Recombination Of Electrons Research Articles

Solvent Effects on Spin-Orbit Charge-Transfer Intersystem Crossing in Aryl-Substituted Boron-dipyrromethene Donor-Acceptor Dyads.

In heavy-atom-free organic molecules, the rate of triplet generation through charge recombination, as dictated by the El-Sayed rule, can be enhanced by 101-102 times compared with the rate of spontaneous spin flipping between π-π* orbitals. This mechanism is known as the spin-orbit charge-transfer intersystem crossing (SOCT-ISC). Within the framework of the SOCT-ISC mechanism, facilitating the generation of charge-separated (CS) states and suppressing the spin-allowed direct charge recombination to the ground state are pivotal for maximizing the efficiency of generating localized triplet states. Herein, a series of orthogonal aryl-substituted boron-dipyrromethene dyads were studied by time-resolved spectroscopy to unravel the multichannel competitive relationships in the SOCT-ISC mechanism. The energy level of the electron donor and the stabilization of the solvent effect to the charge-transfer state are reflected in the Gibbs free energy changes of the electron transfer and recombination reactions, leading to significantly different triplet quantum yields. Additionally, solvation-induced electronic coupling changes in excited states lead to the fact that the spin-allowed charge recombination rate cannot be well simply predicted by the Marcus inverted region but has to consider the specific excited-state dynamics in optimizing the proportion of triplet generation channels based on charge recombination.

Built-In Electric Field Boost Photocatalytic Degradation of Pollutants in Wastewater.

The photocatalysis technique shows significant potential for wastewater degradation; however, the rapid recombination of photogenerated holes and electrons severely limits its photocatalytic efficiency. This situation necessitates the development of effective strategies to tackle these challenges. One well-documented approach is built-in electric field engineering in heterojunctions or composites, which has been shown to enhance electron transfer and thereby reduce the recombination of electrons and holes. This strategy has proven highly effective in significantly improving photocatalytic activity for the degradation of pollutants in wastewater. In this context, we summarize recent advancements in built-in electric field engineering in photocatalysts, highlighting the fundamentals and modifications of this approach, as well as its positive impact on photocatalytic performance in the degradation of wastewater pollutants.

Facet-Engineered BiVO4 Photocatalysts for Water Oxidation: Lifetime Gain Versus Energetic Loss.

A limiting factor to the efficiency of water Oxygen Evolution Reaction (OER) in metal oxide nanoparticle photocatalysts is the rapid recombination of holes and electrons. Facet-engineering can effectively improve charge separation and, consequently, OER efficiency. However, the kinetics behind this improvement remain poorly understood. This study utilizes photoinduced absorption spectroscopy to investigate the charge yield and kinetics in facet-engineered BiVO4 (F-BiVO4) compared to a non-faceted sample (NF-BiVO4) under operando conditions. A significant influence of preillumination on hole accumulation is observed, linked to the saturation and, thus, passivation of deep and inactive hole traps on the BiVO4 surface. In DI-water, F-BiVO4 shows a 10-fold increase in charge accumulation (∼5 mΔOD) compared to NF-BiVO4 (∼0.5 mΔOD), indicating improved charge separation and stabilization. With the addition of Fe(NO3)3, an efficient electron acceptor, F-BiVO4 demonstrates a 30-fold increase in the accumulation of long-lived holes (∼45 mΔOD), compared to NF-BiVO4 (∼1.5 mΔOD) and an increased half-time, from 2 to 10 s. Based on a simple kinetic model, this increase in hole accumulation suggests that facet-engineering causes at least a 50-100 meV increase in band bending in BiVO4 particles, thereby stabilizing surface holes. This energetic stabilization/loss results in a retardation of OER relative to NF-BiVO4. This slower catalysis is, however, offset by the observed increase in density and lifetime of photoaccumulated holes. Overall, this work quantifies how surface faceting can impact the kinetics of long-lived charge accumulation on metal oxide photocatalysts, highlighting the trade-off between lifetime gain and energetic loss critical to optimizing photocatalytic efficiency.

Biochar-Supported Titanium Oxide for the Photocatalytic Treatment of Orange II Sodium Salt

Recent improvements in advanced technology for toxic chemical remediation have involved the application of titanium oxide nanoparticles as a photocatalyst. However, the large energy bandgap associated with titanium oxide nanoparticles (3.0–3.20 eV) is a limitation for their application as a photocatalyst within the solar spectrum. Various structural modification methods have led to significant reductions in the energy bandgap but not without their disadvantages, such as electron recombination. In the current investigation, biochar was made from the leaves of an invasive plant (Acacia saligna) and subsequently applied as a support in the synthesis of titanium oxide nanoparticles. The characterization of biochar-supported titanium oxide nanoparticles was performed using scanning electron microscopy, Fourier transformer infrared, X-ray diffraction, and Brunauer–Emmett–Teller analyses. The results showed that the titanium oxide was successfully immobilized on the biochar’s external surface. The synthesized biochar-supported titanium oxide nanoparticles exhibited the phenomenon of small hysteresis, which represents the typical type IV isotherm attributed to mesoporous materials with low porosity. Meanwhile, X-ray diffraction analysis revealed the presence of a mixture of rutile and anatase crystalline phase titanium oxide. The synthesis of biochar-supported titanium oxide nanoparticles was highly efficient in the degradation of Orange II Sodium dye under solar irradiation. Moreover, 83.5% degradation was achieved when the biochar-supported titanium oxide nanoparticles were used as photocatalysts in comparison with the reference titanium oxide, which only achieved 20% degradation.

Piezo-photocatalysis synergy in γ-GeSe for highly efficient oxygen evolution reaction

Solar-driven semiconductor photocatalysts are highly appealing in applications of environmental remediation and energy conversion. However, photocatalytic reactions, particularly oxygen evolution reaction (OER), are often constrained by the swift recombination of electron–hole pairs, thereby resulting in low reaction efficiency. Although it is effective to separate charge carriers by constructing heterojunctions to form built-in electric field, the lattice mismatch and inefficient interlayer charge transfer of heterojunctions in the photocatalysts limit their further development. Here, we propose a new strategy by constructing an internal electric field for OER through an individual piezoelectric two-dimensional material. The results indicate that the piezoelectric effect regulates the electronic structure, reduces bandgap, improves light absorption efficiency, and that the displacement of positive and negative charge centers is the key factor in the enhanced OER. This research indicates the feasibility of combining piezoelectric properties of two-dimensional materials with OER (1.19 eV), providing new insights and guidance for applying the piezoelectric effect in the OER and opening up a way to promote efficient separation of charge carriers.

Influence of gadolinium substitution on the crystal structure of NiO and its maximized photocatalytic degradation activity on tetracycline and direct yellow pollutants

Gadolinium-substituted NiO crystal structures with excellent stability were utilized for the first time to degrade antibiotic and organic dye pollutants. A simple hydrothermal technique was used to synthesize different concentrations of Gd3+ substituted NiO, and the catalysts were thoroughly characterized using sophisticated techniques to explore the influence of Gd3+ on the crystal structure and optical characteristics of NiO. The 1.5% Gd3+ substituted NiO showed outstanding photocatalytic activity on tetracycline and direct yellow degradation, with percentages of 90.72 and 95.5%, respectively. The improvement of photocatalytic degradation efficiency is primarily due to the suppression of photoinduced electron and hole recombination via the creation of Gd3+ as the inner energy band state below the conduction band. The recycling experiments revealed that the catalyst is more stable, with no indication of loss after ten cycles. Scavenging investigations also demonstrated that superoxide and holes were responsible for the efficient degradation of pollutants.

Steady and transient modeling of dye-sensitive solar cells: The impact of electrode thickness and dye specifications

Investigating the impact of dye compounds on cell performance is crucial for advancing dye-sensitized solar cells (DSSCs). This research focuses on the sensitivity analysis of the effect of critical parameters to enhance DSSC efficiency using a thermo-electric numerical model. These parameters include dye types, trapping parameters, diffusion coefficients, and photoanode thickness. When the type of dye changes, in fact, both physical and chemical properties (molar absorption coefficient, etc.) Change, but to avoid the complexity of solving the equations and only to evaluate the effect of the absorption wavelength range on the cell performance only changes in physical properties are considered. The model calculates steady and transient currents under actual weather conditions and sunlight. It incorporates time/space-dependent relationships for increased accuracy and examines electron, iodide, and triiodide ion interactions under varying environmental conditions. Key concepts include the quasi-Fermi level and the multiple trap model, assuming that trapping processes are faster than electron transport and recombination. The results showed that increasing the trapping parameter can affect the transient current behavior, also increasing the thickness of the photoanode and the wavelength range of the dye increases the efficiency of the cell, so that the N749-BD provides the best performance. The findings provide insights into current–voltage characteristics, electron production, and the effects of photoanode thickness and dye types on cell performance, offering pathways for optimizing DSSC technology.

Interface coupling to improve O2 adsorption and accelerate charge separation for boosting photocatalytic performance of ZnO/ZnIn2S4 composite in H2O2 production and environmental remediation

The key to heterogeneous photo-Fenton technology lies in the efficient generation of hydrogen peroxide (H2O2). Herein, a newly-designed ZnO/ZnIn2S4 composite with heterostructure is synthesized. Benefiting from the formation of built-in electric field, the recombination of photoinduced electrons and holes is suppressed and interfacial charge transfer resistance is reduced. Importantly, the embedding of ZnO in ZnIn2S4 can improve the hydrophobicity and create microscopic three-phase interface, thereby boosting the capture capability for O2 and providing the convenience for the occurrence of O2 reduction reaction. More interestingly, the existence of ZnIn2S4 in the ZnO/ZnIn2S4 composite can reduce the Gibbs free energy (ΔG) of key intermediate (OOH*) formation, which will accelerate the generation of H2O2. As a result, the ZnO/ZnIn2S4 composite displays excellent performance in photocatalytic H2O2 production, and the highest yield was about 897.6 μmol/g/h within 60 min under visible light irradiation. The transfer of photoinduced carriers follows the S-scheme type mechanism. The photogenerated holes can be captured by drug residues (i.e., diclofenac sodium) to accelerate H2O2 production, while generated H2O2 can combine with Fe2+ to construct photo-Fenton system for achieving the advanced degradation of diclofenac sodium, which was mainly related to the formation of OH•. Furthermore, generated H2O2 can be applied for performing the inactivation of pathogenic bacteria. In short, current work will provide a valuable reference for future research.

White afterglow achieved in Eu2+, Ce3+, Dy3+co-doped LiSr4(BO3)3 phosphor

In prior study by our team, orange-yellow afterglow was observed in Eu2+ and Dy3+ co-doped LiSr4(BO3 )3 phosphor due to the emission from Eu2+ center. In this study, further incorporation of Ce3+into the phosphor lead to the observation of white afterglow due to the mixed result of blue light from Ce3+ and orange-yellow light from Eu2+ centers. Upon ultraviolet excitation, the phosphor displays a spectrum characterized from blue emission of Ce3+ at 462nm and orange-yellow emission of Eu2+ at 632nm. Fine-tuning the concentration of Ce3+ enabled the realization of white luminescence in LiSr4(BO3)3: Eu2+, Ce3+ and Dy3+phosphor with chromaticity coordinates of (0.3979, 0.2939). The photoluminescence intensities of the samples could be modulated by incorporating varying amounts of Ce3+ ions, with a critical quenching concentration identified with 0.16 Ce3+. White afterglow is also observed after the removal of the light illumination due to the existence of suitable electron traps with optimal trap depth created by the co-doped Dy3+. The underlying mechanism proposes that the white afterglow is generated by the mixed lights of blue and orange-yellow that are created by the recombination of heat-released electrons from the trap centers with pre-existing holes in the Ce and Eu emission sites.

Study of leakage current degradation based on stacking faults expansion in irradiated SiC junction barrier Schottky diodes

Abstract A comprehensive investigation was conducted to explore the degradation mechanism of leakage current in SiC junction barrier Schottky (JBS) diodes under heavy ion irradiation. We propose and verify that the generation of stacking faults (SFs) induced by the recombination of massive electron--hole pairs during irradiation is the cause of reverse leakage current degradation based on experiments results. The irradiation experiment was carried out based on Ta ions with high linear energy transfer (LET) of 90.5 MeV/(mg/cm2). It is observed that the leakage current of the diode undergoes the permanent increase during irradiation when biased at 20% of the rated reverse voltage. Micro-PL spectroscopy and PL micro-imaging were utilized to detect the presence of SFs in the irradiated SiC JBS diodes. We combined the degraded performance of irradiated samples with SFs introduced by heavy ion irradiation. Finally, three-dimensional (3D) TCAD simulation was employed to evaluate the excessive electron–hole pairs (EHPs) concentration excited by heavy ion irradiation. It was observed that the excessive hole concentration under irradiation exceeded significantly the threshold hole concentration necessary for the expansion of SFs in the substrate. The proposed mechanism suggests that the process and material characteristics of the silicon carbide should be considered in order to reinforcing against the single event effect of SiC power devices.

Enhanced photovoltaic efficiency in TiO2-based CdS quantum dot-sensitized solar cells by the introduction of ZnO:Al3+ nanoparticles

A technique to fabricate quantum dots-sensitized solar cells (QDSSCs) based on Titanium Oxide (TiO2) and Zinc Oxide (ZnO) nanoparticles (NPs) is reported. ZnO nanocubes of around 65 nm were synthesized by the sol–gel precipitation method. ZnO was doped with Al3+ to enhance the photovoltaic efficiency by promoting electron mobility to form an efficient photoelectrode added to TiO2. Current density–voltage (J-V) characterizations indicate that the addition of Al3+ doping in ZnO crystalline structure in the photoelectrode can significantly improve current densities and consequently the photoconversion efficiency (η) of the QDSSCs, achieving maximum η of 3.4 % with five ZnO nanocubes layers with a 0.0005 M Al3+ doping concentration. While with the undoped sample and bare TiO2, the obtained ήs were 2.85 and 1.93 %, respectively. The improved QDSSC photovoltaic performance was attributed to the increased light harvesting due to a large surface area by introducing Al-doped ZnO nanocubes into the available places of the TiO2 lattice. On the other hand, the increased electrical conductivity due to the Al3+ ion doped into the ZnO lattice at the divalent Zn2+ site allows electrons to move readily into the Al-doped ZnO conduction band. Additionally, according to electron lifetime studies, the Al-doped ZnO nanocubes act as a dielectric layer, enhancing the photogenerated charge extraction process due to the introduction of lattice defects, causing intermediate levels to obtain higher electron recombination resistance.

Hole Polaron-Mediated Suppression of Electron-Hole Recombination Triggers Efficient Photocatalytic Nitrogen Fixation.

In the pursuit of successful photocatalytic transformations, challenges persist due to limitations in charge carrier utilization and transfer efficiency, which stemming from rapid recombination. Overcoming these limitations necessitates the exploration of novel mechanisms that enhance the effective separation of photogenerated electron-hole pairs. Herein, deviating from the conventional approach of enhancing carrier migration to separate photogenerated charges and extend their lifetime, the proposal is to directly prevent the recombination of photogenerated electrons and holes by forming hole polarons. Specifically, disordered pores are introduced on the surface of KTaO3 ultrathin sheets, and the clear-cut evidences in electron paramagnetic resonance, photoluminescence, and ultrafast spectroscopy unambiguously confirm the enhanced carrier-phonon coupling, which results in the formation of hole polarons to impede the recombination of photogenerated electron-hole pairs. Taking the challenging nitrogen oxidation reaction as an example, it is found that the hole polarons in atomic-disordered pore KTaO3 ultrathin nanosheets trigger outstanding photo-oxidation performance of nitrogen (N2)to nitrate, with a nitrate-producing rate of 2.1 mg g-1 h-1. This scenario is undoubtedly applicable to a wide variety of photocatalytic reactions due to the common challenge of charge carrier recombination in all photocatalytic processes, manifesting broad implications for promoting photocatalysis performance.

Oxidation cocatalyst/S-scheme junction cooperatively assists photocatalytic H2 production in ternary hybrid: The case of PdO@TiO2-Cu2O

Solar-driven photocatalytic hydrogen production from water splitting holds significant potential in addressing the energy crisis and environmental pollution. However, rapid recombination of photogenerated carriers and insufficient surface catalytic reaction kinetics hinder the photocatalytic process. Constructing the catalytic systems with multi-channel charge-separation can effectively alleviate those issues. In this work, ternary PdO@TiO2-Cu2O composites have been synthesized through precursor calcination and low-temperature reduction, where PdO and Cu2O nanoparticles couple with the TiO2 nanorods. Comparing to single TiO2, binary PdO@TiO2 and TiO2-Cu2O, the PdO@TiO2-Cu2O hybrid exhibits enhanced photocatalytic hydrogen production performance (5831μmol g-1h−1), with a hydrogen production rate more than three times that of single TiO2. Based on the band structures of TiO2 and Cu2O, along with the photochemical/electrochemical, in-situ EPR, Photoluminescence (PL) tests, and work function calculations, the formation of an S-scheme heterojunction at the TiO2-Cu2O interface under light illumination facilitates the recombination of electrons in the conduction band (CB) of TiO2 with holes in the valence band (VB) of Cu2O. In this regard, the established built-in electric field significantly accelerates the transfer of photogenerated charges while preserving their respective strong oxidation and reduction capabilities. Meanwhile, the introduction of PdO enriches the holes and further enhances the rate of charge separation. This S-scheme heterojunction with directional charge transfer and oxidation cocatalyst collectively form multi-channels of charge separation, optimizing charge migration and enabling efficient hydrogen production, thus improving the photocatalytic capability of pristine TiO2. This study provides a rational approach to construct efficient S-scheme heterojunction/oxidation cocatalyst multi-component catalytic systems for water splitting into hydrogen.

Solution-processed quantum dot short-wavelength infrared photodetectors via integrating 2D MXenes into electron transport layer

Solution-processed quantum dots (QDs) have attracted intensive attention in short-wavelength infrared (SWIR) photodetectors due to their excellent optical properties and tunable size-dependent bandgap. However, the intrinsic defects of the widely used ZnO electron-transport layer (ETL) and the inappropriate band alignment at the interface between the ETL and photoactive QDs inevitably impact the optoelectronic performance of the photodetector. Herein, a high-performance self-powered SWIR photodetector is developed by using 2D Ti3C2 MXenes to passivate the defects of ZnO ETL and to tailor the band alignment at the interface of the ETL/photoactive layer through interface engineering. As a result, the SWIR photodetectors demonstrate the ultra-high light-to-dark current (Ilight/Idark) ratio of ∼ 105 and the low dark current density of 8.33 × 10-4 mA/cm2, and the high specific detectivity (D*) of 1.99 × 1011 Jones at 0 V. By the systematic characterizations, it is proofed that 2D MXene can efficiently passivate defects in ZnO and optimize the alignment of energy levels between the ETL and photoactive layer, which will suppress the recombination of electrons and holes and eventually promote photogenerated carrier transfer at the interface and thus improve device performance. This work revealed that the high-performance solution-processed QD based SWIR photodetector enabled by interface engineering will promote the development of optoelectronic devices in the future.

Self-powered multifunctional platform based on dual-photoelectrode for dual-mode detection and inactivation of Salmonella enteritidis

Self-powered photoelectrochemical (PEC) sensing is a novel sensing modality. The introduction of dual-mode sensing and photoelectrocatalysis in a self-powered system enables both detection and sterilization purposes. To this end, herein, a self-powered multifunctional platform for the photoelectrochemical-fluorescence (PEC-FL) detection and in-situ inactivation of Salmonella enteritidis (SE) was constructed. The platform utilized Bi4NbO8Cl/V2CTx/FTO as a photoanode and CuInS2/FTO as a photocathode and incubated quantum dot (QDs) signaling probes on the surface of the photocathode. During detection, the system drives the transfer of photogenerated electrons between the dual photoelectrodes through the Fermi energy level difference. The photoanode amplifies the photoelectric signal, while the photocathode is solely dedicated to the immune recognition process. QDs provide an additional fluorescence signal to the system. Under optimal experimental conditions, the multifunctional platform achieves detection limits of 3.2 and 5.3 CFU/mL in PEC and FL modes respectively, with a detection range of 2.91 × 102 to 2.91 × 108 CFU/mL. With the application of an external bias voltage, it further promotes electron transfer between the dual photoelectrodes, inhibits the recombination of photogenerated electrons and holes. It generates a significant amount of superoxide radicals (·O2−) in the cathodic region, resulting in strong sterilization efficiency (99%). The constructed self-powered multifunctional platform exhibits high sensitivity and sterilization efficiency, it provides a feasible and effective strategy to enhance the comprehensive capability of self-powered sensors.

Boosting visible-light photocatalytic performance of graphitic carbon nitride by regulating its donor-acceptor structure via maleamide

Graphitic carbon nitride (GCN) has attracted much attention due to its many advantages as a kind of photocatalyst, including low cost, easy to prepare, eco-friendly and so on. However, GCN suffers from limited light-absorption capacity and rapid recombination of photogenerated charge carriers. Herein, a new kind of photocatalyst based on GCN has been synthesized by introducing a small molecule compound (maleamide) through a facile thermal polycondensation method (550 ℃ for 180 min) and applied it to photocatalytic removal of bisphenol A (BPA). The optimized GCN-20 (20 mg maleamide in 10 g urea) exhibits the best BPA degradation performance and good stability. The UV–vis test shows that the introduction of maleamide broadens the optical response threshold of GCN from 435 nm to 460 nm. The promoted photocatalytic performance is mainly attributed to enhanced donor-acceptor structure by electron-withdrawing group, which accelerates charge separation and inhibits recombination of free holes and electrons. The active species including superoxide radicals (⋅O2-), hydrogen peroxide (H2O2) and hydroxyl radicals (⋅OH), play dominant roles in the photocatalytic degradation process.

Facile synthesis of a novel CeCO3OH@(H/C–CdS) catalyst with synergistic effect of heterophase junction and heterojunction for enhanced visible-light photocatalytic degradation efficiency at room temperature

A new CeCO3OH@(hexagonal/cubic phases–CdS) (CeCO3OH@(H/C–CdS)) composite catalyst was facilely synthesized by a simple microinjection titration–stirring method, in which CdS nanoparticles were dispersed on the surface of CeCO3OH nanolines. The optimal conditions for the preparation of composite catalysts with high photocatalytic performance were determined by single-factor experiments and response surface experiments. Under these conditions, the degradation rate of 30 mL 2.000 g/L rhodamine B (Rh B) by CeCO3OH@(H/C-CdS) in a photocatalytic reaction for 1 h at 25 °C was up to 86.81 % and its degradation rate in a photocatalytic reaction for 150 min was up to 99.62 %. The degradation rate could be maintained above 80 % even after six times recycling. Especially, the photocatalytic degradation efficiency of 2.000 g/L Rh B on the composite catalyst under sunlight and at room temperature for 30 min reached 97.66 %. Meanwhile, the large size of CeCO3OH considerably alleviated the agglomeration of CdS, providing more adsorption and active sites for visible light-mediated degradation of Rh B. Importantly, the Z-scheme charge transfer realized by CdS and CeCO3OH enhanced the efficient separation of photogenerated electrons and holes, and successfully inhibited the recombination of photogenerated electrons with holes. At the same time, owing to the low energy band difference between the two phases of CdS, charge was transferred between the hexagonal and cubic phases, leaving more effective photogenerated charge to participate in the degradation of Rh B. The synergism of the heterophase junction and heterojunction and the presence of oxygen and sulfur vacancies considerably enhanced the degradation performance of the catalyst. Thus, this study provides a new strategy for the modification and enhanced visible-light catalysis performance of CdS-based catalysts.

Hollow dodecahedral Zn0.3Cd0.7S@NiCo-mixed metal oxide p-n heterojunction with high-efficiency photocatalytic hydrogen production activity

The growing demand for clean and sustainable energy has driven extensive research into efficient photocatalysts for hydrogen production. However, many semiconductor photocatalysts in this field still face the challenges such as wide band gap, limited visible light absorption, and inefficient separation and transport of photoinduced charges. In this study, nickel–cobalt layered double hydroxide (NiCo-LDH) was synthesized using an “etch-and-grow” method with zeolitic imidazolate framework-67 (ZIF-67) as a sacrificial template, followed by high-temperature calcination to produce nickel–cobalt mixed metal oxide (NiCo-MMO). Zn0.3Cd0.7S quantum dots were used to modify NiCo-MMO resulting in a hollow dodecahedral Zn0.3Cd0.7S@NiCo-MMO composite photocatalyst. In hydrogen production performance test, the optimized Zn0.3Cd0.7S@NiCo-MMO exhibited excellent performance (8177.5 μmol·g−1·h−1) and demonstrated good cycling stability. The hollow dodecahedral structure of the Zn0.3Cd0.7S@NiCo-MMO enhanced the light trapping ability and provided large surface area. The p-n heterojunction formed within Zn0.3Cd0.7S@NiCo-MMO accelerated carrier separation and transfer, effectively inhibited the recombination of photogenerated electrons and holes, and significantly improved the hydrogen production activity.

Amorphous NiB layer deposition and piezoelectric field assisted for efficient photocatalytic degradation of Sb2S3

The poor surface charge reaction efficiency and electrical conductivity limit the further application of Sb2S3 in photocatalytic degradation of pollutants. An amorphous NiB layer was deposited on the surface of Sb2S3 by photo-assisted electrodeposition, and the presence of the NiB layer accelerated the charge transport and catalytic reactivity, which greatly enhanced the degradation ability. The photocurrent density of NiB-Sb2S3 was about 0.12 mA/cm2, which was 6 times of that of pure Sb2S3. After increasing the applied mechanical site by ultrasonication, the photocurrent of NiB-Sb2S3 was further increased to 0.19 mA/cm2, which was almost 9.5 times that of pure Sb2S3 under photocatalytic conditions alone. The catalytic kinetic curves show that the degradation rate of RhB by NiB-Sb2S3 under piezoelectric-photocatalytic conditions is significantly increased, being 11.48 times of the degradation rate of Sb2S3 under photocatalytic conditions. The detailed experimental data indicate that the amorphous NiB layer not only changes the electronic structure of the catalyst surface, but also increases the number and activity of the catalyst active sites, and reduces the chance of electron and hole recombination after photoexcitation. The introduction of an applied piezoelectric field provided a driving force for carrier migration to the catalyst surface, which further improved the separation ability. This study provides a new strategy to further improve the photocatalytic degradation.

Plasmonic Pt-PPCN/TiN Ohmic Junction for Photo-Thermo Catalytic Hydrogen Production.

The rational design of photocatalysts for improving the conversion of solar energy into hydrogen is a promising route for achieving carbon neutrality. Herein, we couple plasmonic titanium nitride (TiN) with highly crystalline potassium-doped polymeric carbon nitride (PPCN) to construct a PPCN/TiN ohmic junction. Such an ohmic junction not only broadens the absorption spectrum but also inhibits the recombination of electrons and holes. In addition, Pt nanoparticles are introduced into this ohmic junction to form plasmonic Pt-PPCN/TiN, improving the capture of hot electrons generated by TiN and thereby promoting the dissociation of the O-H bond in H2O. The energy barrier decreases from 0.7 to 0.2 eV. Enhanced separation of carrier, activation of water molecules, and capture of hot electrons are jointly promoting photo-thermo catalytic hydrogen production. Therefore, under full-spectrum irradiation, the hydrogen production rate of Pt-PPCN/TiN reaches 19 085 μmol g-1 h-1. This novel plasmonic photocatalyst is promising for full-spectrum photo-thermo catalytic hydrogen production.