Good Photocurrent Response Research Articles

A "signal-off" anodic photoelectrochemical sensor based on ZnIn2S4/TiO2 heterojunction for dopamine detection

Dopamine (DA) is an important neurotransmitter. Abnormal levels of it in human body can increase the risk of many neurological diseases. Thus, developing a simple, sensitive detection method of DA is crucial. In this paper, we reported a "signal-off" anodic PEC sensor based on fluorine-doped tin oxide (FTO) glass modified ZnIn2S4/TiO2 heterojunction (ZnIn2S4/TiO2/FTO) for DA detection. The experimental results show that the ZnIn2S4/TiO2/FTO electrode prepared by two-step hydrothermal method has a good photocurrent response performance under visible light. After incubation with DA, the photocurrent response decreases significantly because DA can rapidly oxidizes to polydopamine (PDA) through the action of superoxide radical (·O2−) and hydroxyl radical (·OH) intermediate species, which are intermediates produced by the ZnIn2S4/TiO2/FTO electrode under visible light irradiation. The constructed PEC sensor has a good linear relationship in the concentration range from 0.5 to 1000.0 μM, and its detection limit is 0.253 μM. In addition, the results of the proposed PEC sensor in real serum samples are satisfactory. The PEC sensor provides a promising platform for DA detection, laying the foundation for future advances in disease diagnosis and prevention.

Selenium doping to improve internal electric field for excellent photocatalytic efficiency of g-C3N4 nanosheets

Graphitic carbon nitride is a promising photocatalyst to address environmental issues and energy applications. Herein, we develop an efficient defect-containing functionalized system of 2D selenium doped g-C3N4 porous nanosheets via one pot with two-step temperature for the first time. During heat treatment, Se-infused g-C3N4 nanosheets loosen stacking and form thinner nanosheets, which could effectively shorten the electronic path of charge migration. The introduction of nitrogen vacancies creates a midgap energy state below the CB, which improves the light-harvesting efficiency. Moreover, the dual effect of N vacancy and Se doping provides a driving force for the dissociation of excitons and achieves an effective spatial charge separation. High specific surface area (104.1 m2/g), suitable bandgap (2.65 eV), and good photocurrent response (0.45 µA cm−2) help to enhance the photocatalytic efficiency of 1-SeCN remarkably. Henceforth, high photocatalytic H2 production rate of 5441 µmol g−1 h−1 and CO evolution rate of 31.5 µmol g−1 h−1 verifies the effective Se doping enhances the photocatalytic efficiency of g-C3N4. Furthermore, DFT calculations are consistent with experimental results and this facile engineering strategy provides a scalable way to develop a novel, efficient g-C3N4-based photocatalyst for H2 production and CO2 reduction.

Constructing efficient Ti4O7/PbO2 heterostructured photoelectrode for water remediation

Photoelectrocatalytic oxidation (PEC) technology is considered to be an efficient process for the treatment of organic wastewater, and its performance depends on the characteristics of the PEC photoanodes. Therefore, the construction of heterogeneous nanostructured photoelectrodes based on suitable semiconductor materials for fast induced carrier transfer efficiency is essential for a high-performance PEC technique. Herein, titanium suboxide/lead (IV) oxide (Ti4O7/PbO2) ceramic photoelectrode with efficient PEC performance was synthesized by coupling PbO2 nanospheres with Ti4O7 through a hydrothermal method. To maximize the PEC performance of the ceramic electrodes, the Ti4O7/PbO2 nano-heterostructures were optimized by modulating the hydrothermal temperature. The optimized ceramic electrodes possessed a low Tafel slope, a low charge-transfer resistance and a good photocurrent response. Ti4O7/PbO2-110 exhibited an efficient PEC activity (approximately 92.21%) for the degradation of reactive brilliant blue KN-R. The efficient PEC performance of Ti4O7/PbO2-110 arose from the formation of a type II heterojunction between Ti4O7 and PbO2, which achieved efficient photogenerated carrier separation and facilitated the formation of intermediate active species. This work not only validates the efficient performance of Ti4O7/PbO2-110 for PEC water purification but also provides a reference strategy for the preparation of heterostructured ceramic photoelectrodes with a high PEC efficiency.

A 66-Nuclear All-Alkynyl Protected Peanut-Shaped Silver(I)/Copper(I) Heterometallic Nanocluster: Intermediate in Copper-Catalyzed Alkyne-Azide Cycloaddition.

Ligand-protected heterometallic nanoclusters in contrast to homo-metal counterparts show more broad applications due to the synergistic effect of hetero-metals but their controllable syntheses remain a challenge. Among heterometallic nanoclusters, monovalent Ag-Cu compounds are rarely explored due to much difference of Ag(I) and Cu(I) such as atom radius, coordination habits, and redox potential. Encouraged by copper-catalyzed alkyne-azide cycloaddition (CuAAC) reaction, comproportionation reaction of Cu(II)X2 and Cu(0) in the presence of (PhC≡CAg)n complex and molybdate generated a core-shell peanut-shaped 66-nuclear Ag(I)-Cu(I) heterometallic nanocluster, [(Mo4O16)2@Cu12Ag54(PhC≡C)50] (referred to as Ag54Cu12). The structure and composition of Ag-Cu heterometallic nanocluster are fully characterized. X-ray single crystal diffraction reveals that Ag54Cu12 has a peanut-shaped silver(I)/copper(I) heterometallic nanocage protected by fifty phenylacetylene ligands in µ3-modes and encapsulated two mutually twisted tetramolybdates. Heterometallic nanocage contains a 54-Ag-atom outer ellipsoid silver cage decorated by 12 copper inside wall. Nanosized Ag54Cu12 is a n-type narrow-band-gap semiconductor with a good photocurrent response. Preliminary experiments demonstrates that Ag54Cu12 itself and activated carbon supported Ag54Cu12/C are effective catalysts for 1,3-dipole cycloaddition between alkynes and azides at ambient conditions. The work provides not only a new synthetic route toward Ag(I)-Cu(I) nanoclusters but also an important heterometallic intermediate in CuAAC catalytic reaction.

A sandwich-type photoelectrochemical biosensor based on Ru(bpy)32+ sensitized In2S3 for aflatoxin B1 detection.

Aflatoxin B1 (AFB1), classified as a class I carcinogen, is a widespread mycotoxin that poses a serious threat to public health and economic development, and the food safety problems caused by AFB1 have aroused worldwide concern. The development of accurate and sensitive methods for the detection of AFB1 is significant for food safety monitoring. In this work, a sandwich-type photoelectrochemical (PEC) biosensor for AFB1 detection was constructed on the basis of an aptamer-antibody structure. A good photocurrent response was obtained due to the sensitization of In2S3 by Ru(bpy)32+. In addition, this sandwich-type sensor constructed by modification with the antibody, target detector, and aptamer layer by layer attenuated the migration hindering effect of photogenerated carriers caused by the double antibody structure. The aptamer and antibody synergistically recognized and captured the target analyte, resulting in more reliable PEC response signals. CdSe@CdS QDs-Apt were modified as a signal-off probe onto the sensor platform to quantitatively detect AFB1 with a "signal-off" response, which enhanced the sensitivity of the sensor. The PEC biosensor showed a linear response range from 10-12 to 10-6 g mL-1 with a detection limit of 0.023 pg mL-1, providing a feasible approach for the quantitative detection of AFB1 in food samples.

Synthesis, crystal and electronic structures, linear and nonlinear optical properties, and photocurrent response of oxyhalides CeHaVIO4 (Ha = Cl, Br; VI = Mo, W).

Four heteroanionic oxyhalides, CeClMoO4, CeBrMoO4, CeClWO4, and CeBrWO4, have been studied as multifunctional materials, which show a combination of good second harmonic generation (SHG) response and photocurrent signals. Millimeter-sized CeHaVIO4 (Ha = Cl, Br; VI = Mo, W) crystals were grown by halide salt flux. The crystal structure of CeHaVIO4 crystals was accurately determined by single-crystal X-ray diffraction. CeClMoO4, CeBrMoO4, and CeBrWO4 are isostructural to each other, and crystallize in the acentric LaBrMoO4 structure type. CeClWO4 crystallizes in a new structure type with unit cell parameters of a = 19.6059(2) Å, b = 5.89450(10) Å, c = 7.80090(10) Å, and β = 101.4746(8)°. The bandgaps of CeHaVIO4 fall into the range of 2.8(1)-3.1(1) eV, which are much smaller than those of isotypic LaHaVIO4 (Ha = Cl, Br; VI = Mo, W) in the range of 3.9(1)-4.3(1) eV. The narrowing of bandgaps in CeHaVIO4 originates from the presence of partially filled 4f orbitals of cerium atoms, which was confirmed by density functional theory (DFT) calculations. The moderate bandgaps make CeHaVIO4 suitable for infrared nonlinear optical (IR NLO) applications. CeBrMoO4 and CeBrWO4 exhibit moderate SHG responses of 0.58× AGS and 0.46× AGS, respectively, and are both type-I phase-matching materials. Moderate SHG response, easy growth of crystals, high ambient stability, and type-I phase-matching behavior make CeBrMoO4 and CeBrWO4 great materials for IR NLO applications. CeHaVIO4 films also exhibited good photocurrent response upon light radiation. This work demonstrates the rich structural chemistry of the REHaVIO4 (RE = Y, La-Lu; Ha = Cl, Br; VI = Mo, W) family and the potential presence of more multifunctional materials.

Polymer-Derived Carbon Nanofiber and Its Photocurrent-Switching Responses of Carbon Nanofiber/Cu Nanocomposite in Wide Ranges of Excited Light Wavelength.

Transformation into electric or photoelectric functional composite from non-conjugated polymers is a great challenge due to the presence of a large number of locative states. In this paper, carbon nanofiber was synthesized via hydrothermal carbonization utilizing carboxymethyl cellulose as a precursor, and the carbon nanofiber/Cu nanocomposite was constructed for defect passivation. The results indicated that the resulting nanocomposites exhibited good absorbance in visible light range and NIR (near-infrared). The photoconductive responses to typical weak visible light (650 nm et al.) and NIR (808, 980, and 1064 nm) were studied based on Au gap electrodes on flexible polymer substrates. The results exhibited that the nanocomposite's solid thick film showed photocurrent-switching behaviors to visible light and NIR, the switch-ratio was depending on the wavelengths and power of incident lights. The positive and negative photoconductance responses phenomenon was observed in different compositions and changing excited wavelengths. Their photophysical mechanisms were discussed. This illustrated that the nanocomposites easily produce free electrons and holes via low power of incident light. Free electrons and holes could be utilized for different purposes in multi-disciplinary fields. It would be a potential application in broadband flexible photodetectors, artificial vision, simulating retina, and bio-imaging from visible light to NIR. This is a low-cost and green approach to obtain nanocomposite exhibiting good photocurrent response from the visible range to NIR.

Ultrathin mesoporous BiOCl nanosheets-mediated liposomes for photoelectrochemical immunoassay with in-situ signal amplification

Designing new biochemical sensors and achieving selectivity and high-sensitivity analysis is one of main research directions for immunoassays. Herein, a liposome-amplification photoelectrochemical (PEC) immunoassay was developed using ultrathin mesoporous bismuth chloride oxide nanosheets (BiOCl MSCN) for the highly selective and sensitive detection of carcinoembryonic antigen (CEA). Based on good photocurrent response of BiOCl MSCN toward dopamine, a liposome-conjugated secondary antibody loaded with dopamine was added for specific recognition in the presence of CEA. After the lysis treatment, the liberated dopamine was injected into the three-electrode electrolytic cell to enhance the photocurrent of BiOCl MSCN. Under the optimized conditions, the constructed liposome-mediated PEC immunoassay showed high sensitivity against CEA, with a dynamic response in the linear range of 0.05 ng mL−1 to 100 ng mL−1 and a detection limit of 35 pg mL−1. The present study proposes a new approach to the liposome-mediated PEC immunoassay constructed on ultrathin mesoporous BiOCl nanosheets, which can be used to target further the study of the sensing mechanism.

Y2O3 electrodeposited TiO2 nanotube arrays as photoanode for enhanced photoelectrochemical water splitting

Y2O3 deposited TiO2 nanotubes (Y-TNTs) are investigated as photoanodes for efficient photoelectrochemical water splitting. Y2O3 is electrodeposited on TiO2 nanotubes for 5–15 min. The physicochemical and optical properties of Y-TNTs reveal that Y2O3 anchored on the TNTs enhances the visible light absorption. The Y-TNTs show good photocurrent response compared to pristine TNTs. Y2O3 deposition for 10 min on TNTs produces highest photocurrent of 609 μA cm−2 at 1.23 VRHE. Presence of Y2O3 increases the lifetime of the charge carriers as revealed by the Nyquist plot analysis and Mott-Schottky analysis. Y-TNTs-10 min sample shows 2.75 times higher photoconversion efficiency compared to pristine TNTs. Computational analysis shows that Y–TiO2 has negative free energy of adsorption for OER intermediates as compared to bare TiO2 which has positive values. The rare earth metal electrodeposition on TiO2 nanotubes is another approach to improve the photoelectrochemical water splitting activity without distorting the nanotube structure.

High-entropy effect with hollow (ZnCdFeMnCu)xS nanocubes for photoelectrochemical immunoassay

High entropy (HE) compounds with chemically disordered multi-cation structures have become a hot research topic because of their fascinating “cocktail effect”. However, high entropy effect with the efficient photoelectric response has not been reported for photoelectrochemical (PEC) immunoassays. Herein, an innovative PEC immunoassay for the sensitive detection of prostate-specific antigen (PSA) was ingeniously constructed using hollow nanocubic (ZnCdFeMnCu)xS photoactive matrices with high entropic effect via the cation exchange. Initially, a sandwich-type immunoreaction has behaved using dopamine-loaded liposome labeled with anti-PSA secondary antibodies. In the presence of PSA, addition of Triton X-100 caused the liposomal cleavage to release dopamine, which was then detected as a reduced photocurrent on (ZnCdFeMnCu)xS-based photoelectrode. Under optimal condition, the PEC immunoassay showed good photocurrent responses toward target PSA with the dynamic linear range of 0.1–50 ng mL−1 with a limit of detection of 34.1 pg mL−1. Significantly, this system can provide a new platform for the development of PEC immunoassays by coupling with high-entropy photoactive materials.

Enzyme-catalyzed high-performing reaction with in-situ amplified photocurrent on carbon-functionalized inorganic photoanode for immunosensing

An enzyme-catalyzed high-performing reaction with in-situ amplified photocurrent was innovatively designed for the quantitative screening of carcinoembryonic antigen (CEA) in biological fluids by coupling with carbon-functionalized inorganic photoanode. A split-type photoelectrochemical (PEC) immunoassay was initially executed with horseradish peroxidase (HRP)-labeled secondary antibody on the capture antibody-coated microtiter. Then, the photocurrent of carbon-functionalized inorganic photoanode were improved through enzymatic insoluble product. Experimental results revealed that introduction of the outer carbon layer on the inorganic photoactive materials caused the amplifying photocurrent because of the improving light harvesting and separation of photo-generated e-/h+ pairs. Under optimum conditions, the split-type photoelectrochemical immunosensing platform displayed good photocurrent responses within the dynamic range of 0.01 – 80 ng mL-1 CEA, and allowed the detection of CEA as low as a concentration of 3.6 pg mL-1 at the 3Sblank level. The strong attachment of antibodies onto nano label and high-performing photoanode resulted in a good repeatability and intermediate precision down to 9.83%. No significant differences at the 0.05 significance level were encountered in the analysis of six human serum specimens between the developed PEC immunoassay and the commercially available CEA ELISA kits.

A digital multimeter-based portable photoelectrochemical immunoassay for the detection of cardiac troponin I with enzymatic biocatalytic precipitation.

Early diagnosis of acute myocardial infarction (AMI) can significantly reduce mortality, which can be achieved by the highly sensitive detection of AMI-specific cardiac troponin I (cTnI) biomarkers. Herein a highly sensitive and portable photoelectrochemical (PEC) immunoassay for the detection of cTnI was innovatively fabricated based on an efficient photocurrent response of Cu2O coupling with a split-type enzymatic biocatalytic precipitation reaction with a digital multimeter readout. Initially, Cu2O cubic nanomaterials with a good photocurrent response were obtained by facile green room temperature synthesis and dropped on fluorine-doped tin oxide (FTO) plates as photoactive materials (Cu2O/FTO). In the presence of target cTnI, horseradish peroxidase (HRP) on the detection antibody catalyzes the substrate 4-chloro1-naphthol (4-CN) to produce insoluble precipitates of benzo-4-chlorohexadienone (4-CD) on Cu2O/FTO with the assistance of H2O2, resulting in a decrease in the photocurrent of the Cu2O/FTO electrode. To make the whole inspection process more concise and efficient, we used a flashlight and a digital multimeter as the excitation light source and reading device for the PEC sensing system, respectively. Under the optimal conditions of immunoreaction time, pH, and loading, the photocurrent of Cu2O/FTO decreased with increasing target cTnI concentration with a limit of detection (LOD) of 4.7 pg mL-1 in the operating range of 0.01-10 ng mL-1. It is of interest that the developed portable PEC immunoassay is also capable of detecting cTnI in human serum samples with acceptable accuracy compared to the reference cTnI enzyme-linked immunosorbent assay (ELISA) method while maintaining portability and sensitivity.

Photoelectrochemical immunoassay for thyroglobulin on nanogold-functionalized BiVO4 photoanode coupling with enzymatic biocatalytic precipitation

Methods derived from photoelectrochemical (PEC) have been constructed for immunoassays, but most involve the split-type immunoreaction modes, and thus easily cause unpredictable intermediate precision. Herein, we innovatively designed an integrated PEC immunosensing platform for the quantitative monitoring of thyroglobulin (TG) on the gold nanoparticles (AuNPs)-functionalized BiVO4 photoanode coupling with enzymatic biocatalytic precipitation (EBCP). This sensing system could simultaneously implement the immunoreaction and photocurrent measurement. Anti-TG capture antibodies were modified onto AuNPs-decorated BiVO4 photoelectrode. A sandwich-type immunoreaction was carried out in the presence of target TG using horseradish peroxidase (HRP)-conjugated anti-TG detection antibody. The carried HRP molecules catalyzed 4-chloro-1-naphthol (4-CN) to generate an insoluble benzo-4-chlorohexadienone product on the photoanode in the presence of peroxide hydrogen, thereby decreasing the photocurrent. Under optimal conditions, the PEC immunosensors gave good photocurrent responses toward target TG within the dynamic range of 0.01–10 ng mL−1 at a detection limit of 7.6 pg mL−1. Good repeatability and precision, high specificity and acceptable storage stability were acquired during the measurement. No significant differences were encountered for screening 15 human serum specimens between the developed PEC immunoassay and commercially available enzyme-linked immunosorbent assay (ELISA) method for the detection of target TG. Significantly, PEC immunosensing system offers promise for simple and cost-effective analysis of disease-related biomarkers.

Peroxymonosulfate assisted photoelectrocatalytic degradation of pharmaceuticals at a FTO-Bi2WO6 electrode: Mechanism and kinetics studies

Herein, a sulphate enhanced photoelectrochemical degradation method using peroxymonosulfate (PEC/PMS) and FTO-Bi2WO6 as photoanode is reported. The FTO-Bi2WO6 electrode was fabricated through electrodeposition and calcination route. The FTO-Bi2WO6 produced a good photocurrent response of up to 6.62 μAcm−2 with an applied potential of 1.5 V (vs Ag/AgCl). When the electrode was applied for PEC/PMS degradation of pharmaceuticals, 98%, 83% and 79% removal was recorded for sulfamethoxazole, diclofenac chloride and tetracycline, respectively within 90 min with a bias potential of 1.0 V and 3 mM PMS. Hence, the PEC/PMS system with FTO-Bi2WO6 photoanode is suitable for the removal of pharmaceuticals in wastewater.

A Photoelectrochemical Sensor for Firstly the Detection of Amlodipine Besylate Based on an MnC4Pc Coated ZnO Composite Materials

AbstractIn this study, tetracarboxylic manganese phthalocyanine coated nano‐zinc oxide (MnC4Pc‐ZnO) composite material was prepared by in‐situ growth method and modified with indium tin oxide (ITO) glass electrode to construct a photoelectrochemical (PEC) sensor. A PEC sensor for the determination of amlodipine besylate (AB) was developed for the first time based on the principle of precipitation reaction between heavy metal ions and dihydropyridine and the recombination suppression effect of the material. The morphology and optical properties of the MnC4Pc‐ZnO composites were characterized by scanning electron microscopy (SEM) and ultraviolet‐visible diffuse reflectance spectroscopy (UV‐vis DRS). Chronoamperometry (i‐t) and electrochemical impedance spectroscopy (EIS) were used to study the PEC behavior of ITO electrodes modified by MnC4Pc‐ZnO composite material. The study found that the MnC4Pc‐ZnO composite material has a good photocurrent response to AB, and there was a good linear relationship between the concentration range of 75 nM‐250 μM, the linear equation was I(μA)=−5.2×10−8×lgC+3.2×10−8 (r=0.9947), a limit of detection (LOD) of 20 nM. In addition, MnC4Pc‐ZnO/ITO also has good selectivity and stability. The PEC sensor detects amlodipine besylate tablets, amlodipine besylate dispersible tablets, and biological samples, with standard addition recovery rates of 96.11 % and 103.96 %, respectively. The determination result has good accuracy, and the PEC sensor provides a new method for detecting AB.

Turning on High‐Sensitive Organic Electrochemical Transistor‐Based Photoelectrochemical‐Type Sensor over Modulation of Fe‐MOF by PEDOT

AbstractLow‐gate voltages can make large modulations in the drain current. Accordingly, organic electrochemical transistors (OECTs) have attracted considerable interest as amplifying transducers. The use of OECTs in combination with electrochemical analysis promises to promote sensing performance. Herein, an OECT‐based photoelectrochemical‐type (OECT‐PEC) sensor is constructed based on the photo‐induced potential generating variation in the drain current. The as‐constructed OECT‐PEC sensor has high sensitivity because the device incorporated a sensor and an amplifier, providing the benefits of a PEC sensor and an OECT. In addition to the advantages of excellent signal amplification and ease of miniaturization, background signals are also effectively reduced, and possible interferences from electroactive substances are avoided due to the separation of light excitation and the electric output. The OECT‐PEC sensor integrates poly(3,4‐ethylenedioxythiophene) (PEDOT)‐modulated Fe‐metal organic framework (Fe‐MOF) nanocomposites as the photo‐active gating material and poly(3,4‐ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) as the channel material which exhibits a good photocurrent response from the gate electrode and a corresponding 100‐fold expansion channel response. With aptamer as the recognition element, a sensitive OECT‐PEC biosensor is constructed to detect the organophosphorus pesticide malathion. It is found to exhibit a good linear range, a low detection limit, and better sensitivity than the traditional PEC method.

Membraneless Photocatalytic Fuel Cell with Double Photoelectrodes for Simultaneous Electricity Generation and Pollutant Degradation

Environmental pollution and new energy development have become topics of increasing concern. Herein, a visible-light-driven photocatalytic fuel cell (PFC) with double photoelectrodes was constructed for simultaneous electricity generation and pollutant degradation, in which graphitic carbon nitride (g-C3N4) generated on W/WO3 nanorod arrays (W/WNR/g-C3N4) was used as the photoanode and Fe3+-doped CuBi2O4 thin film on indium tin oxide (ITO) conductive glass (ITO/CBFeO) was used as the photocathode. The experimental results showed that the WO3/g-C3N4 Z-scheme structure and one-dimensional WNR rod-like structure could effectively suppress the recombination of photogenerated charge carriers and enable W/WNR/g-C3N4 to present a good photocurrent response under visible light irradiation. The Fermi level mismatch between the W/WNR/g-C3N4 photoanode and ITO/CBFeO photocathode could improve the transfer of photogenerated electrons from the photoanode to the photocathode across the external circuit, enabling the constructed PFC to afford high electricity output and good efficiency for pollutant degradation. The short-circuit current density and maximum power density could reach 620 μA cm−2 and 110 μW cm−2, respectively, while the degradation ratio of oxytetracycline reached 97.6% in 90 min. Therefore, the proposed PFC system provides a new way to generate electric energy and degrade pollutants simultaneously.

Fabrication of Sb2S3 Thin Films by Low-Temperature Plasma-Sulfurizing Metallic Sb Layers

In this work, antimony sulfide (Sb2S3) thin films were prepared by low-temperature plasma (about 190 °C) sulfidation of antimony metal layers, and the sulfidation mechanism was investigated. Solid sulfur powder was used as the sulfur source, and the reaction process did not exhaust toxic gases. The relevant process parameters, including the reaction pressure, radio frequency (RF) power, and sulfurization time, were also optimized. Under conditions of an RF power of 180 W (approximately 190 °C), a curing time of 60 min, and a working pressure of 30 Pa, we prepared a smooth, pinhole-free, (211) preferentially oriented Sb2S3 thin film. The film obtained good photocurrent response and a suitable band gap of 1.74 eV. The properties and structures of the Sb2S3 thin film were characterized by optical emission spectroscopy, high-resolution scanning electron microscopy, energy-dispersive spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and UV and Raman spectroscopies.

Double ion-exchange reaction-based photoelectrochemical immunoassay for sensitive detection of prostate-specific antigen

This work developed a double ion-exchange reaction-based photoelectrochemical (PEC) immunoassay with the split-type detection mode for sensitive detection of prostate-specific antigen (PSA, used as a model). The nanocomposite of cadmium sulfide and nickel sulfide (CdS@NiS nanocomposite), as the photoactive material, was rapidly synthesized by two-step hydrothermal treatment. In the presence of target PSA, the cupric oxide nanoparticle (CuO NP) labeled detection antibody was introduced into the detection system by sandwich immunoreaction and the copper (Cu2+) ions was released from CuO nanoparticles by acid to participate in double ion-exchange reaction. The double ion-exchange reaction on the photoelectric sensing interface between Cu2+ and CdS@NiS nanocomposites formed the weak photoactive material CuxS (x = 1, 2) to reduce the photocurrent. Under optimal conditions, the double ion-exchange reaction-based PEC immunoassay exhibited good photocurrent responses toward target PSA within the dynamic working range from 0.01 ng mL−1 to 50 ng mL−1 at a low limit of detection (LOD) of 2.9 pg mL−1. Besides, our work could achieve good reproducibility and high specificity under the split-type detection mode. Compared with human PSA ELISA kit, the accuracy obtained by our strategy was satisfactory. Importantly, this Cu2+-activated double ion-exchange reaction-based PEC immunoassay provides a promising platform for the detection of biomarkers.

Actuating photoelectrochemical sensing sensitivity coupling core-core-shell Fe3O4@C@TiO2 with molecularly imprinted polypyrrole

Magnetic photocatalyst coupling with molecular imprinting technique is an efficient method for the specific photodegrade organic pollutants. Herein, this method is applied to fabricate a photoelectrochemical sensing platform for bisphenol A (BPA) detection based on electro-polymerization of molecularly imprinting pyrrole (MI-PPy) on the core-shell magnetic nanoparticles, Fe3O4@C@TiO2, which is magnetically adsorbed on magnetic glassy carbon electrode (MGCE). The MI-PPy layer not only provides molecular recognition capabilities for selective absorption of BPA, but also improves the photoelectrochemical behavior because of the heterostructure of TiO2/PPy that accelerated photoelectron transfer, which is a strategy to kill two birds with one stone. Therefore, the fabricated sensor shows a high sensitivity of 3.74 μA μM−1 cm−2 and excellent selectivity for BPA detection. Meanwhile, the electrode could be renewed by the UV irradiation and thus exhibits good recyclability and long-term stability. Under optimum conditions, the as-prepared electrode exhibited good photocurrent response for the detection of BPA, and allowed detection of BPA at a concentration as low as 0.03 μM. The favorable performance for BPA detection in real samples is able to extend more application of photoelectrochemical sensors for sensitive and long-term monitoring of environmental pollutants.