It has long been puzzling regarding the physical origin of the thermally induced red-shift of Raman optical
phonons in group III nitride crystals despite some possible mechanisms such as phonon decay, thermal
expansion, interfacial effects, or their combinations. Here we show that an extension of the recent approach
[Sun, C. Q.; Pan, L. K.; Li, C. M.; Li, S. Phys. Rev.
B
2005, 72, 134301] to the functional dependence of the
frequency of Raman optical modes on the atomic bonding identities (bond length, bond strength, and atomic
coordination numbers) to the temperature domain has enabled us to gain a simple solution with improved
understanding of the thermally induced red-shift of Raman optical phonons. Reproduction of the measured
temperature dependence of the Raman shift of AlN, GaN, and InN reveals that the thermally driven red-shift
arises simply from bond vibration and bond expansion, together with derived information about the mode
cohesive energy.