Charge Separation Research Articles

Visible-light-driven selective cleavage of lignin C-C bonds on the TiO2@g-C3N4 heterostructured photocatalyst.

The selective cleavage of lignin C-C bonds is a highly sought-after process with the goal of obtaining low-molecular-weight aromatic chemicals from renewable resources. However, it remains a challenging task to achieve under mild conditions. Photocatalysis is a potentially promising approach to address this issue, but the development of efficient photocatalysts is still in progress. In this study, we introduce the heterostructured TiO2@g-C3N4 photocatalyst for the development of a visible light photocatalytic procedure for the selective cleavage of lignin C-C bonds under mild conditions. The photocatalyst displays favourable visible light absorption, efficient charge separation efficiency, and promising reusability. A typical β-O-4 dimer model, 2-phenoxy-1-phenylethanol, was effectively (96.0% conversion) and selectively (95.0 selectivity) cleaved under visible light at ambient conditions. This photocatalytic procedure was also effective when subjected to solar irradiation or other lignin dimer models with β-O-4 or β-1 linkages. This reaction occurred through a Cβ-centred radical intermediate and a six-membered transition state with photogenerated holes as the primary active species. The Cα-OH oxidative dehydrogenation of the substrate could also take place but was a relatively minor route. This study provides a new photocatalytic procedure for visible-light-driven lignin valorisation and sheds light on the design of high-performance nanocomposite photocatalysts for C-C bond cleavage.&#xD.

Pd Nanoparticle-Modified BiOBr/CdS S-Scheme Photocatalyst for Enhanced Conversion of CO2.

S-scheme heterojunction photocatalyst-coupled plasma-resonance effect can enhance the response range and absorption of light and charge transfer, and, at the same time, obtain strong redox ability, which is an effective way to improve CO2 conversion. In this work, plasma S-scheme heterojunctions of Pd/BiOBr/CdS with heterogeneous interfaces have been successfully constructed by a simple hydrothermal method. The possible reaction mechanism was proposed by in situ infrared, ultraviolet-visible spectroscopy (UV-vis), electron paramagnetic resonance (ESR), density functional theory (DFT), and electrochemical techniques. It was proved that the plasma S-scheme heterojunction can enhance the charge separation efficiency and improve the photocatalytic activity. When the loading ratio is Pd0.6-10%-BiOBr/CdS, it has the best performance, and the CO yield is 30.24 μmol/g, which is 15 and 30 times that of pure BiOBr and CdS, respectively. The results show that with the strong absorption of photon energy and the special electron transfer mode of S-scheme heterojunction, the charge can be effectively separated and transferred, and the photocatalytic activity is significantly improved. This study provides a useful strategy for charge transfer kinetics of plasma S-scheme heterojunction photocatalysts.

Flexible carbon-coated paper electrokinetic generator with Schottky-junction

Simulating transpiration effect to harvest electricity has attracted continued interest. However, it is limited to directional water/ions transport that shrinks the application scenario. Herein, we propose a new carbon-coated paper electrokinetic generator with Schottky-junction to induce the electricity. The electrical double layer (EDL) forms at carbon-water interface due to the wetting paper that induces an obvious electrical sign. The introduce of Schottky-junction inhibits the carrier recombination that enhances the charge separation. As a result, the output performance is significantly improved. Besides, it breakthroughs the limitation of directional water/ions transport to realize multi-mode energy harvesting due to joint working mechanisms of EDL and Schottky-junction. Consequently, the electrical sign is still remained in the case of full wetting rather than disappearance, showing great potential in practical applications. As a demonstration, it can judge the condition of simulated pipe through the feedback of electrical signal, charges the capacitors to energy storage and powers digital calculator, et al. The cheap and flexible paper-based generators offer a new path to clean energy harvesting and sensor applications.

Cu2WS4 with high-exposure {0 0 1} surfaces promotes efficient charge separation in ZnIn2S4

The spatial segmentation of photogenerated carriers is crucial for achieving efficient photocatalytic H2 production (PHP) rates in photocatalyst. Design studies of crystalline catalyst facets and selective morphology control can facilitate the development of catalysts that expose more advantageous active facets. Herein, Cu2WS4/ZnIn2S4 composites are constructed by growing ZnIn2S4 nanosheets in situ on Cu2WS4 with largely exposed {001} surface. Experiments and density functional theory calculations demonstrate that the electrons of ZnIn2S4 flowed to the {001} surface of Cu2WS4, and the holes vectorially migrated to the {101} surface, during the reaction process, resulting in efficient spatial separation of the photogenerated carriers. The Cu2WS4/ZnIn2S4 achieves a PHP rate of 23.67 mmol g−1 h−1, 13.44-fold increase compared with pure ZnIn2S4. This report combines the advantages of the high-energy activity of the Cu2WS4 {001} surface to morphologically control the ratio of the {001}/{101} surfaces so that ZnIn2S4 can contact a larger area of the {001} surface. Furthermore, under the influence of crystallographic effects on the {001} and {101} surfaces, electrons and holes of ZnIn2S4 are transferred to different crystalline facets, promoting the redox reaction. This paper provides effective ideas for the rational design of photocatalysts with efficient carrier space separation.

Boosting photocatalytic H2 evolution in B-doped g-C3N4/O-doped g-C3N4 through synergistic band structure engineering and homojunction formation

Photocatalytic hydrogen production is a promising method to address the increasing energy demand and depletion of fossil fuels. Among various photocatalysts, g-C3N4 (CN) has attracted significant attention due to its favorable properties and tunable band structure. CN-based heterojunctions have been developed to enhance photocatalytic efficiency through improved charge separation via interfacial charge transfer. However, traditional heterojunctions formed between CN and other semiconductors often face challenges related to material compatibility and stability. In this work, we explored the formation of homojunctions, which involve identical semiconductors and offer superior charge separation and electron mobility due to perfect lattice matching. To further enhance individual oxidation and reduction capabilities, we employed band structure engineering through B doping and O doping. The homojunction between B-doped CN (BCN) and O-doped CN (OCN) was successfully synthesized using simple electrostatic self-assembly, resulting in significantly improved hydrogen production of 519.3 μmol g−1h−1 compared to BCN (34.7 μmol g−1h−1) and CN (167.2 μmol g−1h−1). This approach enhances visible light absorption, charge separation, and mobility, demonstrating the potential for developing advanced CN-based photocatalysts for various applications.

​The structural regulation of photosensitive unit and conjugation in COFs for efficient photocatalytic H2 evolution.

The photosensitive unit and conjugation play a significant role in photocatalytic performance of covalent organic frameworks (COFs). In this work, a series of COFs that introduced the phenyl phenanthridine as photosensitive unit with different planarity of linkages were synthesized and the common regulation between them for photocatalysis hydrogen evolution reaction (HER) was also studied. The results indicate that DHTB-PPD, with 2/3 planarity linkages (β-ketoenamine/imine is 2/3) and the phenyl phenanthridine as building blocks, shows the narrowest bandgap and the strongest charge separation efficiency. Therefore, it shows the highest H2 production rate of 12.13 mmol g-1 h-1. The optimal photocatalytic efficiency of DTHB-PPD can be attributed to the combined effect of the photosensitive unit and the long-range ordering of the COF skeleton. According to The Density Functional Theory (DFT), the O site on β-ketoamine is the most possible H2 generation site, but the photocatalytic efficiency of TP-PPD, with the highest skeletal conjugation and the highest proportion of β-ketoamine is not the most efficient photocatalyst, indicating that the long-range ordering of COFs is important on photocatalytic performance. Thus, these findings provide valuable guidance for the structural design of COFs photocatalysts.

Peptide-Guided Metal-Organic Frameworks Spatial Assembly Sustain Long-Lived Charge-Separated State to Improve Photocatalytic Performance.

The controlled fabrication of spatial architectures using metal-organic framework (MOF)-based particles offers opportunities for enhancing photocatalytic performances. The understanding of the contribution of assembly to a precise photocatalytic mechanism, particularly from the perspective of charge separation and extraction dynamics, still poses challenges. The present report presents a facile approach for the spatial assembly of zinc imidazolate MOF (ZIF-8), guided by β-turn peptides (SAZH). We investigated the dynamics of photoinduced carriers using transient absorption spectroscopy. The presence of a long-lived internal charge-separated state in SAZH confirms its role as an intersystem crossing state. The formation of an assembly interface facilitates efficient electron transfer from SAZH to O2, resulting in approximately 2.6 and 2 times higher concentrations of superoxide (·O2-) and hydrogen peroxide (H2O2), respectively, compared to those achieved with ZIF-8. The medical dressing fabricated from SAZH demonstrated exceptional biocompatibility and exhibited an outstanding performance in promoting wound restoration. It rapidly achieved hemostasis during the bleeding phase, followed by a nearly 100% photocatalytic killing efficiency against the infected site during the subsequent inflammatory phase. Our findings reveal a pivotal dynamic mechanism underlying the photocatalytic activity of control-assembled ZIF-8, providing valuable guidelines for the design of highly efficient MOF photocatalysts.

Unveiling the Dual Impact of CuI Layer and Se Content in Sb2(S, Se)3 Photocathodes for Solar Water Splitting

Sb2(S, Se)3 is a promising photocathode for photoelectrochemical (PEC) conversion of solar energy to hydrogen due to its excellent optoelectronic properties, stability, and low toxicity. For such applications, a p–i–n device architecture is favorable for efficient charge separation, with the p‐type layer improving hole extraction while the n‐type layer facilitates electron injection into the electrolyte for hydrogen evolution reaction. However, the lack of suitable p‐type layers for depositing a uniform layer of Sb2(S, Se)3 photocathode constrains the device architectures for PEC water splitting. In this work, various p‐type materials (e.g., NiO, CuS, and CuI) are investigated. Photocathodes fabricated on CuI demonstrate superior performance due to improved hole extraction and uniform growth of Sb2(S, Se)3 absorber layer. The Se/S ratio is adjusted to further fine‐tune the photocathode's absorption, influencing the efficiency of charge carriers’ injection and separation. The overall PEC performance reaches the maximum value when Se/S = 20%, achieving up to 4.2 mA cm−2 with stable photocurrents sustained for 120 min under standard illumination conditions, achieving the highest‐reported photocurrent among S‐rich‐solution‐processed Sb2(S, Se)3 photocathodes. In this work, new avenues are opened for the design of p–i–n Sb2(S, Se)3 PEC devices.

Constructing type II heterojunction of 2D/1D Pg-C3N4/Ag3VO4 nanocomposite with high interfacial charge separation for boosting photocatalytic CO2 reduction under solar energy

The well-designed, template-free synthesis of 2D protonated g-C3N4 nanosheets (Pg-C3N4) coupled with novel 1D Ag3VO4 nanorods has been investigated to construct 2D/1D interface heterostructures with strong electrostatic interactions between the positively charged 2D Pg-C3N4 nanosheets and the negatively charged 1D Ag3VO4 nanorods. The coupling of Pg-C3N4 and Ag3VO4 with desirable characteristics resulted in a 2D/1D interface heterojunction with a type II charge carrier transfer mechanism, effectively maintaining and utilizing charge carriers. The 2D/1D Pg-C3N4/Ag3VO4 exhibited remarkable photocatalytic performance for CO2 conversion with H2O, resulting in maximum CH4 and dimethyl ether (DME) production of 352.3 and 130.9 µmol/g-cat, respectively. A quantum yield of 0.23 % for CH4 generation was achieved over the 2D/1D Pg-C3N4/Ag3VO4, which was 2.9 and 1.4 times higher than that of the Pg-C3N4 and Ag3VO4 samples, respectively. The improvement in photocatalytic performance primarily stems from the effective interaction between Pg-C3N4 and ternary Ag3VO4, leading to enhanced transfer and separation of photoinduced charge carriers through the creation of a type II heterojunction. The findings of this study are useful in designing template-free heterojunctions for photocatalytic CO2 conversion and other solar energy applications.

Green hydrogen and acetaldehyde production via photo-induced thermal dehydrogenation of bioethanol over a highly dispersed CuS/ TiO2 catalyst

The emergence of global warming issues has triggered the interest in producing carbon-neutral energy sources and fossil-based chemicals from affordable and renewable feedstocks (e.g., bio-ethanol). Herein, the synthesis of highly dispersed CuS/TiO2 photothermal catalysts is reported for simultaneously converting ethanol into hydrogen and acetaldehyde under simulated sunlight. The catalyst achieved a hydrogen evolution rate of 51.61 mmol g−1 h−1 and an acetaldehyde production rate of 48.63 mmol g−1 h−1, with a maximal acetaldehyde selectivity of 97% among carbon-containing products. Compared to pristine TiO2, the introduction of plasmonic CuS largely extended the light adsorption range and enhanced the photothermal performance, whilst the formation of heterojunction structure improved the charge transfer and separation efficiency. The density functional theory calculation results demonstrate that CuS/TiO2 composite interfaces could significantly lower the activation energy of ethanol dehydrogenation reaction and improve hydrogen evolution reaction ability. This study provides deep insight into understanding and optimizing hot carrier dynamics in photothermal catalytic systems.

Tuning Two-Photon Absorption in Rhodopsin Chromophore via Backbone Modification: The Story Told by CC2 and TD-DFT.

We investigate here a systematic way to tune two-photon transition strengths (δ2PA) and two-photon absorption (2PA) cross sections (σ2PA) of the rhodopsin's chromophore 11-cis-retinal protonated Schiff base (RPSB) via the modulation of the methyl groups pattern along its polyene chain. Our team employed the resolution of identity, coupled cluster approximate second order (RI-CC2) method with Dunning's aug-cc-pVDZ basis set, to determine the structural impact on δ2PA, as well as its correlation to both transition dipole moments and permanent electric dipole moments. Seven structures were probed in vacuo, including five-double-bond-conjugated model of the native chromophore, shortened by the β-ionone ring (RPSB5), and its de/methylated analogues: 9-methyl, 13-methyl, planar and twisted models of 9,10-dimethyl and 9,10,13-trimethyl. Our results demonstrate that the magnitude of δ2PA is dictated by both the position and number of methylated groups attached to its polyene chain as well as the degree of dihedral twist that is introduced due to the de/methylation. In fact, a strong correlation between δ2PA enhancement and the presence of a C13-methyl group in the planar RPSB5 species is found. Trends in δ2PA values follow the trends observed in their corresponding changes in the permanent dipole moment upon the S0-S1 excitation nearly exactly. The assessment of four DFT functionals, i.e., M11, MN15, CAM-B3LYP, and BHandHLYP, previously found most successful in predicting 2PA properties in biological chromophores, points to a long-range-corrected hybrid meta-GGA M11 as the top-performing functional, albeit still delivering underestimated δ2PA and σ2PA values by a factor of 3.3-5.3 with respect to the CC2 results. In the case of global-hybrid meta-NGA (MN15), as well as CAM-B3LYP and BHandHLYP functionals, this factor deteriorates significantly to 6.7-20.9 and is mostly related to significantly lower quality of the ground- and excited-state dipole moments.

The preparation technology and catalytic mechanism of PVDF/PVP/a-MoSx porous membrane for water flow driven piezoelectric PMS activation

Piezoelectric catalysis couples with peroxymonosulfate (PMS) activation technology can efficiently increase the yield of reactive oxygen species (ROS). Herein, a novel flexible polyvinylidene difluoride/polyvinyl pyrrolidone/amorphous molybdenum sulfide (PVDF/PVP/a-MoSx) membrane with finger-like pore structure was prepared by non-solvent induced phase separation (NIPS) method. As a result, a-MoSx nanosheets can be exposed out of the pores to provide multiple active sites. The PVDF/PVP/a-MoSx with large dipole moment can form enhanced polarization field under water flow to accelerate the charges separation and transfer, thereby promoting the breakage of the OO bond of PMS. The mechanism of piezo-photocatalytic activated PMS was confirmed by COMSOL multiphysics simulations, electrochemical experiments, contribution of active species and DFT calculations. Moreover, a self-cycling degradation reactor was proved more effective in generating piezoelectric potential and improving the degradation efficiency, supporting the practical potential of this strategy. This study provides a new platform to develop piezoelectric porous membrane for enhanced PMS activation under low density flow water energy.

Guest-Mediated Modulation of Photophysical Pathways in a Coronene Bisimide Cyclophane.

The properties and functions of chromophores utilized by nature are strongly affected by the environment formed by the protein structure in the cells surrounding them. This concept is transferred here to host-guest complexes with the encapsulated guests acting as an environmental stimulus. A new cyclophane host based on coronene bisimide is presented that can encapsulate a wide variety of planar guest molecules with binding constants up to (4.29 ± 0.32) × 1010 M-1 in chloroform. Depending on the properties of the chosen guest, the excited state deactivation of the coronene bisimide chromophore can be tuned by the formation of host-guest complexes toward fluorescence, exciplex formation, charge separation, room-temperature phosphorescence (RTP), or thermally activated delayed fluorescence (TADF). The photophysical processes were investigated by UV/vis absorption, emission, and femto- and nanosecond transient absorption spectroscopy. To enhance the TADF, two different strategies were used by employing suitable guests: the reduction of the singlet-triplet gap by exciplex formation and the external heavy atom effect. Altogether, by using supramolecular host-guest complexation, a versatile multimodal chromophore system is achieved with the coronene bisimide cyclophane.

Exceptional light harvesting in copper doped CaTiO3 nanocuboids with surface nanosteps for the photo remediation of toxic Cr(VI) ions and dyes

Addressing the rising concerns of water pollution caused by harmful inorganic and organic contaminants is very crucial and photocatalysts with exceptional light harvesting capability are a promising way to tackle these issues. This study investigates the transformation of CaTiO3 into a visible light-active photocatalyst via copper doping. Copper-doped CaTiO3 nanocuboids were synthesized via a one-step solvothermal approach, resulting in the formation of distinctive nanostep substructures on the surface. Morphological analysis revealed the successful incorporation of copper ions into the perovskite matrix, as evidenced by the transition from smooth to rough, uneven surface features. X-ray diffraction confirmed the incorporation of Cu2+ ions into the Ti4+ site, while visible range absorption indicated a reduction in the bandgap. Furthermore, doping decreased the rate of charge carrier recombination and increased their average lifetime, prolonging the duration of active species. This modification facilitating efficient absorption of visible light and increase in the charge separation, leads to enhanced photocatalytic activity. The doped catalyst exhibited exceptional performance in the remediation of hexavalent chromium ions (98.5 % Cr6+ ions reduction to Cr3+ ions in 20 min), methylene blue (99.4 % degradation within 120 min), and eosin yellow (99.8 % degradation within 80 min) pollutants. This research underscores the potential of doping as a viable strategy for tailoring photocatalytic properties and addressing water pollution challenges.

The photoelectrochemical properties of FTO/WO3/BiVO4/TiO2 photoanode for water splitting

This work investigates the photoelectrochemical performance of an FTO (Fluorine-doped Tin Oxide) /WO3 (tungsten trioxide) /BiVO4 (bismuth vanadate) /TiO2 (titanium dioxide) photoanode for water splitting. By forming a heterojunction between WO3 and BiVO4, charge separation and transportation are significantly enhanced, resulting in an improved photocurrent density. Surface modification with a thin TiO2 layer further improves the stability of the photoanode without compromising its photocurrent. The SEM, XRD, and XPS analyses confirm the successful formation of the photoanode structure. The photoelectrochemical J-V curves demonstrate that the WO3/BiVO4 composite electrode outperforms single WO3 and BiVO4 electrodes, and the TiO2 coating further enhances its performance. These findings provide valuable insights into optimizing BiVO4-based photoanodes for efficient hydrogen production via water splitting.

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.

Composite dark matter with forbidden annihilation

A dark matter model based on QCD-like SU(Nc) gauge theory with electroweakly interacting dark quarks is discussed. Assuming the dark quark mass m is smaller than the dynamical scale Λd ~ 4πfd, the main component of the dark matter is the lightest G-parity odd dark pion associated with chiral symmetry breaking in the dark sector. We show that nonzero dark quark mass induces the universal mass contribution to both G-parity odd and even pions, and their masses tend to be degenerate. As a result, dark pion annihilation into heavier G-parity even dark pion also affects the dark matter relic abundance. Thus, our setup naturally accommodates forbidden dark matter scenario and realizes heavy dark matter whose mass is O\\documentclass[12pt]{minimal} \\usepackage{amsmath} \\usepackage{wasysym} \\usepackage{amsfonts} \\usepackage{amssymb} \\usepackage{amsbsy} \\usepackage{mathrsfs} \\usepackage{upgreek} \\setlength{\\oddsidemargin}{-69pt} \\begin{document}$$ \\mathcal{O} $$\\end{document}(1–100) TeV, which is different from conventional electroweakly interacting dark matter such as minimal dark matter. We also discuss CP-violation from the θ-term in the dark gauge sector and find that the predicted size of the electron electric dipole moment can be as large as ∼ 10−32e cm.

Advances in the heterostructures for enhanced hydrogen production efficiency: a comprehensive review.

The growing global energy demand and heightened environmental consciousness have contributed to the increasing interest in green energy sources, including hydrogen production. However, the efficacy of this technology is contingent upon the efficient separation of charges, high absorption of sunlight, rapid charge transfer rate, abundant active sites and resistance to photodegradation. The utilization of photocatalytic heterostructures coupling two materials has proved to be effective in tackling the aforementioned challenges and delivering exceptional performance in the production of hydrogen. The present article provides a comprehensive overview of operational principles of photocatalysis and the combination of photocatalytic and piezo-catalytic applications with heterostructures, including the transfer behavior and mechanisms of photoexcited non-equilibrium carriers between the materials. Furthermore, the effects of recent advances and state-of-the-art designs of heterostructures on hydrogen production are discussed, offering practical approaches to form heterostructures for efficient hydrogen production.

Synthesis and characterization of Vs-B/MoS2 with double defects for efficient piezocatalytic antibiotic degradation and bacterial disinfection

Molybdenum disulfide (MoS2) is a promising piezoelectric catalytic material that has garnered extensive research attention. However, its application is hindered by its inherent centrosymmetric structure, leading to comparatively low piezoelectric efficiency. To address this issue, this study proposed a dual-defect (sulfur vacancies and boron-loaded) construction strategy to break the central symmetry of MoS2, and a series of Vs-B/MoS2 catalysts with ultrahigh piezoelectric catalytic efficiency were successfully prepared. The optimized Vs-B3.0/MoS2 catalyst exhibited exceptional piezoelectric catalytic activity, with a piezoelectric force microscopy (PFM) piezoelectric response amplitude of 403.9 pm and a piezoelectric coefficient of 35.1 pC N−1, which is 3.85 and 6.27 times higher than those of Vs-MoS2, respectively. Electrochemical tests and density functional theory calculations indicated that the enhanced piezoelectric performance can be attributed to boron doping and sulfur vacancy formation. These structural defects facilitate charge separation and increase material conductivity, significantly boosting piezoelectric properties. Within 60 min, the Vs-B3.0/MoS2 catalyst efficiently degraded 92.6 % of tetracycline. The electron paramagnetic resonance (EPR) characterization showed that ·OH and ·O2− were the main active radicals of the piezoelectric catalysis. In addition, the material exhibits significant bactericidal properties against E. coli. This study offers novel methods and technological support to enhance the piezoelectric properties of transition metal sulfides and efficiently purify water pollutants.

Effect of Thiophene-Hydrazinyl-Thiazole derivative as an efficient dye sensitizer and performance enhancer of TiO2 toward Rhodamine B photodegradation

Visible-light-driven photocatalysis is an eco-friendly technology for wastewater treatment, where TiO2-based photocatalysts displayed outstanding performance in this regard. Dye sensitization is a promising approach for overcoming the common drawbacks of TiO2 via improving its photocatalytic performance and extending its activity to visible light. Herein, we demonstrate the synthesis of the Thiophene-Hydrazinyl-Thiazole (THT) derivative as a novel organic dye sensitizer to be employed as a visible-light antenna for TiO2 nanoparticles. The physicochemical characteristics of the as-synthesized TiO2-based nanoparticles are examined by different techniques, which revealed the successful fabrication of the proposed THT-TiO2 heterojunction. The incorporation of THT molecules on the TiO2 surface led to slight disorders and deformation in the crystal lattice of TiO2, a remarkable improvement of its absorption in the visible light as a perfect visible-light antenna in the whole visible region, and significant enhancement in the charge transfer. Rhodamine B (RhB) is used as an organic dye model to assess the photocatalytic efficiency of the as-fabricated THT-TiO2 photocatalyst which achieved almost complete degradation (>95% in 150 min) with an observed rate constant (kobs) of 0.0164 min-1; total organic carbon (TOC) measurements suggest ∼75% mineralization. THT-TiO2 achieved 2.1-fold enhancement in photodegradation% and 4.1-fold enhancement in kobs compared to the bare TiO2. THT showed good activity under visible-light irradiation (RhB degradation% was >66% in 150 min and kobs=0.0085 min-1). The influence of the initial pH of the solution was investigated and pH 4 was the optimum pH value for suitable interaction between RhB and the surface of THT-TiO2. Radical quenching experiments were conducted to assess the crucial reactive species where the ∙OH and were the most reactive species. THT-TiO2 showed promising stability over three successive cycles. Finally, the improvement mechanism of the photocatalytic activity of THT-TiO2 was attributed to the electron injection from the excited THT (the dye sensitizer) to TiO2 and enhanced charge separation.