# 2.5: Effective Nuclear Charge

Skills to Develop

• To understand the basics of electron shielding and penetration

For an atom or an ion with only a single electron, we can calculate the potential energy by considering only the electrostatic attraction between the positively charged nucleus and the negatively charged electron. When more than one electron is present, however, the total energy of the atom or the ion depends not only on attractive electron-nucleus interactions but also on repulsive electron-electron interactions. When there are two electrons, the repulsive interactions depend on the positions of both electrons at a given instant, but because we cannot specify the exact positions of the electrons, it is impossible to exactly calculate the repulsive interactions. Consequently, we must use approximate methods to deal with the effect of electron-electron repulsions on orbital energies.

If an electron is far from the nucleus (i.e., if the distance r between the nucleus and the electron is large), then at any given moment, most of the other electrons will be between that electron and the nucleus. Hence the electrons will cancel a portion of the positive charge of the nucleus and thereby decrease the attractive interaction between it and the electron farther away. As a result, the electron farther away experiences an effective nuclear charge (Zeff) that is less than the actual nuclear charge Z. This effect is called electron shielding.

As the distance between an electron and the nucleus approaches infinity, Zeff approaches a value of 1 because all the other (Z − 1) electrons in the neutral atom are, on the average, between it and the nucleus. If, on the other hand, an electron is very close to the nucleus, then at any given moment most of the other electrons are farther from the nucleus and do not shield the nuclear charge. At r ≈ 0, the positive charge experienced by an electron is approximately the full nuclear charge, or ZeffZ. At intermediate values of r, the effective nuclear charge is somewhere between 1 and Z: 1 ≤ ZeffZ. Thus the actual Zeff experienced by an electron in a given orbital depends not only on the spatial distribution of the electron in that orbital but also on the distribution of all the other electrons present. This leads to large differences in Zeff for different elements, as shown in Figure 2.5.1 for the elements of the first three rows of the periodic table. Notice that only for hydrogen does Zeff = Z, and only for helium are Zeff and Z comparable in magnitude.

Figure 2.5.1: Relationship between the Effective Nuclear Charge Zeff and the Atomic Number Z for the Outer Electrons of the Elements of the First Three Rows of the Periodic Table. Except for hydrogen, Zeff is always less than Z, and Zeff increases from left to right as you go across a row.

Because of the effects of shielding and the different radial distributions of orbitals with the same value of n but different values of l, the different subshells are not degenerate in a multielectron atom (compare with Figure 1.6.6). For a given value of n, the ns orbital is always lower in energy than the np orbitals, which are lower in energy than the nd orbitals, and so forth. As a result, some subshells with higher principal quantum numbers are actually lower in energy than subshells with a lower value of n; for example, the 4s orbital is lower in energy than the 3d orbitals for most atoms.

Except for the single electron containing hydrogen atom, in every other element $$Z_{eff}$$ is always less than $$Z$$.

In the next section we will consider a model for estimating the electron shielding, $$S$$. Once we have that estimate, we can calculate an estimate of $$Z_{eff}$$ as follows:

$Z_{eff}=Z-S \tag{2.5.1}$

Figure 2.5.3: Orbital Penetration. A comparison of the radial probability distribution of the 2s and 2p orbitals for various states of the hydrogen atom shows that the 2s orbital penetrates inside the 1s orbital more than the 2p orbital does. Consequently, when an electron is in the small inner lobe of the 2s orbital, it experiences a relatively large value of Zeff, which causes the energy of the 2s orbital to be lower than the energy of the 2p orbital.

## Summary

The calculation of orbital energies in atoms or ions with more than one electron (multielectron atoms or ions) is complicated by repulsive interactions between the electrons. The concept of electron shielding, in which intervening electrons act to reduce the positive nuclear charge experienced by an electron, allows the use of hydrogen-like orbitals and an effective nuclear charge (Zeff) to describe electron distributions in more complex atoms or ions. The degree to which orbitals with different values of l and the same value of n overlap or penetrate filled inner shells results in slightly different energies for different subshells in the same principal shell in most atoms.