Gerhard Martens Thank you very much for your answer, but what confuses me is that there are some differences in the definition of these two indices, the Miller exponent is a concept in crystallography, which is measured in units of the unit sag, while the crystal plane index is a concept in solid state physics, which is measured in units of the original cell sagittal and for the same crystal plane, these two indices are not necessarily the same, in the textbook, there is a formula for how to calculate the plane spacing of the crystal plane index, but when I use this formula to calculate the plane spacing of the Miller index, I find that some of the crystal planes will be missed, For example, for an FCC, the plane spacing of a plane with a Miller index of (110) is different from that of a direct geometric judgment
You wrote above: "some of the crystal planes will be missing".
There are no crystal planes missing; but for example for the case of the FCC lattice the 110 planes are still there and the interplanar distance d110 can be calculated via
dhkl = a * (h2 + k2 + l2)-1/2
but there is no diffraction peak (110).
This is due to the 'selection rules of x-ray diffraction'*).
The structure factor governs the ON and OFF switching of the peaks.
Sorry, maybe my description is a bit of a bother, but what you mentioned is an important phenomenon that we need to be concerned about when it comes to XRD, but what baffles me is some of the problems that arise when using the Miller index to calculate the plane spacing using the plane spacing formula. I searched the literature and described the problem well, but it still seems a bit complicated to solve the problem