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[[Image:Figure1nnew.jpg|thumb|300px|right|Figure 1: Photograph of an AFM system which can be used for chemical force microscopy.]]
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'''Chemical force microscopy''' (CFM) is a variation of [[atomic force microscopy]] (AFM) which has become a versatile tool for characterization of materials surfaces. With AFM, structural morphology is probed using simple tapping or contact modes that utilize [[van der Waals force|van der Waals interactions]] between tip and sample to maintain a constant probe deflection amplitude (constant force mode) or maintain height while measuring tip deflection (constant height mode). CFM, on the other hand, uses chemical interactions between functionalized probe tip and sample. Choice chemistry is typically gold-coated tip and surface with R-SH [[thiol]]s attached, R being the functional groups of interest. CFM enables the ability to determine the chemical nature of surfaces, irrespective of their specific morphology, and facilitates studies of basic chemical bonding enthalpy and surface energy. Typically, CFM is limited by thermal vibrations within the cantilever holding the probe. This limits force measurement resolution to ~1 pN which is still very suitable considering weak COOH/CH<sub>3</sub> interactions are ~20 pN per pair.<ref name=fris>{{cite journal|author=Frisbie, C. D.; Rozsnyai, L. F.; Noy, A.; Wrighton, M. S.; Lieber, C. M. |journal=Science|year=1994|volume=265|page=2071|doi=10.1126/science.265.5181.2071|title=Functional Group Imaging by Chemical Force Microscopy|pmid=17811409|issue=5181|bibcode = 1994Sci...265.2071F }}</ref><ref name=noy>{{cite journal|author=Noy, A.; Vezenov, D. V.; Lieber, C. M.|journal= Annu. Rev. Mater. Sci.|year=1997|volume=27|page=381|doi=10.1146/annurev.matsci.27.1.381|title=Chemical Force Microscopy|bibcode = 1997AnRMS..27..381N }}</ref> Hydrophobicity is used as the primary example throughout this consideration of CFM, but certainly any type of bonding can be probed with this method.
 
==Pioneering work==
CFM has been primarily developed by [[Charles Lieber]] at Harvard University in 1994.<ref name=fris/> The method was demonstrated using hydrophobicity where polar molecules (e.g. COOH) tend to have the strongest binding to each other, followed by nonpolar (e.g. CH<sub>3</sub>-CH<sub>3</sub>) bonding, and a combination being the weakest. Probe tips are functionalized and substrates patterned with these molecules. All combinations of functionalization were tested, both by tip contact and removal as well as spatial mapping of substrates patterned with both moieties and observing the complementarity in image contrast. Both of these methods are discussed below. The AFM instrument used is similar to the one in Figure 1.
 
==Force of adhesion (tensile testing)==
[[Image:Figure2new.png|thumb|400px|right|Figure 2: (Left) Probe tip being pulled from a similarly functionalized patterned area on the substrate to determine adhesion force.
(Right) Typical force profile for adhesion force measurements. The dashed line is indicative of detachment for less probe-substrate interaction versus the solid line.]]
 
This is the simpler mode of CFM operation where a functionalized tip is brought in contact with the surface and is pulled to observe the force at which separation occurs, F<sub>ad</sub> (see Figure 2). The Johnson-Kendall-Roberts (JKR) theory of adhesion mechanics predicts this value as <ref name=fris/><ref name=noy/>
 
(1) <math>F_{ad}=\frac{3}{2}\pi RW_{STM}</math>
 
where W<sub>SMT</sub> = γ<sub>SM</sub>+γ<sub>TM</sub>-γ<sub>ST</sub> with R being the radius of the tip, and γ being various surface energies between the tip, sample, and the medium each is in (liquids discussed below). R is usually obtained from SEM and γ<sub>SM</sub> and γ<sub>TM</sub> from contact angle measurements on substrates with the given moieties. When the same functional groups are used, γ<sub>SM</sub> = γ<sub>TM</sub> and γ<sub>ST</sub> = 0 which results in F<sub>ad</sub> = 3πRγ<sub>SM, TM</sub>. Doing this twice with two different moieties (e.g. COOH and CH<sub>3</sub>) gives values of γ<sub>SM</sub> and γ<sub>TM</sub>, both of which can be used together in the same experiment to determine γ<sub>ST</sub>. Therefore, F<sub>ad</sub> can be calculated for any combination of functionalities for comparison to CFM determined values.
 
For similarly functionalized tip and surface, at tip detachment JKR theory also predicts a contact radius of<ref name=noy/>
 
(2) <math> r=(\frac{3\pi \gamma R^{2}}{K})^{\frac{1}{3}}</math>
 
with an “effective” [[Young's modulus]] of the tip K=(2/3)(E/(1-ν<sup>2</sup>)) derived from the actual value E and the [[Poisson ratio]] ν. If one knows the effective area of a single functional group, A<sub>FG</sub> (e.g. from quantum chemistry simulations), the total number of ligands participating in tension can be estimated as <math>\scriptstyle \pi r^2 /A_{FG}</math>. As stated earlier, the force resolution of CFM does allow one to probe individual bonds of even the weakest variety, but tip curvature typically prevents this. Using Eq 2, a radius of curvature R<10&nbsp;nm has been determined as the requirement to conduct tensile testing of individual linear moieties.<ref name=noy/>
 
[[Image:Figure3.png|thumb|300px|right|Figure 3: (Top) Scan of a patterned surface with regular tip (no functional groups) would produce an image with no contrast because the surface is morphologically uniform.
(Middle) A hydrophilic tip on the hydrophilic functionalized portion of the surface causes the cantilever to bend due to strong interactions which is detected by laser deflection therefore producing a chemical profile image of the surface.
(Bottom) Cantilever functionalization is switched such that the tip is bent when encountering hydrophobic areas of the substrate instead.]]
A quick note to mention is the work corresponding to the hysteresis in the force profile (Figure 2) does not correlate to the bond energy. The work done in retracting the tip is <math>W=\int Fdx\approx \frac{1}{2}F_{max}\Delta x</math>, approximated due to the linear behavior of deformation with F<sub>max</sub> being the force and Δx being the displacement immediately before release. Using the results of Frisbie et al.,<ref name=fris/> normalized to the estimated 50 functional groups in contact, the work values are estimated as 39 eV, 0.25 eV, and 4.3 eV for COOH/COOH, COOH/CH<sub>3</sub>, and CH<sub>3</sub>/CH<sub>3</sub> interactions, respectively. Roughly, intermolecular bond energies can be calculated by: E<sub>bond</sub>=kT<sub>B</sub>, T<sub>B</sub> being the boiling point. According to this, E<sub>bond</sub> = 32.5 meV for [[formic acid]], HCOOH, and 9.73 meV for [[methane]], CH<sub>4</sub>, each value being about 3 orders of magnitude smaller than the experiment might suggest. Even if surface passivation with EtOH were considered (discussed below), the large error seems irrecoverable. The strongest hydrogen bonds are at most ~1 eV in energy.<ref>{{cite journal|author=Emsley|journal=J. Chem. Soc. Rev.|year=1980|volume= 9|page=91|doi=10.1039/cs9800900091|title=Very strong hydrogen bonding}}</ref> This strongly implies that the cantilever has a force constant smaller than or on the order of that for bond interactions and, therefore, it cannot be treated as perfectly rigid. This does open an avenue for increasing the usefulness of CFM if stiffer cantilevers can be used while still maintaining force resolution.
 
==Frictional force mapping==
Chemical interactions can also be used to map prepatterned substrates with varying functionalities (see Figure 3). Scanning of a surface having varying hydrophobicity with a tip having no functional groups attached would produce an image with no contrast because the surface is morphologically featureless (simple AFM operation). Functionalizing a tip to be hydrophilic would cause the cantilever to bend when the tip scans across hydrophilic portions of the substrate due to strong tip-substrate interactions. This is detected by laser deflection in a [[position sensitive detector]] therefore producing a chemical profile image of the surface. Generally, a brighter area would correspond to a greater amplitude of deflection so stronger bonding corresponds to lighter areas of a CFM image map. When the cantilever functionalization is switched such that the tip is bent when encountering hydrophobic areas of the substrate instead, the complementary image is observed.
 
[[Image:Figure4.png|thumb|200px|right|Figure 4: Typical response of frictional force to applied load by the tip. Stronger tip-substrate interactions result in steeper slopes.]]
Frictional force response to the amount of perpendicular load applied by the tip on to the substrate is shown in Figure 4. Increasing tip-substrate interactions produce a steeper slope, as one would expect. Of experimental importance is the fact that contrast between different functionalities on the surface may be enhanced with an application of greater perpendicular force. Of course, this comes at the cost of potential damage to the substrate.
 
==Ambient: measurements in liquids==
Capillary force is a major problem in tensile force measurements since it effectively strengthens the tip-surface interaction. It is usually caused by adsorbed moisture on substrates from ambient environment. To eliminate this additional force, measurements in liquids can be conducted. With X-terminated tip and substrate in liquid L, the addition to F<sub>ad</sub> is calculated using Eq 1 with W<sub>XLX</sub> = 2γ<sub>LL</sub>; that is, the extra force comes from the attraction of liquid molecules to each other. This is ~10 pN for EtOH which still allows for the observation of even the weakest polar/nonpolar interactions (~20 pN).<ref name=noy/> The choice of liquid is dependent on which interactions are of interest. When the solvent is immiscible with functional groups, larger than usual tip-surface bonding exists. Therefore, organic solvents are appropriate for studying van der Waals and hydrogen bonding while electrolytes are best for probing hydrophobic and electrostatic forces.
 
==Applications in nanoscience==
[[Image:Figures5newnew.png|thumb|300px|right|Figure 5: (Left) Utilizing CFM for the unfolding of complex proteins. The force response during strain is shown. (Right) Carbon nanotube terminated tip functionalized at the nanotube end.]] A biological implementation of CFM at the nanoscale level is the unfolding of proteins with functionalized tip and surface (see Figure 5).<ref>{{cite journal|author=Zlatanova, J.; Lindsay, S. M.; Leuba, S. H. |journal=Prog. Biophys. Mol. Biol.|title=Single molecule force spectroscopy using the atomic force microscope|year=2000|pmid=11106806|volume=74|page=37|issue=1-2 | doi = 10.1016/S0079-6107(00)00014-6}}</ref> Due to the increased contact area, the tip and the surface act as anchors holding protein bundles while they separate. As uncoiling ensues, the force required jumps indicating various stages of uncoiling: (1) separation into bundles, (2) bundle separation into domains of crystalline protein held together by van der Waals forces, and (3) linearization of the protein upon overcoming the secondary bonding. Information on the internal structure of these complex proteins, as well as a better understanding of constituent interactions are provided with this method.
A second consideration is one that takes advantage of unique nanoscale materials properties. The high [[aspect ratio]] of [[carbon nanotubes]] (easily >1000) is exploited to image surfaces with deep features..<ref>{{cite journal|author=Wong, S. S.; Joselevich, E.; Woolley, A. T.; Cheung, C. L.; Lieber, C. M.|journal=Nature|year=1998|volume=394|page=52|doi=10.1038/27873|title=Covalently functionalized nanotubes as nanometre- sized probes in chemistry and biology|pmid=9665127|issue=6688|bibcode = 1998Natur.394...52W }}</ref> The use of the carbon material broadens the functionalization chemistry since there are countless routes to chemical modification of nanotube sidewalls (e.g. with diazonium, simple alkyls, hydrogen, ozone/oxygen, and amines). Multiwall nanotubes are typically used for their rigidity. Because of their approximately planar ends, one can estimate the number of functional groups that are in contact with the substrate knowing tube diameter and number of walls which helps in determining single moiety tensile properties. Certainly, this method has obvious implications in [[tribology]] as well.
==References==
{{reflist}}
 
[[Category:Microscopy]]
[[Category:Scanning probe microscopy]]

Latest revision as of 06:43, 2 December 2014

Seasonal Affective Disorder pertains to a depression that is triggered by a lack of sufficient lamp. As winter approaches, circumstance becomes more prominent while the days are shorter. So not only do get low light conditions. Anyone could have longer periods of low light. Compared to the 12-15 hours of sunshine that could be obtained during the warmer months, the number is about 8-10 hours.

Fear to become in crowded places every time you are surrounded with a sea of people, you find yourself vulnerable. What if somebody from using it crowd watches you intently and find out your flaws (whatever you think these are)? What if somebody available in everybody else is poking fun at you? What happens if somebody on the market is judging you? There are no cover, not to protect yourself, no defense.

Many sufferers realize their fears are extreme as well as have even confronted their fears face to face, but they don't just how to to control the online therapist for social anxiety symptoms and overcome them, it just keeps recurring. Usually sufferers will worry where did they were thought about hours following a social event, causing more stress.

I in order to practice what is known in yoga for the reason that Four Part Breath. Review yogic breath itself has four parts: the inhalation (puraka), the retention (kumbhaka), the exhalation (rechaka), and also the absence of breath within the body (shunyata). Just eating becoming associated with their existence and distinction as we breathe, we strengthen and slow our breath.

Afraid getting criticized virtually any reason, whether or not it is irrational. Significantly the above mention and other scenarios, we would tend keep away from standing out, or doing anything in that may any time. This may be just to avoid another issue below.

If carbohydrates learn tips on how to relax you can fight the anxiety attack symptoms, like sweating, racing heartbeat, muscle tension and tremors. Learn techniques like muscle relaxation and meditation and use them to relax when a panic or anxiety attack isn't too far off.

The exact cause is unknown and doctors actually think that several factors can cause outbreaks. Acne outbreaks happen in the oil-producing areas of this body-namely, the face, chest, and back but also occur around neck and upper arms. Adult acne may be caused by hormonal imbalances. Women obviously would scan these changes when pregnant, when using birth control pills extended period of time they their very own menstrual fertility cycle.

You ought to learn to spot when you have problems and ask for the assistance from your family and friends when you need it. Tell them occurred and allowed them to help in order to definitely recover from anxiety problem. If you can, look for advice regarding how you can eliminate the symptoms of anxiety. Support groups can also thought to be good idea and .