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In atomic physics, the effective nuclear charge of an electron in a multi-electron atom or ion is the number of elementary charges an electron experiences by the nucleus. It is denoted by Z eff . The term "effective" is used because the shielding effect of negatively charged electrons prevent higher energy electrons from experiencing the full ...
Trend-wise, as one moves from left to right across a period in the modern periodic table, the electronegativity increases as the nuclear charge increases and the atomic size decreases. However, if one moves down in a group , the electronegativity decreases as atomic size increases due to the addition of a valence shell , thereby decreasing the ...
Other effects of the d-block contraction are that the Ga 3+ ion is smaller than expected, being closer in size to Al 3+.Care must be taken in interpreting the ionization potentials for indium and thallium, since other effects, e.g. the inert-pair effect, become increasingly important for the heavier members of the group.
The first two factors change the effective nuclear charge the most loosely held electron feels. Since the outermost electron of alkali metals always feels the same effective nuclear charge (+1), the only factor which affects the first ionisation energy is the distance from the outermost electron to the nucleus.
An example provided in Slater's original paper is for the iron atom which has nuclear charge 26 and electronic configuration 1s 2 2s 2 2p 6 3s 2 3p 6 3d 6 4s 2.The screening constant, and subsequently the shielded (or effective) nuclear charge for each electron is deduced as: [1]
Core charge is a convenient way of explaining trends in the periodic table. [4] Since the core charge increases as you move across a row of the periodic table, the outer-shell electrons are pulled more and more strongly towards the nucleus and the atomic radius decreases. This can be used to explain a number of periodic trends such as atomic ...
The lanthanide contraction is the greater-than-expected decrease in atomic radii and ionic radii of the elements in the lanthanide series, from left to right. It is caused by the poor shielding effect of nuclear charge by the 4f electrons along with the expected periodic trend of increasing electronegativity and nuclear charge on moving from left to right.
The radii follow general periodic trends: they decrease across the period due to the increase in the effective nuclear charge, which is not offset by the increased number of valence electrons; but the radii increase down the group due to an increase in the principal quantum number.