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Nodes are the points in space around a nucleus where the probability of finding an electron is zero. However, I heard that there are two kinds of nodes, radial nodes and angular nodes. What are they and what information do they provide of an atom?

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    $\begingroup$ Note that nodes are properties of orbitals and wavefunctions (and thus of electrons) and not exactly of atoms. $\endgroup$ – Ben Norris Feb 22 '14 at 13:17
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1. How to get the number and type of nodes for an orbital

As you said, nodes are points of zero electron density. From the principal quantum number $n$ and the azimuthal quantum number $\ell$, you can derive the number of nodes, and how many of them are radial and angular.

$$\text{number of nodes}=n-1$$

$$\text{angular nodes}=\ell$$

$$\text{radial nodes}=(\text{number of nodes})-(\text{angular nodes})$$

So each type of orbital ($s, p, d$ etc) has its own unique, fixed number of angular nodes, and then as $n$ increases, you add radial nodes.

Examples: First shell

For the first shell, $n=1$, which means the number of nodes will be 0.

Examples: Second shell

For the second shell, $n=2$, which yields 1 node.

  • For the $2s$ orbital, $\ell = 0$, which means the node will be radial
  • For the $2p$ orbital, $\ell = 1$, which means the node will be angular

Examples: Third shell

The third shell, $n=3$, yielding $3-1=2$ nodes.

  • The $3s$ orbital still has $\ell = 0$ meaning no angular nodes, and thus the two nodes must be radial
  • The $3p$ orbital still has one angular node, meaning there will be one radial node as well
  • The $3d$ orbital has two angular nodes, and therefore no radial nodes!

2. The difference between radial and angular nodes

Radial nodes are nodes inside the orbital lobes as far as I can understand. Its easiest to understand by looking at the $s$-orbitals, which can only have radial nodes.

Radial nodes of the s-orbitals

To see what an angular node is, then, let's examine the $2p$-orbital - an orbital that has one node, and that node is angular.

Angular nodes of the 2p orbitals

We see that angular nodes are not internal countours of 0 electron probability, but rather is a plane that goes through the orbital. For the $2p_\text{z}$-orbital, the angular node is the plane spanned by the x- and y-axis. For the $2p_\text{y}$-orbital, the angular node is the plane spanned by the z- and x-axis.

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    $\begingroup$ Commenting on the last paragraph. Angular nodes 1) do have zero electron probability density and 2) are not necessarily planes. $\endgroup$ – orthocresol Sep 16 '16 at 9:09
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The accepted answer has nice pictures, but is perhaps somewhat lacking in rigour. Here's a bit more maths.

Atomic orbitals, which are one-electron wavefunctions, are split into two components: the radial and angular wavefunctions

$$\psi_{nlm}(r,\theta,\phi) = R_{nl}(r)Y_{lm}(\theta,\phi)$$

so-called because they only have radial ($r$) and angular ($\theta$,$\phi$) dependencies respectively. If either of these two components are zero, the total wavefunction is zero and the probability density there (given by $\psi^*\psi$) is also zero.

A radial node occurs when the radial wavefunction is equal to zero. Since the radial wavefunction only depends on $r$, this obviously means that each radial node corresponds to one particular value of $r$. (The radial wavefunction may be zero when $r = 0$ or $r \to \infty$, but these are not counted as radial nodes.)

An angular node is analogously simply a region where the angular wavefunction is zero.1 In the case of the p-orbitals, this is a plane, although angular nodes are not necessarily planes.

The number of radial and angular nodes is dictated by the forms of the wavefunctions, which are derived by solving the Schrodinger equation. For a given orbital with quantum numbers $(n,l)$, there are $n-l-1$ radial nodes and $l$ angular nodes, as previously described.

An example

Let's take a look at one of the hydrogen 3d wavefunctions2 with $(n,l) = (3,2)$. $a_0$ is the Bohr radius of the hydrogen atom. We would expect $3-2-1 = 0$ radial nodes and $2$ angular nodes.

$$\mathrm{3d}_{z^2} = \underbrace{\left[\frac{4}{81\sqrt{30}}a_0^{-3/2}\left(\frac{r}{a_0}\right)^2 \exp{\left(-\frac{r}{3a_0}\right)}\right]}_{\text{radial: }R_{32}} \underbrace{\left[\sqrt{\frac{5}{16\pi}}(3\cos^2\theta - 1)\right]}_{\text{angular: }Y_{20}}$$

All the individual terms in the radial wavefunction can never be zero (excluding the cases of $r = 0$ or $r \to \infty$ as I described earlier). Therefore, this orbital has no radial nodes. Surprise, surprise.

The angular nodes are more interesting. The angular wavefunction vanishes when $3 \cos^2\theta - 1 = 0$. Since $\theta$ takes values between $0^\circ$ and $180^\circ$,3 this corresponds to the two solutions $\theta = 54.7^\circ, 125.3^\circ$. Both of these solutions are angular nodes. This is how they look like.4

enter image description here

The dotted lines are the angular nodes. They are not planes, but rather cones. They correspond to one particular value of $\theta$, which in spherical coordinates is the angle made with the positive $z$-axis; I have marked these angles on the diagram.

If you can obtain the forms of the wavefunctions, then it is easy to find the radial nodes. Mark Winter at Sheffield has a great website for this; just click on the orbital you want on the left, then "Equations" near the top-right corner.

Notes and references

1 If we stick to complex atomic orbitals, which are simultaneous eigenfunctions of $H$, $L^2$ and $L_z$, then the dependency on $\phi$ is always of the form $e^{\pm im\phi}$, which can never be zero, so angular nodes never arise due to $\phi$-dependency. However, radial and angular nodes are most commonly discussed in the context of real atomic orbitals, obtained by linear combination of the spherical harmonics. These do have angular nodes that depend on both $\theta$ and $\phi$, but they are often much simpler to express in terms of Cartesian coordinates $(x,y,z)$ (obvious examples being the $\mathrm{2p}_x$ and $\mathrm{2p}_y$ orbitals). The $\mathrm{3d}_{z^2}$ orbital is an exception that was deliberately chose as an example because its angular nodes are not planes.

2 Griffiths, Introduction to Quantum Mechanics, 2nd ed., pp 139, 154.

3 Yes, I am using degrees, not radians.

4 Image source: own work. It was surprisingly difficult to find an appropriate picture online.

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    $\begingroup$ For the angular nodes would it be appropriate to say that theta and phi can form a line in 3D space? This line would also pass through the origin. Hence, all points along this line (towards the selected side of the origin, changing sides would change theta and phi) would have an angular wave function equal to zero. So this line forms a node. I don't see how a plane is formed. Could you please illustrate how a plane could be formed as a node? $\endgroup$ – shre_sudh_97 Oct 2 '16 at 1:05
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    $\begingroup$ The set of all points with $\theta = \pi/2$ forms the xy-plane. $\endgroup$ – orthocresol Oct 2 '16 at 2:27
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If you vibrate a piece of rope then it is quite easy to show that nodes will appear, and when standing waves are produced the nodes are fixed in space and time. Between the nodes the rope oscillates up and down. The n$^{th}$ harmonic has $n-1$ nodes. The more nodes there are, the greater is the energy is required to produce them. In a vibrating rectangular membrane nodal lines are produced and in a vibrating disc nodal rings. The nodal lines, where the amplitude is zero separate normal vibrational modes.

Similarly with atoms and molecules. Nodes are points where the wavefunction crosses zero, and its amplitude is zero. Where the wavefunction gradually approaches zero (at the origin or infinity) are not considered nodes. Nodes naturally appear in all solutions of the Schrodinger equation, even for simple systems such as a particle in a box. Not all wavefunctions have nodes, the lowest energy one does not, (e.g. the S orbital in atoms, zero point vibration and zero rotation in molecules, lowest MO in a molecule). The larger the number of nodes a wavefunction has the greater the energy eigenvalue. Some pictures of wavefunctions and nodes has been given in the answer by @Brian.

There appears to be no special significance to a node, it arises purely out of the solution of the Schrodinger equation and is a consequence of the solutions (hence boundary conditions) we choose to obtain quantisation. Without nodes it is difficult to see how wavefunctions describing different energy eigenvalues could be constructed.

Briefly extending the question to include bond formation. In forming bonds from atomic orbitals the parity of the wavefunction is important. Upon interchanging coordinates, i.e. inversion operator, odd parity (ungerade, u) produces -1 itself and even parity (gerade, g)leaves the orbital indistinguishable. The node in a p orbital causes it to have odd parity, as s orbital even. The symmetry (parity) determines whether two orbitals can combine to form a bonding orbital or anti-bonding one, e.g. $\sigma$ or $\sigma ^*$ or $\pi$ or $\pi ^*$. Anti-bonding orbitals always have nodes.
Nodal planes are also important in Diels Alder addition and similar reactions as here symmetry is important. In spectroscopic transitions in molecules, the nodal structure of the molecular orbitals determine, via symmetry, which transitions are allowed or forbidden.

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