Generation Of Electrons Research Articles

Conical porous hollow g-C3N4 charge separation with high efficiency for enhancing visible-light photocatalytic activity

The performance of the photocatalysts is influenced by factors such as electron generation ability, charge separation rate, and active sites distribution. In this study, needle-shaped precursors were prepared through low-temperature supramolecular self-assembly, and conical porous hollow carbon nitride (PHCN) was obtained after high-temperature pyrolysis. The PHCN not only possesses a thin-walled porous structure but also contains nitrogen defects embedded in its structure, which synergistically enhance the efficiency of photogenerated charge separation and provide more reactive sites. The DFT calculations showed that nitrogen defects and Pt-loading synergistically optimize the intermediate reaction process of graphitic carbon nitride (g-C3N4). PHCN had excellent photocatalytic degradation of tetracycline hydrochloride (TCH) and Rhodamine B (Rh B). The photocatalytic hydrogen evolution rate of PHCN was 20.0 times higher than that of bulk g-C3N4 (BCN). This study elucidated the relationship between crystallization rate and precursor morphology, as well as the influence of their physicochemical properties on photocatalytic performance. It also lays the foundation for constructing materials with nitrogen defects and special morphology through supramolecular self-assembly.

Accelerated peroxidase-like activity of ultrathin amine-tagged bimetallic MOF-74 nanozyme for construction of versatile bioassays from small molecules to enzymes and bacteria

The exquisite design of nanostructures for enzyme-biocatalyzed active sites mimicking has become a prospective method to significantly boost biocatalytic properties, which is profitable to response amplification for bioanalysis scenarios. Metal-organic frameworks (MOFs) with customizable compositions, diverse microstructures and open catalytic sites are considered to deal with challenges in conventional materials of unfriendly microenvironment and inexact coordination. Herein, by combining a metal doping and post-synthetic modification approach, amine-tagged Fe-Ni bimetallic MOF-74 nanozyme (FeNi-MOF-74-NH2) with ultrathin structure and improved peroxidase-mimicking bioactivity is synthesized through a layered double hydroxide (LDH) directed method. The boosted biocatalytic property largely benefits from the synergistic effects of Fe-Ni species, attributing to the dual mechanism (electron transfer and generation of hydroxyl radicals). On the basis of the enhanced enzyme-mimicking property and accessible amino functionalization of FeNi-MOF-74-NH2, versatile applications were carried out for the ultrasensitive detection of analytes from bioactive small molecules (H2O2 and ascorbic acid), biomacromolecules (alkaline phosphatase, ascorbic acid oxidase, and α-glucosidase), and pathogenic bacteria (Staphylococcus aureus). The nanozyme-based biosensing platform without complex enzymatic techniques serves as a proof-of-concept to facilitate the application of MOF nanozymes in biochemical analysis, clinical diagnosis, and biomedical research.

Boosting photocatalytic activity in ternary lamellar hierarchical structured ZnFe2O4/polymeric carbon nitride by constructing an electronic bridge

Photocatalytic technology is one of the ideal approaches for clean energy production and environmental pollution control in the future. However, the rapid recombination of photo-generated charge carriers is a bottleneck problem of low solar energy conversion efficiency. Herein, a magnetic ZnFe2O4/Pt/polymeric carbon nitride (PCN) semiconductor catalyst is designed and prepared for high-performance photocatalytic hydrogen production reaction and photocatalytic degradation rate of RhB. It exhibits 339.31 μmol·g−1·h−1 hydrogen production rate and 96.08 % photocatalytic degradation rate of RhB within 120 min under visible light. The introduction of Pt, constructing an electronic bridge, accelerated the transfer of photo-generated carriers, meanwhile, the smaller band gap of the ternary composites enabled the generation of more photo-generated electrons. The internal electric field accelerated the accumulation of electrons and holes in the conduction band of ZnFe2O4 and valence band of PCN, thus photocatalytic activity is greatly enhanced. The electron-hole separation is also improved and the transport of photo-generated electrons is facilitated by the special structure of the heterojunction and the unique morphology of PCN. In addition, the used catalyst can be recovered through magnetic fields, and this magnetic catalytic system has great application prospects in the fields of photocatalytic hydrogen production and pollutant degradation.

Insight into bay-/end-substituted perylene diimide and its S-scheme heterojunction for enhanced photocatalytic H2O2 production under visible-light irradiation

Here, 1D bis(N-carboxymethyl) peryleneimide (H2PDI), 0D 1,6,7,12-tetrachloro-bis(N-carboxymethyl) peryleneimide (4Cl-H2PDI), and 2D 4Cl-H2PDI/graphene quantum dot (4Cl-H2PDI/GQD) nanostructures are synthesized and carefully analyzed. The effect of bay-/end-substitution and S-scheme heterojunction of PDI-based materials as main catalysts on the photocatalytic H2O2 evolution is first studied through the oxygen reduction reaction (ORR). Under the visible-light irradiation (> 420 nm), 4Cl-H2PDI and 4Cl-H2PDI/GQD as photocatalysts exhibit the ∼7 and ∼16 times H2O2 evolution rate than H2PDI (1059.6 vs. 2484.0 vs. 160.0 µM g−1 h−1), respectively. The systematical experiments reveal that 4Cl-H2PDI and 4Cl-H2PDI/GQD should prefer a two-step single-electron ORR process, while H2PDI may involve a 4e‒ water oxidation and one-step 2e‒ ORR process. Further experiments confirm that the bay-substitution and GQD doping of H2PDI can promote the generation, transportation, and separation of photogenerated electrons and holes, and prolong the carrier lifetime. This work provides insight into PDI-based photocatalytic H2O2 production.

Self-powered sandwich-type dual-mode sensor built on open bipolar electrode

Here, we developed a self-powered bipolar electrode (SP-BPE) based dual-mode sensor with electrochromic (EC) and photoelectrochemical (PEC) techniques for the visualized and sensitive detection of bisphenol A (BPA). An open BPE with the molecularly imprinted polymers (MIPs) modified electron injection area and the Prussian blue (PB) coated electrochromic area was fabricated on an indium tin oxide (ITO) glass. A kind of Zr-based metal-organic framework (UiO-66) coated TiO2 heterojunction (TiO2@UiO-66) was used for aptamer (Apt) immobilization and electron generation. BPA was selectively accumulated by MIPs, and subsequently recognized TiO2@UiO-66-Apt quantitatively, resulting in the formation of MIPs/BPA/Apt-TiO2@UiO-66 “sandwich” structure. Under UV-light, electrons were generated from the captured TiO2@UiO-66. For EC visualization measurements, electrons were injected into the PB film, causing a color change without an external power source. The extent of color change was proportional to the number of generated electrons, which correlated with the amount of captured BPA within a concentration range of 10−6–10−11 M. This allowed for the semi-quantification of BPA by naked eyes. For PEC detection, the BPE was used as the working electrode in a three-electrode system. The generated photocurrents signals could be digitally output for BPA with the concentrations ranging from 10−5 to 10−11 M. The SP-BPE sensors showed low background signal, improved selectivity and anti-interference abilities, and have demonstrated excellent performance in quantitative BPA analysis in water samples. They are particularly useful in scenarios where traditional power sources are limited or unavailable, and they offer opportunities for sustainable and environmentally friendly target detection.

Laser-induced graphene formation on different wood species: Dependence of electronic performance on intrinsic features of certain types of wood

Conductive, 3D, porous graphene can be produced with a CO2 laser from a large variety of materials, including wood, at room temperature, and under inert atmosphere or after treatment for fire protection. Here, we investigated the suitability for direct conversion of 46 typical European and Asian woods into laser-induced graphene (LIG), without pre-treatment. The LIG was characterized by resistance measurements to determine if a conductive layer had formed, and via Raman spectroscopy. Here, we show, for the first time, that it is possible to produce LIG on certain woods under atmospheric conditions without additional fire protection treatment. We determined that the ability to produce LIG on untreated, natural wood under ambient atmosphere is favoured overall by a high density and a diffuse-porous xylem structure, as well as a high soluble lignin content. Some of these characteristics are similar to those required for high yields in char production. Problematic for the production of LIG-based electronics is the presence of pronounced growth rings, or other geometric wood features, with density variations, which can be reduced using specific cuts with minimized growth rings and absence of rays. This is the first time that untreated wood has been directly converted into LIG using a conventional CO2 laser and ambient atmosphere. Our results represent a further step towards the development of a new generation of sustainable electronics relying on natural materials.

Business accounting and information support through the QR- coding system

Business accounting and information support through the QR- coding system

Isolated attosecond electron and hard x-ray pulse generation by ultra-intense spatiotemporal vortex laser

The spatiotemporal optical vortex (STOV) laser pulse, characterized by containing a space-time dependent spiral phase structure and intrinsic transverse orbital angular momentum (OAM), has been of much recent research interest for basic physics as well as potential applications in optical communication and manipulation, as well as the attosecond sciences. Here we consider electron acceleration and generation of attosecond hard x-rays by irradiating a thin foil with intense STOV laser pulse. It is found that the affected foil electrons can be trapped and acquire transverse OAM, or synchrotron-like motion, from the STOV, as well as accelerated forward by the transverse and enhanced axial laser electric fields to form a tiny energetic bunch at the front of the laser pulse and emit short ( ∼400 attosecond) high-flux ( >109 photons per pulse) hard (100–1000 keV) x rays.

Perovskite quantum laser with enhanced population inversion driven by plasmon-induced hot electron transfer under potential shift polarization conditions

The hot electron transfer resulting in fluorescence enhancement is significantly meaningful for theory and experiment of the study on photoelectric devices. However, the laser emission based on direct hot electron transfer is difficult to realize because of the low transfer efficiency. To achieve a laser with a new-generation mechanism based on hot electron transfer, the photoelectric co-excitation is proposed for improving the efficiency of hot electron transfer. The lasing behavior at 532 nm is realized with a threshold of 5 kw cm−2 and 1 μA, which can be considered as the hot electron transfer resulting in population inversion enhancement. Meanwhile, the lasing output power is 0.3 mW. The hot electrons transfer process was described via the transient absorption spectrum according to the improved ground-state bleaching and excited-state absorption signal in device ON. Through comparison with the optical pump only, the quantum efficiencies of hot electron generation (HEG) and hot electron transfer (HET) were increased ∼31% and 31%, respectively. Most importantly, a triple gain mode coupling device including local surface plasmon, hot electron transfer, and array oscillation was presented. Two modes of population inversion enhancement are proposed. This study can provide theoretical and experimental reference for the research of hot electron lasers and devices.

In situ electron generation through Fe/C supported sludge coupled with a counter-diffusion biofilm for electron-deficient wastewater treatment: Binding properties and catalytic competition mechanism of nitrate reductase

A membrane-aerated biofilm-coupled Fe/C supported sludge system (MABR-Fe/C) was constructed to achieve in situ electron production for NO3−-N reduction enhancement in different Fe/C loadings (10 g and 200 g). The anoxic environment formed in the MABR-Fe/C promoted a continual Fe2+release of Fe/C in 120 d operation (average Fe2+concentrations is 1.18 and 2.95 mg/L in MABR-Fe/C10 and MABR-Fe/C200, respectively). Metagenomics results suggested that the electrons generated from ongoing Fe2+ oxidation were transferred via the Quinone pool to EC 1.7.5.1 rather than EC 1.9.6.1 to complete the process of NO3−-N reduction to NO2−-N in Acidovorax, Ottowia, and Polaromonas. In the absence of organic matter, the NO3−-N removal in MABR-Fe/C10 and MABR-Fe/C200 increased by 11.99 and 12.52 mg/L, respectively, compared to that in MABR. In the further NO2−-N reduction, even if the minimum binding free energy (MBFE) was low, NO2−-N in Acidovorax and Dechloromonas preferentially bind the Gln-residues for dissimilatory nitrate reduction (DNR) in the presence of Fe/C. Increasing Fe/C loading (MABR-Fe/C200) caused the formation of different residue binding sites, further enhancing the already dominant DNR. When DNR in MABR-Fe/C200 intensified, the TN in the effluent increased by 3.75 mg/L although the effluent NO3−-N concentration was lower than that in MABR-Fe/C10. This study demonstrated a new MABR-Fe/C system for in situ electron generation to enhance biological nitrogen removal and analyzed the NO3−-N reduction pathway and metabolic mechanism, thus providing new ideas for nitrogen removal in electron-deficient wastewater.

Copolymers of Gelatin-graft-poly(3-hexylthiophene) for Transient Electronics.

As transient electronics continue to advance, the demand for new materials has given rise to the exploration of conducting polymer (CP)-based electronic materials. The big challenge lies in balancing conductivity while introducing controlled degradable properties into CP-based transient materials. In response to this, we present in this work a concept of using conducting polymers attached to an enzymatically biodegradable biopolymer to create transient polymer electronics materials. Specifically, poly(3-hexyl thiophene) (P3HT) is covalently grafted onto biopolymer gelatin, affording graft copolymer gelatin-graft-poly(3-hexyl thiophene) (termed Gel-g-P3HT). The thin films of Gel-g-P3HT that were produced by optimized processing solvent (THF/H2O cosolvent) showed enhanced π-π stacking domains of P3HT, resulting in semiconducting thin films with good electroactivity. Due to the presence of amide bonds in the gelatin backbone, Gel-g-P3HT underwent degradation over a period of 5 days, resulting in the formation of amphiphilic micellar nanoparticles that are biocompatible and nontoxic. The potential of these conductive and degradable graft copolymers was demonstrated in a pressure sensor. This research paves the way for developing biocompatible and enzymatically degradable polymer materials based on P3HT, enabling the next generation of transient polymer electronics for diverse applications, such as skin, implantable, and environmental electronics.

Lithography‐Free Method to Synthesize Quasiperiodic Silicon Inverted‐Pyramid Arrays: A Broadband Light Trapper for High‐Efficiency Thin Silicon Solar Cells

Thin silicon solar cells can be a low‐cost effective photo‐conversion device, if the device can efficiently absorb the solar spectrum. Herein, a new lithography‐free technique is developed for the fabrication of quasiperiodic silicon inverted‐pyramids arrays (SiIPAs), which show a high‐light‐trapping phenomenon in the ultraviolet–visible—near‐infrared (300–2000 nm). Fabricated SiIPA samples show a significant reduction of reflectance (3%) in the silicon absorption band (300–1000 nm). A unique additional absorption of 33–44% compared to the planar silicon is observed in the sub‐bandgap region of silicon (1100–2000 nm) for these samples. Photocurrent response measurement confirms the generation of additional electron–hole pairs in the sub‐bandgap region of silicon for the SiIPA samples in comparison with planar sample. In these results, the effect of field confinement and the creation of optical resonance modes within these structures, qualitatively supported by numerical simulation, are signified. The estimated short‐circuit current density using the experimental absorption spectrum of SiIPAs is 55.46 mA cm−2, which is far higher than the Lambertian limit of ≈43 mA cm−2. The theoretical efficiency of the solar cell can be achieved up to 35.22%, which surpasses the Shockley–Queisser limit of 33.7%.

A Comprehensive Review of Fatigue Strength in Pure Copper Metals (DHP, OF, ETP)

Due to their exceptional electrical and thermal conductivity properties, high-purity copper (Cu-DHP) and copper alloys of similar composition, such as electrolytic tough-pitch (ETP), oxygen-free electronic (OFE) and oxygen-free (OF), have often been used in the manufacture of essential components for the electrical, electronic and power generation industries. Since these components are subject to cyclic loads in service, they can suffer progressive structural damage that causes failure due to fatigue. The purpose of this review is to examine the most relevant aspects of mechanical fatigue in Cu-DHP, ETP, OFE and OF. The impact of many factors on fatigue strength (Se), including the frequency, temperature, chemical environment, grain size, metallurgical condition and load type, were analyzed and discussed. Stress–life (S-N) curves under zero mean stress (σm = 0) were found for high-cycle fatigue (HCF). For non-zero mean stress (σm ≠ 0), stress curves were based on a combination of Gerber, Soderberg and ASME elliptic failure criteria. Stress–life (S-N) curves were also developed to correlate fatigue strength (Se) with stress amplitude (σa), yield strength (Syp) and ultimate strength (Sut). Finally, for low-cycle fatigue (LCF), strain–life (ε-N) curves that establish a relationship between the number of cycles to failure (N) and total strain amplitude (εplastic) were determined. Hence, this review, as well as the proposed curves, provide valuable information to understand fatigue failure for these types of materials.

Volumetric Modification of Transparent Materials with Two-Color Laser Irradiation: Insight from Numerical Modeling.

Traditionally, single-color laser beams are used for material processing and modifications of optical, mechanical, conductive, and thermal properties of different materials. So far, there are a limited number of studies about the dual-wavelength laser irradiation of materials, which, however, indicate a strong enhancement in laser energy coupling to solid targets. Here, a theoretical study is reported that aimed at exploring the volumetric excitation of fused silica with dual-wavelength (800 nm and 400 nm) ultrashort laser pulses focused on the material's bulk. Numerical simulations are based on Maxwell's equations, accounting for the generation of conduction electrons, their hydrodynamic motion in the laser field, and trapping into an excitonic state. It is shown that, by properly choosing the energies of the two laser harmonics successively coupling with the material, it is possible to strongly enhance the laser energy absorption as compared to the pulses of a single wavelength with the same total energy. Laser energy absorption strongly depends on the sequence of applied wavelengths, so that the shorter wavelength pre-irradiation can yield a dramatic effect on laser excitation by the following longer-wavelength pulse. The predictions of this study can open a new route for enhancing and controlling the highly localized absorption of laser energy inside transparent materials for optoelectronic and photonic applications.

Highly efficient SnS2‐based photocatalyst: A green approach to biodiesel production

AbstractBiodiesel, a promising alternative to traditional petroleum fuels, is a green energy solution. Photocatalysis is a facile, novel, economic, and efficient approach to biodiesel synthesis. Metal sulfides have been used extensively for various photocatalytic applications. The present study demonstrates, for the first time, the photocatalytic production of biodiesel using a novel metal sulfide‐based heterogeneous photocatalyst under visible light irradiation.A nano zero‐valent silver doped hydroxyapatite (Ag/HAp) was synthesized using a green bio‐reductant technique and decorated with tin sulfide nanoparticles (SnS2/Ag/HAp or SAH) for photocatalytic biodiesel synthesis. The hydroxyapatite (HAp) was extracted from waste fish scales to minimize the use of chemicals and to utilize waste for useful applications. The prepared SAH photocatalyst was characterized through X‐ray diffraction, UV‐visible diffuse reflectance spectroscopy, photoluminescence spectroscopy, Fourier transform infrared analysis, energy dispersive X‐ray analysis, scanning electron microscopy, high‐resolution transmission electron microscopy and X‐ray photoelectron spectroscopy analysis. The effect of reaction parameters was optimized, and under optimum conditions of 1 wt% photocatalyst loading, and 8:1 methanol‐to‐oleic‐acid ratio, for 60 min, a high yield of 98.0 ± 0.61% could be achieved using a SAH photocatalyst.Scavenger tests indicated the simultaneous generation of photoinduced electrons and holes necessary for photocatalytic biodiesel synthesis. A mechanism for the photocatalytic esterification reaction of oleic acid is proposed. The synthesized SnS2‐based photocatalyst could be easily recoverable and reusable for five consecutive runs, which can replace traditional industrial heterogeneous catalysts in the near future.

Electron acceleration and x-ray generation from near-critical-density carbon nanotube foams driven by moderately relativistic lasers

Direct laser acceleration of electrons in near-critical-density (NCD) carbon nanotube foams (CNFs) has its advantages in the high-efficiency generation of relativistic electrons and broadband x-rays. Here, we report the first simultaneous measurement on the spectra of laser-driven electrons and x-rays from CNFs at moderately relativistic intensities of around 5×1019 W/cm2. The density and thickness of the CNFs were scanned in the experiments, indicating the optimized electron temperature of 5.5 MeV and x-ray critical energy of 5 keV. Two-dimensional particle-in-cell simulations confirm that the electrons, with a temperature significantly higher than the pondermotive scale, are directly accelerated by the laser along the NCD plasma channel, while the bright x-rays are emitted by these electrons through betatron radiation or Thomson backscattering inside the channel. The simultaneously generated electrons and x-rays, automatically synchronized with the femtosecond laser driver, are suitable for applications such as bi-modal radiography.

Radiation reaction kinetics and collective QED signatures

Observing collective effects originating from the interplay between quantum electrodynamics and plasma physics might be achieved in upcoming experiments. In particular, the generation of electron–positron pairs and the observation of their collective dynamics could be simultaneously achieved in a collision between an intense laser and a highly relativistic electron beam through a laser frequency shift driven by an increase in the plasma density increase. In this collision, the radiation of high-energy photons will serve a dual purpose: first, in seeding the cascade of pair generation; and, second, in decelerating the created pairs for detection. The deceleration results in a detectable shift in the plasma frequency. This deceleration was previously studied considering only a small sample of individual pair particles. However, the highly stochastic nature of the quantum radiation reaction in the strong-field regime limits the descriptive power of the average behavior to the dynamics of pair particles. Here, we examine the full kinetic evolution of generated pairs in order to more accurately model the relativistically adjusted plasma density. As we show, the most effective pair energy for creating observable signatures occurs at a local minimum, obtained at finite laser field strength due to the trade-off between pair deceleration and the relativistic particle oscillation at increasing laser intensity. For a small number of laser cycles, the quantum radiation reaction may re-arrange the generated pairs into anisotropic distributions in momentum space, although, in the one-dimensional simulations considered here, this anisotropy quickly decreases.

Working on a dream: bringing up the level of interface spectroscopy to the bulk level

Abstract Liquid interfaces are unique environments in which a variety of fundamental phenomena occur. Therefore, it is important to obtain a molecular-level understanding of liquid interfaces for both basic science and industrial applications. However, it is not an easy task to investigate molecules in the interface region that only has nanometer thicknesses. Second-order nonlinear spectroscopy, or even-order nonlinear spectroscopy more generally, is intrinsically interface-selective because the relevant nonlinear signal is generated only in the region in which the inversion symmetry is broken under the dipole approximation. In the past 2 decades, we have been developing and applying new interface nonlinear spectroscopic methods, aiming to bring up the level of knowledge on interfacial molecules to that on molecules in solution. During this attempt, we developed electronic sum-frequency generation spectroscopy, heterodyne-detected electronic sum-frequency generation spectroscopy, and heterodyne-detected vibrational sum-frequency generation spectroscopy, as well as fourth-order Raman spectroscopy. We also extended the methods to femtosecond time-resolved measurements. Using these methods, we are now able to study the structure and dynamics at liquid interfaces, in particular exposed interfaces such as air/liquid interfaces, at a similar level to the study for solution. I overview our interface research while describing thoughts we had at each turning point.

Tongue-inspired gelatin/poly(acrylate-co-acrylamide)-Fe3+ organic hydrogel with tunable mechanical, electrical, and sensory properties

Conductive hydrogels have emerged as one of the most promising candidates for the next generation of wearable soft electronics. However, they face limitations during practical implementation owing to their unbalanced overall properties. In this study, we present a dynamic cross-linked gelatin/poly(acrylic acid-co-acrylamide) (GxPyFez) hydrogel with tunable mechanical strength, self-healing, freezing resistance, electrical conductivity, and high sensitivity, which was prepared by incorporating Fe3+ ions. The hydrogel was prepared based on the tongue, in which gelatin/poly(acrylic acid-co-acrylamide) and Fe3+ ions mimic the connective tissue and receptor cells of the human tongue. The synergistic effect of reversible crosslinking, along with the modulation of rigid and flexible components enabled tunable flexible structures that exhibit excellent mechanical properties such as elongation at break (569 %) and toughness (8.82 MJ m−3). Notably, the G2P3Fe0.1 hydrogel exhibited remarkable self-healing ability, even at room temperature, while maintaining a good freezing resistance. Furthermore, the G2P3Fe0.1 demonstrated fast response characteristics along with a high sensitivity (GF = 2.75). Consequently, it could be assembled into sensors capable of effectively detecting various movements of the human body; it serves as an electronic skin that responds to diverse external stimuli and monitors underwater motion signals. This study provides new insights into the design of conductive hydrogels with tunable overall properties that can be modified to suit specific application scenarios.

Interfacial carbon quantum dot thin film impacts on morphological and chemical structures of fluorine-doped tin oxide films

Morphology and chemical bonding states, including surface roughness, film density, F-doping, and oxygen vacancy (VO) concentration directly affect the electrical and optical properties of fluorine-doped tin oxide (FTO) films. In this study, morphology and chemical bonding states of FTO films are engineered simultaneously by introducing a carbon quantum dot (CQD) thin film as an interface layer during ultrasonic spray pyrolysis deposition. The abundant oxygen-containing surface functional groups and large surface free energy of the CQD thin film promoted (200) oriented crystal growth and accelerated nucleation of FTO, resulting in smooth and dense FTO film morphology. The abundant carboxyl surface functional groups on the CQDs generate active F− species that are effectively doped into SnO2. Formic acid, formed by dissociation of the carboxyl group, can serve as a strong reducing agent for extracting oxygen atoms from the SnO2 lattice, thereby increasing the VO concentration. The accelerated F-doping and VO concentration result in the generation of additional free electrons. The effects of the optimized CQD on the morphological and chemical structures of FTO films are demonstrated by their superior electrical (sheet resistance of ∼5.7 Ω/□) and optical properties (visible transmittance of ∼85.9 %) compared with bare FTO. Moreover, CQD/FTO used as transparent conducting electrodes in electrochromic (EC) application exhibited improved EC performances, including fast switching speeds (5.3 s and 2.3 s for bleaching and coloration, respectively) and high coloration efficiency (81.1 cm2/C) compared to that of bare FTO.