Surface Electron Research Articles

Quantum Carry Research of Q1D – SE on Helium at Charged Substrate

Known in nano-electronic a solid state quantum - size systems motivate they creating using the surface electrons over helium. The quantum carry of quasi-one-dimensional surface electrons (Q1D-SEs) over superfluid helium is considered here. Research performed according to an electron phase diagram in gas phase at conditions far from electron quantum melting. A substrate is dense row of the light-guide segments where the SEs channels are formed over helium in the fiber gaps. The electrostatic model of substrate profile demonstrates modulation of potential in the electric field leading to possibility of the fibers tops charge thereby improving the Q1D-SEs channels quality. The experiments carried out by a low - frequency electron transport method at the temperature from 1.5 K to 0.5 K and the concentrations of electrons were up to 109cm-2. The SE move transverse to channel satisfies conditions of quantization in sense both the temperature and the relaxation time of electron in a system. According to an experiment lower some temperature the SE conductivity is ladder-like. The differential of SE conductivity is peak-like corresponding qualitatively to an electron states density. The distance between peaks accords to the 1D energy spectrums in some approach. Possibility of apply the 1D-SEs quantized energy levels (vibration levels) as quantum bits of quantum computer is considered.

Variable‐Range Hopping Conduction in Amorphous, Non‐Stoichiometric Gallium Oxide

AbstractAmorphous, non‐stoichiometric gallium oxide (a‐GaOx, x < 1.5) is a promising material for many electronic devices, such as resistive switching memories, neuromorphic circuits and photodetectors. So far, all respective measurements are interpreted with the explicit or implicit assumption of n‐type band transport above the conduction band mobility edge. In this study, the experimental and theoretical results consistently show for the first time that for an O/Ga ratio x of 0.8 to 1.0 the dominating electron transport mechanism is, however, variable‐range hopping (VRH) between localized states, even at room temperature and above. The measured conductivity exhibits the characteristic exponential temperature dependence on T−1/4, in remarkable agreement with Mott's iconic law for VRH. Localized states near the Fermi level are confirmed by photoelectron spectroscopy and density of states (DOS) calculations. The experimental conductivity data is reproduced quantitatively by kinetic Monte Carlo (KMC) simulations of the VRH mechanism, based on the ab‐initio DOS. High electric field strengths F cause elevated electron temperatures and an exponential increase of the conductivity with F1/2. Novel results concerning surface oxidation, magnetoresistance, Hall effect, thermopower and electron diffusion are also reported. The findings lead to a new understanding of a‐GaOx devices, also with regard to metal|a‐GaOx Schottky barriers.

Structure-activity relationship between crystal plane and pyrite-driven autotrophic denitrification efficacy: Electron transfer and metagenome-based microbial mechanism

Pyrite-driven autotrophic denitrification (PAD) has been recognized as a promising treatment technology for nitrate removal. Although the occurrence of PAD has been found in recent years, there is a knowledge gap about effects of crystal plane of pyrite on the performance and mechanism of PAD system. Here, this study investigated the effects of crystal planes ({100}, {111} and {210}) of single-crystal pyrite on denitrification performance, electron transfer, and microbial mechanism in PAD system. The removal efficiency of nitrate in B-{210} reached 100%, which was 1.67-fold and 2.86-fold higher than that of B-{100} and B-{111}, respectively. X-ray photoelectron spectroscopy and electrochemical results indicated that Fe-S bonds of pyrite with {210} crystal plane were more susceptible to breakage by Fe3+ oxidation assault, and leaching microbially available Fe2+ and sulfur intermediates to drive autotrophic denitrification. Metagenomic results suggested that community of functional pyrite-driven denitrifiers varied in response to crystal plane, and abundances of N-S transformation and EET-related microbes and genes in B-{210} notably up-regulated compared to B-{100} and B-{111}. In addition, this work proposed a dual-mode for electron transfer pathway during pyrite oxidation and nitrogen transformation in PAD system. In B-{210}, Fe(II)- and sulfur-driven denitrifiers obtained electron after pyrite oxidation-dissolution, and the enrichment of pyrite-oxidizing bacteria in B-{210} could enhance the electron transfer from pyrite through electron shuttles. This work highlighted that stronger surface reactivity and electron shuttle effect in B-{210} enhanced electron transfer, leading to favorable PAD performance in B-{210}. Overall, this study provides novel insights into the structure-activity relationship between the crystal plane structure of pyrite and denitrification activity in PAD system.

Quantum efficiency enhancement of reflective GaAs photocathodes with exponential-doping structure generating a favorable built-in electric field

The rapid development of GaAs photocathodes has led to an increased focus on the attainment of high quantum efficiency. Three types of exponential-doping structures with a high to low doping concentration distribution from the interior to the surface are proposed for reflective GaAs emission layers. These three structures generate different built-in electric fields that facilitate photoelectron emission. The one-dimensional continuity equations for the increasing, constant, and decreasing types of built-in electric fields are derived, respectively. The electron concentration distribution and quantum efficiency varying with the wavelength are solved numerically by the finite difference method. The simulation results indicate that the quantum efficiency of the GaAs photocathode with the increasing type of built-in electric field is superior to that with the constant built-in electric field, while the GaAs photocathode with the decreasing type of built-in electric field shows the worst performance. Then, the designed GaAs photocathodes with the increasing and constant types of built-in electric fields are grown by metal-organic chemical vapor deposition and activated by cesium-oxygen alternating deposition. The measured spectral response curves show that the quantum efficiency of the GaAs photocathode with the increasing type of built-in electric field is higher in the whole band than that with the constant type of built-in electric field. In addition, the exponential-doping structure generating the increasing type of built-in electric field is beneficial for improving the surface potential barrier and increasing the surface electron escape probability.

Electrochemical Determination of Tinidazole and Brucine Using Poly (l‐Glutamic Acid) Modified Carbon Nanotube Paste Electrode

AbstractThis study developed an electrochemical method for the selective and sensitive detection of Tinidazole (TZ) by modifying a bare carbon nanotube paste electrode (BCNTPE) with electrochemically polymerized l‐Glutamic acid (P(L‐GA)/MCNTPE). The modified carbon nanotube paste electrode (MCNTPE) achieved optimal detection with an irreversible peak in a 0.2 M phosphate buffer solution (PBS) at pH 3.5. Characterization of both the P(L‐GA)/MCNTPE and BCNTPE was carried out using techniques such as scanning electron microscopy (SEM), electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and linear sweep voltammetry (LSV). The sensor effectively identified possible interferences from different metals and organic compounds, with scan rate studies indicating that the reaction was controlled by diffusion. The effects of pH and concentration variations were also thoroughly investigated. The active surface area of the P(l‐GA)/MCNTPE and BCNTPE were found to be 0.471 cm2 and 0.217 cm2 respectively. The P(l‐GA)/MCNTPE displayed excellent electrochemical properties, with a limit of detection (LOD) of 0.06 µM and a limit of quantification (LOQ) of 0.2 µM, along with good reproducibility, repeatability, and stability. This study presents a P(l‐GA) MCNTPE that significantly enhances the sensitivity and selectivity for simultaneous detection of TZ and bare carbon nanotube (BCN). The improved electroactive surface area and electron transfer dynamics demonstrate its potential for practical applications in pharmaceutical analysis.

Studies on the retarded recrystallization of tungsten in CIMPLE-PSI exposed under very-high target temperature and long He+-fluence

Abstract Experiments are carried out in CIMPLE-PSI, to understand the recrystallization behavior of tungsten (W) exposed under very-high target temperature and ITER relevant long He+-fluence. The effect of helium bubbles on possible retardation of the recrystallization process is also studied. W samples are simultaneously exposed under He plasma and annealed by the plasma heat-load, in contrast to previously reported experiments in literature, which were carried out sequentially. Exposed samples are characterized by field emission scanning electron microscopy (FESEM), Vickers surface micro-hardness, nano-hardness and electron backscattered diffraction (EBSD). It is observed that the sample exposed to plasma under the highest temperature (1866 K) suffered acute retarded grain growth. This also contained small, unrecovered grains on the exposed surface. FESEM imaging of the cross-sections confirm relatively smaller helium bubbles still form even at the very high temperature conditions, which can impede the grain growth locally, whenever they are forming right on the grain boundaries. This results in an inhomogeneous mixture of surface grains with sizes from few micrometer to few tens of micrometer. EBSD estimates that the plasma exposed surface was only 34% recrystallized. The second sample exposed at a lower temperature (1699 K) but for three times higher fluence (ion fluence: 1.19×1027 m-2) was almost fully recrystallized, which shows retardation diminishes very fast with the duration of the exposure. Hardness measurements were undertaken to understand the variation with plasma exposure/annealing temperature and the extent of recrystallization, with three different probing length scales, spanning from few hundreds of nanometer to several micrometers. Both helium plasma exposed W samples are observed to undergo retarded softening up to a depth of few hundred nanometers from the surface, compared to when the metal may be recrystallized by simple heating, without any plasma exposure.

Research progress of nanoscale zero-valent iron in synergistic combinations of denitrifying bacteria for nitrate removal

Nitrate (NO3--N) is a common inorganic nitrogen pollutant in water. Excessive NO3--N can lead to water eutrophication and threaten human health. Nanoscale zero-valent iron (nZVI) has attracted much attention in NO3--N removal due to its high specific surface and excellent electron donor properties. The combination of nZVI and denitrifying bacteria (DNB) demonstrates high efficiency in converting NO3--N into N2. This approach not only substantially enhances the removal rate of NO3--N but also exhibits superior environmental sustainability compared with conventional chemical denitrification methods. Accordingly, it holds substantial promise for mitigating NO3--N pollution and warrants further exploration in the pollution control. Therefore, it is necessary to understand the interaction mechanism between nZVI and DNB for NO3--N removal. This paper details the factors affecting the removal of NO3--N by nZVI combined with DNB, reviews the latest research progress in this field, elaborates on the interaction mechanism between nZVI and DNB for NO3--N removal, and discusses the challenges and future research directions of NO3--N removal by nZVI combined with DNB. This review aims to provide a theoretical basis for the development of efficient approaches for the remediation of NO3--N pollution.

Creating Spin Channels in SrCoO3 through Triagonal‐to‐Cubic Structural Transformation for Enhanced Oxygen Evolution/Reduction Reactions

Oxygen evolution and reduction reactions (OER and ORR) play crucial roles in energy conversion processes such as water splitting and air batteries, where spin dynamics inherently influence their efficiency. However, the specific contribution of spin has yet to be fully understood. In this study, we intentionally introduce a spin channel through the transformation of trigonal antiferromagnetic SrCoO2.5 into cubic ferromagnetic SrCoO3, aiming to deepen our understanding of spin dynamics in catalytic reactions. Based on the results from spherical‐aberration‐corrected microscope, synchrotron absorption spectra, magnetic characterizations, and density functional theory calculations, it is revealed that surface electron transfer is predominantly governed by local geometric structures, while the presence of the spin channel significantly enhances the bulk transport of spin‐polarized electrons, particularly under high current densities where surface electron transfer is no longer the limiting factor. The overpotential for OER is reduced by at least 70 mV at 150 mA cm‐2 due to the enhanced conductivity from spin‐polarized electrons facilitated by spin channels, with an expectation of even more significant reductions at higher current densities. This work provides a clearer picture of the role of spin in oxygen‐involved electrocatalysis, providing critical insights for the design of more efficient catalytic systems in practical applications.

Creating Spin Channels in SrCoO3 through Triagonal-to-Cubic Structural Transformation for Enhanced Oxygen Evolution/Reduction Reactions.

Oxygen evolution and reduction reactions (OER and ORR) play crucial roles in energy conversion processes such as water splitting and air batteries, where spin dynamics inherently influence their efficiency. However, the specific contribution of spin has yet to be fully understood. In this study, we intentionally introduce a spin channel through the transformation of trigonal antiferromagnetic SrCoO2.5 into cubic ferromagnetic SrCoO3, aiming to deepen our understanding of spin dynamics in catalytic reactions. Based on the results from spherical-aberration-corrected microscope, synchrotron absorption spectra, magnetic characterizations, and density functional theory calculations, it is revealed that surface electron transfer is predominantly governed by local geometric structures, while the presence of the spin channel significantly enhances the bulk transport of spin-polarized electrons, particularly under high current densities where surface electron transfer is no longer the limiting factor. The overpotential for OER is reduced by at least 70 mV at 150 mA cm-2 due to the enhanced conductivity from spin-polarized electrons facilitated by spin channels, with an expectation of even more significant reductions at higher current densities. This work provides a clearer picture of the role of spin in oxygen-involved electrocatalysis, providing critical insights for the design of more efficient catalytic systems in practical applications.

ZIF‐8 as Potential Vector for Enhanced Target Delivery of Sulfathiazole for the Treatment of Bovine Ruminal Acidosis

The aim of this paper is enlarging the potential use of ZIF‐8 MOF as drug delivery system (DDS) for antimicrobial molecules, in particular for sulfathiazole, to be employed for the treatment of Subacute Ruminal Acidosis (SARA) in dairy cows. We therefore optimized (from milligrams to grams) the synthesis methodology for ZIF‐8 MOF, moving from organic solvents to aqueous solution, deeply characterizing the prepared material with X‐ray diffraction (XRD), surface area analyses (BET), electron microscopy (SEM), and thermogravimetric analyses (TGA). Once proved that the synthesis is also reproducible, we tested the stability of the material at physiological and acid pH, controlling material stability over time by checking their crystallinity with XRD. We then optimized sulfathiazole entrapment method to obtain the best material, checking the effective loading with UV‐vis spectroscopy. Afterwards, we checked the effective entrapment vs physical mixture by means of XRD, SEM and ATR‐MIR spectroscopy. Finally we tested the pH‐responsive drug release by dialyzing the sulfathiazole@ZIF‐8 by UV spectroscopy on the dialysis solution, confirming the strong pH‐dependence of release time of sulfathiazole.

Effect of Tungsten Doping on the Properties of Titanium Dioxide Dye-Sensitized Solar Cells

Tungsten-doped TiO2 thin films were prepared by sol–gel method on fluorine-doped tin oxide-coated substrates as working electrodes of dye-sensitized solar cells. The influences of different W doping (0, 2, 4, 6, and 8 at%) on the microstructure, optical, and photovoltaic properties of the W-TiO2 thin-film DSSCs were studied by the measurement of X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET) analysis, and electrochemical impedance spectroscopy (EIS). An optimal DSSCs performance was observed with a 6 at% W-doped TiO2 thin film, resulting in a Voc of 0.68 V, a Jsc of 20.2 mA/cm2, an FF of 68.6%, and an efficiency (η) of 9.42%. The efficiency of DSSCs with 6 at% W-doped TiO2 photoanode improved by 75%. This is because the 6 at% W-doped TiO2 thin film increases the specific surface area and electron transfer rate.

Comparative analysis of microwave radiation generated by the interaction between electron beam and plasma under different methods

This article presents a physical model that describes the interaction between surface electron beams and plasma. The dispersion relations for beam plasma interactions were derived using perturbation method and field matching methods. The study investigates how different parameters affect radiation frequency and bandwidth. The results indicate that as electron beam velocity increases, the associated kinetic energy also rises, leading to an increase in both the maximum radiation frequency and bandwidth at high frequencies. Conversely, the radiation bandwidth at low frequencies decreases. Similarly, a higher plasma density results in a greater maximum radiation frequency, but the high-frequency bandwidth decreases, while the low-frequency bandwidth increases. Additionally, when the electron density and electron velocity of the electron beam remain constant, increasing the plasma density can increase the microwave radiation frequency However, there exists a plasma density threshold, beyond which high-frequency electromagnetic waves are no longer radiated.

Te2− modulated heterogeneous remodeling of S atoms in ultrathin ZnIn2S4 nanosheets containing S vacancies synergistically enhances CO2 photoreduction

Reconfiguration of in situ heterojunction composites without interfacial resistance by substitution of homologous anions for the formation of gradient work function differences inducing the formation of built-in electric field is an effective strategy to enhance the charge separation efficiency. Herein, Te2−/ZnIn2S4-VS (Te2−/ZIS-VS) in situ heterojunction was synthesized by substitution of Te2− ions for S2− in ultrathin ZIS containing S vacancies, which can significantly promote photogenerated charge separation, surface electron enrichment, and CO2 adsorption/activation. The presence of S vacancies and adjacent Te2−/S2− double anions, the double active sites constructed by defect engineering promote the desorption of *CO molecules while inhibiting the protonation toward *CHO, which was more favorable for selective CO2 photoreduction to CO. The experimental results showed that the CO yield of Te2−/ZIS-VS was significantly increased to 672.1 μmol g−1 h−1 compared with pristine ZIS (54.3 μmol g−1 h−1) and the CO selectivity was close to 83 %. Notably, the life cycle assessment (LCA) of Te2−/Znln2S4 nanosheets with S-vacancy was performed. The evaluation results showed that most of the 17 impact categories showed low overall impact values and were environmentally friendly. Based on the results of this LCA, suggestions were put forward to further optimize the product to reduce carbon emissions.

The surface electron transfer strategy promotes the hole of PDI release and enhances emerging organic pollutant degradation

In semiconductor photocatalysts, the easy recombination of photogenerated carriers seriously affects the application of photocatalytic materials in water treatment. To solve the serious problem of electron−hole pair recombination in perylene diimide (PDI) organic semiconductors, we loaded ferric hydroxyl oxide (FeOOH) on PDI materials, successfully prepared novel FeOOH@PDI photocatalytic materials, and constructed a photo-Fenton system. The system was able to achieve highly efficient degradation of BPA under visible light, with a degradation rate of 0.112 min−1 that was 20 times higher than the PDI system, and it also showed universal degradation performances for a variety of emerging organic pollutants and anti-interference ability. The mechanism research revealed that the FeOOH has the electron trapping property, which can capture the photogenerated electrons on the surface of PDI, effectively reducing the compounding rate of photogenerated carriers of PDI and accelerating the iron cycling and H2O2 activation on the surface of FeOOH at the same time. This work provides new insights and methods for solving the problem of easy recombination of carriers in semiconductor photocatalysts and degrading emerging organic pollutants.

Sulfur doping and oxygen vacancy in In2O3 nanotube co-regulate intermediates of CO2 electroreduction for efficient HCOOH production and rechargeable Zn-CO2 battery

By manipulating the distribution of surface electrons, defect engineering enables effective control over the adsorption energy between adsorbates and active sites in the CO2 reduction reaction (CO2RR). Herein, we report a hollow indium oxide nanotube containing both oxygen vacancy and sulfur doping (Vo-Sx-In2O3) for improved CO2-to-HCOOH electroreduction and Zn-CO2 battery. The componential synergy significantly reduces the *OCHO formation barrier to expedite protonation process and creates a favorable electronic micro-environment for *HCOOH desorption. As a result, the CO2RR performance of Vo-Sx-In2O3 outperforms Pure-In2O3 and Vo-In2O3, where Vo-S53-In2O3 exhibits a maximal HCOOH Faradaic efficiency of 92.4% at −1.2 V vs. reversible hydrogen electrode (RHE) in H-cell and above 92% over a wide window potential with high current density (119.1 mA cm−2 at −1.1 V vs. RHE) in flow cell. Furthermore, the rechargeable Zn-CO2 battery utilizing Vo-S53-In2O3 as cathode shows a high power density of 2.29 mW cm−2 and a long-term stability during charge-discharge cycles. This work provides a valuable perspective to elucidate co-defective catalysts in regulating the intermediates for efficient CO2RR.

An analytical I-V model of SiC double-gate junctionless MOSFETs

Silicon carbide(SiC) double gate junctionless metal oxide semiconductor field-effect transistors(DG JL MOSFETs) have attracted significant attention due to their ideal high temperature characteristics and radiation resistance. Therefore, it is meaningful to exploit an I-V model for SiC DG JL MOSFETs. In this article, we make a linear approximation to describe the relationship between the surface mobile charge density and the surface electron concentration of the device. Based on this approximation and using the one-dimensional Poisson’s equation, we solve for the potential distribution of a SiC DG JL MOSFET in the subthreshold region. From this solution, we derived a functional relationship between the surface mobile charge density in the channel and the channel quasi-Fermi potential. Then we successfully developed a unified I-V model for the SiC DG JL MOSFETs. Based on the drain to source current calculation formula, the calculation expressions for the device’s transconductance and output conductance are derived. By comparing our model with the results from the two-dimensional numerical simulation software Silvaco Atlas, our model’s calculations closely match the two-dimensional numerical simulation results from the subthreshold region to the accumulation region. This model has reference significance for SiC DG JL MOSFETs in the high temperature electronic circuit application field.

Boosting oxygen storage capacity of Fe-Cu bimetallic catalysts through sulfide modification for efficient and selective molecular oxygen activation

Molecular oxygen (O2), a reactive oxygen species precursor, has great potential for water purification, but its spin-forbidden resistance hinders its direct involvement in the redox reactions of organic compounds under mild ambient conditions. In this study, a facile strategy was employed to synthesize sulfide-modified Fe-Cu bimetallic catalysts (FeCu-S) to enhance the activation efficiency of O2. The results showed that the FeCu-S material exhibited a tenfold increase in O2 activation compared to that of the control group, primarily attributed to the increased specific surface area of the catalysts with an optimized Fe/Cu site distribution and promoted generation of Cu-containing crystalline phases (e. g., CuFeS2 and CuO) to significantly enhanced the oxygen storage capacity. Moreover, such Cu-containing crystalline phases strengthened surface electron transfer, thus remarkably promoting the selective generation of singlet oxygen (1O2) for sulfamethoxazole (SMX) degradation. The FeCu-S/O2 system maintained high activity after the fifth recycle with stable reaction pH and negligible leaching of Cu and Fe ions, also exhibited great performance in the advanced treatment of the real biological effluent and ultrafiltration effluent from landfill leachate, confirming its great potential for practical water purification applications.

Effective activation of PMS by encapsulating monodispersed Fe3O4 within N, S heteroatoms co-doped carbon chamber for ROX removal dominated by the non-radical pathway

Developing the eco-friendly catalyst-adsorption iron-based materials with improved catalytic activity and minimal Fe leaching is fascinating for roxarsone (ROX) removal. Herein, Fe3O4 nanoparticles were encapsulated in flexible N, S-modified carbon chamber (Fe3O4@NS4C) through the “hydrothermal + pyrolysis” process to form a catalyst with multi-active sites. ROX could be degraded nearly 100 % at pH 5.0 − 11.0 and secondary inorganic As species concentration is lower than 0.09 mg/L by efficient adsorption. Especially, the Fe ion leaching concentration in Fe3O4@NS4C/PMS after ROX removal is decreased to 0.08 mg/L. Combined with quenching experiment, EPR, Raman spectroscopy and electrochemical analysis, the non-radical activation mechanism dominated by 1O2 and electron transfer was determined. The synergistic interaction between the N doped sites and the S anchored sites within the carbon matrix not only improves the adsorption of PMS on the catalyst but also facilitates the direct activation of PMS to 1O2, while the surface electron transfer improves the Fe2+/Fe3+ redox cycling in PMS activation. The active sites of ROX attacked by 1O2 were examined through Fukui function computations. Combined with HPLC-MS, the ROX degradation pathway was determined, and the toxicity of intermediates was evaluated. Furthermore, the removal performance of ROX in Fe3O4@NS4C/PMS system was also assessed in different environment for practical application, indicating that the advantages in the synergy between N, S co-doping carbon chamber and encapsulated iron oxide for water purification.

Novel electron activation of pollutants for driving its energy to boost H2O2 generation and wastewater purification

Dual-photocatalysis for synchronous H2O2 production with contaminant degradation presents a promising approach to addressing the energy crisis and environmental pollutantion that prevails in the indirect conversion of pollutant energy into chemical energy. Herein, a novel activation strategy that leverages visible-light and the n-state sites to harness antibiotic electrons to generate H2O2 in a dual-photocatalysis process is demonstrated. With n-state sites on g-C3N4 (CBCN), ciprofloxacin (CIP) molecules tend to be absorbed on their surface and transfer electrons to the n-state site to lower the surface energy of CIP-CBCN. These electrons stored in the n-state site are then activated by visible-light to reduce molecular oxygen into H2O2. As CIP loses electrons, its degradation is accelerated. Therefore, in this novel electron activation process, the CIP energy is converted into chemical energy, driving the self-degradation of CIP. This results in a remarkable H2O2 yield of 95 μmol L−1 achieved synchronously with 99.9 % CIP removal after 40 min of visible-light irradiation.

Enhancing Built‐In Electric Field via Defect‐Mediated Interfacial Chemical Bond Construction in Chalcogenide Heterojunction for Alcohol Photooxidation Coupled with H2 Production

AbstractRationally designing nanostructures based on an adequate understanding of structure‐performance relationships is key for directional charge transfer regulation in heterojunction photocatalysts. A general strategy is developed for synthesizing bifunctional Sv‐chalcogenide/Ti3C2 Schottky junctions (Sv = sulfur vacancies, chalcogenides containing CdS, CdIn2S4, ZnIn2S4, ZnS, CuInS2) featuring a giant built‐in electric field (BIEF) via defect‐mediated heterocomponent anchorage, which consists of sulfur vacancy modulation of chalcogenides and Ti3C2 nanoparticle anchoring at defects via interfacial Metal─Oxygen (M─O) bonds. These heterojunctions have the distinctive interface structure of semicoherent phase boundaries and a directionally aligned BIEF pointing from chalcogenides to Ti3C2. The enhanced BIEF creates an asymmetrical charge distribution, which not only governs the charge migration behavior by enabling charge carrier localization and delocalized electron transport continuity but also regulates the molecular catalytic behavior by optimizing pivotal intermediate adsorption/activation (*Ar‐CH(R2)‐OH in dehydrogenation and H* in H2 evolution) in selective alcohol photooxidation coupled with H2 generation. Encouragingly, Sv‐chalcogenide/Ti3C2 exhibits unprecedented performance (up to 13.34‐fold higher efficiency than unmodulated chalcogenides) and good substrate compatibility for various alcohols. This work demonstrates the synergistic effects of surface electron density control and interfacial interaction modulation in regulating BIEFs, elucidating the substantial impact of reinforced BIEF on carrier transport properties and molecular catalytic behavior.