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The physical origin of dielectric loss is shown to be sum of n number ofsubunits relaxation of a molecule, where n=1,2,3.. For each subunit relaxation,the idea of intermolecular dipole-dipole interactions triggered non-Debyedipole, ($\bf G$)$_{n}$=((1-g$_d$)$\bf G$$_{0}$)$_{n}$, and the ensuing dualdipole ($\bf G$$_{\pm}$)$_n$=($\bf G$$_0$$\pm$$\bf G$)$_n$, relaxationprocesses is proposed, where $\bf G$$_{-}$=g$_{d}$$\bf G$$_{0}$, $\bfG$$_{+}$=(2-g$_{d}$)$\bf G$$_{0}$, and $\bf G$$_{0}$ is a Debye dipole. Eachsubunit motion is statistically highly independent process and discriminated byDebye and non-Debye relaxation (NDR) time, where g$_d$ is an exponent 0<g$_d$<1and signifies interaction strength with a redistribution and conservation ofDebye dielectric loss energy. The proposed concept provides a new insight forthe NDR and discloses the physical origin of $\alpha$, $\beta$, $\gamma$,$\delta$ relaxations and excess wing of glass formers, plastic crystals, drugs,etc., with an excellent agreement with experimental results.

Novel Concept of Non-Debye Dipole Relaxation Processes for the  Interpretation of Physical Origin of Dielectric Loss in the Glass Formers,  Drugs, Polymers and Plastic Crystals