Photocurrent Intensity Research Articles

Engineering fluorene-based covalent organic framework photocatalysts toward efficient and selective aerobic oxidation of amines

Covalent organic frameworks (COFs) have attracted significant interest due to diverse applications, relying on their versatile molecular building blocks like fluorenes. However, the twisted structures of fluorenes pose substantial challenges for the construction of porous crystalline materials like COFs. Here, the couplings of 1,3,5-triformylphloroglucinol (Tp) with 9H-fluorene-2,7-diamine (DAF), 9,9-dimethyl-9H-fluorene-2,7-diamine (MFC) and 9,9-difluoro-9H-fluorene-2,7-diamine (FFC) with a pyrrolidine catalyst afford three fluorene-based COFs, TpDAF-COF, TpMFC-COF and TpFFC-COF, respectively. The resulting COFs, with distinct functional groups, exhibit high crystallinity and porosity. Optoelectronic tests reveal that TpFFC-COF demonstrates the most intense photocurrent density and the lowest interfacial charge transfer resistance. When applied to the selective aerobic oxidation of amines to imines, the efficiency follows the order of TpFFC-COF > TpMFC-COF > TpDAF-COF, consistent with the observed optoelectronic properties. Additionally, the TpFFC-COF photocatalyst showcases excellent reusability and broad applicability. This work illuminates the potential of engineering COFs with functional groups toward efficient photocatalysts.

Upconverting particles in near-infrared light-induced TiO2 photocatalysis: towards the optimal architecture of upconverter/photocatalyst systems.

Preparation of highly active core-shell/hybrid materials based on up-converting particles combined with semiconductors for photocatalytic application usually requires sophisticated and multi-step synthesis procedures. We propose a new design of a highly efficient NIR-driven photocatalytic system composed of spatially separated thin films of upconverting NaYF4:Yb,Tm particles (UCPs), and TiO2. Several samples of UCPs were prepared in the form of thin films and suspensions, directly coated with a titania layer or mixed with P25. Photocatalytic and photoelectrochemical studies have shown that thin film samples achieved significantly higher photocatalytic activity than their suspended counterparts. Moreover, the sample consisting of spatially separated layers of UCPs and P25 presented a significant photocatalytic activity and generated the highest photocurrent intensity. Separating the photocatalyst and upconverter layers allows for an interchangeable photocatalytic system active in a wide range of light.

Development of photoelectrochemical immunosensor based on halide perovskite protected by organometallic compounds for determining interleukin-17A (IL-17A).

The overexpression of interleukin-17A (IL-17A) is closely associated with the pathogenesis of autoimmune diseases and cancer, rendering precise identification of IL-17A level critical for disease diagnosis and prognosis monitoring. In this study, CsPbBr3 nanoclusters (NCs) were embedded in C16H14Br2O6Pb2 organometallic compound (Pb-MA MOC) via a hot injection approach. Through this way, the issue of CsPbBr3 NCs susceptible to decomposition in water was solved, and the photocurrent intensity that isgenerated by CsPbBr3 was significantly enhanced. A highly sensitive photoelectrochemical (PEC) sensor for detecting IL-17A in human serum was developed using CsPbBr3/Pb-MA as the photoactive material. The electrode was initially modified with CsPbBr3/Pb-MA. Then, antibody-modified Fe3O4 magnetic nanoparticles (MNs) with target analyte IL-17A captured, and IL-17A antibody-modified Au@CuNi diatomic catalyst (DAC) formed sandwich immune complex structure on theelectrode. The existence of CuNi DAC led to a substantial reduction in photoelectric signal intensity due to oxidation of ascorbic acid in thesupporting electrolyte. The photocurrent intensity exhibited linear correlation with IL-17A concentration within the range 15-750pg/mL, and achieving an impressive detection limit of1pg/mL. Moreover, the sensor was successfully applied to the determination of IL-17A in human serum, suggesting its potential clinical applications.

Assembly of Eosin Y in-situ intercalated Zr-MOF composite for decontaminating Cr(VI) and reactive dyes via physical capture and photochemical purification

Post-modification based on highly water stable Zr-MOF introduces a novel dimension of functional regulation, offering a fresh perspective for the advancement of pragmatic photocatalysts in the water treatment field. In this study, an entirely novel Zr-MOF (NU-1400-py), featuring a topological network identical to that of NU-1400, has been assembled. The main difference is the replacement of TPTC's central benzene ring with a pyrimidine ring. Utilizing the inherent porosity and semiconducting properties, this Zr-MOF possesses the capability to physically trap Cr2O72- ions (136.43 mg/g), achieving photochemical purification of Cr(VI) and K-, X-, M-type reactive dyes from water. Moreover, another novel heterojunction material EY@Zr-MOF, has been fabricated via in-situ intercalation of luminescent Eosin Y (EY) species within Zr-MOF. Due to the sensitization of embedded EY molecules, EY@Zr-MOF exhibits significantly optimized interface resistance, transient photocurrent intensity and carrier migration efficiency compared to pristine Zr-MOF. Notably, the photochemical purification efficiencies of EY@Zr-MOF towards Cr2O72- (99.66 %, 30 min), RB13 (90.18 %, 120 min), RR2 (92.40 %, 300 min) and RR11 (84.80 %, 90 min) have been dramatically elevated, offering the considerably accelerated reaction kinetics of 1.24, 4.82, 2.48 and 6.23 times, respectively, compared to pristine Zr-MOF, the photochemical purification efficiencies of Zr-MOF towards Cr2O72- (97.88 %, 30 min), RB13 (85.55 %, 450 min), RR2 (71.38 %, 450 min) and RR11 (53.16 %, 240 min). Additionally, its photocatalytic REDOX mechanisms in eliminating target contaminants were proposed tentatively. This contribution offers a viable pathway for designing multi-functional materials aimed at solving some intractable environmental issues caused by Cr(VI) and reactive dyes.

Polarization photodetectors with configurable polarity transition enabled by programmable ferroelectric-doping patterns

Advances in symmetry-breaking engineering of heterointerfaces for optoelectronic devices have garnered significant attention due to their immense potential in tunable moiré quantum geometry and enabling polarization light detection. Despite several proposed approaches to breaking the symmetry of low-dimensional materials, there remains a lack of universal methods to create materials with prominent polarization detection capabilities. Here, we introduce a reliable strategy for manipulating the symmetry of low-dimensional materials through a programmable ferroelectric-doping patterns technique. This method introduces a spontaneous photocurrent and enables the detection of linearly polarization light in isotropic 2H-MoTe2. The 2H-MoTe2 photodetector exhibits a significant short-circuit photocurrent intensity (Jsc = 29.9 A/cm2) and open-circuit voltage Voc of 0.12 V ( ~ 3 × 105 V/cm). Under a specific bias, the polarization ratio transitions from 1 to ∞/−∞, shifting from a positive state (unipolar regime) to a negative state (bipolar regime). These findings underscore the potential of ferroelectric-doping patterns as a promising approach to creating composite materials with artificial bulk photovoltaic effect and achieving high-performance polarization light detection.

A novel metal-free nanomaterial P-CN/BC/NCDs preparation and its performance of photocatalytic degradation

The development of photocatalysts with high charge separation and migration efficiencies for environmental remediation using sunlight had been a research priority. In this study, a ternary composite photocatalyst, P-CN/BC/NCDs, was successfully synthesized by thermal condensation and hydrothermal methods, incorporating graphitic carbon nitride (P-CN), biochar (BC), and nitrogen-doped carbon quantum dots (NCDs). Alizarin red S (ARS) was selected as the model pollutant to evaluate the photocatalytic degradation performance. P-CN/BC/NCDs exhibited enhanced photocatalytic degradation performance under visible light irradiation, with a 4.5-fold improvement compared to P-CN alone. The optimally NCDs-loaded P-CN/BC nanocomposites exhibited high visible light absorption and high specific surface area. The increased photocatalytic activity was further confirmed by the increase in photocurrent intensity and the decrease in fluorescence intensity and resistance. XPS and FT-IR tests showed that NCDs, as co-catalysts of P-CN/BC, effectively promoted charge separation through ether bonds and electrostatic interactions. It was experimentally verified by free radical trapping experiments and EPR tests that •O2− was the primary active species in the photocatalytic process, while •OH served as an auxiliary site during the degradation process. Cyclic experiments demonstrated high reusability and excellent stability, with an activity exceeding 93.8 %. Decomposition intermediates and reaction pathways were identified by liquid-quality analysis. Photocatalyst pervasiveness was evaluated by using different pollutants including methyl orange (MO), rhodamine B (Rh B) under similar conditions. This design concept of functional synergistic modification of P-CN materials holds promise for application in various fields.

Multipath collaboration-based signal amplification on Z-scheme In2O3/g-C3N4 heterojunction photoelectrode for sensitive photoelectrochemical immunoassay

The ideal photoelectrode and efficient signaling strategy are pivotal to achieve sensitive photoelectrochemical (PEC) analysis. Here, a multipath collaborative signal amplification-based PEC immunosensor was constructed for the ultrasensitive detection of cytokeratin 19 fragment 21-1. Specifically, the photoelectrode fabricated by Z-scheme In2O3/g-C3N4 heterojunction showed enhanced photocurrent intensity in response to visible light. Meanwhile, the signal probe, horseradish peroxidase functionalized dopamine-melanin nanosphere@Au nanoparticles (HRP-Dpa-melanin NS@AuNPs), were introduced into the system. When the target exists, the signal probe can induce multiple quenching of the photocurrent due to the competition of light absorption, steric hindrance and HRP-mediated biocatalytic precipitation, which effectively inhibit light, electron donor, and electron access to the photoelectrode. The fabricated immunosensor exhibits a wide linear range from 1.0 × 10−3 - 1.0 × 102 ng mL−1 with the detection limit of 0.35 pg mL−1 (S/N = 3) for cytokeratin 19 fragment 21-1 detection. The study enhances sensitivity for PEC detection by utilizing the superior Z-scheme heterojunction photoelectrode, providing a valuable method that combines multiple signal pathways for a synergistic effect in bioanalysis.

Construction of SnO2/Cu2O heterojunctions for enhanced photocatalytic degradation of moxifloxacin

Herein, SnO2/Cu2O heterojunction composites were prepared using a hydrothermal method for moxifloxacin removal from water. Cu2O and SnO2 were detected in the composite samples, which exhibited between the two semiconductors. The introduction of SnO2 into pure Cu2O, forming a heterojunction structure, can enhance device charge conversion, improve photocurrent intensity and photogenerated electron-hole separation efficiency, and greatly improve photocatalytic performance. Moxifloxacin degradation by SnO2/Cu2O composites reached 86.4 %. The proposed catalytic mechanism was based on radical scavenging, with • O2‐ identified as the main active species. In addition, the moxifloxacin degradation intermediates were analyzed, with possible degradation pathways suggested.

Mechanism Exploration of the Photoelectrochemical Immunoassay for the Integration of Radical Generation with Self-Quenching.

Photoelectrochemical (PEC) sensing mechanisms based on enzyme-catalyzed strategies primarily achieve the quantitative analysis of biomolecules through the enhancement or attenuation of photocurrent signals. However, there are still no reports that delve into the principles of photocurrent signaling conversion in the reaction between photoactive materials and the biomolecules. In this work, we demonstrated that indium oxysulfide InOS-0.5 heterojunction has excellent peroxidase activity to catalyze the reaction of H2O2-generated hydroxyl radicals (•OH) with the self-generated electrons, thereby resulting in synergistic quenching of the photocurrent signal. Based on the above principles, we coupled InOS-0.5 with a sandwich-type immunoassay to introduce H2O2 production catalyzed by glucose oxidase for the development of a PEC immunosensing platform. H2O2 reacted with InOS-0.5 to produce •OH with strong oxidizing properties, thus quenching the photogenerated electrons and realizing the PEC detection of the carcinoembryonic antigen (CEA, as a model analyte). The photocurrent intensity decreases with the logarithmic increase in CEA concentration (0.02-50 ng mL-1), with a remarkable limit of detection of 8.9 pg mL-1 (S/N = 3). This study further investigates the mechanism of hydrogen peroxide-induced photocurrent quenching, providing deeper insights into the mechanisms of electron-hole transport in hollow porous semiconductor materials and paving the way for the development of efficient PEC sensors.

Optimizing photocurrent intensity in layered SiGe heterostructures

Abstract We study the dependence of photo-spectral intensity on tri- and multilayers of SiO2/[SiGe [ d SiGe ]/SiO2] N with repetitions N = 1 to 10 and thicknesses d SiGe = 5 –100 nm. Photocurrent analysis reveals a bimodal spectral feature. A comparison of the photocurrent analysis between tri- and multilayers shows that in the multilayer structures, the photo-spectral intensity increases with increasing repetition N. The change in intensity could then be further tuned by changing the thickness of the SiGe layers d SiGe . We attribute the change in intensity to an increase in tensile strain, along with increased Ge atomic concentration and reduced SiGe-nano cluster size.

Enhanced photodegradation performance of Zn-BiPO4 on RhB and TC under the synergistic effect of oxygen vacancies and built-in electric field

In this work, Zn2+ ions doped BiPO4 photocatalyst was successfully prepared by one-step hydrothermal method for the first time. The degradation rates of the optimal sample on RhB and TC solution reached 91.5 % and 81.25 % under simulated sunlight exposure for 3 and 5 hours, respectively, while pure BiPO4 only reached 59.22 % and 49.4 %. The improved photocatalytic performance was due to the synergistic effect of oxygen vacancies and built-in electric field. The EPR test demonstrated the generation of more oxygen vacancies in the optimal sample. Additionally, the electrochemical experiments showed that the photocurrent intensity of the optimal sample was about 3 times than that of pure BiPO4, indicating an enhanced carrier separation and transfer ability after doping Zn2+ ions. Through density functional theory (DFT), the incorporated Zn2+ ions caused the contraction of crystal structure and the redistribution of charges, leading to a built-in electric field. As few studies pay attention to the relationship between oxygen vacancies and the built-in electric field. This study has enlightening significance for the construction of photocatalysts with oxygen vacancies and built-in electric field through doping engineering.

Near zero background noise photoelectrochemical sensor based on sensitized signal probe CdS QDs-Dox intercalating double-stranded DNA for PEDV detection

The highly sensitive detection method for porcine epidemic diarrhea virus (PEDV) is crucial for promptly identify infected pigs and effectively control the spread of the virus. In this study, the sensitization enhancement of organic photoactive material was combined with near zero background noise strategy for PEDV sensitive detection. A novel sensitized signal probe CdS quantum dots-doxycycline complex (CdS QDs-Dox) was prepared serving as a photoelectrochemical (PEC) probe embedded in dsDNA. Subsequently, a thiol-modified upstream inner primer (SH-FIP) was immobilized on the surface of electrode modified with gold nanoparticles (Au NPs) via Au–S bonding, enabling the loop-mediated isothermal amplification (LAMP) of PEDV on the electrode surface. The PEC probe (CdS QDs-Dox) embedded in the amplified dsDNA groove showed an increasing photocurrent signal with the rise of PEDV concentration, establishing a near-zero background LAMP-PEC sensing platform for PEDV detection. Under optimized conditions, the photocurrent intensity of this platform exhibited a good linear relationship with PEDV concentrations ranging from 0.0005 pg/μL to 10 pg/μL, achieving a detection limit as low as 0.17 fg/μL. This platform demonstrates outstanding specificity and sensitivity, thereby enabling precise quantitative detection of diverse pathogens.

Strong absorption of silica over full solar spectrum boosted by interfacial junctions and light–heat–storage of Mg(OH)2–(CrOx–SiO2)

Strong absorption of near-infrared (NIR) light is essential for efficient solar energy applications. NIR absorption primarily depends on the surface plasmon resonance of incident light with free charge carriers (FCCs). We demonstrated that S-scheme interfacial junctions (IJs) can substantially enhance FCC density, light-harvesting, photocurrent intensity, long lifetime of the charge carriers and photothermal effects, paving a way for novel light-material design. Abundant S–scheme IJs are constructed in CrOx–SiO2 nanoparticles, which increase the FCCs outstandingly and enhance light absorption exceptionally over the entire solar spectrum. IJs’ construction enables silica to harvest solar energy strongly. Doped with multifunctional CrOx–SiO2 nanoparticles, the photothermal-dehydration conversion and the stored heat of Mg(OH)2 can be improved by 7.0- and 5.1-times upon 30-min irradiation, respectively. The reversibility of the photothermal charge–discharge cycles of Mg(OH)2 improves 19.3 times. The thermal-storage kinetics is substantially improved owing to the reduction of the dehydration activation energy (−15.2 %). Mg(OH)2–CrOx–SiO2 composite is an excellent one-step system of light–heat–storage.

Interface coupling of octahedron Cu2O with reduced graphene oxide for enhanced photocatalytic and photoelectrochemical activity

Graphene oxide (GO) has been recognized as an ideal substrate material of semiconductor photocatalysts to achieve superior properties. Herein, Cu2O/reduced graphene oxide hetero-structures (Cu2O/rGO), featured by octahedron Cu2O with highly exposed {111} facets in-situ anchored on the framework of rGO nanosheets, were constructed via a green wet chemistry route at room temperature. During the reactions, Cu2+ ions that were adsorbed on GO could act as the nucleation sites of Cu2O while GO was further converted into rGO under the reduction of glucose, forming a robust hetero-interface of C–O–Cu bonding. Owning to the improved photon capture ability and carrier separation efficiency, the optimized Cu2O/rGO exhibits about 3.5 and 9.3 times enhancement of photocurrent intensity and photocatalytic activity, respectively, as compared to those of pure Cu2O. Meanwhile, the correlation among rGO content, structure and photocatalytic activity of Cu2O/rGO was demonstrated. This work presents a rational route and deep insight for the interface coupling within metal oxide/carbon material hetero-structures for advanced catalytic applications.

Synergistic photocatalysis for bacteria inactivation and organic pollutant removal by S-scheme heterojunction InVO4/Bi5O7I: Performance evaluation and mechanism investigation

The low efficiency of charge carrier separation is a major limitation hindering the application of photocatalytic technology. Constructing S-scheme heterojunction photocatalysts not only effectively promotes the separation of charge carriers, but also maximizes the oxidative and reductive capabilities of the two monomers. In this study S-scheme heterogeneous InVO4/Bi5O7I photocatalyst was synthesized by hydrothermal method combined with calcination. The optimal sample 20 % InVO4/Bi5O7I can completely deactivate Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) in 30 min, remove 20 mg/L TC 76.0 % in 60 min and 20 mg/L BPA 93.0 % in 90 min. Intermediate products of TC and BPA degradation were detected using LC-MS, and possible degradation pathways were proposed. The photocurrent and electrochemical impedance spectroscopy (EIS) tests confirm that InVO4/Bi5O7I exhibits excellent photocurrent intensity and photocarrier migration ability, which are crucial reasons for the enhancement of the photocatalytic performance of the InVO4/Bi5O7I composite. Capture experiments indicate that OH, O2−, h+ and e−are reactive species. EPR further confirms the generation of OH and O2−. Combined with Kelvin probe force microscopy (KPFM) and band structure analysis, it is proposed that InVO4/Bi5O7I has an S-scheme charge transfer mechanism.

Enzymatically Mediated In Situ Generation of Z-Scheme Bi2S3/Bi2MoO6 Heterojunction-Based Organic Photoelectrochemical Transistor for METTL3/METTL14 Detection.

The OPECT biosensing platform, which connects optoelectronics and biological systems, offers significant amplification and more possibilities for research in biological applications. In this work, a homogeneous organic photoelectrochemical transistor (OPECT) biosensor based on a Bi2S3/Bi2MoO6 heterojunction was constructed to detect METTL3/METTL14 protein activity. The METTL3/METTL14 complex enzyme was used to catalyze adenine (A) on an RNA strand to m6A, protecting m6A-RNA from being cleaved by an E. coli toxin (MazF). Alkaline phosphatase (ALP) catalyzed the conversion of Na3SPO3 to H2S through an enzymatic reaction. Due to the adoption of the strategy of no fixation on the electrode, the generated H2S was easy to diffuse to the surface of the ITO electrode. The Bi2S3/Bi2MoO6 heterojunction was formed in situ through a chemical replacement reaction with Bi2MoO6, improving photoelectric conversion efficiency and realizing signal amplification. Based on this "signal on" mode, METTL3/METTL14 exhibited a wide linear range (0.00001-25 ng/μL) between protein concentration and photocurrent intensity with a limit of detection (LOD) of 7.8 fg/μL under optimal experimental conditions. The applicability of the developed method was evaluated by investigating the effect of four plasticizers on the activity of the METTL3/METTL14 protein, and the molecular modeling technique was employed to investigate the interaction between plasticizers and the protein.

Enhancing methane production from corn straw via illumination-assisted Fe3O4/g-C3N4 nanocomposite in anaerobic digestion

This study proposes a novel anaerobic digestion (AD) strategy combining recyclable photoactivated nanomaterials with illumination to enhance electronic transfer for anaerobic microorganisms. Results showed that 7000 Lux illumination increased methane production yield and rate. Incorporating Fe3O4 into graphite carbon nitride (g-C3N4) created a recyclable Fe3O4/g-C3N4 (FG) nanocomposite with improved light absorption, conductivity, redox properties, and methane promotion. The highest methane yield from corn straw was achieved with 7000 Lux and 1.5 g/L FG nanocomposite, 22.6% higher than the dark control. The AD system exhibited increased adenosine triphosphate content, improved redox performance, reduced electron transfer resistance, and higher photocurrent intensity. These improvements bolstered the microorganisms and key genes involved in hydrolysis and acidification, which in turn optimized the acetoclastic pathway. Furthermore, this strategy promoted microorganisms associated with direct interspecies electron transfer, fostering a favorable environment for methanogenic activities, paving the way for future anaerobic reactor developments.

Partial Photoelectrocatalytic Oxidation of 3‐Methylpiridine in Green Conditions by Nanotube/Nanowire Ti/TiO2 Plates Prepared in Aqueous, Glycerol, or Ethylene Glycol Medium

AbstractNanotube/nanowire structured TiO2 samples on Ti plates were prepared by anodic oxidation in aqueous, glycerol or ethylene glycol medium under different experimental conditions and characterized by XRD, SEM‐EDX, electrochemical methods (photocurrent profiles and electrochemical impedance spectroscopy). The nanostructured TiO2 was built on relatively large Ti plates, and consequently, in some preparation conditions, different morphologic properties were observed in the underside and upside zones of the electrodes, especially in ethylene glycol medium. The electrodes were tested for selective photoelectrocatalytic oxidation of 3‐methylpyridine to 3‐pyridinemethanol, 3‐pyridinemethanal and vitamin B3 in water under UVA irradiation. The best performance was found with the electrode prepared in ethylene glycol/water/NH4F (98/2/0.3 w/w) medium at 36 V potential for 3 h, while the worst was that prepared in aqueous medium which showed the shortest nanostructure length. Unlike photoelectrocatalysis and photocatalysis, no aromatic alcohol/carbonyl products were obtained in electrocatalytic and photolytic experiments. The selectivity values of the products were similar for the various electrodes, while the morphology of the nanotubes/nanowires and their quantity which affects the total active surface area were essential for the substrate conversion. The results also show that the photocurrent intensity, XRD peak intensity, and electrical conductivity are correlated with photoelectrocatalytic activity of the Ti/TiO2 electrodes.

Studies on the development and performance of natural dye-sensitised solar cell

ABSTRACT Dye-sensitised solar cells (DSSCs) have gained popularity as a cost-effective alternative to silicon-based solar cells. The present study, provides a unique approach for the construction of DSSCs using anatase titanium dioxide (TiO2) as the photoelectrode material and natural fruit extracts (blackcurrent and pomegranate) as photosensitisers. To generate a compact and homogenous TiO2 anatase layer, nanoparticles are deposited onto a transparent conducting fluorine-doped tin oxide glass. Subsequently, natural fruit extracts were added to the TiO2 anatase film, functioning as photosensitisers to absorb sunlight and start the electron transfer process. Each fruit extract unique chemical makeup adds to the absorption of various wavelengths, widening the DSSC's light absorption spectrum. A thin graphite coating was applied to a conducting material for the generation of a counter electrode, which completes the DSSC structure. The sensitised TiO2 anatase layer and counter electrode are joined together, with a redox electrolyte filling the gap between them. Current–voltage measurements used to characterise the manufactured DSSC during simulated solar irradiation. The DSSC's efficiency was calculated as 0.4–18% based on the produced photocurrent and incident light intensity. The study’s finding shows that a DSSC can be successfully fabricated because of its low manufacturing cost and low harmful. It has wide applicability in renewable energy sectors.

Preparation and photocatalytic performance of BiOCl nanosheet–TiO2 nanotube array composites

Combining BiOCl with TiO2 nanomaterials is beneficial to enhance the photocatalytic activity and optoelectronic activity. In this paper, BiOCl nanosheet–TiO2 nanotube array composites were synthesized to enhance the photocatalytic degradation performance for methyl orange (MO) of TiO2 under ultraviolet light irradiation. BiOCl nanosheets were deposited on TiO2 nanotube arrays by the straightforward impregnation method. X-ray diffraction, scanning electron microscopy, energy dispersive x-ray spectroscopy, transmission electron microscopy, x-ray photoelectron spectroscopy, and photocurrent (i–t) were used to evaluate the composites of BiOCl nanosheets–TiO2 nanotube arrays. The results showed that the tetragonal BiOCl nanosheets clustered together on the surface of the TiO2 nanotubes and grew along the (110) crystal plane. The composites outperformed pure TiO2 regarding outstanding structure and overall photocatalytic performance, and the MO photocatalytic degradation rate was 98.5%. For the 30-BiOCl–TiO2, its photocurrent intensity (58 µA) was 4.5 higher than TiO2 (13 µA). The degradation rate of 87% can still be reached after three cycles.