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. 2014 Mar 21;4:4426. doi: 10.1038/srep04426

Bismuthoxyiodide Nanoflakes/Titania Nanotubes Arrayed p-n Heterojunction and Its Application for Photoelectrochemical Bioanalysis

Wei-Wei Zhao 1, Zhao Liu 2, Shu Shan 1, Wen-Wen Zhang 2, Jing Wang 1, Zheng-Yuan Ma 1, Jing-Juan Xu 1,a, Hong-Yuan Chen 1,b
PMCID: PMC3961734  PMID: 24651880

Abstract

We have developed sensitive detection of cancer biomarker vascular endothelial growth factor (VEGF) using the p-n heterojunction comprised of p-type BiOI nanoflakes (NFs) array and n-type TiO2 nanotubes (NTs) array. Due to the unique arrayed structure and the synergy effect of photoelectrochemistry in the formed p-n junction, the synthesized configuration has superior excitation efficiency and thus excellent photoresponsibility. Then, the fabricated p-n heterojunction was integrated with an exquisite bioassay protocol for addressing VEGF using a sandwich immunoassay with glucosedehydrogenase (GDH) as the enzyme tags. Due to the excellent performance of BiOI NFs array/TiO2 NTs array and the ingenious signaling mechanism, the proposed system could achieve the sensitive and specific VEGF detection. This work not only presents a simple BiOI NFs array/TiO2 NTs array p-n heterojunction for general applications in the broad photochemistry areas, but also opens a different horizon for current development of advanced PEC biomolecular detection.

The newly emerged photoelectrochemical (PEC) bioanalysis has rapidly becoming a current research hotspot due to its desirable properties and attractive potential in future bioassay1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20. From the very beginning of such technique, the exploitation of various functional semiconductive materials and its utilization for advanced bioanalytical protocols has been a focus of substantial research since these efforts would probably underlie elegant routes for probing biological events. Of late, nafion-functionalized CdS–methyl viologen quantum dots (QDs) was equipped on ITO electrode for the ultrasensitive PEC detection of cysteine4. More recently, ZnO/ZIF-8 nanorods architecture was successfully synthesized and examined for selective PEC chemosensing9. Soon afterwards, IrO2−Hemin−TiO2 nanowire arrays was proposed for the sensitive PEC detection of glutathione10. Although these previous work have achieved remarkable results, the investigation on this field is still in its early stage due to the short development time and new versatile semiconductive electrode is yet of urgent need for application in advanced PEC biomolecular detection.

With unique photophysical features, semiconductor heterostructures have been a highly exploited subject in a plethora of areas21,22 including photocatalyst or solar cells. For example, CdS/Cu2S p–n junction nanowire was fabricated for efficient photovoltaic cells23. The CdS/CuGaSe2 p–n junction was successfully synthesized for stable PEC hydrogen evolution24. However, such p–n junction architecture has seldom been exploited for PEC bioanalysis application. Obviously, to develop new p–n junction with unique structure and/or enhanced properties would be desirable for application in future PEC analysis.

As known, numerous TiO2 nanostructures have long been used for bioanalysis purposes due to their good biocompatibility and chemical/thermal stability as well as environmental benignity. In particular, the TiO2 nanotubes (NTs), a well-known n-type semiconductor (with band gap of ~3.2 eV) with regular oriented structure and high surface area, has received much attention due to its outstanding merits in manifold fields including PEC detection. We previously had exploited CdS QDs/TiO2 NTs hybrid for PEC bioassay application17. BiOI is an attractive ternary p-type semiconductor with a narrow band gap (~1.8 eV) and strong absorption in the visible region (with absorption edge of ~680 nm) which currently begins its career in the field of photocatalysis25,26,27. In fact, comparing with other semiconductive materials, to date there is surprisingly little research on BiOI in spite of its interesting PEC properties28. So, of particular interest here is the possibility of developing a new BiOI/TiO2 p-n junction heterostructure and using as a versatile visible-light-active hybrid for biomolecular detection purposes. If possible, such hybrid is supposed to possess great advantages due to their synergic effect and harnessing this type material would in principle allow the operation of PEC detection with higher effiency, the success of which could provide great opportunities for further biosensing construction.

In this work, we for the first time fabricated a simple and versatile p-n heterojunction architecture comprised of BiOI crossed nanoflakes (NFs) array/TiO2 NTs array, which was then exploited for advanced PEC biomolecular detection toward vascular endothelial growth factor (VEGF), an important cancer biomarker for breast cancer, lung cancer, colorectal cancer, as well as rheumatoid arthritis. Structurally, as illustrated in Figure 1A, the synthesized hybrid was expected to function as a “light collector”, i.e., the p-type BiOI NFs array with large surface area could facilitate the efficient light harvesting while the n-type TiO2 NTs array would provide an effective directional pathway for rapid electron transportation. Significantly, the distinct photoelectrochemistry in the formed p-n junction would behave like a spontaneous “exciton pump” that additionally is advantageous for the resulting performance. As shown in Figure 1B, the BiOI NFs array/TiO2 NTs array was then used for VEGF detection by an ingenious PEC immunoassay protocol. In detail, after anchoring the first antibodies via the chitosan-glutaraldehyde (CS-G) bridging, an immunosandwich assembly was formed on the biofunctional electrode with glucosedehydrogenase (GDH) as the enzyme tags through the biotin-streptavidin (B-SA) affinity system (experimental details see the ESI). The subsequent reaction of the GDH with glucose substrate in the presence of its NAD+ cofactor would lead to the enzymatic product of NADH, which could neutralize the holes localized on p-type BiOI and hence boost charge separation and photocurrent generation. In such system, increased VEGF concentration leads to the enhanced GDH loading and thus promotes the NADH generation for improved photocurrent responding. Due to the excellent performance of BiOI NFs array/TiO2 NTs array and the exquisite signaling mechanism, the proposed system could achieve the sensitive and specific VEGF detection. To the best of our knowledge, both the fabricated BiOI NFs array/TiO2 NTs array structure and the proposed PEC bioanalytical strategy have never been reported.

Figure 1.

Figure 1

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(A) Schematic Illustration for fabricating crossed BiOI NFs/TiO2 NTs arrayed structure. (B) Schematic diagram of the immunoanalysis principle using the novel BiOI/TiO2 NTs arrayed p–n junction photoelectrode.

Results

Experimentally, to achieve the hierarchical structure of designed BiOI NFs array/TiO2 NTs array, successive ionic layer adsorption and reaction (SILAR) was used to build the BiOI array onto the TiO2 NTs fabricated by electrochemical anodization firstly. Such direct SILAR growth of BiOI flake membranes onto TiO2 NTs can be performed at room temperature, atmospheric pressure with good convenience and repeatability. Specifically, the self-organized TiO2 NTs were grown by anodization of Ti foils in a 0.5 wt% hydrofluoric acid solution at 20 V for 60 min. Thereafter, BiOI NFs were coated onto the TiO2 NTs by alternately immersing the latter into two different ionic precursor solutions containing Bi3+ and I− ions, respectively (experimental details see supporting information). Figure 2A shows a typical scanning electron microscopy (SEM) image of the as-obtained self-organized TiO2 NTs, which exhibited a one-dimensional (1D) perpendicularly aligned and highly ordered porous structure. A high-magnification SEM image further displayed that the average inner and outer pore diameter were ca. 100 and 140 nm, respectively. Figure 2B demonstrates the morphology of the three-dimensional (3D) crossed BiOI NFs on TiO2 NTs, it possessed unique layered structures (with lateral dimension in the micrometer size, height of several hundred nm and average thickness of ca. 10 nm, as shown in Figure 1B inset) with the internal static electric field perpendicular to each layer, which can induce the effective separation of photo-generated electron–hole pairs. Figure S1 and S2 provides insight into the effect that the SILAR cycles have on the location and growth density of crossed BiOI NFs on TiO2 NTs. X-ray photoelectron spectroscopy (XPS) was further performed to study the surface chemical compositions and oxidation states of BiOI NFs/TiO2 NTs. The obtained survey spectrum is depicted in Figure 2C, and the corresponding high-resolution XPS spectra of Bi 4f, O 1s and I 3d are illustrated and discussed with Figure S3. The phase structure of the sample was further identified by X-ray diffraction (XRD), as shown in Figure 2C inset, quantitative analysis of the pattern would index all the observed peaks to the TiO2 anatase phase (JCPDS file No: 21-1272, a = 3.7852 Å, c = 9.5139 Å, space group: I41/amd (141)), tetragonal structure of BiOI (JCPDS file No: 10-0445, a = 3.994 Å, c = 9.149 Å, space group: P4/nmm (1129)), and the Ti metal phase (JCPDS file No: 44-1294, a = 2.951 Å, c = 4.683 Å, space group: P63/mmc (194)), respectively, suggesting that no Bi and I related impurities exist in the BiOI/TiO2 NTs hybrid. Transient photocurrent responses of the samples were also investigated upon intermittent visible light irradiation of 470 nm with the results shown in Figure 2D. As shown in curve a, the Ti foil exhibited no photoresponse. In contrast to the weak response of bare TiO2 NTs (curve b), the absolute intensity (the illuminated current subtracts dark current) of such novel array-array heterostructure (curve c) enhanced greatly from 1.0 × 10−8 to 1.67 × 10−7 A, indicating the strong coupling effect between BiOI NFs and TiO2 NTs. Significantly, comparing curve e and c, we would find that the presence of electron donor nicotinamide adenine dinucleotide (NADH) in the solution can greatly amplify the response of the samples, indicating that NADH can neutralize the generated holes and hence contribute to the photocurrent production. Figure 2D inset shows the effect of SILAR cycles of BiOI on the resulting hybrids, with the increased loading of BiOI on the TiO2 NTs up to 30 cycles, the response of the hybrid enhanced correspondingly. Further increase of the SILAR cycles to 45 cycles led to the signal reduction, which may be caused by the too dense distribution of BiOI NFs that impaired interfacial mass and electron communication.

Figure 2.

Figure 2

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(A) SEM of the self-organized TiO2 NTs, the inset: high-magnification SEM image (B) SEM of the 3D interlaced network of BiOI layer on TiO2 NTs, the inset: high-magnification SEM image, (C) XPS spectrum of the hybrid, the inset: XRD pattern of the developed TiO2 NTs (a) and BiOI/TiO2 hybrid (b), (D) Transient photocurrent response of the samples, the bare Ti foil (a), the TiO2 NTs (b, d) and BiOI/TiO2 hybrid (c, e) in 0.10 M tris-HCl (pH 7.8) without (b, c) and with (d, e) 1.0 × 10−3 M NADH, the inset: the effect of SILAR cycles of BiOI on the resulting hybrids. All photocurrent responses were recorded with 0 V working potential and 470 nm light wavelength on and off.

For comparison, other two structures composed of BiOI NFs on TiO2 nanoparticles (NPs) film on indium tin oxide (ITO) electrode (BiOI NFs/TiO2 NPs/ITO) and BiOI coating on TiO2 NTs tube wall (BiOI coating/TiO2 NTs) were then constructed (experimental details see ESI). Figure 3A depicts the SEM images of the as-prepared samples. As shown, in the two samples, optimized TiO2 NPs film14 (Figure 3A-a) and BiOI coating26 (Figure 3A-d) were used in place of the TiO2 NTs array and the BiOI NFs array, respectively. To clarify how the architecture affects the performance, Figure 3B demonstrates the photocurrent responses of all the three samples under visible-light irradiation of 470 nm. As shown, compared to BiOI coating/TiO2 NTs, the outstanding behavior of BiOI NFs/TiO2 NTs could be attributed to the presence of NFs structure that permits higher efficiency of light harvesting. As to the difference between the TiO2 NPs and TiO2 NTs-based samples, although 1D architectures also change how the film absorbs light, the primary mechanism for improvement is the enhanced residence lifetime29. To further pinpoint how BiOI species are contributing to broadband photocurrent, the incident-photon-to-carrier efficiency (IPCE) is then determined by using the expression (1):

graphic file with name srep04426-m1.jpg

where Isc(λ) is the wavelength dependent short-circuit photocurrent density in A/cm2, I(λ) is the wavelength dependent incident light intensity in W/cm2, and λ is the excitation wavelength in nm. Upon analysis, the results of 25.3%, 5.01% and 1.79% were obtained for BiOI NFs/TiO2 NTs, BiOI NFs/TiO2 NPs/ITO and BiOI coating/TiO2 NTs, respectively. Incidentally, the IPCE 5.01% of the sample BiOI NFs/TiO2 NPs was near the 4% of a similar structure on fluorine-doped tin oxide (FTO) electrode30. These value further identified that the superior performance of the proposed hybrid was of intimate relevance to the proposed arrayed structure.

Figure 3.

Figure 3

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(A) SEM images of the as-prepared (a) TiO2 NPs film, (b) BiOI NFs/TiO2 NPs/ITO, (c) TiO2 NTs, (d) BiOI film/TiO2 NTs. (B) The photocurrent responses of the (a) BiOI NFs/TiO2 NTs, (b) BiOI NFs/TiO2 NPs/ITO, (c) BiOI coating/TiO2 NTs. All the tests were performed in 0.10 M PBS containing 0.10 M ascorbic acid with 0 V working potential and 470 nm excitation light.

Apparently, due to its unique configuration and property, the developed p-n heterojunction has great potential for application in the broad field of photochemistry such as photocatalysis or solar cells. As mentioned above, here its opportunity to the important field of molecular detection was examined. As shown in Figure 1B, on basis of the developed photoelectrode, an innovative sandwich protocol was then designed for probing the immunocomplexing toward VEGF. As far as we known, GDH has never been used as enzymatic labels for PEC detection before. Previous experiment had demonstrated that the response of the developed photoelectrode could be obviously enhanced by NADH. Figure 4A manifests the photoresponse of the immunosystem to VEGF at a level of 1.0 × 10−6 g/mL in the absence and presence of glucose (10 mM). As expected, in the absence of glucose, the response of the system was weaker (cure b) than that of the bare hybrid electrode (cure a), which related to the formation of insulating protein layer that affected the efficient hole scavenging. By contrast, in the presence of substrate, the system exhibited enhanced photoresponse (cure c), which could be attributed to that the existence of glucose could in situ induce NADH production and thus the attenuated charge recombination. Apparently, the signal intensity correlates intimately with VEGF concentration; our preliminary results have shown that the VEGF determination can be accomplished by following the signal variation. As shown in Figure 4B, the signal climbs along with the VEGF concentration ascends up to 1.0 ng/mL, and the detection limit was experimentally found to be 10 pg/mL. As shown in Figure 4B inset, the selectivity was assessed by using another two head and neck squamous cell carcinoma (HNSCC) biomarkers, i.e., interleukin 6 (IL-6) and interleukin 8 (IL-8) as interfering agents, the results indicated that these interfering agents could not cause an apparent signal increase and thus the satisfactory selectivity. The reproducibility of this PEC immunoassay was then evaluated by intra-assay relative standard deviation (RSD). At the level of 1.0 ng/mL, the RSD was 7.3%, suggesting an acceptable reproducibility of the proposed protocol. The result of real plasma sample test was 82.7 pg/mL, which was slightly higher than the 76.3 pg/mL of the commercial ELISA test. These results indicated the potential of the developed immunoassay for practical applications.

Figure 4.

Figure 4

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(A) Photocurrent response of (a) the bare BiOI/TiO2 NTs electrode, the developed immunosystem in the (b) absence and (c) presence of 10 mM glucose in 0.10 M tris-HCl (pH 7.8) containing 10 mM NAD+ cofactor (corresponding to 1.0 × 10−6 g/mL of VEGF). (B) Plot of the photocurrent vs VEGF concentration. ΔI is the photocurrent enhancement corresponding to variable VEGF concentration. Inset: Selectivity of the proposed immunoassay to VEGF by comparing it to the interfering proteins at 1.0 ng/mL, IL-6 and IL-8.

Discussion

The reasons for the excellent property of the as-fabricated electrode are threefold: (1) the arrayed architecture of the hybrid. The 3D interlaced network of BiOI layer with large surface areas would allow extended light harvesting, while the well-aligned 1D features of TiO2 NTs array could provide an effective directional electron percolation pathway and hence the enhanced carrier mobility and lifetime17. (2) the peculiar activity of TiO2 NTs. As known, generally TiO2 is a wide band gap semiconductor and not photoactive under visible light illumination. However, the vertically oriented structure would endow TiO2 NTs with distinct responsibility in a specific visible range31. (3) the formation of p-n junction. The contact of p-type BiOI and n-type TiO2 could form the p-n heterojunction, rendering the rise of Fermi level and whole energy band of BiOI while the descent of those of TiO2 till a new stable equilibrium, wherein the reformed conduction band (CB) edge of BiOI exceeds that of latter. So, when upon visible irradiation, the p-n junction would facilitate the effective separation and quick transportation of the photogenerated excitions. Specifically, as illustrated in Figure 5, charge separation could occur simultaneously both in BiOI NFs and TiO2 NTs. Then, the photoelectrons of p-type BiOI would promptly inject into the CB of n-type TiO2, while the holes of latter would transfer to the valence band (VB) of the former. These injected electrons on the CB of TiO2 NTs were then rapidly collected by the Ti substrate as photocurrent due to the efficient charge transport within the arrayed tubes. The synergy effect of these factors could substantially promote the spatial charge separation and the subsequent migration of these carriers, impeding the charge recombination and thus improving the excitation and conversion efficiency.

Figure 5. Schematic diagrams for the energy bands of p-type BiOI and n-type TiO2 before and after coupling, as well as the specific charge transfer process at the formed p-n junction under visible-light irradiation.

Figure 5

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The following assay confirmed the excellence of the developed p-n junction architecture and also the feasibility of the proposed sensing protocol. Further work will modulate the experimental conditions to optimize the property of the hybrid and exploit its utilization for other bioanalysis application. In summary, a distinct p-n heterojunction has been constructed on basis of coupling p-type crossed BiOI NFs array to n-type TiO2 NTs array. Due to the unique arrayed structure consisted of 3D interlaced network of BiOI NFs layer and the 1D configuration of TiO2 NTs, the developed hybrid possessed excellent photo-to-electric conversion efficiency. By means of an immunosandwich protocol, we further demonstrated that this hybrid enabled novel PEC biomolecular detection toward protein marker which could be extended to other biorecognition events. These results not only offered a unique BiOI NFs/TiO2 NTs p-n heterojunction which has a wide application prospects in the broad photochemistry, but also opened a different perspective for current development of advanced PEC biomolecular detection.

Methods

Fabrication of the 3D BiOI Crossed NFs Array/1D TiO2 NTs array p-n heterojunction electrodes

The utilized TiO2 NTs were fabricated by the technique of electrochemical anodic oxidation according to our previous report17. In detail, prior to anodization, Ti sheets were mechanically polished with different abrasive papers and rinsed in an ultrasonic bath of cold distilled water for 10 min. Then the cleaned Ti sheets were soaked in a mixture of HF and HNO3 acids for 1 min (the mixing ratio of HF:HNO3:H2O is 1:4:5 in volume). Using 0.5 wt% hydrofluoric acid as the electrolyte, the cleaned titanium sheets was anodized at 20 V at room temperature for 60 min in a conventional two-electrode system with a platinum electrode as the cathode. Anodized Ti sheets were washed with ultrapure water and then annealed at 500°C for 1 h in ambient atmosphere to crystallize the amorphous tubes to obtain the well-ordered and uniform TiO2 NTs array. On basis of the developed TiO2 NTs, the 3D BiOI crossed NFs array/1D TiO2 NTs array p-n heterojunction electrode was then prepared by a successive ionic layer adsorption and reaction (SILAR) approach. Briefly, before use, the TiO2 NTs substrates were cleaned by ultrasonication in distilled water and ethanol, subsequently. Then, BiOI flakes were coated onto the TiO2 NTs by alternately immersing the latter into 5 mM Bi(NO3)3 and 5 mM KI solutions for 10 s each, respectively. The films were carefully washed with doubly distilled water after each dipping step. After certain cycles of SILAR, the resulting BiOI NFs array/TiO2 NTs array was dried at room temperature.

Fabrication of the BiOI NFs/TiO2 NPs/ITO and BiOI coating/TiO2 NTs Electrodes

0.1 g TiO2 powder was dispersed ultrasonically in 20 mL water (the concentration of the suspension is 5.0 mg/mL), and then 40 μL of the suspension was applied onto a piece of freshly cleaned ITO slice with fixed area of ~0.25 cm2. After drying in air, the film was sintered in a Muffle furnace at 500°C for 30 min and finally cooled down to room temperature14. The BiOI NFs/TiO2 NPs was then prepared by the successive ionic layer adsorption and reaction (SILAR) approach under the same experimental conditions. To fabricate BiOI coating/TiO2 NTs, BiOI was coated onto the TiO2 NTs by an impregnating hydroxylation method using BiI3 as the precursor26. In a typical synthesis, 0.94 g of BiI3 was added into 20 mL of absolute ethanol solutions containing 2 drops of 35% HCl. The TiO2 NTs were first immersed in BiI3 solution for 30 min followed by a slight rinse with ethanol and then dried in an oven at 80°C for 1 h to ensure that BiI3 was adhered to the tube wall uniformly. Subsequently, the TiO2 NTs were immersed in distilled water, and BiOI was deposited on the nanotube wall by hydroxylation of BiI3.

Immunoassay development

A chitosan film was firstly coated on the BiOI NFs/TiO2 NTs to offer abundant –NH2 that covalently links to the –NH2 of antibodies via the reaction with glutaraldehyde. Specifically, chitosan (CS) solution (0.5 wt%) was prepared by ultrasonically dissolving CS powder in 1% acetic acid. 20 μL CS solution was dropped on hybrid electrode and dried at 50°C. After the electrode was washed with 0.1 M NaOH and distilled water, respectively, it was dipped in 5.0% GLD solution diluted in phosphate buffer (pH 7.4) at room temperature for 30 min. The electrode was rinsed with distilled water thoroughly to remove physically adsorbed GLD. Then, 25 μL of 0.1 mg/mL Ab1 dissolved in 0.01 M PBS (pH 7.4) was spread onto the GLD-activated electrode surface at 4°C in a moisture atmosphere to avoid evaporation of solvent. After incubation for 16 h, the electrode was rinsed with the washing buffer to remove physically adsorbed Ab1 and then blocked with 25 μL blocking solution for 2 h at 4°C to block non-specific binding sites, followed by washing with the washing buffer thoroughly. Next, 25 μL of Ag with different concentrations were dropped onto the Ab1 modified electrodes for an incubation of 60 min at 37°C followed by washing with washing buffer. Biotinylated Ab2-streptavidin-biotinylated GDH was prepared through reaction of 100 μL 0.1 mg/mL streptavidin solution (0.01 M PBS, pH 7.4) with 100 μL 0.1 mg/mL biotinylated GDH solution (0.01 M PBS, pH 7.4) for 30 min at room temperature, followed by addition of 100 μL 0.1 mg/mL biotinylated Ab2 solution (0.01 M PBS, pH 7.4) for another 30 min at room temprature. After the binding reaction between Ab1 and the Ag, the electrodes were allowed for labeling by additional incubation with 25 μL of the obtained biotinylated Ab2-streptavidin-biotinylated GDH solution for 60 min, and again the electrodes were washed thoroughly with water to remove nonspecifically bound conjugations. Finally, the assembled electrodes were allowed for 30 min incubation at room temperature in the freshly prepared 0.1 M Tris-HCl solution (pH 7.8) containing 10 mM glucose and 10 mM NAD+ at room temperature, followed by the respective PEC measurements.

Author Contributions

W.W.Z., J.J.X. and H.Y.C. proposed and designed the project, W.W.Z., Z.L., S.S. and W.W.Z. performed the experiments, J.W. and Z.Y.M. performed characterizations, W.W.Z., J.J.X. and H.Y.C. analyzed data and wrote the manuscript. All the authors participated in discussions of the research.

Supplementary Material

Supplementary Information

Bismuthoxyiodide Nanoflakes/Titania Nanotubes

srep04426-s1.pdf (553.6KB, pdf)

Acknowledgments

This work was supported by the 973 Program (2012CB932600), the National Natural Science Foundation of China (Nos. 21327902, 21135003, 21121091 and 21305063), the Natural Science Funds of Jiangsu Province (BK20130553) and the open fund of SKLACLS (0205119005).

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Supplementary Materials

Supplementary Information

Bismuthoxyiodide Nanoflakes/Titania Nanotubes

srep04426-s1.pdf (553.6KB, pdf)

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