Heterostructure of Fe-Doped CoMoOx/CoMoOx as an Efficient Electrocatalyst for Oxygen Evolution Reaction.

Oxygen evolution reaction (OER) plays a crucial role as a counter half-reaction for both electrochemical hydrogen production through water splitting and the generation of valuable carbon compounds via CO2 reduction. To overcome the sluggish kinetics of the OER, significant efforts have been devoted to developing cost-effective, sustainable, and efficient electrocatalysts, with transition-metal-based catalysts emerging as promising candidates. Herein, we successfully synthesized a core-shell type nanostructure of Fe-doped CoMoOx/CoMoOx (CMFO), which exhibits excellent electrocatalytic properties for OER. The presence of an amorphous layer of Fe-doped CoMoOx with abundant oxygen vacancies, along with the stability of a key OER intermediate, *O, contributes to the enhanced activity of CMFO catalyst compared to pristine CoMoOx (CMO). The optimized catalyst of CMFO-550 achieved much lower overpotential and Tafel slope and also exhibited better remarkable long-term stability for over 90 h compared to CMO-550. These findings highlight the potential of CMFO-550 as a cost-effective and highly efficient electrocatalyst for the OER. The successful development of this core-shell nanostructure opens up a new opportunity for the design and synthesis of advanced electrocatalysts for the OER, with implications for various applications in energy conversion and storage.

A self-powered mechanical energy harvester based on CH3NH3PbI3 doped P(VDF-HFP)/PANI composite films.

Piezoelectric polymers, particularly poly(vinylidene fluoride) (PVDF) and its copolymers attract attention from researchers due to their stretchability, flexibility, lightweight, and most importantly their biocompatible nature. In this research work, we report on the preparation of polymer composite films as flexible piezoelectric generators (PGs) and their electroactive phase (ß- and γ-phase) formation. The piezoelectric properties of copolymer poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) have been enhanced by incorporating polyaniline (PANI) and methylammonium lead iodide (CH3NH3PbI3) into it for a higher yield of the electroactive phases where a traditional electrical poling treatment was avoided. The remarkable enhancement in the piezoelectric phase (i.e., ß-phase) of the P(VDF-HFP) copolymer has been reported in this work, and it is found that the overall improvement of the piezoelectric ß-phase and the conversion of the degree of crystallinity is governed by the incorporation of the PANI and CH3NH3PbI3 fillers as revealed by the attenuated total reflectance (ATR) and X-ray diffraction (XRD) analysis. The X-ray photoelectron spectroscopy (XPS) analysis further confirmed the interfacial dipole-dipole interaction of PANI with the P(VDF-HFP) copolymer matrix. Piezoelectric generators (PGs) fabricated from the composite films show an open circuit piezoelectric voltage output of 5 volts and an output power of 8.2 nW. The capacitor charging capability by simple repetitive finger touch and release motions (a pressure amplitude of ∼14 kPa) of the flexible PGs promises their applicability as a piezoelectric-based energy harvester where different mechanical vibrations can be utilized.

Natural Sugar-Assisted, Chemically Reinforced, Highly Durable Piezoorganic Nanogenerator with Superior Power Density for Self-Powered Wearable Electronics.

Natural piezoelectric materials are of increasing interest, particularly for applications in biocompatible, implantable, and flexible electronic devices. In this paper, we introduce a cost-effective, easily available natural piezoelectric material, that is, sugar in the field of wearable piezoelectric nanogenerators (PNGs) where low electrical output, biocompatibility, and performance durability are still critical issues. We report on a high-performance piezoorganic nanogenerator (PONG) based on the hybridization of sugar-encapsulated polyvinylidene fluoride (PVDF) nanofiber webs (SGNFW). We explore the crucial role of single-crystal sugar having a fascinating structure along with the synergistic enhancement of piezoelectricity during nanoconfinement of sugar-interfaced macromolecular PVDF chains. As a consequence, the SGNFW-based PONG exhibits outstanding electricity generation capability (e.g., ∼100 V under 10 kPa human finger impact and maximum power density of 33 mW/m2) in combination with sensitivity to abundantly available different mechanical sources (such as wind flow, vibration, personal electronics, and acoustic vibration). Consequently, it opens up suitability in multifunctional self-powered wearable sensor designs for realistic implementation. In addition, commercially available capacitors are charged up effectively by the PONG because of its rapid energy storage capability. The high performance of the PONG not only offers "battery-free" energy generation (several portable units of light-emitting diodes and a liquid crystal display screen are powered up without using external storage) but also promises its use in wireless signal transmitting systems, which widens the potential in personal health care monitoring. Furthermore, owing to the geometrical stress confinement effect, the PONG is proven to be a highly durable power-generating device validated by stability test over 10 weeks. Therefore, the organic nanogenerator would be a convenient solution for portable personal electronic devices that are expected to operate in a self-powered manner.

The preparation of γ-crystalline non-electrically poled photoluminescant ZnO-PVDF nanocomposite film for wearable nanogenerators.

Polyvinylidene fluoride (PVDF) films are filled with various mass fractions (wt%) of zinc oxide nanoparticles (ZnO-NPs) to fabricate the high performance of a wearable polymer composite nanogenerator (PCNG). The ZnO-NPs can induced a fully γ-crystalline phase in PVDF, where traditional electrical poling is not necessary for the generation of piezoelectric properties. The PCNG delivers up to 28 V of open circuit voltage and 450 nA of short circuit current by simple repeated human finger imparting (under a pressure amplitude of 8.43 kPa) that generates sufficient power to turn on at least 48 commercial blue light emitting diodes (LEDs) instantly. Furthermore, it also successfully charged the capacitors, signifying practical applicability as a piezoelectric based nanogenerator for self-powering devices. The applicability of PCNG by wearable means is clarified when it gives rise to a sensible response, say up to 400 mV of output voltage synchronized with the PCNG embedded human finger in a bending and releasing gesture. UV-visible absorption spectral analysis revealed the possibility of estimating a change in the optical band gap value (E g), refractive index (n) and optical activation energy (E a) in different concentrations of ZnO-NP incorporated PVDF nanocomposite films, and it possesses a useful methodology where ZnO-NPs can be used as an optical probe. Near blue light emission is observed from photoluminescence spectra, which are clearly shown from a Commission Internationale de L'Eclairage (CIE) diagram. The piezoelectric charge coefficient of the nanocomposite film is estimated to be -6.4 pC/N, where even electrical poling treatment is not employed. In addition, dielectric properties have been studied to understand the role of molecular kinetic and interfacial polarization occurring in nanocomposite films at different applied frequencies.

Cerium(III) Complex Modified Gold Electrode: An Efficient Electrocatalyst for the Oxygen Evolution Reaction.

Exploring efficient and inexpensive electrocatalysts for the oxidation of water is of great importance for various electrochemical energy storage and conversion technologies. In the present study, a new water-soluble [Ce(III)(DMF) (HSO4)3] complex was synthesized and characterized by UV-vis, photoluminescence, and high-resolution X-ray photoelectron spectroscopy techniques. Owing to classic 5d → 4f transitions, an intense photoluminescence in the UV region was observed from the water-soluble [Ce(III)(DMF) (HSO4)3] complex. A stacking electrode was designed where self-assembled l-cysteine monolayer modified gold was immobilized with the synthesized cerium complex and was characterized by scanning electron microscopy, electrochemical impedance spectroscopy, and cyclic voltammetry. The resulting electrode, i.e., [Ce(III)(DMF) (HSO4)3]-l-cysteine-Au stacks shows high electrocatalytic water oxidation behavior at an overpotential of η ≈ 0.34 V under neutral pH conditions. We also demonstrated a way where the overpotential is possible to decrease upon irradiation of UV light.

Design of In Situ Poled Ce(3+)-Doped Electrospun PVDF/Graphene Composite Nanofibers for Fabrication of Nanopressure Sensor and Ultrasensitive Acoustic Nanogenerator.

We report an efficient, low-cost in situ poled fabrication strategy to construct a large area, highly sensitive, flexible pressure sensor by electrospun Ce(3+) doped PVDF/graphene composite nanofibers. The entire device fabrication process is scalable and enabling to large-area integration. It can able to detect imparting pressure as low as 2 Pa with high level of sensitivity. Furthermore, Ce(3+)-doped PVDF/graphene nanofiber based ultrasensitive pressure sensors can also be used as an effective nanogenerator as it generating an output voltage of 11 V with a current density ∼6 nA/cm(2) upon repetitive application of mechanical stress that could lit up 10 blue light emitting diodes (LEDs) instantaneously. Furthermore, to use it in environmental random vibrations (such as wind flow, water fall, transportation of vehicles, etc.), nanogenerator is integrated with musical vibration that exhibits to power up three blue LEDs instantly that promises as an ultrasensitive acoustic nanogenerator (ANG). The superior sensing properties in conjunction with mechanical flexibility, integrability, and robustness of nanofibers enabled real-time monitoring of sound waves as well as detection of different type of musical vibrations. Thus, ANG promises to use as an ultrasensitive pressure sensor, mechanical energy harvester, and effective power source for portable electronic and wearable devices.

An Effective Electrical Throughput from PANI Supplement ZnS Nanorods and PDMS-Based Flexible Piezoelectric Nanogenerator for Power up Portable Electronic Devices: An Alternative of MWCNT Filler.

We demonstrate the requirement of electrical poling can be avoided in flexible piezoelectric nanogenerators (FPNGs) made of low-temperature hydrothermally grown wurtzite zinc sulfide nanorods (ZnS-NRs) blended with polydimethylsiloxane (PDMS). It has been found that conductive fillers, such as polyaniline (PANI) and multiwall carbon nanotubes (MWCNTs), can subsequently improve the overall performance of FPNG. A large electrical throughput (open circuit voltage ∼35 V with power density ∼2.43 µW/cm(3)) from PANI supplement added nanogenerator (PZP-FPNG) indicates that it is an effective means to replace the MWCNTs filler. The time constant (τ) estimated from the transient response of the capacitor charging curves signifying that the FPNGs are very much capable to charge the capacitors in very short time span (e.g., 3 V is accomplished in 50 s) and thus expected to be perfectly suitable in portable, wearable and flexible electronics devices. We demonstrate that FPNG can instantly lit up several commercial Light Emitting Diodes (LEDs) (15 red, 25 green, and 55 blue, individually) and power up several portable electronic gadgets, for example, wrist watch, calculator, and LCD screen. Thus, a realization of potential use of PANI in low-temperature-synthesized ZnS-NRs comprising piezoelectric based nanogenerator fabrication is experimentally verified so as to acquire a potential impact in sustainable energy applications. Beside this, wireless piezoelectric signal detection possibility is also worked out where a concept of self-powered smart sensor is introduced.

DNA-Assisted ß-phase Nucleation and Alignment of Molecular Dipoles in PVDF Film: A Realization of Self-Poled Bioinspired Flexible Polymer Nanogenerator for Portable Electronic Devices.

A flexible nanogenerator (NG) is fabricated with a poly(vinylidene fluoride) (PVDF) film, where deoxyribonucleic acid (DNA) is the agent for the electroactive ß-phase nucleation. Denatured DNA is co-operating to align the molecular -CH2/-CF2 dipoles of PVDF causing piezoelectricity without electrical poling. The NG is capable of harvesting energy from a variety of easily accessible mechanical stress such as human touch, machine vibration, football juggling, and walking. The NG exhibits high piezoelectric energy conversion efficiency facilitating the instant turn-on of several green or blue light-emitting diodes. The generated energy can be used to charge capacitors providing a wide scope for the design of self-powered portable devices.

The influence of hydrogen bonding on the dielectric constant and the piezoelectric energy harvesting performance of hydrated metal salt mediated PVDF films.

Polyvinylidene fluoride (PVDF) films are filled with various mass fractions (wt%) of hydrated metal salt (MgCl2·6H2O) (Mg-salt) to fabricate high performance piezoelectric energy harvesters (PEHs). They deliver up to 4 V of open circuit voltage by simply repeated human finger imparting (under a pressure of ∼4.45 kPa) and also generate sufficient power to turn on at least ten commercial blue light emitting diodes (LEDs) instantly. The enhanced piezo-response is attributed to the combined effect of the change in the inherent dipole moment of the electroactive phase containing PVDF itself and H-bonding arising between the Mg-salt filler and PVDF via electrostatic interactions. Furthermore, it also successfully charged the capacitors, signifying practical applicability as a piezoelectric based energy harvester power source. UV-visible optical absorption spectral analysis revealed the possibility to estimate a change in the optical band gap value at different concentrations of Mg-salt filler added PVDF films that possess a useful methodology where the Mg-salt can be used as an optical probe. In addition dielectric properties have been studied to understand the role of molecular kinetic and interfacial polarization occurs in H-bond PVDF films at different applied frequencies at room temperature.

The co-operative performance of a hydrated salt assisted sponge like P(VDF-HFP) piezoelectric generator: an effective piezoelectric based energy harvester.

We have prepared hydrated salt filler assisted sponge like P(VDF-HFP) micro-porous electroactive films to fabricate a high performance flexible piezoelectric generator (FPG). These FPGs deliver up to 8 V of open circuit voltage under external stress and also generate enough power to turn on at least fifteen commercial blue light emitting diodes (LEDs) instantly. Furthermore, capacitors have been successfully charged by repeated finger touches indicating the potential of the FPGs to be used as self-powered devices where different types of mechanical vibrations can be applied. The high performance of FPGs might be attributed to the co-operative contribution from the porous electret structure and electroactive nature of the P(VDF-HFP) film, as they also enhance the dielectric permittivity. This approach is simple, cost-effective, and well-suited for large-scale fabrication of high-performance FPGs.

Self-poled transparent and flexible UV light-emitting cerium complex-PVDF composite: a high-performance nanogenerator.

Cerium(III)-N,N-dimethylformamide-bisulfate [Ce(DMF)(HSO4)3] complex is doped into poly(vinylidene fluoride) (PVDF) to induce a higher yield (99%) of the electroactive phases (ß- and γ-phases) of PVDF. A remarkable enhancement of the output voltage (∼32 V) of a nanogenerator (NG) based on a nonelectrically poled cerium(III) complex containing PVDF composite film is achieved by simple repeated human finger imparting, whereas neat PVDF does not show this kind of behavior. This high electrical output resembles the generation of self-poled electroactive ß-phase in PVDF due to the electrostatic interactions between the fluoride of PVDF and the surface-active positive charge cloud of the cerium complex via H-bonding and/or bipolar interaction among the opposite poles of cerium complex and PVDF, respectively. The capacitor charging capability of the flexible NG promises its applicability as piezoelectric-based energy harvester. The cerium(III) complex doped PVDF composite film exhibit an intense photoluminescence in the UV region, which might be due to a participation of electron cloud from negative pole of bipolarized PVDF. This fact may open a new area for prospective development of high-performance energy-saving flexible solid-state UV light emitters.