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Electron affinity is the measure of the energy change when an electron is added to a neutral atom to form a negative ion., Eea, of an atom or molecule is the amount of energy required to detach an electron from a singly charged negative ion,[1] i.e., the energy change for the process

X- → X + e

An equivalent definition is the energy released (Einitial − Efinal) when an electron is attached to a neutral atom or molecule.

The electron affinities of the noble gases have not been conclusively measured, so they may or may not have slightly negative EAs. Atoms whose anions are more stable than neutral atoms have a greater Eea. Chlorine most strongly attracts extra electrons; mercury most weakly attracts an extra electron. Eea of noble gases are close to 0.

Although Eea vary in a chaotic manner across the table, some patterns emerge. Generally, nonmetals have more positive Eea than metals.

Contents

[edit] Values for the elements

The following data are quoted in kJ/mol. Elements marked with an asterisk are expected to have electron affinities close to zero on quantum mechanical grounds. Elements marked with a dotted box are synthetically made elements—elements not found naturally in the environment.

Group → 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
↓ Period
1 H
73

He
*
2 Li
60
Be
*

B
27
C
122
N
*
O
141
F
328
Ne
*
3 Na
53
Mg
*

Al
42
Si
134
P
72
S
200
Cl
349
Ar
*
4 K
48
Ca
2
Sc
18
Ti
8
V
51
Cr
65
Mn
*
Fe
15
Co
64
Ni
112
Cu
119
Zn
*
Ga
41
Ge
119
As
79
Se
195
Br
324
Kr
*
5 Rb
47
Sr
5
Y
30
Zr
41
Nb
86
Mo
72
Tc
*
Ru
101
Rh
110
Pd
54
Ag
126
Cd
*
In
39
Sn
107
Sb
101
Te
190
I
295
Xe
*
6 Cs
46
Ba
14
*
Hf
 
Ta
31
W
79
Re
*
Os
104
Ir
150
Pt
205
Au
223
Hg
*
Tl
36
Pb
35
Bi
91
Po
 
At
 
Rn
*
7 Fr
 
Ra
 
**
Rf
 
Db
 
Sg
 
Bh
 
Hs
 
Mt
 
Ds
 
Rg
 
Uub
 
Uut
 
Uuq
 
Uup
 
Uuh
 
Uus
 
Uuo
 

* Lanthanides La
45
Ce
92
Pr
 
Nd
 
Pm
 
Sm
 
Eu
 
Gd
 
Tb
 
Dy
 
Ho
 
Er
 
Tm
99
Yb
 
Lu
33
** Actinides Ac
 
Th
 
Pa
 
U
 
Np
 
Pu
 
Am
 
Cm
 
Bk
 
Cf
 
Es
 
Fm
 
Md
 
No
 
Lr
 
Chemical series of the periodic table
Alkali metals Alkaline earth metals Lanthanides Actinides Transition metals
Poor metals Metalloids Nonmetals Halogens Noble gases

[edit] Periodic trends

Eea generally increases across a period (row) in the periodic table. This is caused by the filling of the valence shell of the atom; a group 7A atom releases more energy than a group 1A atom on gaining an electron because it obtains a filled valence shell.

A trend of decreasing Eea going down the groups in the periodic table would be expected. The additional electron will be entering an orbital farther away from the nucleus, and thus would experience a lesser effective nuclear charge. However, a clear counterexample to this trend can be found in group 2A, and this trend only applies to group 1A atoms. Electron affinity follows the trend of electronegativity. So F has a higher electron affinity than oxygen and so on.

[edit] Molecular electron affinities

Eea is not limited to the elements but also applies to molecules. For instance the electron affinity for benzene is negative, as is that of naphthalene, while those of anthracene, phenanthrene and pyrene are positive. In silico experiments show that the electron affinity of hexacyanobenzene surpasses that of fullerene[2].

[edit] EA of Surfaces

The electron affinity measured from a material's surface is a function of the bulk material as well as the surface condition. Often negative electron affinity is desired to obtain efficient cathodes that can supply electrons to the vacuum with little energy loss. The observed electron yield as a function of various parameters such as bias voltage or illumination conditions can be used to describe these structures with band diagrams in which EA is one parameter. For one illustration of the apparent effect of surface termination on electron emission, see Figure 3 in Marchywka Effect.

[edit] See also

[edit] References

  1. ^ International Union of Pure and Applied Chemistry. "Electron affinity". Compendium of Chemical Terminology Internet edition.
  2. ^ Remarkable electron accepting properties of the simplest benzenoid cyanocarbons: hexacyanobenzene, octacyanonaphthalene and decacyanoanthracene Xiuhui Zhang, Qianshu Li, Justin B. Ingels, Andrew C. Simmonett, Steven E. Wheeler, Yaoming Xie, R. Bruce King, Henry F. Schaefer III and F. Albert Cotton Chemical Communications, 2006, 758 - 760 Abstract

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