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Topic:Janus nanoparticles

Jajarawiki (talk) 22:23, 22 September 2011 (UTC)

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Rcl1963 (talk) 18:15, 25 September 2011 (UTC)

Introduction[edit]

A schematic view of a basic spherical Janus particle with two distinct faces. Sides A and B represent two surface with different physical or chemical properties.

Janus nanoparticles are a special type of nanoparticle whose surface has two or more distinct types of properties.[1] This unique surface of Janus nanoparticles allows two different types of chemistry to occur on the same particle. The simplest case of a Janus nanoparticle is achieved by dividing the nanoparticle into two distinct parts, each of them either made of a different material, or bearing different functional groups.[2]For example, a Janus nanoparticle may have one half of its surface composed of hydrophilic groups and the other half hydrophobic groups.[3] This gives these particles unique and fascinating properties related to their asymmetric structure and/or functionalization.

History[edit]

Originally the term Janus particle was coined by C. Casagrande et al. in 1988[4] to describe spherical glass particles with one of the hemispheres hydrophilic and the other hydrophobic. In that work the amphiphilic beads were synthesized by protecting one hemisphere with varnish and chemically treating the other hemisphere with a silane reagent. This method resulted in a particle with equal hydrophilic and hydrophobic areas.[5] In 1991, Pierre-Gilles de Gennes mentioned the term "Janus" particle in his Nobel lecture. Janus particles are named after the two faced Roman god Janus because these particles may be said to have "two faces" since they possess two distinct types of properties.[6] de Gennes pushed for the advancement of Janus particles by pointing out that these "Janus grains" have the unique property of densely self-assembling at liquid-liquid interfaces while allowing material transport to occur through the gaps between the solid amphiphilic particles.[7] Although the term "Janus particles" was not yet used, Lee and coworkers reported the first particles matching this description in 1985.[8] They introduced asymmetric polystryene/polymethylmethacrylate lattices from seeded emulsion polymerization. One year later, Casagrande and Veyssie reported the synthesis of glass beads that were made hydrophobic on only one hemisphere using octadecyl trichlorosilane, while the other hemisphere was protected with a cellulose varnish.[5] The glass beads were studied for their potential to stabilize emulsification processes. Then several years later, Binks and Flechter investigated the wettability of Janus beads at the interface between oil and water.[9] They concluded that Janus particles are both surface active and amphiphilic, whereas homogeneous particles are only surface active. Twenty years later, a plethora of Janus particles of different sizes and shapes and properties with applications in textile[10], sensors[11], stabilization of emulsions[12], and magnetic field imaging[13] have been reported.

Synthesis[edit]

The synthesis of Janus nanoparticles requires the ability to selectively create each side of a nanometer sized particle with different chemical properties in a cost effective and reliable way that produces the particle of interest in high yield. Initially this was difficult task, however with in the last 10 years, methods have been refined to make this possible. Currently, three major methods are utilized in the synthesis of Janus nanoparticles.[2]

Masking[edit]

Schematic view of the synthesis of Janus nanoparticles via masking. 1) Homogeneous nanoparticles are placed in or on a surface in such a way that only one hemisphere is exposed. 2) The exposed surface is exposed to a chemical 3) which change it's properties. 4) The masking agent is then removed releasing the Janus nanoparticles.

Masking was one of the first techniques developed for the synthesis of Janus nanoparticles.[14] This technique was developed by simply taking synthesis techniques of larger Janus particles and scaling down to the nanoscale.[14] [15] [16] Masking, as the name suggests, involves the protection of one side of a nanoparticle followed by the modification of the unprotected side and the removal of the protection. Two masking techniques are common to produce Janus particles, evaporative deposition and a technique where the nanoparticle is suspended at the interface of two phases. However, only the phase separation technique scales well to the nanoscale.[17]

The phase interface method involves trapping homogeneous nanoparticles at the interface of two immiscible phases. These methods typically involve the liquid-liquid and liquid-solid interfaces, however a gas-liquid interface method has been described.[18][19]

The liquid-liquid interface method is best exemplified by Gu et al. who made an emulsion from water and an oil and added nanoparticles of magnetite. The magnetite nanoparticles aggregated at the interface of the water-oil mixture forming a Pickering emulsion. Then silver nitrate was added to the mixture resulting in the deposition of silver nanoparticles on the surface of the magnetite nanoparticles. These Janus nanoparticles were then functionalized by the addition of various ligands with specific affinity for either the iron or silver.[20] This method can also utilize gold or iron-platinium nanoparticles instead of magnetite nanoparticles.[2]

A similar method is the gas-liquid interface method developed by Pradhan et al. In this method, hydrophobic alkanethiolate gold nanoparticles were placed in water causing the formation of a monolayer of the hydrophobic gold nanoparticles on the surface. Air pressure was then increased forcing the hydrophobic layer to be pushed into the water decreasing the contact angle. When the contact angle was at the desired level, a hydrophillic thiol, 3-mercaptopropane-1,2-diol, was added to the water causing the hydrophillic thiol to competitively replace the hydrophobic thiols resulting in the formation of amphiphilic Janus nanoparticles.[19]

The liquid-liquid and gas-liquid interface methods do have an issue where the nanoparticles can rotate in solution causing the deposition of silver on more than one face.[21]. A liquid-liquid/liquid-solid hybrid interface method was first introduced by Granick et al. as a solution to this liquid-liquid method problem. In this method, the oil was substituted for molten parrifin wax and the magnetite for silica nanoparticles. When the solution was cooled the wax solidified trapping half of each silica nanoparticle in the wax surface leaving the other half of the silica nanoparticle exposed. The water was then filtered off and the wax trapped silica nanoparticles were then exposed to a methanol solution containing (amino- propyl)triethoxysilane which reacted with the exposed silica surface of the nanoparticles. The methanol solution was then filtered off and the wax was dissolved with chloroform, freeing the newly made Janus particles. Liu et al. has reported the synthesis of acorn and mushroom shaped silica-aminopropyl-trimethoxysilane Janus nanoparticles utilizing the hybrid liquid-liquid/liquid-solid method developed by Granick et al. They exposed homogenous aminopropyl-trimethoxysilane functionalized silica nanoparticles embedded in wax to an ammonium fluoride solution which etched away the exposed surface. The liquid-liquid/liquid-solid hybrid method also has some drawbacks, when exposed to the second solvent for functionalization some of the nanoparticles may be released from the wax resulting in homogenous nanoparticles instead of Janus nanoparticles. This can partially be corrected by using waxes with higher melting points or performing functionalization at lower temperatures. However, these modifications still result in significant loss. Granick et al. in another paper demonstrated a possible fix by utilizing a liquid-liquid/gas-solid phase hybrid method by first immobilizing silica nanoparticles in paraffin wax using the previously discussed liquid-solid phase interface method and then filtering off the water. The resulting immobilized nanoparticles were then exposed to silanol vapor produced by bubbling nitrogen or argon gas through liquid silanol causing the formation of a hydrophillic face. The wax was then dissolved in chloroform releasing the Janus nanoparticles.[18]

An example of a more traditionial liquid-solid technique has been described by Sardar et al. by beganing with the immobilization of gold nanoparticles on a salinized glass surface. Then the glass surface was exposed to 11-mercapto-1-undecanol which bound to the exposed hemisphere of the gold nanoparticle. The nanoparticles were then removed from the slide using ethanol containing 16-mercaptohexadecanoic acid which functionalized the previously masked hemisphere of the nanoparticle.[22]

Self Assembly[edit]

Block copolymers[edit]
Schematic representation of the synthesis of Janus nanoparticles utilizing the Block Copolymer self assembly method

This method utilizes the well studied methods of producing block copolymers with well defined geometries and composition across a large variety of substrates.[2][23] Synthesis of Janus particles by self assembly via block copolymers was first described in 2001 by Erhardt et al. . They produced a triblock polymer from polymethylacrylate, polystyrene and low molecular weight polybutadiene.The polystyrene and polymethylacrylate formed alternating layers in between which polybutadiene sat in nanosized spheres. The blocks were then cross-linked and dissolved in THF and after several washing steps yielded spherical Janus particles with polystyrene on one face and polymethylacrylate)on the other with a polybutadiene core. [24] The production of Janus spheres, cylinders, sheets, and ribbons is possible using this method by adjustment of the starting material's molecular weights and degree of cross-linking.[2][25]

Competitive adsorption[edit]

The key aspect of competitive absorption involves two substrates that phase-separate due to one or more opposite physical or chemical proprieties. When these substrates are mixed with a nanoparticle, typically gold, they maintain their separation and form two faces.[2][26] A good example of this technique has been demonstrated by Vilain et al. where phosphinine coated gold nanoparticles were exposed to long chain thiols resulting in substitution of the phosphinine ligands in a phase separated manner producing Janus nanoparticles. Phase separation was proven by showing the thiols formed one locally pure domain on the nanoparticle utilizing FT-IR.[26] Jakobs et al. demonstrated a major issue with the competitive adsorption method when they attempted to synthesize amphiphilic gold Janus nanoparticles utilizing the competitive adsorption of hydrophobic and hydrophilic thiols.[27] The synthesis demonstrated was quiet simple and only involved two steps. First gold nanoparticles capped with tetra-n-octylammonium bromide were produced. Then the capping agent was removed followed by the addition of various ratios of hydrophilic disulfide functionalized ethylene oxide and hydrophobic disulfide functionalized oligo(p-phenylenevinylene). They then attempted to prove that phase separation on the particle surface occurred by comparing the contact angles of water on the surface of a monolayer of the Janus particles with nanoparticles made with only the hydrophobic or hydrophobic ligands. Instead the results of this experiment showed that while there was some phase separation, it was not complete. [27] This result highlights that the ligand choice is extremely important and any changes may result in incomplete phase separation. [2][27]

Phase Separation[edit]

Scheme of the basic principle of phase separation method of producing Janus nanoparticles.Two incompatible substances (A and B) ware mixed forming a nanoparticle. A and B then separate into their own domains while still part of a single nanoparticle.

This method involves the mixing of two or more incompatible substances which then separate into their own domains while still part of a single nanoparticle. These methods can involve the production of Janus nanoparticles of two inorganic as well as two organic substances.[2]

Typical organic phase separation methods use co-jetting of polymers to produce Janus nanoparticles. This technique is exemplified by the work of Yoshid et al. to produce Janus nanoparticles where one hemisphere has affinity for human cells while the other hemisphere has no affinity for human cells. This was achieved by co-jetting polyacrylamide/poly(acrylic acid) co-polymers which have no affinity for human cells with biotinylated polyacrylamide/poly(acrylic acid) co-polymers which when exposed to streptavidin modified antibodies obtain an affinity for human cells.[11]

The inorganic phase separation methods are diverse and vary greatly depending on the application.[2] The most common method utilizes the growth of a crystal of one inorganic substance on or from another inorganic nanoparticle.[2][28] A unique method for doing this has been developed by Gu et al. where iron-platinum nanoparticles were coated with sulfur reacted with cadmium acetylacetonate, trioctylphosphineoxide, and hexadecane-1,2-diol at 100oC producing nanoparticles with a Fe-Pt core and an amorphous CdS shell. The mixture was then heated to 280oC resulting in a phase transition and a partial eruption of the Fe-Pt from the core creating a pure Fe-Pt sphere attached to the CdS coated nanoparticle.[28] A new method of synthesizing inorganic Janus nanoparticles by phase separation has recently been developed by Zhao and Gao. In this method, they explored the use of the common homogeneous nanoparticle synthetic method of flame synthesis. They found that when a methanol solution containing ferric triacetylacetonate and tetraethylorthosilicate was burned, the iron and silicon components form an intermixed solid which undergoes phase separation when heated to approximately 1100oC producingmaghemite-silica Janus nanoparticles. Additionally, they found that it was possible to modify the silica after producing the Janus nanoparticles making it hydrophobic by reacting it with oleylamine. [29]

Properties and Applications[edit]

Self Assembly Behavior of Janus Nanoparticles[edit]

Janus particles' two or more distinct faces give them special properties in solution. In particluar, Janus particles have been observed to self-assemble in specific way in aqueous or organic solutions. In the case of spherical Janus micelles having hemispheres of polystyrene (PS) and poly(methyl methacrylate) (PMMA), aggregation into clusters has been observed in various organic solvents, such as tetrahydrofuran. Similarly, Janus discs composed of sides of PS and poly(tert-butyl methacrylate) (PtBMA) can undergo back-to-back stacking into superstructures when in an organic solution[14]. It is interesting that these particular Janus particles form aggregates in organic solvents considering that both sides of these particles are soluble in the organic solvent. It appears that the slight selectivity of the solvent is able to induce self-assembly of the particles into discrete clusters of Janus particles. This type of aggregation does not occur for either standard block copolymers nor for homogeneous particles and thus is a feature specific to Janus particles[14].

Additionally, the behavior of Janus particle in aqueous solutions is also very interesting. In an aqueous solution two kinds of biphasic particles can be distinguished. The first type are particles which are truly amphiphilic and possess one hydrophobic and one hydrophilic side. The second type has two water soluble yet chemically distinct sides. To illustrate the first case, extensive studies have been carried out with spherical Janus particles composed of one hemisphere of water-soluble poly(methacrylica cid) (PMAA) and another side of non water soluble polystyrene. In these studies, it was found that the Janus particles aggregate on two hierarchical levels. The first type of self assembled aggregates look like small clusters, similar to what you would find for the case of Janus particles in an organic solution. The second type of self assembled structure is noticeably larger than the first and is has been termed 'super micelle'. Unfortunately, the structure of the supermicelles is unknown so far; however, it was suggested that they may be similar to multilamellar vesicles[14].

For the second case of Janus particles which contain two distinct, but still water soluble sides the work of Granick’s group provides some insight. Granick's research deals with the clustering of dipolar (zwitterionic) micronsized Janus particles, whose two sides are both fully water soluble[30]. Zwitterionic Janus particles are interesting because they do not behave like classical dipoles, since their size is much larger than the distance at which electrostatic attractions are strongly felt. The study of zwitterionic janus particles once again demonstrates janus particles ability to form defined clusters. However, this particular type of janus particle prefers to aggregate into larger clusters since this is more energetically favorable because each cluster carries a macroscopic dipole which allows the aggregation of already formed clusters into larger assemblies. Compared to aggregates formed through van der waals interactions for homogenous particles, the shapes of the zwitterionic janus nanoclusters are different and the janus clusters are less dense and more asymmetric[14].

Self Assembly Modification using pH[edit]

The self assembly of certain types of Janus particles may be controlled via modifying the pH of the solution that they are in. Lattuada et al. prepared nanoparticles with one side coated with a pH responsive polymer (polyacrylic acid, PAA) and the other with either a positively charged polymer (Poly dimethylamino ethyl methacrylate, PDMAEMA), a negatively charged pH-insensitive polymer, or a temperature responsive polymer (Poly N-isopropyl Acryl amide, PNIPAm)[2]. In changing the pH of their solution, they noticed a change in the clustering of their Janus nanoparticles. At very high pH values, where PDMAEMA is uncharged while PAA is highly charged the Janus nanoparticles were very stable in solution. However, below a pH of 4, when PAA is uncharged and PDMAEMA is positively charged they formed finite clusters. At intermediate pH values, they found that the janus nanoparticles were unstable due to dipolar interaction between the positively and negatively charged hemispheres[2]

Reversibility of Cluster Formation and Control of Cluster Size[edit]

Control of cluster size for in the aggregation of janus nanoparticles has also been demonstrated. Lattuada et al. achieved control of the cluster size of janus particles with one face PAA and the other either PDMAEMA or PNIPAm by mixing small amounts of these Janus nanoparticles with PAA coated particles[2]. One unique feature of these clusters was that stable particles could be recovered reversibly when high pH conditions were restored. Furthermore, Janus nanoparticles functionalized with PNIPAm showed that controlled and reversible aggregation could be achieved by increasing the temperature above the lower critical solubility temperature of PNIPAm.

Amphiphilic Properties[edit]

A significant characteristic of Janus nanoparticles is the capability of having both hydrophilic and hydrophobic parts. Many research groups have investigated the surface activities of nanoparticles with amphiphilic properties. In 2006, Janus nanoparticles, made from gold and iron oxide, were compared with their homogeneous counterparts by measuring the ability of the particles to reduce the interfacial tension between water and n-hexane.[31] Experimental results indicated that Janus nanoparticles are considerably more surface active than homogeneous particles of comparable size and chemical nature. Furthermore, increasing the [amphiphile|amphiphilic]] character of the particles can increase the interfacial activity. The ability of Janus nanoparticles to lower interfacial tension between water and n-hexane confirmed previous theoretical predictions on the ability of Janus nanoparticles to stabilize Pickering emulsions.

In 2007, the amphiphilic nature of the Janus nanoparticles was examined by measuring the adhesion force between the atomic force microscopy (AFM) tip and the particle surface.[32] The stronger the interactions between the hydrophilic AFM tip and the hydrophilic side of the Janus nanoparticles were reflected by a greater adhesion force. The Janus nanoparticles were dropcast onto both hydrophobically and hydrophilically modified substrates. The hydrophobic hemisphere of the Janus particles was exposed when a hydrophilic substrate surface was used, resulting in disparities in adhesion force measurements. Thus, the Janus nanoparticles adopted a conformation that maximized the interactions with the substrate surface.

The nature of amphiphilic Janus nanoparticles to orient themselves spontaneously at the interface between oil and water has been well known.[33][34][35] This behavior allows considering [amphiphile|amphiphilic]] Janus nanoparticles as analogues of molecular surfactants for the stabilization of emulsions. In 2005, spherical silica particles with amphiphilic properties were prepared by partial modification of the external surface with an alkylsilane agent. These particles form spherical assemblies encapsulating water-immiscible organic compounds in aqueous media by facing their hydrophobic alkylsilylated side to the inner organic phase and their hydrophilic side to the outer aqueous phase, thus stabilizing oil droplets in water.[36] In 2009, hydrophilic surface of silica particles was made partially hydrophobic by adsorbing cetyltrimethylammonium bromide. These amphiphilic nanoparticles spontaneously assembled at the water-dichloromethane interface.[37] In 2010, Janus particles composed from silica and polystyrene, with the polystyrene portion loaded with nanosized magnetite particles, were used to form kinetically stabile oil-in-water emulsions that can be spontaneously broken on application of an external magnetic field.[38] Such Janus materials will find applications in magnetically controlled optical switches and other related areas. The first real applications of Janus nanoparticles were in polymer synthesis. In 2008, it was shown that spherical amphiphilic Janus nanoparticles, having one polystyrene and one poly(methyl methacrylate) side, were effective as compatibilizing agents of multigram scale compatibilization of two immiscible polymer blends, polystyrene and poly(methyl methacrylate).[12] The Janus nanoparticles oriented themselves at the interface of the two polymer phases, even under high temperature and shear conditions, allowing the formation of much smaller domains of poly(methyl methacrylate) in a polystyrene phase. The performance of the Janus nanoparticles as compatibilizing agents was significantly superior to other state-of-the-art compatibilizers, such as linear block copolymers.

Stabilizers in Emulsion[edit]

A similar application of Janus nanoparticles as stabilizers was shown in emulsion polymerization. In 2008, spherical amphiphilic Janus nanoparticles was applied for the first time to the emulsion polymerization of styrene and n-butyl acrylate.[39] The polymerization did not require additives or mini-emulsion polymerization techniques, as do other Pickering emulsion polymerizations. Also, by applying Janus nanoparticles the emulsion polymerization produced very well controlled particle sizes with low polydispersities.

Catalyst in Hydrogen Peroxide Decomposition[edit]

In 2010, spherical silica Janus nanoparticles with one side coated with platinum were used for the first time to catalyze the decomposition of hydrogen peroxide (H2O2).[40] The platinum particle catalyzes the surface chemical reaction: 2H2O2 → O2 + H2O. The decomposition of hydrogen peroxide created Janus catalytic nanomotors, the motion of which was analyzed experimentally and theoretically utilizing computer simulations. The motion of the spherical Janus nanoparticles was found to agree with the predictions of computed simulations. Ultimately, catalytic nanomotors have practical applications in delivering chemical payloads in microfluidic chips, eliminating pollution in aquatic media, removing toxic chemicals within biological systems, and performing medical procedures.

Water Repellent Fibers[edit]

In 2011, Janus nanoparticles were shown to be applicable in textiles. Water repellent fibers can be prepared by coating polyethylene terephthalate fabric with amphiphilic spherical Janus nanoparticles.[10] The Janus particles bind with the hydrophilic reactive side to the textile surface, while the hydrophobic side exposed to the environment, thus providing the water repellent behavior. Janus particle size of 200 nm was found to deposit on the surface of fibers and were very efficient for the design of water repellent textiles.

Applications in Biological Sciences[edit]

The groundbreaking progress in the biological sciences has led to a drive towards custom made materials with precisely designed physical/chemical properties at the nanoscale level. Inherently Janus nanoparticles play a crucial role in such applications. In 2009, a new type of bio-hybrid material composed of Janus nanoparticles with spatially controlled affinity towards human endothelial cells was reported.[11] These nanoparticles were synthesized by selective surface modification with one hemisphere exhibiting high binding affinity for human endothelial cells and the other hemisphere being resistant towards cell binding. The Janus nanoparticles were fabricated via electrohydrodynamic jetting of two polymer liquid solutions. When incubated with human endothelial cells, these Janus nanoparticles exhibited expected behavior, where one face binds toward human endothelial cells, while the other face was non-bonding. These Janus nanoparticles not only bound to the top of the human endothelial cells, but also associated all around the perimeter of cells forming a single particle lining. The biocompatibility between the Janus nanoparticles and cells was excellent. The concept is to eventually design probes based on Janus nanoparticles to attain directional information about cell-particle interactions.

Nanocorals[edit]

In 2010, a new type of cellular probe synthesized from Janus nanoparticles called a nanocoral, combining cellular specific targeting and biomolecular sensing, was presented.[41] Nanocoral is comprised of a polystyrene hemisphere and a gold hemisphere. The polystyrene hemisphere of the nanocoral was selectively functionalized with antibodies to target receptors of specific cells. This was demonstrated by functionalizing the polystyrene region with antibodies that specifically attached to breast cancer cells. The gold region of the nanocoral surface was utilized for detecting and imaging. Thus, the targeting and sensing mechanisms were decoupled and could be separately engineered for a particular experiment. Additionally, the polystyrene region may also be used as a carrier for drugs and other chemicals by surface hydrophobic adsorption or encapsuation, making the nanocoral a possible multifunctional nanosensor.

Imaging and Magnetolytic Therapy[edit]

Also in 2010, Janus nanoparticles synthesized from hydrophobic magnetic nanoparticles on one side and poly(styrene-block-allyl alcohol) on the other side were used for imaging and magnetolytic therapy.[13] The magnetic side of the Janus nanoparticles responded well to external magnetic stimuli. The nanoparticles were quickly attached to the cell surface using a magnetic field. Magnetolytic therapy was achieved through magnetic field modulated cell membrane damage. First, the nanoparticles were brought close in contact with the tumor cells, and then a spinning magnetic field was applied. After 15 minutes, the majority of the tumor cells were killed. Magnetic Janus nanoparticles could serve as the basis for potential applications in medicine and electronics. Quick responses to external magnetic fields could become an effective approach for targeted imaging, therapy in vitro and in vivo, and cancer treatment. Similarly, a quick response to magnetic fields is also desirable to fabricate smart displays, opening new opportunities in electronics and spintronics.

In 2011, silica coated Janus nanoparticles, composed of silver and iron oxide (Fe2O3), were prepared in one-step with scalable flame aerosol technology.[42] These hybrid plasmonic-magnetic nanoparticles bear properties that are applicable in bioimaging, targeted drug delivery, in vivo diagnosis, and therapy. The purpose of the nanothin SiO2 shell was to reduce the release of toxic Ag+ ions from the nanoparticle surface to live cells. As a result, these hybrid nanoparticles showed no cyctotoxicity during bioimaging and remained stable in suspension with no signs of agglomeration or settling, thus enabling these nanoparticles as biocompatible multifunctional probes for bioimaging. Next, by labeling their surface and selectively binding them on the membrane of live-tagged Raji and HeLa cells, this demonstrated the nanoparticles as biomarkers and their detection under dark-field illumination was achieved. These new hybrid Janus nanoparticles overcame the individual limitations of Fe2O3 (poor particle stability in suspension) and of Ag (toxicity) nanoparticles, while retaining the desired magnetic properties of Fe2O3 and the plasmonic optical properties of Ag.

Applications in electronics[edit]

The potential application of Janus particles was first demonstrated by Nisisako et al., who made use of the electrical anisotropy of Janus particles filled with white and black pigments in both hemispheres.[43] These particles were used to make switchable screens by placing a thin layer of these spheres between two electrodes. Upon changing the applied electric field, the particles orient their black sides to the anode and their white sides to the cathode. Thus the orientation and the color of the display can be changed by simply reversing the electric field. With this method it may be possible to make very thin and environmentally friendly displays.

Janus particles handling by dielectrophoresis[edit]

Janus particles Au/fluorescent polystyrene are fabricated and their flip/flop rotational effect is studied in a microfluidic channel thanks to dielectrophoresis, providing a new type of local light switch. A method for producing large amounts more than 10^6 particles/ml of Janus particles is first presented. Those particles were then injected in an electromicrofluidic chip and stabilized in the fluid by a dielectrophoretic trap. The spanning frequency of this trap allowed performing a “flip-flop” effect of the Janus particles by recording their fluorescent intensities. Flip Au top side and flop PS top side frequencies are identified. Experiments were performed on the time triggered commutations between flip and flop frequencies to define the capability of each Janus particle to sustain speed control of their flip-flop. [44], [45]

External links[edit]

References[edit]

  1. ^ Li, Fan; Josephson, David P.; Stein, Andreas (2011-01-10). "Colloidal Assembly: The Road from Particles to Colloidal Molecules and Crystals". Angewandte Chemie International Edition. 50 (2): 360–388. doi:10.1002/anie.201001451. ISSN 1521-3773. PMID 21038335. Retrieved 2011-09-23.
  2. ^ a b c d e f g h i j k l m Lattuada, Marco; Hatton, T. Alan (1 June 2011). "Synthesis, properties and applications of Janus nanoparticles". Nano Today. 6 (3): 286–308. doi:10.1016/j.nantod.2011.04.008.
  3. ^ Granick, Steve; Jiang, Shan; Chen, Qian (2009). "Janus particles". Physics Today. 62 (7): 68–69. doi:10.1063/1.3177238. ISSN 0031-9228. Retrieved 2011-09-15.
  4. ^ Casagrande C., Veyssie M., C. R. Acad. Sci. (Paris), 306 11, 1423, 1988.
  5. ^ a b Casagrande. C., Fabre P., Veyssie M., Raphael E., Europhys. Lett., 9, 251, 1989.
  6. ^ de Gennes, Pierre‚ÄêGilles (1992-07-01). "Soft Matter (Nobel Lecture)". Angewandte Chemie International Edition in English. 31 (7): 842–845. doi:10.1002/anie.199208421. ISSN 1521-3773. Retrieved 2011-09-23.
  7. ^ de Gennes, Pierre-Gilles (1997-07-15). "Nanoparticles and Dendrimers: Hopes and Illusions". Croatica Chemica Acta. 71 (4): 833–836. Retrieved 2011-10-04.
  8. ^ Cho, Iwhan; Lee, Kyung-Woo (1985-05-01). "Morphology of latex particles formed by poly(methyl methacrylate)'Äêseeded emulsion polymerization of styrene". Journal of Applied Polymer Science. 30 (5): 1903–1926. doi:10.1002/app.1985.070300510. ISSN 1097-4628. Retrieved 2011-10-05.
  9. ^ Binks, B. P. (2011-10-05). "Particles Adsorbed at the Oil'àíWater Interface:'Äâ A Theoretical Comparison between Spheres of Uniform Wettability and 'ÄúJanus'Äù Particles". Langmuir. 17 (16): 4708–4710. doi:10.1021/la0103315. ISSN 0743-7463. Retrieved 2011-10-05. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  10. ^ a b Synytska, Alla; Khanum, Rina; Ionov, Leonid; Cherif, Chokri; Bellmann, C. (2011-09-25). "Water-Repellent Textile via Decorating Fibers with Amphiphilic Janus Particles". ACS Appl. Mater. Interfaces. 3 (4): 1216–1220. doi:10.1021/am200033u. ISSN 1944-8244. PMID 21366338. Retrieved 2011-09-25.
  11. ^ a b c Yoshida, Mutsumi; Roh, Kyung-Ho; Mandal, Suparna; Bhaskar, Srijanani; Lim, Dongwoo; Nandivada, Himabindu; Deng, Xiaopei; Lahann, Joerg (2009-12-28). "Structurally Controlled Bio'Äêhybrid Materials Based on Unidirectional Association of Anisotropic Microparticles with Human Endothelial Cells". Advanced Materials. 21 (48): 4920–4925. doi:10.1002/adma.200901971. ISSN 1521-4095. PMID 25377943. Retrieved 2011-09-25.
  12. ^ a b Walther, Andreas; Matussek, Kerstin; Müller, Axel H. E. (2011-09-25). "Engineering Nanostructured Polymer Blends with Controlled Nanoparticle Location using Janus Particles". ACS Nano. 2 (6): 1167–1178. doi:10.1021/nn800108y. ISSN 1936-0851. PMID 19206334. Retrieved 2011-09-25.
  13. ^ a b Hu, Shang-Hsiu; Gao, Xiaohu (2011-09-25). "Nanocomposites with Spatially Separated Functionalities for Combined Imaging and Magnetolytic Therapy". J. Am. Chem. Soc. 132 (21): 7234–7237. doi:10.1021/ja102489q. ISSN 0002-7863. PMID 20459132. Retrieved 2011-09-25.
  14. ^ a b c d e f Walther, Andreas; Müller, Axel H. E. (1 January 2008). "Janus particles". Soft Matter. 4 (4): 663–668. doi:10.1039/b718131k. PMID 32907169.
  15. ^ Perro, Adeline; Reculusa, Stéphane; Ravaine, Serge; Bourgeat-Lami, Elodie; Duguet, Etienne (1 January 2005). "Design and synthesis of Janus micro- and nanoparticles". Journal of Materials Chemistry. 15 (35–36): 3745. doi:10.1039/b505099e.
  16. ^ Lu, Yu; Xiong, Hui; Jiang, Xuchuan; Xia, Younan; Prentiss, Mara; Whitesides, George M. (1 October 2003). "Asymmetric Dimers Can Be Formed by Dewetting Half-Shells of Gold Deposited on the Surfaces of Spherical Oxide Colloids". Journal of the American Chemical Society. 125 (42): 12724–12725. doi:10.1021/ja0373014. PMID 14558817.
  17. ^ Jiang, Shan; Chen, Qian; Tripathy, Mukta; Luijten, Erik; Schweizer, Kenneth S.; Granick, Steve (27 January 2010). "Janus Particle Synthesis and Assembly". Advanced Materials. 22 (10): 1060–1071. doi:10.1002/adma.200904094. PMID 20401930.
  18. ^ a b Jiang, Shan; Schultz, Mitchell J.; Chen, Qian; Moore, Jeffrey S.; Granick, Steve (16 September 2008). "Solvent-Free Synthesis of Janus Colloidal Particles". Langmuir. 24 (18): 10073–10077. doi:10.1021/la800895g. PMID 18715019.
  19. ^ a b Pradhan, S.; Xu, L.; Chen, S. (24 September 2007). "Janus Nanoparticles by Interfacial Engineering". Advanced Functional Materials. 17 (14): 2385–2392. doi:10.1002/adfm.200601034.
  20. ^ Gu, Hongwei; Yang, Zhimou; Gao, Jinhao; Chang, C. K.; Xu, Bing (1 January 2005). "Heterodimers of Nanoparticles: Formation at a Liquid−Liquid Interface and Particle-Specific Surface Modification by Functional Molecules". Journal of the American Chemical Society. 127 (1): 34–35. doi:10.1021/ja045220h. PMID 15631435.
  21. ^ Hong, Liang; Jiang, Shan; Granick, Steve (1 November 2006). "Simple Method to Produce Janus Colloidal Particles in Large Quantity". Langmuir. 22 (23): 9495–9499. doi:10.1021/la062716z. PMID 17073470.
  22. ^ Sardar, Rajesh; Heap, Tyler B.; Shumaker-Parry, Jennifer S. (1 May 2007). "Versatile Solid Phase Synthesis of Gold Nanoparticle Dimers Using an Asymmetric Functionalization Approach". Journal of the American Chemical Society. 129 (17): 5356–5357. doi:10.1021/ja070933w. PMID 17425320.
  23. ^ Kim, Jaeup U.; Matsen, Mark W. (1 February 2009). "Positioning Janus Nanoparticles in Block Copolymer Scaffolds". Physical Review Letters. 102 (7): 078303. doi:10.1103/PhysRevLett.102.078303. PMID 19257718.
  24. ^ Erhardt, Rainer; Böker, Alexander; Zettl, Heiko; Kaya, Håkon; Pyckhout-Hintzen, Wim; Krausch, Georg; Abetz, Volker; Müller, Axel H. E. (1 February 2001). "Janus Micelles". Macromolecules. 34 (4): 1069–1075. doi:10.1021/ma000670p.
  25. ^ Wolf, Andrea; Walther, Andreas; Müller, Axel H. E. (3 November 2011). "Janus Triad: Three Types of Nonspherical, Nanoscale Janus Particles from One Single Triblock Terpolymer". Macromolecules. 44 (23): 9221–9229. doi:10.1021/ma2020408.
  26. ^ a b Vilain, Claire; Goettmann, Frédéric; Moores, Audrey; Le Floch, Pascal; Sanchez, Clément (1 January 2007). "Study of metal nanoparticles stabilised by mixed ligand shell: a striking blue shift of the surface-plasmon band evidencing the formation of Janus nanoparticles". Journal of Materials Chemistry. 17 (33): 3509. doi:10.1039/b706613a.
  27. ^ a b c Jakobs, Robert T. M.; Van Herrikhuyzen, Jeroen; Gielen, Jeroen C.; Christianen, Peter C. M.; Meskers, Stefan C. J.; Schenning, Albertus P. H. J. (1 January 2008). "Self-assembly of amphiphilic gold nanoparticles decorated with a mixed shell of oligo(p-phenylene vinylene)s and ethyleneoxide ligands". Journal of Materials Chemistry. 18 (29): 3438. doi:10.1039/b803935f.
  28. ^ a b Gu, Hongwei; Zheng, Rongkun; Zhang, Xixiang; Xu, Bing (1 May 2004). "Facile One-Pot Synthesis of Bifunctional Heterodimers of Nanoparticles: A Conjugate of Quantum Dot and Magnetic Nanoparticles". Journal of the American Chemical Society. 126 (18): 5664–5665. doi:10.1021/ja0496423. PMID 15125648.
  29. ^ Zhao, Nan; Gao, Mingyuan (12 January 2009). "Magnetic Janus Particles Prepared by a Flame Synthetic Approach: Synthesis, Characterizations and Properties". Advanced Materials. 21 (2): 184–187. doi:10.1002/adma.200800570.
  30. ^ Hong, Liang; Cacciuto, Angelo; Luijten, Erik; Granick, Steve (2006). "Clusters of Charged Janus Spheres". Nano Letters. 6 (11): 2510–2514. doi:10.1021/nl061857i. PMID 17090082.
  31. ^ Glaser, Nicole (2006). "Janus Particles at Liquid'àíLiquid Interfaces". Langmuir. 22 (12): 5227–5229. doi:10.1021/la060693i. ISSN 0743-7463. PMID 16732643. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  32. ^ Xu, Li-Ping; Pradhan, Sulolit; Chen, Shaowei (2007). "Adhesion Force Studies of Janus Nanoparticles". Langmuir. 23 (16): 8544–8548. doi:10.1021/la700774g. ISSN 0743-7463. PMID 17595125.
  33. ^ Binks, B. P.; Lumsdon, S. O. (2000). "Catastrophic Phase Inversion of Water-in-Oil Emulsions Stabilized by Hydrophobic Silica". Langmuir. 16 (6): 2539–2547. doi:10.1021/la991081j. ISSN 0743-7463.
  34. ^ Dinsmore, A. D.; Hsu, Ming F.; Nikolaides, M. G.; Marquez, Manuel; Bausch, A. R.; Weitz, D. A. (2002-11-01). "Colloidosomes: Selectively Permeable Capsules Composed of Colloidal Particles". Science. 298 (5595): 1006–1009. doi:10.1126/science.1074868. PMID 12411700. Retrieved 2011-11-20.
  35. ^ Aveyard, Robert; Binks, Bernard P.; Clint, John H. (2003-02-28). "Emulsions stabilised solely by colloidal particles". Advances in Colloid and Interface Science. 100–102: 503–546. doi:10.1016/S0001-8686(02)00069-6. ISSN 0001-8686. Retrieved 2011-11-20.
  36. ^ Takahara, Yoshiko K.; Ikeda, Shigeru; Ishino, Satoru; Tachi, Koji; Ikeue, Keita; Sakata, Takao; Hasegawa, Toshiaki; Mori, Hirotaro; Matsumura, Michio; Ohtani, Bunsho (2005). "Asymmetrically Modified Silica Particles:'Äâ A Simple Particulate Surfactant for Stabilization of Oil Droplets in Water". J. Am. Chem. Soc. 127 (17): 6271–6275. doi:10.1021/ja043581r. ISSN 0002-7863. PMID 15853333.
  37. ^ Perro, Adeline; Meunier, Fabrice; Schmitt, Véronique; Ravaine, Serge (2009-01-05). "Production of large quantities of 'ÄúJanus'Äù nanoparticles using wax-in-water emulsions". Colloids and Surfaces A: Physicochemical and Engineering Aspects. 332 (1): 57–62. doi:10.1016/j.colsurfa.2008.08.027. ISSN 0927-7757. Retrieved 2011-10-30.
  38. ^ Teo, Boon M.; Suh, Su Kyung; Hatton, T. Alan; Ashokkumar, Muthupandian; Grieser, Franz (2010). "Sonochemical Synthesis of Magnetic Janus Nanoparticles". Langmuir. 27 (1): 30–33. doi:10.1021/la104284v. ISSN 0743-7463. PMID 21133341.
  39. ^ Walther, Andreas; Hoffmann, Martin; Müller, Axel H. E. (2008-01-11). "Emulsion Polymerization Using Janus Particles as Stabilizers". Angewandte Chemie International Edition. 47 (4): 711–714. doi:10.1002/anie.200703224. ISSN 1521-3773. PMID 18069717. Retrieved 2011-10-30.
  40. ^ Valadares, Leonardo F.; Tao, Yu-Guo; Zacharia, Nicole S.; Kitaev, Vladimir; Galembeck, Fernando; Kapral, Raymond; Ozin, Geoffrey A. (2010-02-22). "Catalytic Nanomotors: Self'ÄêPropelled Sphere Dimers". Small. 6 (4): 565–572. doi:10.1002/smll.200901976. ISSN 1613-6829. PMID 20108240. Retrieved 2011-10-30.
  41. ^ Wu, Liz Y.; Ross, Benjamin M.; Hong, Soongweon; Lee, Luke P. (2010-02-22). "Bioinspired Nanocorals with Decoupled Cellular Targeting and Sensing Functionality". Small. 6 (4): 503–507. doi:10.1002/smll.200901604. ISSN 1613-6829. PMID 20108232. Retrieved 2011-11-05.
  42. ^ Sotiriou, Georgios A.; Hirt, Ann M.; Lozach, Pierre-Yves; Teleki, Alexandra; Krumeich, Frank; Pratsinis, Sotiris E. (2011). "Hybrid, Silica-Coated, Janus-Like Plasmonic-Magnetic Nanoparticles". Chem. Mater. 23 (7): 1985–1992. doi:10.1021/cm200399t. ISSN 0897-4756. PMC 3667481. PMID 23729990.
  43. ^ Nisisako, T.; Torii, T.; Takahashi, T.; Takizawa, Y. (2006). "Synthesis of Monodisperse Bicolored Janus Particles with Electrical Anisotropy Using a Microfluidic Co-Flow System". Adv. Mater. 18 (9): 1152–1156. doi:10.1002/adma.200502431.
  44. ^ Thibault Honegger, O. Lecarme, K. Berton and D. Peyrade, Microelectron. Eng., 2010, 87, 756–759.
  45. ^ Thibault Honegger, O. Lecarme, K. Berton and D. Peyrade, J. Vac. Sci. Technol., B, 2010, 5, 1 – 3.
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