Electricity out of electronic trash: Triboelectric nanogenerators from discarded smartphone displays for biomechanical energy harvesting.

In the context of escalating electronic waste (e-waste) generated by the rapid evolution of electronic devices, particularly smartphones/mobiles, the imperative for effective e-waste management to mitigate adverse environmental and health consequences has become increasingly apparent. Herein, novel mobile phone-based triboelectric nanogenerators (M-TENGs) are fabricated from discarded smartphone displays of eight different brands (B1-B8) for harvesting electrical energy. Analytical characterization techniques such as SEM and EDS are employed for morphological investigation. The tribopositivity and tribonegativity of the smartphone display layers are confirmed using the FTIR technique and test materials. The percentage tensile strength of the selected triboactive layers is measured to assess the mechanical durability. The electrical measurements are performed for all eight M-TENG devices, notably the device constructed from B8 smartphone display layers outperforms other brands by generating about three and five times higher voltage and current than the M-TENG device composed of B1 layers. Further, the optimized device is subjected to frequency, force, and stability tests, and also the impact of fluctuating humidity on the device performance is analyzed. Moreover, the M-TENG demonstrates its versatility by efficiently charging commercial electrolytic capacitors, powering LEDs, and effectively harvesting biomechanical energy. Thus, the present study represents a significant step towards mitigating the challenges posed by electronic smartphone waste disposal while simultaneously offering a viable pathway to harvest electricity and power a variety of applications.

Fabrication of cadmium chloride PVA polymer composite for γ-ray shielding.

Reducing the effect of exposure to radiation in places such as radiation labs, nuclear reactors, radiotherapy facilities, industries involving radiation, etc., is essential for the health of radiation workers. In such cases materials having flexibility added with high attenuation coefficient of radiation is required for manufacturing wearables. Even though materials such as lead compounds, building materials, etc., have high attenuation coefficient, they are toxic and rigid, making them unsuitable for this purpose. In this regard, blending compounds with polymers would lead to flexible materials with high shielding capability. In the present work, 25 wt% cadmium chloride in polyvinyl alcohol (PVA) polymer composite has been prepared using solution casting method. The obtained polymer composite is characterised by energy dispersive X-ray spectroscopy. The mass attenuation coefficients (µ/ρ) and half value layer (HVL) of gamma radiations were measured at various energies 511, 661, 1173 and 1332 keV using calibrated gamma ray spectrometer with NaI(Tl) detector and compared to WinXCom-calculated theoretical values. The measured µ/ρ and HVL are 0.089, 0.078, 0.064, 0.061 cm2/g and 0.685, 0.778, 0.985, 1.003 cm, respectively. It is found that the obtained experimental values are in good agreement with theoretical values within the experimental errors. Also, it is observed that the µ/ρ decreases and HVL increases with increase in energy. Even though PVA is not radiation resistant, when it is blended with 25 wt% cadmium chloride it shows good shielding property. Thus, the fabricated cadmium chloride-PVA polymer composite can be used for radiation shielding instead of toxic and expensive materials.

Polyvinyl alcohol-based economical triboelectric nanogenerator for self-powered energy harvesting applications.

Triboelectric nanogenerators (TENGs) have emerged as a promising alternative for powering small-scale electronics without relying on traditional power sources, and play an important role in the development of the internet of things (IoTs). Herein, a low-cost, flexible polyvinyl alcohol (PVA)-based TENG (PVA-TENG) is reported to harvest low-frequency mechanical vibrations and convert them into electricity. PVA thin film is prepared by a simple solution casting technique and utilized to serve as the tribopositive material, polypropylene film as tribonegative, and aluminum foil as electrodes of the device. The dielectric-dielectric model is implemented with an arch structure for the effective working of the PVA-TENG. The device showed promising electrical output by generating significant open-circuit voltage, short-circuit current, and power . Also, PVA-TENG is subjected to a stability test by operating the device continuously for 5000 cycles. The result shows that, the device is mechanically durable and electrically stable. Further, the as-fabricated PVA-TENG is demonstrated to show feasible applications, such as charging two commercial capacitors with capacitances 1.1 and 4.7µF and powering green light-emitting diodes. The stored energy in the 4.7µF capacitor is utilized to power a digital watch and humidity and temperature sensor without the aid of an external battery. Thus, the PVA-TENG facilitates ease of fabrication, robustness, and cost-effective strategy in the field of energy harvesting for powering lower-grid electronics by demonstrating their potential as a sustainable energy source.

Loop-mediated fluorescent probes for selective discrimination of parallel and antiparallel G-Quadruplexes.

Herein we report simple pyridinium (1-3) and quinolinium (4) salts for the selective recognition of G-quadruplexes (G4s). Among them, the probe 1, interestingly, selectively discriminated parallel (c-KIT-1, c-KIT-2, c-MYC) G4s from anti-parallel/hybrid (22AG, HRAS-1, BOM-17, TBA) G4s at pH 7.2, through a switch on response in the far-red window. Significant changes in the absorption (broad 575 nm â†’ sharp 505 nm) and emission of probe 1 at 620 nm, attributed to selective interaction with parallel G4s, resulted in complete disaggregation-induced monomer emission. Symmetrical push/pull molecular confinements across the styryl units in probe 1 enhanced the intramolecular charge transfer (ICT) by restricting the free rotation of CC units in the presence of sterically less hindered and highly accessible G4 surface/bottom tetrads in the parallel G4s, which is relatively lower extent in antiparallel/hybrid G4s. We confirm that the disaggregation of probe 1 was very effective in the presence of parallel G4-forming ODNs, due to the presence of highly available free surface area, resulting in additional π-stacking interactions. The selective sensing capabilities of probe 1 were analyzed using UV-Vis spectroscopy, fluorescence spectroscopy, molecular dynamics (MD)-based simulation studies, and 1H NMR spectroscopy. This study should afford insights for the future design of selective compounds targeting parallel G4s.

Medium Energy Carbon and Nitrogen Ion Beam Induced Modifications in Charge Transport, Structural and Optical Properties of Ni/Pd/n-GaN Schottky Barrier Diodes.

The irradiation effects of carbon and nitrogen medium energy ions (MEI) on charge transport, structural and optical properties of Ni/Pd/n-GaN Schottky barrier diodes are reported. The devices are exposed to 600 keV C2+ and 650 keV N2+ ions in the fluence range of 1 × 1013 to 1 × 1015 ions cm-2. The SRIM/TRIM simulations provide quantitative estimations of damage created along the trajectories of ion beams in the device profile. The electrical parameters like Schottky barrier height, series resistance of the Ni/Pd/n-GaN Schottky barrier diodes decreases for a fluence of 1 × 1013 ions cm-2 and thereafter increases with an increase in fluence of 600 keV C2+ and 650 keV N2+ ions. The charge transport mechanism is influenced by various current transport mechanisms along with thermionic emission. Photoluminescence studies have demonstrated the presence of yellow luminescence in the pristine samples. It disappears at higher fluences due to the possible occupancy of Ga vacancies. The presence of the green luminescence band may be attributed to the dislocation caused by the combination of gallium vacancy clusters and impurities due to MEI irradiation. Furthermore, X-ray diffraction studies reveal that there is a decrease in the intensity and shift in the diffraction peaks towards the lower side of two thetas. The reductions in the intensity of C2+ ion irradiation is more when compared to N2+ ion irradiation, which may be attributed to change in the mean atomic scattering factor on a given site for light C2+ ion as compared to N2+ ion.

Dry-Coated Graphite onto Sandpaper for Triboelectric Nanogenerator as an Active Power Source for Portable Electronics.

Developing an eco-friendly, flexible and recyclable micro-structured dry electrode for sustainable life is essential. In this work, we have developed irregular, micro-structured sandpaper coated with graphite powder as an electrode for developing a simple, low-cost, contact-separation mode graphite-coated sandpaper-based triboelectric nanogenerator (GS-TENG) as a self-powered device and biomechanical sensor. The as-fabricated GS-TENG is a dielectric-conductor model. It is made up of a bottom layer with polytetrafluoroethylene (PTFE) as a triboelectric layer, which is attached onto a graphite-coated sandpaper-based electrode and a top layer with aluminum as another triboelectric layer as well as an electrode. The forward and reverse open-circuit voltages reach upto ~33.8 V and ~36.62 V respectively, and the forward and reverse short-circuit currents are ~2.16 µA and ~2.17µA, respectively. The output generated by GS-TENG can power 120 blue light-emitting diodes connected in series, liquid crystal display and can charge commercial capacitors along with the rectifier circuit. The capacitor of 22 µF is charged upto 5 V and is sufficient to drive digital watch as wearable electronics. Moreover, the device can track signals generated by human motion, hence it scavenges biomechanical energy. Thus, GS-TENG facilitates large-scale fabrication and has potential for future applications in wearable and portable devices.