Structure and bonding properties of gold (Au) nanoparticles (NPs) are of great interest due to the unique size-dependent quantum-confinement effect exhibited by structures on the nanoscale. As such, Au NPs have demonstrated their potential use in a variety of fields (e.g. imaging, drug delivery, catalysis). The popularity of Au NPs is largely due to its versatility in synthesizing different NP compositions and surfaces. In this thesis, structure and bonding in Au NPs was examined from both surface functionalization/ligand and composition/metal bonding perspectives. Functionalization of Au-surface with model biomolecule ligands enables formation and electroless deposition of Au NPs onto a biocompatible Ti substrate. Through variation of model biomolecule size and concentration with respect to a Au precursor, insight was gained into the formation mechanisms of Au NPs, and the processes that lead to deposition upon the Ti substrate. Furthermore, using extended X-ray absorption fine-structure (EXAFS) with sample spinning and glancing angle setup allowed us to resolve small differences in coordination, leading to new findings on fine-tuning of peptide-coated Au NP size on Ti substrates. To explicitly analyze Au NP structure and bonding from a metallic perspective, NP model systems with precisely controlled compositions were studied with ab initio calculations to compare local environment and electronic character. It was determined that while surface features may be structurally similar, the effect of local environment and geometry can affect the electronic character of these features. Finally, small Au NP samples were studied to understand the alloying effect. The position of a heteroatom dopant Pt atom within Au25 has been a disputed issue, with no definitive means of determination. Using a combination of EXAFS spectra and ab initio calculations, it was possible to determine that the Pt atom resides in the central position of the icosahedral core. Furthermore, Pt doping in Au25 resulted in a contraction of the surface Au structure, an unobserved phenomenon until now. Through the careful and systematic comparison of Au NP systems, this thesis will contribute to a better understanding of Au local structure and bonding in ligand-functionalized substrate-supported Au NPs, as well as compositionally precise Au nanoclusters.

This research proposes a novel polymer-based optical waveguide made with Polydimethylsiloxane (PDMS) for optical detection applications. Alternative to other fiber-based sensor, the proposed optical sensor uses PDMS waveguide as the main sensing component. PDMS has excellent optical properties which is essential for bio-photonic detection, including highly optical transparency, good flexibility and high bio-compatibility. Uncured PDMS polymer is cast in a Teflon tubing to form the PDMS rod. Since the reflective index of PDMS is as high as 1.43, that the bare PDMS can be an optical waveguide while the reflective index of the surrounding media is smaller than 1.43. The cast PDMS waveguide is then connect with plastic optical fibers to form the proposed optical waveguide system. In order to improve the optical performance of the PDMS waveguide, a surface coating process is used to reduce the surface roughness of the PDMS waveguide. The measured insertion loss with and without performing the surface coating procedure is 1.14 and 1.71dB/cm, respectively. Once the PDMS waveguide is formed, Au nanoparticles (Au-Nps) were coated on the PDMS surface with the assistance of a positive charge polymer of PDDA to form an optical waveguide capable of localized SPR detection. In addition, an atmospheric plasma treating process is used to enhance the coating ratio and speed of Au-Nps. UV-VIS spectrum and the SEM observation of the Au-particle coated PDMS waveguide confirm that the plasma treatment process significantly improves the coating results of Au-Nps. Liquid samples with different refractive index were used to demonstrate the LSPR sensing ability of the fabricated optical waveguide. The label free DNA detection was demonstrated by the system. The thiolated single strand DNA was modify on the PDMS optical waveguide as a DNA probe and bound with target DNA by DNA hybridization. The detection limit is as low as 10 pM. This research provides a simple and fast fabrication method to fabricate waveguide-based LSPR sensors.

As a result of increasing demand of power in the modern society, energy storage/consumption is playing a more important role on future economics. Therefore energy storage systems which are more environmentally friendly, low-cost and high-performance have attracted much attention. Among electrochemical systems, supercapacitors are considered as a prominent candidate for the modern energy storage systems due to the high power density, high charge/discharge rate, and long lifetimes. Nevertheless, the performance of supercapacitors is limited by the significant disadvantage of low energy density. Metal oxides with high pseudocapacitance such as MnO2 are used as the electrode materials for supercapacitors to resolve the lack of energy density in supercapacitors. The specific capacitance is notably enhanced by the metal oxides because of the reversible redox reactions. Previous studies confirmed that only a thin layer of MnO2 is involved in the redox process and is electrochemically active, which makes surface area a critical factor of energy storage. To increase surface area of MnO2, ZnO nanostructure is introduced in the electrode material as a template for electrodeposition of MnO2. In the first part of the research, we synthesize a nanomaterial which combines 0-1-2 dimensional properties of different nanostructures and significantly increases the energy capacity of MnO2. iv In the second part of the research, we demonstrate an in situ synthesis of a hybrid device that combines two materials to investigate the individual characteristic of two nanomaterials. In this study, a ZnO nanorod interface on Au nanoparticle arrays is fabricated, and results in the photo-modulation of the array characteristics. We find the use of nanoparticle arrays as electrochemical systems by electrodepositing ZnO on Au nanoparticle arrays. The method expands their potential use in sensors, multifunctional materials, single electron transistors and nanoscale energy systems. Characteristic behavior of Au nanoparticle arrays including Coulomb blockade at room temperature, single electron charging effects and a power law dependence in current-voltage were observed, and Schottky behavior and photocurrent generation due to the ZnO nanorods were also proved. From the modulation of the threshold voltage of the Au array due to the electron-hole pairs generated by photo excitation in the ZnO rods, it can be seen that the system also has coupling between the Au nanoparticles and ZnO rods other than the individual characteristics. Au nanoparticles can be used as electrochemical systems with both structural and spatial confinement of the synthesized material. The possibility of using Au nanoparticle chains as electroactive sites significantly expands their potential use in sensors, multifunctional materials, single electron transistors and nanoscale energy systems.

京都大学 / 0048 / 新制・課程博士 / 博士(工学) / 甲第18979号 / 工博第4021号 / 新制||工||1619(附属図書館) / 31930 / 京都大学大学院工学研究科マイクロエンジニアリング専攻 / (主査)教授 鈴木 基史, 教授 木村 健二, 教授 蓮尾 昌裕 / 学位規則第4条第1項該当 / Doctor of Philosophy (Engineering) / Kyoto University / DFAM

This thesis describes novel research using Portobello mushroom spores (PMS) as a biotemplate and reducing agent that may be used to produce nanocomposites and replicas with societal benefits. First, the use of PMS as a green eco-friendly bioreagent for the biosynthesis of Ag, Au and TiOx nanoparticles (NPs) and their hybrids is described. These have been characterised using SEM, TEM, XRD, FTIR, UV, SIMS, DLS and TGA (where a full list of acronyms is to be found on page iv). The spherical shape, location and mean diameter of the PMS-held (5-30nm) Ag and Au NPs were confirmed. PMS functional groups are comparable with those in plant sources and allow them to act as reducing/capping/stabilising agents. Second, the sequential biosynthesis of PMS-held Ca2+, CaCO3 and nanohydroxyapatite (nHAp) is described where surface nucleation and growth are facilitated by biotemplate surface hydrophilic polar groups (-OH and -COO-). XRD and HRTEM suggest that the nHAp so formed has lower crystallinity and greater directed growth in the (002) direction than commercial nHAp (e.g. Bio-Oss), making PMS-routes useful for the delivery of artificial bone (after subsequent PMS removal). Furthermore, PMS-held nHAp showed more rapid in-vitro mineralization in simulated body fluid (SBF). Third, it is shown that ascorbic acid (AA), haemoglobin (Hb) and insulin (In) can be loaded into/released by PMS through its cell walls faster than with synthetic hydrogels (PVA); the transdermal use of PMS nanocomposites is considered in the context of drug delivery nanotechnology, avoiding size-dependent toxicity. Fourth, it is shown by traditional diffusion and novel methods that the antimicrobial activity especially of Ag/PMS, but also TiOx/PMS and Ag-TiOx/PMS (but not Au/PMS) is good in the inhibition of the growth of E.coli and S.aureus bacteria. The highest activity of Ag/PMS is attributed to Agx+ release. Fifth, the synthesis of NPs/PMS and biomimetic TiOx/PMS has shown to lead to good photocatalysis for the removal of coloured organic pollutants (e.g. methyl orange) from water, with faster rates of removal in molecules/mg/s and turnover numbers (TON) (s-1) than commercial anatase-rutile TiO2 (P25) possibly as the texture of the titania replicas raises the number of multiple reflections of light.

A controlled assembly of natural beta-cyclodextrin modified Au NPs mediated by dopamine is demonstrated. Furthermore, a simple and sensitive colorimetric detection for dopamine is established by the concentration-dependent assembly.

Master of Science / Department of Chemistry / Jun Li / With the worldly consumption of energy continually increasing and the main source of this energy, fossil fuels, slowly being depleted, the need for alternate sources of energy is becoming more and more pertinent. One promising approach for an alternate method of producing energy is using solar cells to convert sunlight into electrical energy through photovoltaic processes. Currently, the most widely commercialized solar cell is based on a single p-n junction with silicon. Silicon solar cells are able to obtain high efficiencies but the downfall is, in order to achieve this performance, expensive fabrication techniques and high purity materials must be employed. An encouraging cheaper alternative to silicon solar cells is the dye-sensitized solar cell (DSSC) which is based on a wide band gap semiconductor sensitized with a visible light absorbing species. While DSSCs are less expensive, their efficiencies are still quite low compared to silicon. In this thesis, Grätzel cells (DSSCs based on TiO2 NPs) were fabricated and optimized to establish a reliable standard for further improvement. Optimized single layer GSCs and double layer GSCs showing efficiencies >4% and efficiencies of ~6%, respectively, were obtained. Recently, the incorporation of metallic nanoparticles into silicon solar cells has shown improved efficiency and lowered material cost. By utilizing their plasmonic properties, incident light can be scattered, concentrated, or trapped thereby increasing the effective path length of the cell and allowing the physical thickness of the cell to be reduced. This concept can also be applied to DSSCs, which are cheaper and easier to fabricate than Si based solar cells but are limited by lower efficiency. By incorporating 20 nm diameter Au nanoparticles (Au NPs) into DSSCs at the FTO/TiO2 interface as sub wavelength antennae, average photocurrent enhancements of 14% (maximum up to ~32%) and average efficiency enhancements of 13% (maximum up to ~23% ) were achieved with well dispersed, low surface coverages of nanoparticles. However the Au nanoparticle solar cell (AuNPSC) performance is very sensitive to the surface coverage, the extent of nanoparticle aggregation, and the electrolyte employed, all of which can lead to detrimental effects (decreased performances) on the devices.

PhD thesis - Faculty of Science / The main aim of this thesis has been to study the way in which Fe(III) and Co(II) incorporation into Si-MCM-41 synthesis gels affects the properties of the unmodified material. Another aim was to investigate the influence of these hetero-atoms on the dispersion and particle size distribution as well as the catalytic activity of supported Au nanoparticles in the CO oxidation reaction. Si-MCM-41 has been successfully synthesized in this work using mixtures containing CTAB as a structure-directing agent (SDA) and water-glass as a SiO2 source. Replacement of water-glass with pre-calcined Si-MCM-41 for SiO2 source in the secondary synthesis step has produced Si-MCM-41 with improved structural properties (XRD, HRTEM and Raman spectroscopy), including restructured and more crystalline pore walls (Raman spectroscopy). The conventional shortcomings of Si-MCM-41 as a support for catalyticallyactive (transition) metal components such as low hydrothermal stability, low PZC, lack of cation exchange capacity and no reducibility have been partially addressed by modification with Fe(III) and Co(II). The premodification was achieved both during framework synthesis and after synthesis by the incipient wetness impregnation (IWI) method. As opposed to the one-pot synthesis of metal-containing derivatives, the IWI method gave materials with high metal loadings and maximal retention of the properties of pristine Si-MCM-41. On the other hand, metal incorporation during synthesis to a loading of ~8.8 wt% using aqueous solutions of metal precursors showed some collapse of the mesostructure. Consequently methods were sought to incorporate this amount of metal (and up to double, i.e., 16 wt%) with maximal retention of the MCM-41 characteristics. These methods included (i) using Si-MCM-41 as a SiO2 source, (ii) dissolving the metal precursors in an acid solution before inclusion into the synthesis gel, and (iii) using freshly precipitated alkali slurries of the metal precursors. The first method produced a highly ordered 16wt% Fe-MCM-41 material with excellent reducibility (TPR showed three well-resolved peaks) and pore-wall structure (Raman spectroscopy). Like the aqueous route, the acid-mediated metal incorporation route did not produce ordered materials at metal contents of ~16 wt%. The base precipitate route produced highly ordered composite materials up to 16 wt% metal content, with characteristics similar to those of Si-MCM-41 (XRD, BET and HRTEM), although some metal phases were observed as a separate phase on the SiO2 surface. Thus, metal-containing MCM-41 materials could be obtained with conservation of MCM-41 mesoporosity. Raman spectroscopic studies have shown that the effect of transition metal incorporation in MCM-41-type materials is to strengthen the pore walls (shift of Si-O-Si peaks to higher frequencies), while TPR studies revealed that the essentially neutral framework of Si-MCM-41 could be rendered reducible by transition metal incorporation. Gold-containing mesoporous nanocomposites were prepared by both direct synthesis and post-synthetically. Catalysts prepared by direct hydrothermal synthesis were always accompanied by formation of large Au particles because of the need to calcine the materials at 500 oC in order to remove the occluded surfactant template. The presence of transition metal components in Me-MCM-41 (Me = Fe and Co) has been found to play a significant role in the particle size distribution and also the dispersion of Au nanoparticles when these materials were used as supports. In general, a base metal-containing support was found to produce smaller Au nanoparticles than the corresponding siliceous support. It has been proposed that the transition metal components serve as anchoring or nucleation sites for the Au nanoparticles, which are likely to sinter during calcination. The anchoring sites thus retard the surface mobility of Au at calcination temperatures above their TTammann. The use of the Au/Me-MCM-41 materials as catalysts in the CO oxidation reaction has led to the following observations: (i) catalyst on metal-containing supports showed better activity than those on Si-MCM-41, probably due to the induced reducibility in metal-MCM-41, (ii) catalysts prepared by direct synthesis showed inferior activity owing to large Au particles, (iii) increasing Au content improves the catalytic performance, (iv) increasing the Fe content of the support at constant Au improves the catalytic performance, and (v) changing the base metal component of the support from Fe to Co led to a significant improvement in catalytic activity. The similarity of the apparent activation energies (Ea) for the 5 wt% Au-containing 5 wt% Fe- and 5 wt% Co-MCM-41 suggested that the difference in catalytic activity is associated with the number of active sites possessed by each catalyst system. The observed order of catalytic activity of these 5 wt% Au-containing systems in terms of the support type is: Co-MCM-41 > Fe-MCM-41 > Si-MCM-41. This was further supported by the average Au particle size, which, in terms of the support, followed the order Co-MCM-41 < Fe-MCM-41 < Si-MCM-41. Thus, metal-support interactions between Au and MCM-41 have been enhanced by introducing Fe(III) and Co(II), which also induced framework charge, ion exchange capacity (IEC) and reducibility in the neutral siliceous support.

Com o desenvolvimento de novos nanomateriais têm-se descoberto propriedades eletrônicas, elétricas, ópticas e catalíticas únicas para aplicações nanotecnológicas. Entre estes nanomateriais com caraterísticas singulares, estão as nanopartículas (Np) Core&alpha;Shell, as quais combinam propriedades físico-químicas de dois materiais diferentes, provendo maior eficiência em aplicações como nanoeletrônica, sensoreamento, biossensoreamento e biomédicas. Neste trabalho, Np Core&alpha;Shell são sintetizada com núcleo (Core) de Np Fe&#8323;O&#8324; e com casca (Shell) de Np Au, formando as Nps Fe&#8323;O&#8324;&alpha;Au na presença do dendrímero poli(amidoamina) geração 4.0 (Pamam G4). As propriedades físico-químicas do nanomaterial core-shell são estudadas através de análises espectroscópicas, microscopias e eletroquímicas, além de medidas de magnetização. Essas técnicas revelam a formação das Nps Au nas cavidades do Pamam G4 e as interações eletrostáticas entre os grupos funcionais do Pamam G4 e os grupos OH &#8315; e H &#8314; da superfície das Nps magnéticas, as quais dão uma forte estabilidade na configuração da Np Fe&#8323;O&#8324;&alpha;Au. Evidencia-se propriedades óticas da Np Au e propriedades superparamagnéticas da Np Fe &#8323; O &#8324;, as quais podem ser usadas para aplicações em nanomedicina. As propriedades electrocatalíticas das Nps são utilizadas na detecção de dopamina (DA). Foram fabricados sensores eletroquímicos das Nps Fe&#8323;O&#8324;&alpha;Au, Nps Fe&#8323;O&#8324; e Nps Au, e caracterizados por técnicas de voltametria cíclica e voltametria de pulso diferencial. A fabricação dos sensores consistiu na deposição de camadas alternadas entre as nanopartículas com o poliânion poly(ácido vinil sulfônico) (PVS) no eletrodo de ITO, levando à configuração de três arquiteturas; ITO - (Fe&#8323;O&#8324;&alpha;Au &frasl; PV S), ITO - (Fe&#8323;O&#8324; &frasl; PV S) e ITO - (Au &frasl; PV S). Um problema encontrado na detecção de DA é que esta tem potenciais de oxidação aproximadamente iguais ao ácido ascórbico (AA) e ao ácido úrico (AU). Portanto, os sensores utilizados na detecção de DA, devem ser altamente seletivos a DA em relação a seus interferentes. Os sensores desenvolvidos aqui mostraram uma boa seletividade e velocidade de resposta na detecção de DA, sendo o sensor ITO - (Fe&#8323;O&#8324;&alpha;Au &frasl; PV S) o mais eficiente. As Nps Fe&#8323;O&#8324;&alpha;Au revelam maior citotoxicidade nas células cancerígenas comparadas com as células saudáveis, já que as células cancerígenas são mais sensíveis ao estresse oxidativo produzido pelas nanopartículas no interior da célula. / Along with the development of nanomaterials came the knowledge and design of their unique eletronic, optical and catalitycal properties which may be used for a variety of nanotecnological applications. A special class of nanomaterials with interesting characteristics is represented by the Core&alpha;Shell nanoparticles, which combine the physicochemical properties of two differerent nanomaterials (including oxides, metals, semiconductors or polymers). This combination provides greater efficiency in applications such as nanoelectronics, sensing, biosensing and biomedical areas. This study reports the synthesis of Fe&#8323;O&#8324; Np, which in the presence of the polyamido amine generation 4.0 (Pamam G4), is covered with Au Np forming the Fe&#8323;O&#8324;&alpha;Au Nps. The nanomaterials had been characterized using spectroscopic, microscopic and electrochemical techniques. The results revealed the formation of Au Nps in the cavities of PAMAM G4 and showed that the electrostatic interactions between the PAMAM functional groups and the OH &#8315; and H &#8314; groups on the surface of the magnetic nanoparticles lead to a strong stability in the configuration of Fe&#8323;O&#8324;&alpha;Au Nps. The optical properties of the Au Np (namely the Plasmon resonance band at 542 nm) as well as the superparamagnetic properties of the Fe&#8323;O&#8324; Np were present in the core-shell nanostrutures. Due to their electrocatalytical properties, the core-shell nanoparticles were employed as active elements for dopamine (DA) detection. The fabrication of the modified electrodes for DA detection consisted in the deposition by LbL technique of alternating layers of nanoparticles and poly(vinyl sulfonic acid) (PVS) on the ITO eletrode, in three distinct architectures: ITO - (Fe&#8323;O&#8324;&alpha;Au Fe&#8323;O&#8324; PV S), ITO - (Fe&#8323;O&#8324; &frasl; PV S) and ITO - (Au &frasl; PV S). We found a good selectivity and rapid response toward the detection of DA, being the sensor ITO - (Fe&#8323;O&#8324;&alpha;Au &frasl; PV S) the most efficient. The effect of Fe&#8323;O&#8324;&alpha;Au Nps showed a higher cytotoxicity in cancer cells compared to healthy cells, because cancer cells are more sensitive to oxidative stress produced by the nanoparticles.

Com o desenvolvimento de novos nanomateriais têm-se descoberto propriedades eletrônicas, elétricas, ópticas e catalíticas únicas para aplicações nanotecnológicas. Entre estes nanomateriais com caraterísticas singulares, estão as nanopartículas (Np) Core&alpha;Shell, as quais combinam propriedades físico-químicas de dois materiais diferentes, provendo maior eficiência em aplicações como nanoeletrônica, sensoreamento, biossensoreamento e biomédicas. Neste trabalho, Np Core&alpha;Shell são sintetizada com núcleo (Core) de Np Fe&#8323;O&#8324; e com casca (Shell) de Np Au, formando as Nps Fe&#8323;O&#8324;&alpha;Au na presença do dendrímero poli(amidoamina) geração 4.0 (Pamam G4). As propriedades físico-químicas do nanomaterial core-shell são estudadas através de análises espectroscópicas, microscopias e eletroquímicas, além de medidas de magnetização. Essas técnicas revelam a formação das Nps Au nas cavidades do Pamam G4 e as interações eletrostáticas entre os grupos funcionais do Pamam G4 e os grupos OH &#8315; e H &#8314; da superfície das Nps magnéticas, as quais dão uma forte estabilidade na configuração da Np Fe&#8323;O&#8324;&alpha;Au. Evidencia-se propriedades óticas da Np Au e propriedades superparamagnéticas da Np Fe &#8323; O &#8324;, as quais podem ser usadas para aplicações em nanomedicina. As propriedades electrocatalíticas das Nps são utilizadas na detecção de dopamina (DA). Foram fabricados sensores eletroquímicos das Nps Fe&#8323;O&#8324;&alpha;Au, Nps Fe&#8323;O&#8324; e Nps Au, e caracterizados por técnicas de voltametria cíclica e voltametria de pulso diferencial. A fabricação dos sensores consistiu na deposição de camadas alternadas entre as nanopartículas com o poliânion poly(ácido vinil sulfônico) (PVS) no eletrodo de ITO, levando à configuração de três arquiteturas; ITO - (Fe&#8323;O&#8324;&alpha;Au &frasl; PV S), ITO - (Fe&#8323;O&#8324; &frasl; PV S) e ITO - (Au &frasl; PV S). Um problema encontrado na detecção de DA é que esta tem potenciais de oxidação aproximadamente iguais ao ácido ascórbico (AA) e ao ácido úrico (AU). Portanto, os sensores utilizados na detecção de DA, devem ser altamente seletivos a DA em relação a seus interferentes. Os sensores desenvolvidos aqui mostraram uma boa seletividade e velocidade de resposta na detecção de DA, sendo o sensor ITO - (Fe&#8323;O&#8324;&alpha;Au &frasl; PV S) o mais eficiente. As Nps Fe&#8323;O&#8324;&alpha;Au revelam maior citotoxicidade nas células cancerígenas comparadas com as células saudáveis, já que as células cancerígenas são mais sensíveis ao estresse oxidativo produzido pelas nanopartículas no interior da célula. / Along with the development of nanomaterials came the knowledge and design of their unique eletronic, optical and catalitycal properties which may be used for a variety of nanotecnological applications. A special class of nanomaterials with interesting characteristics is represented by the Core&alpha;Shell nanoparticles, which combine the physicochemical properties of two differerent nanomaterials (including oxides, metals, semiconductors or polymers). This combination provides greater efficiency in applications such as nanoelectronics, sensing, biosensing and biomedical areas. This study reports the synthesis of Fe&#8323;O&#8324; Np, which in the presence of the polyamido amine generation 4.0 (Pamam G4), is covered with Au Np forming the Fe&#8323;O&#8324;&alpha;Au Nps. The nanomaterials had been characterized using spectroscopic, microscopic and electrochemical techniques. The results revealed the formation of Au Nps in the cavities of PAMAM G4 and showed that the electrostatic interactions between the PAMAM functional groups and the OH &#8315; and H &#8314; groups on the surface of the magnetic nanoparticles lead to a strong stability in the configuration of Fe&#8323;O&#8324;&alpha;Au Nps. The optical properties of the Au Np (namely the Plasmon resonance band at 542 nm) as well as the superparamagnetic properties of the Fe&#8323;O&#8324; Np were present in the core-shell nanostrutures. Due to their electrocatalytical properties, the core-shell nanoparticles were employed as active elements for dopamine (DA) detection. The fabrication of the modified electrodes for DA detection consisted in the deposition by LbL technique of alternating layers of nanoparticles and poly(vinyl sulfonic acid) (PVS) on the ITO eletrode, in three distinct architectures: ITO - (Fe&#8323;O&#8324;&alpha;Au Fe&#8323;O&#8324; PV S), ITO - (Fe&#8323;O&#8324; &frasl; PV S) and ITO - (Au &frasl; PV S). We found a good selectivity and rapid response toward the detection of DA, being the sensor ITO - (Fe&#8323;O&#8324;&alpha;Au &frasl; PV S) the most efficient. The effect of Fe&#8323;O&#8324;&alpha;Au Nps showed a higher cytotoxicity in cancer cells compared to healthy cells, because cancer cells are more sensitive to oxidative stress produced by the nanoparticles.