Detecting the spread of valence-band Wannier functions by optical sum rules

The spread of valence-band Wannier functions in semiconductors and insulators is a characteristic property that gives a rough estimation of how insulating is the material. We elaborate that the gauge-invariant part of the spread can be extracted experimentally from optical conductivity and absorbance, owing to their equivalence to the quantum metric of the valence band states integrated over momentum. Because the quantum metric enters the matrix element of optical conductivity, the spread of valence-band Wannier functions in the gapped 3D materials can be obtained from the frequency-integration of the imaginary part of the dielectric function. We demonstrate this practically for typical semiconductors like Si and Ge, and for topological insulators like Bi2Te3. In 2D materials, the spread of Wannier functions in the valence bands can be obtained from the absorbance divided by frequency and then integrated over frequency. Applying this method to graphene reveals a finite spread caused by intrinsic spin-orbit coupling, which may be detected by absorbance in the microwave range. The absorbance of twisted bilayer graphene in the millimeter wave range can be used to detect the formation of the flat bands and quantify their quantum metric. Finally, we apply our method to hexagonal transition metal dichalcogenides MX2 (M=Mo,W; X=S,Se,Te) and demonstrate how other effects like excitons and higher energy bands can affect the spread of Wannier function.