Cadmium Sulfide Nanowires Research Articles

Novel Phenothiazine and Coumarin based Sensitizers: Design, Synthesis and Photoelectrochemical Application by Anchoring on CdS Nanowires

Novel metal-free organic dyes (E)-2-cyano-3-(10-(prop-2-yn-1-yl)-10H-phenothiazin-3-yl)acrylic acid (PPC) and (E)-2-cyano-3-(10-((1-((7-methyl-2-oxo-2H-chromen-4-yl)methyl)-1H-1,2,3-triazol-4-yl)methyl)-4a,10a-dihydro-10H-phenothiazin-3-yl)acrylic acid (PCTC) was synthesized and then anchored to 1D cadmium sulfide nanowires (1D CdS NWs) for application in photoelectrochemical dye-sensitized solar cell (DSSC). The 1D CdS nanowires were interconnected into a nanonetwork using solution chemistry in a straightforward and efficient manner. The UV-visible spectroscopy, cyclic voltammetry and density functional theory (DFT) were effectively employed to analyze the characteristics of PPC and PCTC. The sensitizer-anchored CdS nanowires have a broader range of light absorption in the UV-visible spectrum compared to bare CdS nanowires. The complete device has the assembly FTO, compact CdS, CdS nanowires, synthesized dye and counter electrode. In photovoltaic assessment, the PCTC and PPC devices yield 3.19 and 3.04 times, respectively, more efficiency than naked CdS nanowires under conventional sunshine illumination (100 mW/cm2, AM 1.5G). The obtained results provide strong evidence supporting the presence of rising external quantum efficiency (EQE) and show a high level of consistency with the optical tests.

Spatial orientation of CdS nanowiresbased on second harmonic generation spectroscopy and microscopic Imaging

The second harmonic generation (SHG), as a nonlinear optical effect, has a wide range of applications in obtaining information such as material composition, structure, and properties due to its good polarization sensitivity. Although SHG spectroscopy or SHG microscopy has been used to explore the precise positioning or tracking of nanowires, there are few reports on the combination of SHG spectroscopy and SHG microscopy to study the structure of nanomaterials and the spatial orientation of crystal axes. In this work, we investigate the spatial orientation and crystal axis orientation of cadmium sulfide (CdS) nanowires by combining SHG spectroscopy and microscopic imaging. Firstly, we experimentally and theoretically study the spectral intensity of the SHG of CdS nanowires with the polarization direction of the incident light based on the all-optical analysis method proposed by the predecessors. We also analyze the influence of the azimuth angle of the crystal axis γ, ω and φ on the pattern of the SHG of CdS nanowires in detail. Secondly, through the mutual verification of theoretical calculations and experimental measurement results, we successfully determine the three axial orientations of a single CdS nanowire. Finally, we also investigate the spatial orientation of a single CdS nanowire by using the polarization-dependent SHG microscopic imaging method. It is shown that different parts of the CdS nanowire have different SHG responses when the polarization is changed. These results provide a new idea and an important reference for studying the application of SHG spectroscopy and microscopic imaging in the research of high-precision spatial positioning of nanomaterials. This study provides important enlightenment for realizing the potential applications of nanomaterials in biomedicine.

Novel 1,2,4-triazole sensitizers using N-arylsydnone as Synthon: Synthesis, Spectral, electrochemical, DFT and photovoltaic properties

Two novel 1,2,4-triazolone derivatized triphenylamine (TPA) and phenothiazine (PTZ) based metal-free organic dyes have been designed, synthesized and anchored on 1D CdS nanowires to serve as photoelectrochemical (PEC) dye-sensitized solar cells (DSSCs). Solution chemistry is employed simply and efficiently to link cadmium sulfide nanowires (CdS NWs) into a nano-network. Optical, electrochemical and density functional theory (DFT) have been well utilized to examine the properties of synthesized dyes (TPA and PTZ). In the visible range, sensitizer-anchored CdS NWs exhibit a wider region of light absorption referenced to naked CdS NWs. Comprehensive photovoltaic assessment showed that TPA and PTZ devices respectively showed IPCE 3.02 and 3.13 times more efficient than bare CdS NWs under standard sunlight (100 mW/cm2, AM 1.5G) illumination. The collected findings offer solid evidence for the existence of increasing external quantum efficiency (EQE) and exhibit good agreement with the optical experiments.

Design of Metal Free Fluorescent Pyridine Dyes Anchored on Cadmium Sulfide Nanowires: Optical, Electrochemical and Photovoltaic Applications.

Through a facile two-step synthetic procedure, three metal-free organic dyes having D-π-A kind of structure, belonging to chalcone family have been designed, produced and anchored on one dimensional cadmium sulfide nanowires (1D CdS NWs) to serve as a light energy harvester through dye-sensitized solar cells (DSSC) assembly. In order to anchor dye on CdS NWs nano-network, solution chemistry has been used in an easy and effective manner. The sensitizing capability of synthesized materials has been evaluated using optical and electrochemical studies, density functional theory (DFT) simulations, and photovoltaic performances. In line with a detailed analysis of fabricated Dye sensitized solar cells containing T4PC a photovoltaic efficiency yields 4.35 times (0.487%) more than that of bare CdS NWs (0.112%), while the other devices having T3PC and T2PC have shown 3.0 (0.338%) and 2.40 (0.273%) times greater photovoltaic efficiencies, respectively under standard light illumination. The obtained results offer solid evidence in favour of boosting external quantum efficiency (EQE) and reflect good agreement with the optical studies.

Highly Selective Photocatalytic Conversion of 5‐Hydroxymethyl‐2‐furfural to 2,5‐Diformylfuran over Gold Ion Exchanged Cadmium Sulfide Nanowire

Abstract5‐Hydroxymethyl furfural (HMF) obtained from biomass can be converted to 2,5‐diformylfuran (DFF), a valuable chemical intermediate. However, the typical HMF oxidation process requires energy consumption such as high temperature and oxygen pressure. Herein, Au2S decorated CdS nanowires (denoted as Au2S@CdS NWs) are fabricated by a simple ion exchange method and applied as a heterostructure photocatalyst system for HMF oxidation under mild conditions. Under visible light irradiation, the photocatalytic performance of Au2S@CdS NWs is significantly enhanced compared with pristine CdS NWs, in which Au2S (0.25%)@CdS NWs achieve the high DFF yield (≈95%) for 4 h reaction time. This result means that the heterogeneous interface formed between CdS NWs and Au2S promotes the separation efficiency of photogenerated charges, which leads to high catalytic activity. Moreover, Au2S (0.25%)@CdS NWs work well for HMF conversion to DFF under anaerobic and aerobic conditions. Control experiments and characterization are conducted to investigate each reaction mechanism. Consequently, it is found that the photogenerated hole directly oxidizes HMF to DFF under anaerobic conditions and the1O2produced from oxygen is the active species for HMF conversion to DFF under aerobic conditions.

Facile three-step strategy to design CdS@Bi2Se3 core-shell nanostructure: An efficient electrode for supercapacitor application

In this study, we utilized a successive ionic layer adsorption and reaction (SILAR) route to attach bismuth selenide (Bi2Se3) nanoparticles on one dimensional (1D) cadmium sulfide nanowires (CdS NWs) at ambient temperature (27 °C) to design CdS@Bi2Se3 core-shell nanostructure towards active electrode for supercapacitor application. To verify and explore the retrieved surface configuration, structural, elemental, compositional, and surface morphological investigations were performed. The designed CdS@Bi2Se3 core-shell nanostructure not only offers the tremendous number of active areas, but also a continuous and quick one directional electron transport channels, demonstrating noticeable electrochemical performance with specific capacitance of 198 F g−1 (aerial capacitance 59.5 mF/cm2) with 80% cyclic retention @ 2000 cycles. Superior electrochemical activity was enhanced through the mutualistic involvement of Na+ ion insertion/extraction via non-stoichiometric bismuth selenide, which was well supported through electrochemical impedance (EIS) studies.

Tunable Selectivity of Photocatalytic Benzyl Alcohol Transformation over Ag-Ion-Exchanged CdS Nanowires

Existing methods for the photocatalytic transformation of aromatic alcohols to value-added products via C–C cross-coupling are inefficient and insufficiently selective. Herein, a series of cadmium sulfide nanowires (CdS NWs) loaded with Ag2S (denoted as Ag2S@CdS NWs) are constructed via a simple Ag+ exchange protocol for the photocatalytic transformation of benzyl alcohol. We successfully demonstrated that the selectivity toward specific products in the photocatalytic transformation of benzyl alcohol over Ag+-exchanged CdS NWs is controlled by varying the amount of exchanged Ag+ ions. Notably, the product of the photocatalytic reaction was dependent on the amount of Ag+ ions exchanged: with a Ag+ exchange of <5 mol %, the C–C coupling product was obtained with >90% selectivity and >95% transformation yield owing to photoinduced electron transfer from the conduction band of CdS to Ag2S. Conversely, with a Ag+ exchange of >7 mol %, a cocatalyst in which Ag2S and Ag are mixed was produced, and benzaldehyde was obtained with >90% selectivity and >90% transformation yield because of photoinduced hole transfer from the valence band of CdS to Ag2S/Ag. This study proves that Ag2S@CdS NWs can be used as a basis for the development of heterojunction photocatalysts for the conversion of aromatic alcohols into value-added products via C–C cross-coupling reactions or photooxidation toward aromatic aldehyde.

C3N4 and C3N5 Nanosheets As Passivation Layers and Carrier Extractors for Inorganic Semiconductor Nanowires and Quantum Dots

Inorganic semiconductor nanowires and quantum dots made of chalcogenides, III-V semiconductors and halide perovskites offer exciting potential for optoelectronic devices. The orthogonalization possible in nanowires between the normally competing processes of charge generation and charge separation have been used to project very high operating performance exceeding that of thin films and single crystals in light harvesting devices such as solar cells, photodetectors, photocatalysts and photoelectrolyzers. Likewise, inorganic quantum dots with size-tunable absorption and emission spectra are excellent candidates for light emitting devices as well as light harvesting devices. However, the practical performance of inorganic nanowire based optoelectronic devices has significantly lagged theoretical predictions. A major reason for the discrepancy between theory and experiment is the presence of surface traps and defects in nanowires and quantum dots, which exhibit a large surface area to volume ratio. Several chemical treatments and annealing regimens have been employed to heal surface defects in nanowires and quantum dots. One popular strategy involves wrapping nanowires and/or quantum dots with a thin coating of a molecular monolayer (e.g. alkanethiols) or an atomic layer deposited conformal oxide. While such core-shell architectures are frequently effective in reducing surface defects, the surface passivation is invariably accompanied by a deterioration in optoelectronic properties due to the difficulty experienced by charge carriers in tunneling through the thin shell layer. The resulting trade-off between surface passivation and carrier extraction limits performance improvements in light harvesting devices. Thus there is a strong need for passivating layers that do not negatively impact carrier extraction.Herein, we show that graphitic carbon nitride coatings are highly effective in passivating the surfaces of inorganic nanowires and quantum dots while preserving excellent carrier transport and extraction. Three illustrative examples are provided together with in-depth spectroscopic and electrical characterization:(1) Cesium lead bromide (CsPbBr3) quantum dots passivated by g-C3N4 nanosheets and performing spectacularly as CO2 photoreduction catalysts and water-splitting photoanodes(2) The double helical ternary semiconductor SnIP passivated by g-C3N4 nanosheets which experienced a remarkable improvement in photoelectrochemical performance(3) Cadmium sulfide (CdS) nanowires passivated by C3N5 nanosheets resulting in a superior photocatalytic performance

NO2 sensing with CdS nanowires at room temperature under green light illumination

Detection of ppb-level NO2 gas under atmosphere is urgent to meet the requirements of the rapidly developing internet of things. Compared with traditional sensing methods, light illumination has been considered as a key approach for excellent gas sensor performance under moderate conditions. Herein, we developed a green-light-assisted gas sensor based on cadmium sulfide nanowires (CdS NWs) that has good NO2 sensing capability at ambient temperature. The response values of NO2 are 236% and 11% to 10 ppm and 12.5 ppb, respectively. Furthermore, the CdS NWs sensor has a high selectivity for NO2 over a variety of interference gases, as well as good stability. The cleaning light activation and the sulfur vacancy-trapped charge behavior of CdS NWs are observed, which suggest a light-assisted sensing mechanism. These results suggest that light-induced charge separation behavior might significantly improve gas-sensing characteristics.

Photoelectron Transfer Mediated by the Interfacial Electron Effects for Boosting Visible-Light-Driven CO2 Reduction

Imine-linked covalent organic frameworks (COFs) are popular candidates for photocatalytic CO2 reduction, but high polarization of the imine bond is less efficient for π-electron delocalization between the linked building units, leading to low intramolecular electron transfer and poor photocatalytic efficiency. Herein, we present a structural and electronic engineering strategy through integrating the imine-linked COF consisting of Zn–porphyrin and Co–bipyridyl units with cadmium sulfide (CdS) nanowires to form a CdS@COF core–shell structure. The experimental and theoretical results have validated that CdS serves as the electron transfer channel through the interfacial electron effects, which induces photoelectron transfer from Zn–porphyrin to CdS and subsequent injection into Co–bipyridyl units for CO2 reduction. The as-prepared CdS@COF generates 4057 μmol g–1 CO in 8 h under visible-light irradiation, which is considerably higher than those of its neat CdS and imine-linked COF counterparts. This work provides protocols to tackle intramolecular charge transfer across polar linkages between photosensitizers and active sites for solar-to-chemical energy conversion.

Passive near-field optical scanning imaging based on semiconductor nanowire/tapered microfiber probe

&lt;sec&gt;In this paper, we propose a passive near-field scanning imaging system by using the structure of cadmium sulfide (CdS) nanowire/tapered microfiber probe, which combines the near-field scanning structure and the nanowire/microfiber coupling technology. In the passive near-field scanning imaging system, a passive nanoprobe is adopted to detect the intensity change of the reflected light field on the sample surface, which not only retains the advantage of the nanoprobe for the strong restriction of the reflected light on the sample surface, but also reduces the interference of strong excitation light during detection. Through the high efficiently evanescent field coupling between the CdS nanowire and the tapered microfiber, the collected light signal is transmitted to the photodetector in the far field, and finally the imaging of the target sample morphology can be realized.&lt;/sec&gt;&lt;sec&gt;At first, the light field model of the nanowire/tapered microfiber probe structure is verified by the finite element analysis method. The calculated collection efficiency from the sample to the probe is about 4.65‰ and the transmission efficiency from the nanowire to the tapered microfiber is about 74.47%. The collection efficiency is improved by an order of magnitude compared with traditional metal-coated near-field probe. In the experiments, a scanning step of 20 nm and a probe-sample distance of 230 nm are selected. The nanowire/tapered microfiber probe and traditional tapered fiber probe are both used to measure the widths of different CdSe nanoribbons samples, and the atomic force microscopy measurement is used as the benchmark to calculate their measurement error, which is increased about 3 times. By changing the angle &lt;i&gt;θ&lt;/i&gt; between the probe and the sample, it is found that the resolution obtained using the designed nanowire/microfiber probe is always higher than only using the tapered microfiber probe. Comparing with the tapered microfiber probe scheme, the measurement error is reduced to a value less than 7.2%.&lt;/sec&gt;&lt;sec&gt;In addition, compared with the active luminescence probe scheme, this passive near-field scanning scheme reduces the preparation complexity of the optical probe and the detection structure complexity of the optical system. The large microscopic illumination area can avoid the influence of the small laser spot size on imaging, and the imaging range is determined only by the travel distance of the linear stage. Therefore, our work may provide an attractive approach for developing new near-field scanning microscopy systems in the future.&lt;/sec&gt;

Orientation and ellipticity dependence of high-order harmonic generation in nanowires

It has been predicted that high-order harmonic generation (HHG) in nanowires has the potential to scale up photon energy and harmonic yield. However, studies on HHG in nanowires are still theoretical and no relevant experimental results have been reported as yet. Our experimental observation of the high-order harmonic in cadmium sulfide nanowires (CdS NWs) excited by a mid-infrared laser is, to our knowledge, the first of such study, and it verifies some of the theoretical results. Our experimental results show that the observed harmonics are strongest when a pump laser is parallel to the nanowires. Therefore, the theoretical prediction that harmonics are strongest under the nanowires parallel to the laser field is confirmed experimentally, and this can be used to determine the orientation of the nanowire. In addition, harmonics are sensitive to the variation of pump light ellipticities. This orientation dependence opens new opportunities to access the ultrafast and strong-field physics of nanowires.

Strong coupling of a plasmonic nanoparticle to a semiconductor nanowire

Abstract By placing a single Au nanoparticle on the surface of a cadmium sulfide (CdS) nanowire, we demonstrate strong coupling of localized surface plasmon resonance (LSPR) modes in the nanoparticle and whispering gallery modes (WGMs) in the nanowire. For a 50-nm-diameter Au-nanosphere particle, strong coupling occurs when the nanowire diameter is between 300 and 600 nm, with a mode splitting up to 80 meV. Using a temperature-induced spectral shift of the resonance wavelength, we also observe the anticrossing behavior in the strongly coupled system. In addition, since the Au nanosphere has spherical symmetry, the supported LSPR mode can be selectively coupled with transverse electric (TE) and transverse magnetic (TM) WGMs in the nanowire. The ultracompact strong-coupling system shown here may provide a versatile platform for studying hybrid “photon–plasmon” nanolasers, nonlinear optical devices, and nanosensors.

Orbital-Angular-Momentum-Controlled Hybrid Nanowire Circuit.

Plasmonic nanostructures can enable compact multiplexing of the orbital angular momentum (OAM) of light; however, strong dissipation of the highly localized OAM-distinct plasmonic fields in the near-field region hinders on-chip OAM transmission and processing. Superior transmission efficiency is offered by semiconductor nanowires sustaining highly confined optical modes, but only the polarization degree of freedom has been utilized for their selective excitation. Here we demonstrate that incident OAM beams can selectively excite single-crystalline cadmium sulfide (CdS) nanowires through coupling OAM-distinct plasmonic fields into nanowire waveguides for long-distance transportation. This allows us to build an OAM-controlled hybrid nanowire circuit for optical logic operations including AND and OR gates. In addition, this circuit enables the on-chip photoluminescence readout of OAM-encrypted information. Our results open exciting new avenues not only for nanowire photonics to develop OAM-controlled optical switches, logic gates, and modulators but also for OAM photonics to build ultracompact photonic circuits for information processing.

Synthesis of metal free organic dyes: Experimental and theoretical approach to sensitize one-dimensional cadmium sulphide nanowires for solar cell application

Synthesis of metal-free organic dyes PDR and PDP based on the phenothiazine core unit have been attempted through solution chemistry approach and anchored on to one dimensional cadmium sulphide nanowires (CdS NWs) to be used as light harvesters in dye sensitized solar cell (DSSC) device application. Simple and cost effective solution chemistry approach leads to enable CdS NWs interconnected nano network. Synthesized dyes have been investigated through optical and electrochemical studies in addition to theoretical calculations using density functional theory (DFT). Dye anchored CdS films cover wider light absorption than bare CdS in the visible part of solar spectrum. The complete device configuration has been assembled as FTO/CdS compact/CdS NWs/Organic dye/electrolyte/Platinum electrode. PDR and PDP sensitized CdS NWs yield 0.24 and 0.28% efficiency which are 2.36 and 2.77 times as compared to bare CdS NWs (0.10%) with sun light of standard conditions of illuminations. External quantum efficiency enhancement is well supported with the obtained results and correlated well with the absorption studies. The present work successfully demonstrates the use of novel synthesized organic dyes as light harvesters.

Scaling-up photocatalytic activity of CdS from nanorods to nanowires for the MB degradation

The development of a scalable and facile method for the synthesis of visible light driven photocatalytic materials to degrade toxic organic dyes is highly challenging and essential. In this regards, cadmium sulfide (CdS) nanorods and nanowires with controlled aspect ratio, grain size, surface area, and bandgap were synthesized by a simple solvothermal method, and their photocatalytic performances were exploited for the photo-degradation of methylene blue (MB) under simulated solar light. Extensive structural characterizations to identify the origin of the activities were performed. The photocatalytic activity measurements showed that the degradation of MB was 94.41%, 97.24%, 97.88%, and 99.82% for CdS prepared by following four different synthesis routes and increasing trend showed a correlation with the nanostructure morphology changing from nanorod and nanowires with increasing aspect ratio. It has been found that CdS nanowires show more pronounced photocatalytic activity due to the efficient separation of photo-generated electron-hole pairs induced by increased the aspect ratio and higher active surface area.

Facile synthesis of Zn-doped CdS nanowires with efficient photocatalytic performance

ABSTRACT In this study, one-dimensional zinc (Zn)-doped cadmium sulphide (CdS) nanowires were synthesised by a solvothermal method. The Zn doping concentrations were varied from 1 to 5 mol% (Zn x Cd1− x S where x = 0.001, 0.003 and 0.005). As-prepared materials were characterised by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray (EDX) spectroscopy and UV–visible spectroscopy. Electrochemical impedance spectroscopy (EIS) was conducted to measure the charge transfer resistance. The photocatalytic performance of prepared materials was evaluated by the photodegradation of methylene blue (MB) dye. The result showed that 5% Zn-doped CdS is more photoactive as compared to other corresponding doped and undoped CdS. The increase in photocatalytic performance is due to improvement in the charge separation.

Hierarchically 1D CdS decorated on 2D perovskite-type La2Ti2O7 nanosheet hybrids with enhanced photocatalytic performance

In this paper, a heterojunction of hierarchically one-dimensional (1D) cadmium sulfide (CdS) nanowires decorated on the two-dimensional (2D) La2Ti2O7 (LTO) has been fabricated by a simple two-step hydrothermal process. The structure, morphology and surface chemical composition of CdS/LTO were studied by a variety of characterizations, in which the X-ray photoelectron spectroscopy (XPS) results showed a strong interaction between CdS and LTO through S–O bonds. The type II band alignment of CdS/LTO for favorable electron transfer from CdS to LTO and hole transfer from LTO to CdS was clarified by ultraviolet–visible (UV–Vis) diffuse reflectance spectroscopy and Mott–Schottky (M–S) plot measurements. In the absence of any co-catalyst, H2 production from water splitting and Rhodamine B (RhB) decomposition in aqueous solution were carried out to evaluate the photocatalytic activities, showing that the photocatalytic performance of CdS/LTO was superior to that of pure LTO and CdS under visible light and simulated sunlight. The optimal CdS content in the CdS/LTO system was determined to be 7.5 wt%. The present results show an effective pathway to design a 1D/2D heterojunction photocatalyst in the face of overwhelming problems of energy crisis and environmental pollution.

Enhanced photocatalytic hydrogen evolution using green carbon quantum dots modified 1-D CdS nanowires under visible light irradiation

Photoluminescent carbon quantum dots (CQD) have drawn intense attention due to its excellent optical properties, strong confinement effect, and good electrical conductivity. However, sustainable synthesis of CQD from green carbon sources and its application in water splitting has not been well explored. Herein, we synthesized CQD from orange peels and embedded them onto one-dimensional (1-D) cadmium sulfide (CdS) nanowires (average diameter 30 nm and length 2–4 µm) via a facile chemical adsorption method. The synthesized photocatalysts were thoroughly characterized using various spectroscopic, microscopic, diffraction, and photoelectrochemical techniques. The photocatalysts were tested for water-splitting reaction under visible light. The effect of mass fraction of CQD in CdS on water splitting performance has been investigated both in the presence and absence of sacrificial reagents. The reusability of the photocatalyst has also been tested. The optimal catalyst, 0.4CQD/CdS, exhibited the highest H2 production rate of 309 mmol g−1h−1 (apparent quantum yield of 32.6%) which is 1.5 times higher than that with bare CdS. The excellent photocatalytic performance of CQD/CdS was due to the existence of sulfur vacancies and the formation of cadmium oxide with effective charge transfer and separation. The higher photostability of CQD/CdS compared to that of CdS in three consecutive cycles can be attributed to suppression of photocorrosion of CdS in the presence of CQD.

An On-chip Chemiluminescent Immunoassay for Bacterial Detection using in Situ-synthesized Cadmium Sulfide Nanowires with Passivation Layers

The passivation layers of an in situ-synthesized cadmium sulfide (CdS) nanowire (NW) photosensor were prepared for two reasons: (1) to improve the physical stability of the NW on an interdigitated electrode and (2) to enhance the immobilization efficiency of proteins for the on-chip immunoassay. The passivation layer was estimated to have suitable optical properties, and the photoresponse of photosensor was increased after the formation of passivation layer. The immobilization efficiency of a parylene-H film through covalent bonding was compared with the immobilization of Z-domains through physical adsorption. Finally, on-chip chemiluminescent immunoassay of bacteria was carried out by immobilizing antibodies against Escherichia coli through Z-domains for the orientation control of antibodies. The limit of detection was determined to be less than 104E. coli/mL (n=3), and the sensitivity of bacterial detection was estimated to be 0.339 pA/E. coli/mL (n=3) with a linearity factor (R2) of 0.999. These results showed that the on-chip chemiluminescent immunoassay for bacterial detection could be performed using passivation layer coated CdS NW photosensor.