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'''Chemisorption''' is a kind of [[adsorption]] which involves a chemical reaction between the surface and the adsorbate.  New chemical bonds are generated at the adsorbant surface. Examples include macroscopic phenomena that can be very obvious, like [[corrosion]], and subtler effects associated with [[heterogeneous catalysis]]. The strong interaction between the [[adsorbate]] and the [[Substrate (chemistry)|substrate]] [[surface]] creates new types of electronic [[chemical bond|bonds]].<ref name="oura">{{cite book |first=K. |last=Oura |coauthors=V. G. Lifshits; A. A. Saranin; A. V. Zotov; M. Katayama |title=Surface Science, An Introduction |publisher=Springer |location=Berlin |year=2003 |isbn=3-540-00545-5}}</ref>
 
In contrast with chemisorption is [[physisorption]], which leaves the chemical species of the [[adsorbate]] and surface intact. It is conventionally accepted that the energetic threshold separating the [[binding energy]] of "physisorption" from that of "chemisorption" is about 0.5 eV per adsorbed [[Chemical species|species]].
 
Due to specificity, the nature of chemisorption can greatly differ, depending on the chemical identity and the surface structure.
 
==Uses==
An important example of chemisorption is in [[heterogeneous catalysis]] which involves molecules reacting with each other via the formation of chemisorbed intermediates.  After the chemisorbed species combine (by forming bonds with each other) the product desorbs from the surface.
[[Image:Hydrogenation on catalyst.png|thumb|[[Hydrogenation]] of an [[alkene]] on a solid catalyst entails chemisorption of the molecules of hydrogen and alkene, which form bonds to the surface atoms.]]
 
==Self-assembled monolayers==
[[Self-assembled monolayer]]s (SAMs) are formed by chemisorbing reactive reagents with metal surfaces.  A famous example involves [[thiol]]s (RS-H) absorbing onto the surface of [[gold]].  This process forms strong Au-SR bonds and releases H<sub>2</sub>.  The densely packed SR groups protect the surface. 
 
==Gas-surface Chemisorption==
===Adsorption Kinetics===
As an instance of adsorption, chemisorption follows the adsorption process.  The first stage is for the adsorbate particle to come into contact with the surface.  The particle needs to be trapped onto the surface by not possessing enough energy to leave the gas-surface [[potential well]]. If it elastically collides with the surface, then it would return to the bulk gas.  If it loses enough [[momentum]] through an [[inelastic collision]], then it “sticks” onto the surface, forming a precursor state bonded to the surface by weak forces, similar to physisorption.  The particle diffuses on the surface until it finds a deep chemisorption potential well.  Then it reacts with the surface or simply desorbs after enough energy and time.<ref name="rettner">{{cite journal |doi=10.1021/jp9536007 |first=C.T |last=Rettner |coauthors=Auerbach, D.J. |year=1996 |title=Chemical Dynamics at the Gas-Surface Interface |journal=Journal of Physical Chemistry |volume=100 |issue=31 |pages=13021–13033}}</ref>
 
The reaction with the surface is dependent on the chemical species involved. Applying [[Gibbs free energy]] equation for reactions:
 
:<math>\Delta G = \Delta H - T\Delta S</math>  
 
General [[thermodynamics]] states that for spontaneous reactions at constant temperature and pressure, the change in free energy should be negative.  Since a free particle is restrained to a surface, and unless the surface atom is highly mobile, entropy is lowered.  This means that the [[enthalpy]] term must be negative, implying an [[exothermic reaction]].<ref name="gasser">Gasser, R.P.H.; (1985) ''An introduction to chemisorption and catalysis by metals'', Clarendon Press, Oxford</ref>
 
<!-- [[Image:ljgraph.PNG|thumb|Figure 1: Graph of energy curves of physisorption (W-O<sub>2</sub>) and chemisorption (W-O). Chemisorption has a deeper energy well.  The graphs are shown to either cross above the zero-energy line or below it.]] Deleted file/image-->
Figure 1 is a graph of physisorption and chemisorption energy curves of [[tungsten]] and [[oxygen]].  Physisorption is given as a [[Lennard-Jones potential]] and chemisorption is given as a [[Morse potential]].  There exists a point of crossover between the physisorption and chemisorption, meaning a point of transfer. It can occur above or below the zero-energy line (with a difference in the Morse potential, a), representing an [[activation energy]] requirement or lack of.  Most simple gases on clean metal surfaces lack the activation energy requirement.
 
===Modeling===
 
For experimental setups of chemisorption, the amount of adsorption of a particular system is quantified by a sticking probability value.<ref name="gasser" />
 
However, chemisorption is very difficult to theorize.  A multidimensional [[potential energy surface]] (PES) derived from [[Effective medium approximations|effective medium theory]] is used to describe the effect of the surface on absorption, but only certain parts of it are used depending on what is to be studied. A simple example of a PES, which takes the total of the energy as a function of location:
 
:<math>E(\{R_i\}) = E_{el}(\{R_i\}) + V_{\text{ion-ion}}(\{R_i\})</math>
 
where <math>E_{el}</math> is the [[Energy eigenstates|energy eigenvalue]] of the [[Schrödinger equation]] for the electronic degrees of freedom and <math>V_{ion-ion}</math> is the ion interactions.  This expression is without translational energy, [[rotational energy]], vibrational excitations, and other such considerations.<ref name="norskov">{{cite journal |doi=10.1088/0034-4885/53/10/001 |first=J.K. |last=Norskov |year=1990 |title=Chemisorption on metal surfaces |journal=Reports on Progress in Physics |volume=53 |issue=10 |pages=1253–1295}}</ref>
 
There exist several models to describe surface reactions: the [[Langmuir adsorption model|Langmuir-Hinschelwood mechanism]] in which both reacting species are adsorbed, and the [[Reactions on surfaces|Eley-Rideal mechanism]] in which one is adsorbed and the other reacts with it.<ref name="gasser" />
 
Real systems have many irregularities, making theoretical calculations more difficult:<ref name="clark">Clark, A.; (1974); ''The Chemisorptive Bond: Basic Concepts'', Academic Press, New York and London</ref>
 
* Solid surfaces are not necessarily at equilibrium. 
* They may be perturbed and irregular, defects and such. 
* Distribution of adsorption energies and odd adsorption sites. 
* Bonds formed between the adsorbates.
 
Compared to physisorption where adsorbates are simply sitting on the surface, the adsorbates can change the surface, along with its structure.  The structure can go through relaxation, where the first few layers change interplanar distances without changing the surface structure, or reconstruction where the surface structure is changed.<ref name="clark" />
 
<!-- [[Image:stm-OCu.JPG|thumb|Figure 2: [[Scanning tunneling microscope|STM]] image of oxygen adsorbed onto Cu(110). Several defects can be seen, gaps and missing rows.  The oxygen is arrayed in the 001 direction.]] Deleted file/image-->
For example oxygen can form very strong bonds (~4 eV) with metals, such as Cu(110).  This comes with the breaking apart of surface bonds in forming surface-adsorbate bonds. A large restructuring occurs by missing row as seen in Figure 2.
 
===Dissociation Chemisorption===
 
A particular brand of gas-surface chemisorption is the [[Dissociation (chemistry)|dissociation]] of [[Diatomic molecule|diatomic]] gas molecules, such as [[hydrogen]], [[oxygen]], and [[nitrogen]].  One model used to describe the process is precursor-mediation.  The absorbed molecule is adsorbed onto a surface into a precursor state.  The molecule then diffuses across the surface to the chemisorption sites.  They break the molecular bond in favor of new bonds to the surface. The energy to overcome the activation potential of dissociation usually comes from the translational energy and vibrational energy.<ref name="rettner" />
 
And example is the hydrogen and [[copper]] system, one that has been studied many times over.  It has a large activation energy of .35 - .85 eV. The vibrational excitation of the hydrogen molecule promotes dissociation on low index surfaces of copper.<ref name="rettner" />
 
==See also==
*[[Adsorption]]
*[[Physisorption]]
 
== References ==
 
{{Reflist}}
 
[[Category:Physical chemistry]]
[[Category:Catalysis]]

Revision as of 00:08, 1 November 2013

Chemisorption is a kind of adsorption which involves a chemical reaction between the surface and the adsorbate. New chemical bonds are generated at the adsorbant surface. Examples include macroscopic phenomena that can be very obvious, like corrosion, and subtler effects associated with heterogeneous catalysis. The strong interaction between the adsorbate and the substrate surface creates new types of electronic bonds.[1]

In contrast with chemisorption is physisorption, which leaves the chemical species of the adsorbate and surface intact. It is conventionally accepted that the energetic threshold separating the binding energy of "physisorption" from that of "chemisorption" is about 0.5 eV per adsorbed species.

Due to specificity, the nature of chemisorption can greatly differ, depending on the chemical identity and the surface structure.

Uses

An important example of chemisorption is in heterogeneous catalysis which involves molecules reacting with each other via the formation of chemisorbed intermediates. After the chemisorbed species combine (by forming bonds with each other) the product desorbs from the surface.

Hydrogenation of an alkene on a solid catalyst entails chemisorption of the molecules of hydrogen and alkene, which form bonds to the surface atoms.

Self-assembled monolayers

Self-assembled monolayers (SAMs) are formed by chemisorbing reactive reagents with metal surfaces. A famous example involves thiols (RS-H) absorbing onto the surface of gold. This process forms strong Au-SR bonds and releases H2. The densely packed SR groups protect the surface.

Gas-surface Chemisorption

Adsorption Kinetics

As an instance of adsorption, chemisorption follows the adsorption process. The first stage is for the adsorbate particle to come into contact with the surface. The particle needs to be trapped onto the surface by not possessing enough energy to leave the gas-surface potential well. If it elastically collides with the surface, then it would return to the bulk gas. If it loses enough momentum through an inelastic collision, then it “sticks” onto the surface, forming a precursor state bonded to the surface by weak forces, similar to physisorption. The particle diffuses on the surface until it finds a deep chemisorption potential well. Then it reacts with the surface or simply desorbs after enough energy and time.[2]

The reaction with the surface is dependent on the chemical species involved. Applying Gibbs free energy equation for reactions:

General thermodynamics states that for spontaneous reactions at constant temperature and pressure, the change in free energy should be negative. Since a free particle is restrained to a surface, and unless the surface atom is highly mobile, entropy is lowered. This means that the enthalpy term must be negative, implying an exothermic reaction.[3]

Figure 1 is a graph of physisorption and chemisorption energy curves of tungsten and oxygen. Physisorption is given as a Lennard-Jones potential and chemisorption is given as a Morse potential. There exists a point of crossover between the physisorption and chemisorption, meaning a point of transfer. It can occur above or below the zero-energy line (with a difference in the Morse potential, a), representing an activation energy requirement or lack of. Most simple gases on clean metal surfaces lack the activation energy requirement.

Modeling

For experimental setups of chemisorption, the amount of adsorption of a particular system is quantified by a sticking probability value.[3]

However, chemisorption is very difficult to theorize. A multidimensional potential energy surface (PES) derived from effective medium theory is used to describe the effect of the surface on absorption, but only certain parts of it are used depending on what is to be studied. A simple example of a PES, which takes the total of the energy as a function of location:

where is the energy eigenvalue of the Schrödinger equation for the electronic degrees of freedom and is the ion interactions. This expression is without translational energy, rotational energy, vibrational excitations, and other such considerations.[4]

There exist several models to describe surface reactions: the Langmuir-Hinschelwood mechanism in which both reacting species are adsorbed, and the Eley-Rideal mechanism in which one is adsorbed and the other reacts with it.[3]

Real systems have many irregularities, making theoretical calculations more difficult:[5]

  • Solid surfaces are not necessarily at equilibrium.
  • They may be perturbed and irregular, defects and such.
  • Distribution of adsorption energies and odd adsorption sites.
  • Bonds formed between the adsorbates.

Compared to physisorption where adsorbates are simply sitting on the surface, the adsorbates can change the surface, along with its structure. The structure can go through relaxation, where the first few layers change interplanar distances without changing the surface structure, or reconstruction where the surface structure is changed.[5]

For example oxygen can form very strong bonds (~4 eV) with metals, such as Cu(110). This comes with the breaking apart of surface bonds in forming surface-adsorbate bonds. A large restructuring occurs by missing row as seen in Figure 2.

Dissociation Chemisorption

A particular brand of gas-surface chemisorption is the dissociation of diatomic gas molecules, such as hydrogen, oxygen, and nitrogen. One model used to describe the process is precursor-mediation. The absorbed molecule is adsorbed onto a surface into a precursor state. The molecule then diffuses across the surface to the chemisorption sites. They break the molecular bond in favor of new bonds to the surface. The energy to overcome the activation potential of dissociation usually comes from the translational energy and vibrational energy.[2]

And example is the hydrogen and copper system, one that has been studied many times over. It has a large activation energy of .35 - .85 eV. The vibrational excitation of the hydrogen molecule promotes dissociation on low index surfaces of copper.[2]

See also

References

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    The data offered is for normal info purposes only and isn't supposed to be personalised investment or monetary advice. Motley Fool Singapore contributor Stanley Lim would not personal shares in any corporations talked about. Singapore private home costs increased by 1.eight% within the fourth quarter of 2012, up from 0.6% within the earlier quarter. Resale prices of government-built HDB residences which are usually bought by Singaporeans, elevated by 2.5%, quarter on quarter, the quickest acquire in five quarters. And industrial property, prices are actually double the levels of three years ago. No withholding tax in the event you sell your property. All your local information regarding vital HDB policies, condominium launches, land growth, commercial property and more

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  3. 3.0 3.1 3.2 Gasser, R.P.H.; (1985) An introduction to chemisorption and catalysis by metals, Clarendon Press, Oxford
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    In its statement, the singapore property listing - website link, government claimed that the majority citizens buying their first residence won't be hurt by the new measures. Some concessions can even be prolonged to chose teams of consumers, similar to married couples with a minimum of one Singaporean partner who are purchasing their second property so long as they intend to promote their first residential property. Lower the LTV limit on housing loans granted by monetary establishments regulated by MAS from 70% to 60% for property purchasers who are individuals with a number of outstanding housing loans on the time of the brand new housing purchase. Singapore Property Measures - 30 August 2010 The most popular seek for the number of bedrooms in Singapore is 4, followed by 2 and three. Lush Acres EC @ Sengkang

    Discover out more about real estate funding in the area, together with info on international funding incentives and property possession. Many Singaporeans have been investing in property across the causeway in recent years, attracted by comparatively low prices. However, those who need to exit their investments quickly are likely to face significant challenges when trying to sell their property – and could finally be stuck with a property they can't sell. Career improvement programmes, in-house valuation, auctions and administrative help, venture advertising and marketing, skilled talks and traisning are continuously planned for the sales associates to help them obtain better outcomes for his or her shoppers while at Knight Frank Singapore. No change Present Rules

    Extending the tax exemption would help. The exemption, which may be as a lot as $2 million per family, covers individuals who negotiate a principal reduction on their existing mortgage, sell their house short (i.e., for lower than the excellent loans), or take part in a foreclosure course of. An extension of theexemption would seem like a common-sense means to assist stabilize the housing market, but the political turmoil around the fiscal-cliff negotiations means widespread sense could not win out. Home Minority Chief Nancy Pelosi (D-Calif.) believes that the mortgage relief provision will be on the table during the grand-cut price talks, in response to communications director Nadeam Elshami. Buying or promoting of blue mild bulbs is unlawful.

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  5. 5.0 5.1 Clark, A.; (1974); The Chemisorptive Bond: Basic Concepts, Academic Press, New York and London