Titania Nanofibers Research Articles

Photo-annealed electrospun TiO2 nanofibers as ion-storage layer for self-rechargeable Zn-based electrochromic energy storage device

Developing a self-rechargeable transparent electrochromic energy storage device (EESD) is highly demanding for advancing electrochromic technology and energy harvesting capabilities. In this study, we introduce a room-temperature photo-annealing method to fabricate electrospun titanium oxide (TiO2) nanofibers, serving as an ion-storage layer (ISL) on the counter electrode. By monitoring the composition and morphology of the precursor before and after ultraviolet/ozone irradiation, we confirm the formation of oxide nanostructures in electrospun TiO2 nanofibers, which enhances ion transport in the fabricated EESDs. The structural and surface properties of the photo-annealed ISL are comprehensively analyzed using various characterization techniques. Enhanced electrochromic performances are evidenced through cyclic voltammetry, spectroelectrochemical measurements, and charge storage assessments. The Zn-based EESDs with ISL (ISL Zn-EESDs) display rapid electrochemical kinetics, high charge-storing capacities, and long lifespans, with open-circuit potential of 1.2 V, optical contrast of 77 %, discharge capacity of 92 mA h/g, coloration efficiency of 58.63 cm2/C, and 99.9 % efficiency retention up to 250 cycles in both flat and bent states. Furthermore, the practical viability of the ISL Zn-EESDs is demonstrated by powering an LED lamp for several minutes. This approach highlights the potential of ISL Zn-EESDs for developing flexible smart windows, opening up a range of promising applications.

Nanofiber array growth mechanism based on dealloying of Ti-Cu/Cu multilayer precursor film

Metal oxide nanofiber array materials are a type of material with outstanding performance and application potential. Recently, an efficient dealloying method using Ti–Cu/Cu multilayer film as a precursor was proposed to prepare titanium oxide nanofiber array structure. However, the growth mechanism and formation process of such an oxide nanofiber array grown on multilayer-film is not clear. In this work, we use Ti-Cu/Cu multilayer film as the precursor, NaOH solution as the dealloying corrosion solution, and free dealloying at room temperature. On the basis of successfully obtaining TiO2 nanofiber array films, the morphology formation and evolution process of the nanoarray were carefully monitored, and the atomic percentage changes of Ti, Cu and O elements in the dealloying precursor films were tested, as well as the formation and crystalline phase evolution trends of TiO2. Based on the experimental data, we tried to draw a schematic diagram of the formation process of this TiO2 nanofiber array, and proposed that the growth mechanism of the TiO2 nanofiber array is the precipitation growth process both with Ostwald Ripening and Oriented Attachment mechanisms. Then, the photocurrent response characteristics of the obtained nanofiber array structure samples were analyzed, and it was found that the nanofiber array structure had a certain effect on the photocurrent response performance. The completion of the present work is expected to provide a theoretical reference for the preparation and application of other metal oxide nanofiber array by dealloying method.

Enhanced photocatalytic performance of coaxially electrospun titania nanofibers comprising yolk-shell particles

The present paper reports the fabrication of novel types of hybrid fibrous photocatalysts by combining block copolymer (BCP) templating, sol–gel processing, and coaxial electrospinning techniques. Coaxial electrospinning produces core–shell nanofibers (NFs), which are converted into hollow porous TiO2 NFs using an oxidative calcination step. Hybrid BCP micelles comprising a single plasmonic nanoparticle (NP) in their core and thereof derived silica-coated core–shell particles are utilized as precursors to generate yolk-shell type particulate inclusions in photocatalytically active NFs. The catalytic and photocatalytic activity of calcined NFs comprising different types of yolk-shell particles is systematically investigated and compared. Interestingly, calcined NFs comprising silica-coated yolk-shells demonstrate enhanced catalytic and photocatalytic performance despite the presence of silica shell separating plasmonic NP from the TiO2 matrix. Electromagnetic simulations indicate that this enhancement is caused by a localized surface plasmon resonance and a confinement effect in silica-coated yolk-shells embedded in porous TiO2 NFs. Utilization of the coaxially electrospun TiO2 NFs in combination with yolk-shells comprising plasmonic NPs reveals to be a potent method for the photocatalytic decomposition of numerous pollutants. It is worth noting that this study stands as the first occurrence of combining yolk-shells (Au@void@SiO2) with porous electrospun NFs (TiO2) for photocatalytic purposes and gaining an understanding of plasmon and confinement effects for photocatalytic performance. This approach represents a promising route for fabricating highly active and up-scalable fibrous photocatalytic systems.

Potential investigation of poly (lactic acid)–curcumin–titanium dioxide nanofibers as bioactive wound dressings: characterization and cellular assessments

Potential investigation of poly (lactic acid)–curcumin–titanium dioxide nanofibers as bioactive wound dressings: characterization and cellular assessments

Sn(IV)porphyrin-Incorporated TiO2 Nanotubes for Visible Light-Active Photocatalysis.

In this study, two distinct photocatalysts, namely tin(IV)porphyrin-sensitized titanium dioxide nanotubes (SnP-TNTs) and titanium dioxide nanofibers (TNFs), were synthesized and characterized using various spectroscopic techniques. SnP-TNTs were formed through the hydrothermal reaction of NaOH with TiO2 (P-25) nanospheres in the presence of Sn(IV)porphyrin (SnP), resulting in a transformation into Sn(IV)porphyrin-imbedded nanotubes. In contrast, under similar reaction conditions but in the absence of SnP, TiO2 (P-25) nanospheres evolved into nanofibers (TNFs). Comparative analysis revealed that SnP-TNTs exhibited a remarkable enhancement in the visible light photodegradation of model pollutants compared to SnP, TiO2 (P-25), or TNFs. The superior photodegradation activity of SnP-TNTs was primarily attributed to synergistic effects between TiO2 (P-25) and SnP, leading to altered conformational frameworks, increased surface area, enhanced thermo-chemical stability, unique morphology, and outstanding visible light photodegradation of cationic methylene blue dye (MB dye). With a rapid removal rate of 95% within 100 min (rate constant = 0.0277 min-1), SnP-TNTs demonstrated excellent dye degradation capacity, high reusability, and low catalyst loading, positioning them as more efficient than conventional catalysts. This report introduces a novel direction for porphyrin-incorporated catalytic systems, holding significance for future applications in environmental remediation.

Electrospun synthesis of polyaniline and titanium dioxide nanofibers as potential electrode materials in electrochemical hydrogen storage

To meet the imperative of advancing sustainable energy, prioritizing storage systems for clean energy, such as hydrogen, is crucial. However, challenges exist in hydrogen storage, and focusing on nanofibers that incorporate appropriate nanoparticles emerges as a promising approach to enhance storage capacity. In this study, polyaniline/polyvinyl alcohol (PANI/PVA) nanofibers and polyaniline/polyvinyl alcohol/titanium dioxide (PANI/PVA/TiO2) nanofibers were synthesized using the electrospinning method under constant conditions. After characterization of the nanofibers by various techniques, the nanocomposites were used as novel electrode materials for a first time for electrochemical hydrogen energy. Electrochemical tests were conducted on the synthesized nanofibers, and an optimal current of 1.5 mA was determined. The electrochemical analyses obtained revealed a significant improvement in the maximum hydrogen storage capacity with the presence of TiO2 nanoparticles. It increased from 654.8 mAh/g for PANI/PVA nanofibers to 1250 mAh/g for PANI/PVA/TiO2 nanofibers. The difference in storage capacity is attributed to the addition of TiO2 nanoparticles.

Efficient removal of trace thallium from NH4ReO4 solutions using titanium dioxide nanofibers

A highly effective, stable, and recyclable adsorbent based on titanium dioxide nanofibers (TNFs) was fabricated via a one-step hydrothermal synthesis. The application of TNFs for the deep removal of thallium (Tl) from ammonium perrhenate (NH4ReO4) solutions was investigated. The effect of different factors, including hydrothermal temperature and time (120–170 °C, 4–10 h), adsorbent surface area (3–12 cm2), initial concentration of Tl(III) (2–10 mg/L) and pH (2–10) on the removal performance, was analyzed using batch adsorption experiments. Kinetic analysis revealed that the removal process followed a pseudo-first-order model. The adsorption data of TNFs were analyzed using Freundlich and Langmuir isotherms, with the Langmuir isotherm showing the best fit and indicating a theoretical maximum adsorption capacity of 767.2 mg m−2. Thermodynamic studies demonstrated the adsorption process was characterized by physisorption, being spontaneous, and exothermic. Under optimized conditions, TNFs demonstrated successful removal of Tl(III) from NH4ReO4 solutions with limited adsorption of rhenium (Re) and arsenic (As) ions. Acidity and reusability tests confirmed the significant stability and excellent recoverability of TNFs. The proposed TNFs serve as an effective, and stable adsorbent with a high affinity for Tl(III), offering a viable and efficient approach for the purification of NH4ReO4 solutions.

Self-cleaning SiO2–TiO2 ceramic membrane for enhanced oil–water separation

An efficient and practical method is proposed for the separation of oil–water mixtures and emulsions in sustainable water ecosystems, facilitating energy recovery. The construction of flexible ceramic fiber membranes with high throughput and self-cleaning capabilities has proven effective but challenging. This study reports a novel approach combining the sol–gel and electrospinning techniques to synthesize flexible silicon dioxide (SiO2)–titanium dioxide (TiO2) nanofiber membranes (STNFMs). These membranes possess nanoscale rough structures, granting them superhydrophilicity and underwater superoleophobicity (155°). Exploiting the photocatalytic properties of titanium dioxide, STNFMs-4 not only demonstrates excellent separation performance but also exhibits remarkable self-cleaning abilities. After 2 h of ultraviolet light irradiation, the membrane flux returns to its original level. STNFMs provide a promising solution for highly efficient separation of oil–water mixtures and emulsions, with the potential to play a significant role in water treatment and resource recovery.

Curcumin loaded as prepared electrospun titania nanofibers for post breast cancer surgeries

In the present study, curcumin-loaded titania nanofibers were synthesized by the conventional sol-gel method via the electrospinning technique using polyvinyl pyrrolidone and characterized via SEM, FTIR, and XRD. Moreover, their contact angle measurement, degradability, water uptake, and mechanical strength were investigated, besides their antibacterial activity, antioxidant activity, sustained drug release, and cytotoxicity against normal cells and breast cancer cell lines. It can be observed that as the concentration of curcumin increased, the mechanical characteristics of the samples were enhanced. The antibacterial results declared that the increase in curcumin concentration enhanced the inhibitory effect against the different pathogens. Moreover, the viability of cells of the normal cell line, seeded on the samples was in the range from 61.4 to 86.5% which indicated its safety on normal cells. However, the cell viability on the cancerous cell line was found to be 33.8, 19.7, 17.9 and 0% for 0, 1, 3, and 5% loaded TiO2/PVP respectively. This lethal effect of the prepared mats on breast cancer cells with nearly no cytotoxic effect on normal cells, favors the usage of the prepared 5% curcumin-loaded TiO2/PVP mat as anticancerous wound healing bandages for postoperative breast cancer surgeries.Graphical

Silver infusion: Enhancing physical and photocatalytic properties of titanium dioxide nanofibers

We report here titanium dioxide (TiO2) and silver-doped titanium dioxide (Ag/TiO2) nanofibers in a polyvinyl pyrrolidone (PVP) matrix. The unique hygroscopic nature of PVP enabled better networking of ethanol-dissolved precursors. X-ray diffraction (XRD) and RAMAN spectroscopy were used to study the phase transformation of the TiO2 nanofibers due to doping, while field emission scanning electron microscopy (FE-SEM) provided the surface morphology. The Ag/TiO2 nanofibers transformed from anatase to rutile phase, resulting in better conductive and photocatalytic properties. Dielectric studies suggested phase transformation related charge delocalization and enhanced mobility with increasing Ag content. The photocatalytic properties of the Ag/TiO2 nanofibers were observed via degradation of Congo Red (CR). The increasing Ag content and conversion to the rutile phase enhanced the degradation efficiency from 36 to 92% under Ultra-violet (UV)-light irradiation.

Boosted Photocatalytic Performance for Antibiotics Removal with Ag/PW12/TiO2 Composite: Degradation Pathways and Toxicity Assessment.

Photocatalyst is the core of photocatalysis and directly determines photocatalytic performance. However, low quantum efficiency and low utilization of solar energy are important technical problems in the application of photocatalysis. In this work, a series of polyoxometalates (POMs) [H3PW12O40] (PW12)-doped titanium dioxide (TiO2) nanofibers modified with various amount of silver (Ag) nanoparticles (NPs) were prepared by utilizing electrospinning/photoreduction strategy, and were labelled as x wt% Ag/PW12/TiO2 (abbr. x% Ag/PT, x = 5, 10, and 15, respectively). The as-prepared materials were characterized with a series of techniques and exhibited remarkable catalytic activities for visible-light degradation tetracycline (TC), enrofloxacin (ENR), and methyl orange (MO). Particularly, the 10% Ag/PT catalyst with a specific surface area of 155.09 m2/g and an average aperture of 4.61 nm possessed the optimal photodegradation performance, with efficiencies reaching 78.19% for TC, 93.65% for ENR, and 99.29% for MO, which were significantly higher than those of PW12-free Ag/TiO2 and PT nanofibers. Additionally, various parameters (the pH of the solution, catalyst usage, and TC concentration) influencing the degradation process were investigated in detail. The optimal conditions are as follows: catalyst usage: 20 mg; TC: 20 mL of 20 ppm; pH = 7. Furthermore, the photodegradation intermediates and pathways were demonstrated by HPLC-MS measurement. We also investigated the toxicity of products generated during TC removal by employing quantitative structure-activity relationship (QSAR) prediction through a toxicity estimation software tool (T.E.S.T. Version 5.1.2.). The mechanism study showed that the doping of PW12 and the modification of Ag NPs on TiO2 broadened the visible-light absorption, accelerating the effective separation of photogenerated carriers, therefore resulting in an enhanced photocatalytic performance. The research provided some new thoughts for exploiting efficient and durable photocatalysts for environmental remediation.

The application of Sn(IV)Cl2 and In(III)Cl porphyrin-dyed TiO2 nanofibers in photodynamic antimicrobial chemotherapy for bacterial inactivation in water

The World Health Organization has reported that antimicrobial resistance is one of the top 10 health threats that humanity faces today. Due to this, alternative therapies to the common antimicrobials are being explored and among these is photodynamic antimicrobial chemotherapy, where a combination of light, a photosensitizer and reactive oxygen species can be used to target microbial cells. In this research, free base, tin (IV) and indium (III) tetramethoxyporphyrins photosensitizers are adsorbed onto inorganic titanium dioxide nanofibers in an effort to create reusable fibers that are effective against Staphylococcus aureus. The photodynamic antimicrobial chemotherapy studies indicate that the metalloporphyrin adsorbed nanofibers exhibit good photodynamic antimicrobial activity against Staphylococcus aureus where the Cl2Sn(IV) tetramethoxyporphyrin dyed TiO2 exhibited 100% bacterial inhibition after a 30 min irradiation period.

Synthesis of 0D/1D electrospun titania nanofibers incorporating CuO nanoparticles for tetracycline photodegradation and modeling and optimization of the removal process

Air-calcined electrospun CuO nanoparticles embedded in TiO2 nanofibers were synthesized and examined for tetracycline photodegradation. The electrospun nanofibers were characterized by XRD, FESEM, ICP, EDX, N2 adsorption–desorption, PL, and UV–DRS techniques. Elemental analysis, crystalline phase identification method, and FESEM images proved electrospun 0D/1D composite nanofiber fabrication. Composite nanofibers have mesoporous structure, extended light response range, limited band gap energy, promoted light absorption, and efficient charge transfer. Excess CuO produces a surface covering of TiO2 nanofibers, which decreases textural characteristics and increases agglomerations. CuO inclusion caused a hump-like variation in tetracycline UV photodegradation, culminating at 10 wt.%. RSM-CCD optimized process parameters for photocatalytic performance. A quadratic model (Adj. R2 = 0.9986, p-value < 0.0001) predicted experimental data and interpreted system behaviour. TiO2-CuO (10%) nanofibers eliminated 86% and 77% of tetracycline under UV and simulated sun light, respectively, under optimum conditions (photocatalyst dose of 1.4 g.L-1, initial solution pH of 6.14, and 75 min irradiation).

Comparison of Electrospun Titania and Zinc Oxide Nanofibers for Perovskite Solar Cells and Photocatalytic Degradation of Methyl Orange Dye

ZnO and TiO2 are both well-known electron transport materials; however, an exact comparison of their performance, when fabricated under the same synthesis conditions, is missing in the literature. Considering this, we introduced a viable electrospinning route for the development of highly polycrystalline TiO2 and ZnO nanofibers for an electron transport material (ETM) of perovskite solar cells and photocatalysts for textiles. Thanks to the effective tuning of band structure and morphology of TiO2, a significant improvement in performance as compared to ZnO was observed when both were used as photoanodes and photocatalysts. X-ray diffraction detected polycrystalline structural properties and showed that peaks are highly corresponding to TiO2 and ZnO. Morphological analysis was carried out with a scanning electron microscope, which revealed that nanofibers are long, uniform, and polycrystalline, having diameter in the nano regime. TiO2 nanofibers are more aligned and electron-supportive for conduction as compared to ZnO nanofibers, which are dense and agglomerated at some points. Optoelectronic properties showed that TiO2 and ZnO show absorption values in the range of ultraviolet, and visible range and band gap values for TiO2 and ZnO were 3.3 and 3.2 eV, respectively. The TiO2 band gap and semiconductor nature was more compatible for ETL as compared to ZnO. Electrical studies revealed that TiO2 nanofibers have enhanced values of conductivity and sheet carrier mobility as compared to ZnO nanofibers. Therefore, a higher photovoltaic conversion efficiency and antibacterial activity was achieved for TiO2 nanofibers (10.33%), as compared to ZnO (8.48%). In addition, the antibacterial activity of TiO2 was also recorded as better than ZnO. Similarly, compared to ZnO nanofibers, TiO2 nanofibers possess enhanced photoactivity for antimicrobial and dye degradation effects when applied to fabrics.

Enhanced degradation of methylene blue dye using flexible SiO2–TiO2 nanofiber membranes

Titanium dioxide (TiO2) is widely regarded as one of the most extensively applied photocatalytic semiconductor materials. However, conventional powdered titanium dioxide exhibits certain limitations, including relatively weak light absorption capability, a small surface area and insufficient active sites. This study successfully prepared flexible and porous silicon dioxide (SiO2)–titanium dioxide nanofiber membranes (NFMs) by implementing electrospinning technology and calcination processes. The porous membranes demonstrate remarkable performance in water treatment, featuring a high specific surface area (49 m2/g) and porosity, enabling efficient adsorption and removal of organic pollutants in water. Remarkably, the NFMs-800 variant exhibits outstanding photocatalytic performance, achieving complete removal of adsorbed organic compounds under ultraviolet irradiation. The design and fabrication methods of this porous membrane are simple and scalable, providing a potential solution for practical water-treatment applications. Consequently, the silicon dioxide–titanium dioxide porous membrane holds significant prospects in the field of water treatment, offering a promising contribution to the attainment of efficient and sustainable water resource management.

Mechanistic insight into the enhanced photodegradation by black titanium dioxide nanofiber-graphene quantum dot composites

The photocatalytic activity of black titanium dioxide nanofibers (bTiO2 NFs) can be enhanced through composition with carbon nanomaterials. However, it is unclear whether enhanced charge separation or increased surface adsorption of organic pollutants to the nanocomposite surfaces is the dominant contributor. This knowledge gap was filled when we sought to enhance the surface contact of carbon with the bTiO2 NFs by using graphene quantum dots (GQDs) hypothesizing that this would further enhance photocatalytic activity. The results showed a similar Rhodamine B (RhB) photodegradation rate between the optimal loadings of GQDs and RGO we reported previously. This allowed for further elucidation of the enhancement mechanism, where charge carrier separation enhancement at the photocatalyst surface is the dominant effect, whereas RhB adsorption does not make significant contribution. This significant insight enhances our understanding towards engineering highly efficient composite photocatalysts for organic pollutant removal in water.

Efficiency enhancement of perovskite-sensitized solar cell based on electrospun titania nanofibers coated in organic-inorganic hybrid metal trihalide nanocrystals

In this work, we have developed highly efficient, flexible, and thermally stable photoanode materials for perovskite-sensitized solar cells (PSCs). Methylammonium lead iodide (MAPbI3 or CH3NH3PbI3) coated TiO2 nanofibers (TNFs) were prepared by two step process. The cubic crystalline nature of MAPbI3 and the semi-crystalline nature of TNFs were confirmed by X-ray diffraction. The functional groups present in the photoanode materials were identified by Fourier-transform infrared spectroscopy. From UV–visible spectral studies, the absorption maximum of MAPbI3-coated TNFs was observed at 754 nm. High-resolution transmission electron microscopy and scanning electron microscopy images of MAPbI3 and TNFs showed a polycrystalline nature and uniform fiber structures, respectively. The highest electrical conductivity of 5.29 × 10−4 S/cm was achieved by the MAPbI3-coated TNFs photoanode, as measured by electrochemical impedance spectroscopy at room temperature. MAPbI3-coated TNFs, Spiro-OMeTAD, and gold chloride were used as the photoanode, hole transport material, and back electrode, respectively, in a PSC. A PSC constructed with MAPbI3-coated TNFs yielded an efficiency of 13.12%, bettering the 11.48% efficiency of a PSCs constructed from MAPbI3-coated TiO2 nanoparticles.

Photovoltaic Measurement Under Different Illumination of the Dye-Sensitized Solar Cell With the Photoanode Modified by Fe2O3/g-C3N4/TiO2 Heterogeneous Nanofibers Prepared by Electrospinning With Dual Jets

In this study, iron oxide (Fe2O3)/graphitic carbon nitride (g-C3N4)/titanium dioxide (TiO2) nanofibers (NFs) were used as an additional layer on photoanode in dye-sensitized solar cells (DSSCs) to improve the photovoltaic performance of DSSCs. The nanofibers were prepared by electrospinning with double jets. The heterogeneous nanofiber composite mainly includes Fe2O3, g-C3N4, and TiO2. The Fe2O3/g-C3N4/TiO2 NFs were characterized by X-ray diffractometer (XRD), and the surface morphology was observed by a field emission scanning electron microscope (Fe-SEM). The electrochemical impedance spectroscopy (EIS) was applied to analyze the impedance of the cell. The incident photon current efficiency (IPCE) measurements were applied to determine the quantum efficiency, and ultraviolet-visible (UV-Vis) spectrophotometer was applied to observe the dye adsorption and absorption wavelength. To understand the performance of the modified photoanodes in DSSCs, we analyzed the photovoltaic parameters. The results suggest that the addition of Fe2O3/g-C3N4/TiO2 NFs is able to improve the conversion efficiency of the modified DSSCs to 4.81%. In addition, the efficiency under different illumination was also analyzed, and the highest conversion efficiency was 6.81% at 30 mW/cm2.

Pseudocapacitive sodium-ion storage in one-dimensionally structured anatase TiO2 nanofiber anode for high performance sodium-ion batteries

Nanofibers provide high surface area to volume ratio, vectoral conduction, fast ionic diffusion, and short pathways for sodium ions. Titania nanofibers exhibit excellent electrochemical performance when used for sodium-ion storage. One-dimensional titania nanofiber was synthesized by an electrospinning process as an anode material for high capacity sodium-ion batteries. The electrochemical kinetics of titania nanofiber for sodium-ion storage were examined. Titania nanofiber exhibited pseudocapacitive capacitive properties with high rate performance, giving capacity of 97 mA h g−1 after 1000 cycles with a current density of 1000 mA g−1. Even when current rate returned to the initial current density of 50 mA g−1, titania nanofiber electrode capacity climbed to 206 mA h g−1 again without capacity fading, which indicated good rate performance, superior sodium insertion/extraction reaction, and high reversible capacity.

Piezo/Triboelectric Nanogenerator from Lithium-Modified Zinc Titanium Oxide Nanofibers to Monitor Contact in Sports

The need for technological innovation in competitive sports is crucial for self-monitoring and smart decision making. In this work, we demonstrate how intelligent sports and smart decision making can be achieved in cricket and boxing using lithium-modified zinc titanium oxide (LZTO) nanofibers based on piezoelectric nanogenerators (PENGs) and triboelectric nanogenerators (TENGs). Zinc titanium oxide (ZTO) nanofibers synthesized using electrospinning followed by a calcination technique are modified with lithium to increase the output of the nanogenerator. An optimized PENG is fabricated using 25 wt % loading of LZTO (d33 = 214 pm/V) in a poly(vinylidene fluoride) (PVDF) matrix as a double-layered structure and yields an open-circuit voltage (Voc) of 35 V and a short-circuit current (Isc) of 1.6 μA by manual tapping. To fabricate the TENG, Kapton and LZTO are used as negative and positive tribolayers, while Cu and adhesive polymer tape are used as the electrode and spacer, respectively. Furthermore, a hybrid nanogenerator (HNG) is fabricated by combining the PENG and TENG to produce a rectified voltage, current, and power density of up to 75 V, 3.2 μA, and 240 μW/cm2, respectively. These HNGs are integrated with a punching bag and demonstrated to differentiate among the six types of punches in boxing. Furthermore, PENGs are used in cricket to monitor the number of balls middled on the bat during practice and the contact of the ball with the bat and stumps for smart decision making. All kinds of lab-scale testing are done for these applications, which pave a way for exploring the frontiers in nanogenerator applications in sports as maintenance-free and self-powered sensing technology.