the applied voltage increases due to the use of a discharge gas containing a large amount of monomer vapors and doping materials. The results of field-emission scanning electron microscopy (FE-SEM) and Fourier transformation infrared spectroscopy (FT-IR) show that the polyaniline (PANI) films are successfully deposited on the silicon (Si) substrates, and that the crosslinking pattern of the synthesized nanoparticles is predominantly vertically aligned. In addition, the in-situ I₂-doped PANI film fabricated by the proposed AP plasma reactor exhibits excellent electrical resistance without electrical aging behavior. The developed AP plasma reactor proposed in this study is more advantageous for the polymerization and in-situ I₂ doping of conductive polymer films than the existing AP plasma reactor with a dielectric barrier.

We have executed a cost-effective approach to produce a high-performance multifunctional human–machine interface (HMI) humidity sensor. The designed sensors were ecofriendly, flexible, and highly sensitive to variability in relative humidity (%RH) in the surroundings. In this study, we have introduced a humidity sensor by using carbon paper (as both a substrate and sensing material) and a silver (Ag) conductive ink pen. The carbon paper-based humidity sensor was developed by using a simple handwriting approach and the resulting devices exhibited excellent results including fast response/recovery times (12/24 s), a wide sensing range (30 to 85%), small hysteresis (1.1%), high stability (1 month), and repeatability. This high-performance humidity response could be attributed to the highly porous, hydrophilic, and permeable nature of carbon paper. Besides these features, the sensor offered high flexibility (100 bending cycles across different radii) and adaptability for uses like breath monitoring (through mouth and nose), proximity sensing (from multiple distances ranging from 1 to 10 cm), and depicting Morse code. This research work is a significant step forward in humidity sensing technology and the sustainable future of electronic devices by using a cost-effective, fast, and simple fabrication technique.

The use of low-voltage-driven plasma in atmospheric pressure (AP) plasma polymerization is considered as a simple approach to reducing the reactivity of the monomer fragments in order to prevent excessive cross-linking, which would have a negative effect on the structural properties of the polymerized thin films. In this study, AP-plasma polymerization can be processed at low voltage by an AP-plasma reactor with a wire electrode configuration. A bare tungsten wire is used as a powered electrode to initiate discharge in the plasma area (defined as the area between the wide glass tube and the substrate stand), thus allowing plasma polymerization to proceed at a lower voltage compared to other AP-plasma reactors with dielectric barriers. Thus, transparent polyaniline (PANI) films are successfully synthesized. The surface morphology, roughness, and film thickness of the PANI films are characterized by field emission scanning electron microscopy and atomic force microscopy. Thus, the surface of the polymerized film is shown to be homogenous, smooth, and flat, with a low surface roughness of 1 nm. In addition, the structure and chemical properties of the PANI films are investigated by Fourier transform infrared spectroscopy, thus revealing an improvement in the degree of polymerization, even though the process was performed at low voltage.