Polyaniline Layer Research Articles

Coupling hole-transporting polyaniline layer with a cobalt phthalocyanine cocatalyst to boost photoelectrochemical water oxidation of bismuth vanadate photoanodes

Though bismuth vanadate (BiVO4) exhibits a promising potential as a semiconductor photoanode toward photoelectrochemical (PEC) water oxidation, its PEC performance is still limited by the poor charge carrier transport and sluggish oxygen evolution kinetics. Herein, the polyaniline (PANI) and cobalt coordinated-phthalocyanines (CoTcPc) were introduced onto the BiVO4 semiconductor substrate, constructing the integrated CoTcPc/nPANI/BiVO4 (n = 30, 60 and 90, n represents the deposition time for PANI with the unit of s) composite photoanodes. It is demonstrated that the PEC water oxidation activity of BiVO4 is significantly boosted by the incorporation of PANI and CoTcPc, stemming from the improved electron/hole transfer, enhanced charge separation efficiency, and accelerated carrier mobility and water oxidation kinetics. CoTcPc/60PANI/BiVO4 composite photoanode with the optimized compositions exhibits an enhanced photocurrent density of 4.03 mA/cm2 at 1.23 V vs. RHE under illumination, ranking among the best records reported recently. Furthermore, the roles of electrodeposition time to generate PANI are also distinguished through experimental studies. These results reveal the crucial role of engineering the hole transfer layer to optimize the semiconductor photoanodes toward efficient PEC water oxidation.

Graphene oxide-titanium oxide-polyaniline hybrid materials for high-performance dye-sensitized solar cells

A new solar cell that comprises a graphene oxide and titanium oxide nanoparticle (NP) composite with graphitized polyaniline (PANI) has been tested in polymer solar cells (PSCs). In this study, a series of conjugated polymers were synthesized and evaluated as the absorber and hole-transport layer materials in organic solar cells, demonstrating the significant impact of the chemical structure of the polymers on solar cell performance. The incorporation of graphene oxide (GOX) and titanium oxide TiO2 NP in conjugated polymers, particularly when graphitized within the PANI layer, led to improved open-circuit voltages compared to structurally similar polymers without NP. The morphology of the composite films was analyzed and related to the photovoltaic performance of polymers synthesized with polyaniline PANI-base and PANI-salt. Optimal NP addition in PANI-salt, PANI-base, PANI-base-TiO2, and PANI-base-GOX resulted in open-circuit voltages and efficiencies of 433 mV and 3.67%, 250 mV and 0.595%, 310 mV and 1.358%, and 520 mV and 2.366%, respectively. This study underscores the importance of polymer film uniformity in the performance of PSCs, with the highest efficiency obtained using a conjugated polymer with the best PANI-salt and PANI-base-GOX films. The research sheds light on the relationship between polymer structure and device photovoltaic performance, which is crucial for the design of new polymeric materials for efficient use and stable OSCs and PSCs.

Anionic Dye Removal with a Thin Cationic Polyaniline Coating on Cellulosic Biomaterial.

This paper reports the development of novel adsorbent materials using polyaniline (PANI) grafted onto Posidonia (POS) fibers, aimed at efficiently removing phenol red (PSP), an anionic dye, from aqueous solutions. The synthesis involved the copolymerization of aniline grafted on the surface of the POS and aniline monomer in solution, resulting in a chemically bound thin PANI layer on the POS bioadsorbent. Structural characteristics and binding affinities of these adsorbents with PANI under its emeraldine salt (POS@PANI-ES) or emeraldine base (POS@PANI-EB) forms are reported. The rapid adsorption kinetics observed are attributed to enhanced accessibility to PANI adsorption sites on the POS surface. The binding percentages of PSP to POS@PANI-ES and POS@PANI-EB materials were found to be 97 and 50%, respectively, after 15 min of contact time. The Langmuir model for localized adsorption sites and the Volmer model for nonlocalized adsorption as a mobile layer were fitted to the experimental adsorption isotherms of PSP to POS@PANI-EB and POS@PANI-ES, yielding the thermodynamic parameters of adsorption. The adsorption capacities of PSP on POS@PANI-EB and POS@PANI-ES were 37.8 and 71.5 μmol g-1, respectively. The adsorption of PSP remained above 80% at moderate salt concentrations of around 0.1 mol L-1; however, higher concentrations of NaCl and CaCl2 in PSP solutions significantly reduced the adsorption on POS@PANI-ES.

High energy capability in poly(vinylidene fluoride-co-chlorotrifluoroethylene) nanocomposite incorporated with Ag@polyaniline@covalent organic framework core–shell nanowire

The development of polymer film with large electrical displacement is essential for the applications of lightweight and compact energy storage. The dielectric diversity at interface of polymer composite should be addressed to realize the film capacitor with high energy density and dielectric reliability. In this work, poly(vinylidene fluoride-co-chlorotrifluoroethylene) (P(VDF-CTFE)) nanocomposite was incorporated by core–shell nanowire with covalent organic framework (COF) outer coating to alleviate the dielectric mismatch at interface. After the preparation of Ag nanowire through polyol reduction, polyaniline (PANI) and COF layers were sequentially deposited to construct core–shell Ag@polyaniline@covalent organic framework (Ag@PANI@COF) nanowire. According to the unique core–shell architecture, the COF framework is utilized to suppress the remanent polarization while high electrical displacement is preserved by the center Ag nanowire. The maximum energy density of 25.0 J/cm3 at 425 MV/m is obtained in 0.1 wt% stretched Ag@PANI@COF/P(VDF-CTFE) nanocomposite. The presence of core–shell nanowire depresses the distribution distortion of electric field and the diffusion of charge carriers under high field. This work demonstrates an effective method to develop the polymer film with large electrical displacement, and sheds a light on insightful exploration of interfacial polarized mechanism in polymer dielectric composite.

Controlling the morphology and properties of electrodeposited polyaniline layer on TiO2 nanotubes

Polyaniline (PANI) layers were electrodeposited, as the conductive emeraldine salt phase (PANI (ES)), on the surface of titanium dioxide nanotubes (TiO2 NTs) to evaluate the protective and photo(electro)chemical performance. TiO2 NTs plates were obtained by anodization, in a two-electrode in the undivided cell. The adjustment of the electropolymerization parameters (e.g. aniline concentration, cycles number in cyclic voltammetry, TiO2 cathodic polarization) allowed the control of the PANI (ES) morphology and film thickness, changing the charge recombination dynamics on the PANI (ES)/TiO2 and PANI (ES)/liquid interfaces. It was observed that lower aniline concentrations resulted in the best control of the electropolymerization process, which ensured the deposition of thin films. The TiO2 NTs/PANI (ES) interface was characterized by absorption and vibrational spectroscopies, and scanning electron microscopy. Electronic and photo(electro)chemical properties of the TiO2 NTs/PANI (ES) films were characterized by photoelectrochemical measurements and electrochemical impedance spectroscopy.

Innovative modification of cellulose fibers for paper-based electrode materials using metal-organic coordination polymers

Cellulosic paper-based electrode materials have attracted increasing attention in the field of flexible supercapacitor. As a conductive polymer, polyaniline exhibits high theoretical pseudocapacitive capacitance and has been applied in paper-based electrode materials along with cellulose fibers. However, the stacking of polyaniline usually leads to poor performance of electrodes. In this study, metal-organic coordination polymers of zirconium-alizarin red S and zirconium-phytic acid are applied to modulate the polyaniline layer to obtain high-performance cellulosic paper-based electrode materials. Zirconium hydroxide is firstly loaded on cellulose fibers while alizarin red S and phytic acid are introduced to regulate the morphology of polyaniline through doping and coordination processes. The results show that the introduction of dual coordination polymers is effective to regulate the morphology of polyaniline on cellulose fibers. The performances of the paper-based electrode materials, including electrical conductivity and electrochemistry, are apparently improved. It provides a promising strategy for the potential development of economical and green electrode materials in the conventional paper-making process.

Analogous Confinement Effect Enables High Stability and High Capacity Ammonium Storage in Polyaniline@Poly(o-fluoroaniline)@Carbon Layer.

Rechargeable aqueous ammonium ion (NH4 +) batteries have attracted much attention due to the unique properties of NH4 +. Polyaniline (PA) with outstanding conductivity is a potential cathode material, but it can be oxidized to pernigraniline (PG) rapidly, resulting in its poor stability. In this study, polyaniline@poly(o-fluoroaniline)@carbon layer (PA@POFA@C) is prepared for excellent and durable NH4 + storage. PA@POFA@C exhibits a high capacity of 208 mAh g-1 at 0.2 A g-1 and maintains 126 mAh g-1 at 10 A g-1. More importantly, an excellent capacity retention rate of 88.24% is achieved after 2000 cycles with ≈100% coulombic efficiency. Spectroscopy studies suggest analogous confinement effect can effectively limit the escape of hydrogen in imine group, and form the hydrogen-restricted region between the PA and POFA layer which can provide H+ for the complete reduction of PG. Meanwhile, the hydrophobic effect of POFA effectively restrains the hydrolysis of PG. Interestingly, the introduction of C layer improves the hydrophilicity of electrode and shortens the activation process, serving as the outermost protective layer of the electrode. Finally, PA@POFA@C achieves desirable electrochemical performances with analogous confinement effect. This research provides ideas for the preparation of advanced polymer electrodes for aqueous NH4 + batteries.

Conductivity-Based Gas Sensors Using Tamarindus indica Polysaccharide-Capped Gold Nanoparticles for the Detection of Volatile Gases.

Gold nanoparticles (nAu) were synthesized by a sustainable approach utilizing tamarind seed polysaccharide (TSP). Polysaccharides are naturally occurring polymers derived from tamarind seeds, which function both as capping and reducing agents. Polyaniline (PANI) was subsequently capped over the as-prepared gold nanoparticles in order to facilitate the sensor property. The TSP-nAu-PANI film was fabricated by Methods I and II and utilized in the investigation of active sensor devices for the detection of organic pollutants such as benzene, toluene, and chloroform. The synthesized gold nanoparticles and the TSP-nAu-PANI films were analyzed using several analytical and spectral tools. Among the two methods, the Method II (TSP-nAu-PANI) film has a high sensing response toward benzene (105.69%), toluene (96.99%), and chloroform (74.98%). TSP is also a proton-conducting biopolymer, which enhances the conductivity of the material. The combination with the PANI layer of the film adsorbs the vapors easily and the prepared film material is more effective and ideal for sensing toxic gases.

Preparation and performance of a bamboo-based electromagnetic wave absorber by interfacial polymerization of graphene oxide/polyaniline

Excellent electromagnetic wave absorption ability and effective absorption bandwidth have been the development direction of electromagnetic wave absorbing materials. In this paper, a rational structural design is proposed. Graphene oxide (GO)/polyaniline (PANI) layer was formed on the surface of the natural material bamboo powder (BP) by an interfacial polymerization process. The combination of GO and PANI improves the impedance mismatch of the conductive polymer PANI. Enhanced dielectric storage and loss capability of the composite GO/PANI/BP. The addition of BP brings more electromagnetic wave loss channels to the composite GO/PANI/BP. This unique structure facilitates the construction of a three-dimensional electromagnetic wave-reflecting cavity, which improves the absorptive capacity of the composite by introducing effective multiple reflections. The conductivity of GO/PANI/BP was 1.78 (±0.06) S/cm. When filled to 30 wt%, a minimum reflection loss (RLmin) of −44 dB at 9.36 GHz and a thickness of 3 mm, and an effective absorption bandwidth (<-10 dB) of up to 5.36 GHz in the frequency range 12.64–18 GHz and at a thickness of 2 mm. Exhibits superior loss capability compared to most previous PANI-based electromagnetic wave absorbing materials. In addition, the design structure of this three-dimensional electromagnetic wave reflecting cavity can provide inspiration for the design of other electromagnetic wave absorbing materials and expands the candidate range of green and efficient electromagnetic wave absorbers.

Highly efficient polyaniline based flexible electrochemical sensor for bisphenol a detection

We report herein a novel label-free polyaniline (PANI) based bisphenol A (BPA) electrochemical sensor fabricated on a flexible polyethylene terephthalate (PET) substrate. The PANI layer was electrochemically deposited on a gold-coated PET substrate using the facile amperometric (current–time transient) technique. A thorough investigation of the PANI sensing layer was done using Raman spectroscopy and field emission scanning electron microscopy (FESEM) characterization techniques. The sensing properties of the implanted matrix for BPA detection were investigated through cyclic voltammetry (CV). The fabricated electrochemical sensor showed linearity in the concentration range of 0.05–––5.0 µM, a higher sensitivity of ∼ 56.69 A/M and a lower limit of detection (LOD) of ∼ 1.06 nM. The sensor exhibited excellent flexibility and a better shelf life of 20 weeks. The results highlight the importance of PANI thin film as an attractive matrix for the realization of electrochemical sensor for BPA detection.

Electrochemical preparation and features of newly cross-stacking multi-layered reduced graphene oxide (rGO) and polyaniline (PANI) modified carbon-based electrode

Carbon-based electrode as an economically benign choice is widely used in electrochemical or bio-electrochemical systems. However, its poor electrical conductivity that leading high overpotential and energy loss, especially in large scale facilities, remains a bottleneck for its application. Herein, a unique cross-stacking multi-layered reduced graphene oxide (rGO) and polyaniline (PANI) modified carbon brush is fabricated via one-step electro-depositing. In particular, the top-most layer of the modified electrode is orientated controlled to be rGO or PANI layer by adjusting the initial CV scanning in the positive or negative direction. As was indicated by cyclic voltammetry, the improved electrochemical activity is achieved by coupling the advantages of the highly conductive network offered by graphene with desirable stability provided by the well-dispersed deposition of nanoscale PANI particles. In comparison, the modified electrode with rGO on the top-most layer (LrGO) showed higher degree of sp2-hybridized -C-C- ordered structure in Raman profile, lower O/C ratio in XPS analysis, higher Zeta potential (−2.05 mV) and more hydrophilic than unmodified one. Moreover, benefiting from the unique cross-stacking multi-layered matrix of rGO and PANI, the best electrochemical performance was achieved on the electrode LrGO with high exerted electrochemical active surface area (ECSA) of 0.85 mF cm−2, and the charge transfer resistance as low as 0.32 Ω. The findings of this study provide a guidance for the modification and application of carbon-based electrode using rGO and PANI, which potentially enables the scaling-up of carbon-based electrode in various (bio-) electrochemical systems with high electrochemical performance.

Improving the corrosion protection of plasma electrolysis-treated light metal by polymeric functionalization

Suppressing the rate of corrosive degradation has been the primary challenge in the widespread use of lightweight metals across a variety of potential applications because their native passive layer is still susceptible to chemical attacks in aqueous or humid environments. This work explores the roles of polyaniline in tandem with a TiO2 layer in improving the corrosion properties of pure Ti. The anodic TiO2 surface is a result of a plasma electrolysis treatment in a non-acidic, phosphate-based electrolyte. The emeraldine base form of the polymer is subsequently applied to modify the surface properties of the plasma-electrolyzed Ti samples to further protect the surface against polar species that might interact with TiO2. The deposition of the thin layer of polyaniline retains the original surface microstructure of the plasma electrolysis layer. Nevertheless, the presence of polyaniline successfully reduces the corrosion current density and passive current density of plasma-electrolyzed Ti by ~50%. The corrosion protection mechanism is explained in the context of equivalent circuit models based on impedance measurements.

Hydrogen Video Imaging System for Visualizing Microstructure-Dependent Hydrogen Diffusion Behaviors in Polycrystalline Metals

Hydrogen diffusion in polycrystalline metals is known to depend on microstructure. The hydrogen-microstructure interactions have been extensively studied last decades, but the microstructure-dependent hydrogen diffusion behavior is still unclear. To clarify the hydrogen diffusion behavior, it is necessary to visualize the time variations of the microscopic hydrogen distribution in polycrystalline metals. Thus, we developed a hydrogen video imaging system (HVIS) in this study to analyze the hydrogen distribution in polycrystalline metals with sub-micrometer spatial and video-rate time resolutions. The inexpensive and atmospheric-control-free system is expected to be widely used as a versatile approach for analyzing the hydrogen-microstructure interaction in detail.Pure polycrystalline Ni (thickness: 125 µm) was used as a specimen. The specimen was electrochemically polished at a constant voltage of 50 V in a mixed solution of perchloric acid and acetic acid. The thickness was approximately 110 µm after polishing. Subsequently, a polyaniline layer (PANI) was polymerized on one side of pure Ni. The specimen was set to the acrylic cell, which is used to preserve a 0.1 M NaOH aqueous solution. So, only the bare Ni side of the specimen was exposed to the 0.1 M NaOH solution. Electrochemical hydrogen charging was conducted at the bare Ni side of the specimen at a constant current density of -10 A / m2. An inverted optical microscope was used to observe the color distribution of the PANI side. In our previous studies,1-3) it has been clarified that PANI changes its color due to the reaction with hydrogen in metals. Thus, the distribution of hydrogen permeated through pure polycrystalline Ni can be observed as a color distribution of PANI during hydrogen charging.The color of PANI was purple before the hydrogen charging. After 20 h of hydrogen charging, the color of PANI partially turned white. If PANI reacts with hydrogen, the color changes from purple or dark blue to yellow or transparent.1,2) Therefore, the local whitening of PANI is thought to be caused by the reaction with atomic state hydrogen permeated through pure polycrystalline Ni. The number of color changed areas increased with time during hydrogen charging. After 120 h of hydrogen charging, the specimen was immersed in a 1 M NaOH aqueous solution to remove PANI. Subsequently, the microstructure of pure polycrystalline Ni was analyzed using FE-SEM and EBSD. It was found that the color changed area of PANI corresponded to the grain boundaries (GBs) of pure Ni. This suggests that the GBs in pure Ni are preferential hydrogen diffusion paths. Furthermore, the clear color change of PANI was observed at the random GBs, while the whitening scarcely occurred at the Σ3 GBs, indicating that the preferential hydrogen diffusion mainly occurred at the random GBs. The results showed that HVIS can clarify the microstructure-dependent hydrogen diffusion in polycrystalline metals.

Low-Cost Optical pH Sensor with a Polyaniline (PANI)-Sensitive Layer Based on Commercial Off-the-Shelf (COTS) Components.

In this paper, we presented a novel, compact, conceptually simple, and fully functional low-cost prototype of a pH sensor with a PANI thin film as a sensing layer. The PANI deposition process is truly low-cost; it performs from the liquid phase, does not required any specialized equipment, and comprises few processing steps. The resulting PANI layer has excellent stability, resistance to solvents, and bio- and chemical compatibility. The pH sensor's sensing part includes only a few components such as a red-light-emitting diode (LED) as a light source, and a corresponding photodiode (PD) as a detector. Unlike other PANI-based sensors, it requires no sophisticated and expensive techniques and components such lasers to excite the PANI or spectrometry to identify the PANI color change induced by pH variation. The pH sensor is sensitive in the broad pH range of 3 to 9, which is useful for numerous practical applications. The sensor requires a tiny volume of the test specimen, as little as 55 µL. We developed a fully integrated packaging solution for the pH sensor that comprises a limited number of components. The pH sensor comprises exclusively commercial off-the-shelf (COTS) components and standard printed circuit boards. The pH sensor is assembled using standard surface mounting technology (SMT).

A flexible self-powered ultra-violet photodetector based on sandwiched zinc oxide nanorods between polyaniline layers

A flexible self-powered ultra-violet photodetector based on sandwiched zinc oxide nanorods between polyaniline layers

In situ visualization of misorientation-dependent hydrogen diffusion at grain boundaries of pure polycrystalline Ni using a hydrogen video imaging system

Hydrogen, the key element for solving the major environmental issues, exhibits rapid diffusion and localization in lattice defects of metals, which leads to embrittlement. However, the microstructure-hydrogen interactions in metallic materials are poorly understood. Therefore, a technique for capturing the microstructure-dependent hydrogen diffusion in real-time has long been targeted by researchers. Here, we successfully visualized the preferential hydrogen diffusion at grain boundaries (GBs) of pure Ni using a hydrogen video imaging system. A thin polyaniline layer was utilized as a hydrogenochromic sensor, and the hydrogen distribution was analyzed based on the color distribution of polyaniline. The system revealed the misorientation-dependent hydrogen flux at GBs of pure polycrystalline Ni with a micrometer-scale spatial resolution. It suggests that the geometrical structure of the GBs is a critical factor for preferential hydrogen diffusion. The use of the hydrogen video imaging system further advances the mechanistic understanding of hydrogen-material atomic interactions in polycrystalline metals and critically facilitates the development of hydrogen-related materials.

Preparation of ZnO Nanosheet Array and Research on ZnO/PANI/ZnO Ultraviolet Photodetector.

High-performance ultraviolet photodetectors have important scientific research significance and practical application value, which has been the focus of researchers. In this work, we have constructed a highly photosensitive UV photodetector with a unique "sandwich" structure, which was mainly composed of two layers of ZnO nanosheet arrays and one layer of polyaniline (PANI). The results showed that the UV current of ZnO/PANI devices was 100 times higher than that of pure ZnO devices under the same UV irradiation time. At a 365 nm wavelength, the device had excellent photocurrent responsiveness and photoconductivity. This high performance was attributed to the large specific surface area of ZnO nanosheets and the p-n junction formed between P-type PANI nano-porous film and N-type ZnO nanosheets. This provides a solid theoretical basis for the application of ZnO nanosheets in ultraviolet detection, and possesses significance for the development of ultraviolet photodetectors.

Fabrication and characterization of PANI-based sandwiched photodetector devices on n-Si and ZnO nanorods: Performance evaluation

This study focuses on the fabrication and characterization of simple sandwiched photodetector devices based on polyaniline (PANI) with various configurations: ITO/PANI/n-silicon, and ITO/PANI/ZnO nanorods (NRs)/n-silicon. The PANI polymer was synthesized from the polymerization of aniline, and the ZnO NRs were grown via hydrothermal method. The fabricated devices were analyzed via field emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), diffuse reflectance spectroscopy (DRS), and current-voltage (I-V) measurements. FESEM analysis revealed distinct PANI structures at the center and edge of the samples, with dendrites forming at the edge and mesh-like structure at the center due to solvent effect during deposition. The addition of PANI as an interlayer in the nSi/ITO junction enhanced the contact and improved carrier separation. However, the performance of the PANI-ZnO NRs devices was mixed, whereby performing better than ITO/ZnO NRs/nSi at zero bias voltage but otherwise at higher bias voltages. The thick PANI layer improved light absorption and reduced dark current but allowed increased hole-electron recombination, reducing overall performance. ITO/PANI/nSi recorded the highest normalized photocurrent-to-dark current ratio (NPDR) at 0 V bias of 50870 W−1 under 385 nm illumination. ITO/ZnO NRs/nSi sandwiched device obtained the highest responsivity value at 0.253 A W−1 at − 8 V bias under 385 nm illumination.

Performance of Polyaniline Thin Film as a Functional Material of Acid Vapor Sensors

Polyaniline (PANI) is a conductive polymer that can be produced by the electrodeposition process. The purpose of this research is to evaluate the performance of PANI sensors on hydrochloric acid (HCl) and acetic acid (CH3COOH) vapor using a scan rate of 100 mV/s and ten cycles, a thin PANI layer was created on the surface of the ITO substrate. The PANI spectroscopic test results before and after CH3COOH vapor exposure revealed no differences and remained within the PANI functional group range. A four-point probe (FPP) test was performed to evaluate the sensing performance of the PANI thin film against analyte gas. The results of recovery time, response time, and sensitivity tended to increase as analyte concentration increased. The quickest CH3COOH sensing (1 ppm) has a reaction time of 29.7 seconds, a recovery time of 21.9 seconds, and a sensitivity of 5.11%. The greatest CH3COOH sensing (10 ppm) resulted in a reaction time of 50.3 seconds, a recovery time of 39.7 seconds, and a sensitivity of 13.64%. The reaction time for the lowest HCl sensing (1 ppm) was 42.6 s, the recovery time was 32.4 s, and the sensitivity was 7.82%. The greatest level of CH3COOH sensing (10 ppm) resulted in a response time of 60.6 s, a recovery time of 55.3 s, and a sensitivity of 16.31%. As a result, the PANI thin film is a functional material for acid gas sensors.

Amplifying electrical outputs of polyaniline-based Schottky DC generators through single polarity charge injection

Schottky direct-current (DC) generators have gained attention for their ability to produce DC output directly without rectification. However, a major challenge is their limited voltage output, often below 1 V, and difficulty in simultaneously increasing both voltage and current outputs. This study develops a new design concept to improve the voltage and current outputs of a conducting polymer/metal Schottky DC generator by injecting a single type of charges from the Schottky unit's exterior to either its semiconductor or metal components. By utilizing a polyaniline-coated fabric and a metal Al plate to create a Schottky DC generator, as well as a single-mode triboelectric device such as PTFE film/metal Al, PTFE film/PA6 nanofiber membrane, or PA6-Ni/Cu plate as the external charge supplier, we demonstrate that injecting positive tribo charges to the Schottky Al electrode or negative charges to the polyaniline results in a significant increase in both the voltage and current outputs of the Schottky generator. The resultant Schottky unit showcased an exceptional peak open circuit voltage increasing to 4.88 ± 0.20 V, and an equally impressive peak short circuit current output peaking at 154.97 ± 5.20 μA (6.20 ± 0.21 μA/cm2). Remarkably, this configuration delivered an outstanding power density of up to 7.37 μW/cm2. These output metrics surpass those of standalone PANI/Al Schottky DC generator counterparts (1.09 ± 0.03 V, 67.32 ± 6.52 μA, and 0.66 μW/cm²), and also surpass most other Schottky DC generators previously reported. Incorporating nano Coulombs of charge into the Schottky generator resulted in an impressive micro Coulombs of charge migration within the Schottky device, achieving a remarkable fourfold amplification of voltage outputs and twofold amplification of current outputs, all while preserving the inherent DC output characteristics intrinsic to Schottky generators. Moreover, we have observed that the amount external tribo charges have a direct relationship with the voltage and current output increases of the Schottky DC generators. These phenomena were consistent, whether introducing positive charges to the Al layer of the Schottky unit or infusing negative charges into the polyaniline layer. Furthermore, alternative triboelectric devices connected to the Schottky generators yielded similar outcomes, thereby corroborating the robustness of our approach. This novel approach shows promise in enhancing power generation efficiency in Schottky DC generators and has potential applications in various fields requiring efficient and direct DC power generation.