Tuning ZnO-based piezoelectric nanogenerator efficiency through n-ZnO/p-NiO bulk interfacing.

ZnO based piezoelectric nanogenerators (PENG) hold immense potential for harvesting ambient vibrational mechanical energy into electrical energy, offering sustainable solutions in the field of self-powered sensors, wearable electronics, human-machine interactions etc. In this study, we have developed flexible ZnO-based PENGs by incorporating ZnO microparticles into PDMS matrix, with ZnO concentration ranging from 5 to 25 wt%. Among these, the PENG containing 15 wt% ZnO exhibited the best performance with an open-circuit output voltage/short-circuit current of ~ 42.4 V/2.4 µA. To further enhance the output performance of PENG, p-type NiO was interfaced with ZnO in a bulk hetero-junction geometry. The concentration of NiO was varied from 5 to 20 wt% with respect to ZnO and incorporated into the PDMS matrix to fabricate the PENGs. The PENG containing 10 wt% NiO exhibits the best performance with an open-circuit output voltage/short-circuit current of ~ 65 V/4.1 µA under loading conditions of 30 N and 4 Hz. The PENG exhibiting the best performance demonstrates a maximum instantaneous output power density ~ 37.9 µW/cm2 across a load resistance of 20 MΩ under loading conditions of 30 N and 4 Hz, with a power density per unit force and Hertz of about ~ 0.32 µW/cm2·N·Hz. The enhanced output performance of the PENG is attributed to the reduction in free electron concentration, which suppresses the internal screening effect of the piezopotential. To assess the practical utility of the optimized PENG, we tested the powering capability by charging various commercial capacitors and used the stored energy to illuminate 10 LEDs and to power a stopwatch displays. This work not only presents a straightforward, cost-effective, and scalable technique for enhancing the output performance of ZnO-based PENGs but also sheds light on its underlying mechanism.

Enhancing the Features of DNA Mimic Foldamers for Structural Investigations.

DNA mimic foldamers based on aromatic oligoamide helices bearing anionic phosphonate side chains have been shown to bind to DNA-binding proteins sometimes orders of magnitude better than DNA itself. Here, we introduce new features in the DNA mimic foldamers to facilitate structural investigations of their interactions with proteins. Thirteen new foldamer sequences have been synthesized and characterized using NMR, circular dichroism, molecular modeling, and X-ray crystallography. The results show that foldamer helix handedness can be quantitatively biased by means of a single stereogenic center, that the foldamer structure can be made C2-symmetrical as in palindromic B-DNA sequences, and that associations between foldamer helices can be promoted utilizing dedicated C-terminal residues that act as sticky ends in B-DNA structures.

Surfactant gel-based method: A universal soft method for the exfoliation of 2D materials.

HYPOTHESIS: Fluidic micelles and reverse micelles have served as exfoliation mediums. However, an additional force, such as extended sonication, is required. Gelatinous cylindrical micelles that are formed once desired conditions are achieved can be an ideal medium for the quick exfoliation of 2D materials without the need for any external force. The quick formation of gelatinous cylindrical micelles can rip off layers from the 2D materials suspended in the mixture leading to the quick exfoliation of 2D materials. EXPERIMENTS: Herein, we introduce a quick universal method capable of delivering high-quality exfoliated 2D materials cost-effectively using CTAB-based gelatinous micelles as an exfoliation medium. The approach is devoid of harsh treatment, such as prolonged sonication and heating, and a quick exfoliation of 2D materials is completed using this approach. FINDINGS: We successfully exfoliated four 2D materials (MoS2, Graphene, WS2, and BN) and investigated their morphology, chemical, and crystal structure along with optical and electrochemical properties to probe the quality of the exfoliated product. Results revealed that the proposed method is highly efficient in exfoliating 2D materials in a quick time without causing any significant damage to the mechanical integrity of the exfoliated materials.

Determination of stability and degradation in polysilanes by an electronic mechanism.

Polysilanes are potential candidates for active materials in light emitting diodes because of possible emission in the near-ultraviolet to blue region. Unfortunately, they degrade rapidly upon exposure to light because of scission of sigma bonds. Relative stability of four polysilanes, for example, poly(di-n-butylsilane) (PDBS), poly(di-n-hexylsilane) (PDHS), poly(methylphenylsilane) (PMPS), and poly[bis(p-butylphenyl)silane] (PBPS), which have been reported as active materials in light emitting diodes, have been investigated theoretically through semiempirical (AM1) and ab initio (HF/6-31g) methods and density functional theory using B3LYP parametrization. The AM1 level of calculation predicts the absorption maxima reasonably, but it fails to explain the relative stabilities of the four polysilanes in the excited state. However, calculations based on configuration interaction with single excitation and time-dependent density functional theory suggest additional stabilization in the excited states through intersystem crossing to triplets for PMPS and PBPS, consistent with the experimental observation. In contrast, no such stabilization is predicted for PDBS and PDHS. Furthermore, the existence of a stable triplet state in PMPS may also explain the visible emission observed experimentally in PMPS.