Enhanced functional integration in modern electron devices requires an accu
rate modeling of energy transport in semiconductors in order to describe hi
gh-field phenomena such as hot electron propagation, impact ionization and
heat generation in the bulk material. The standard drift-diffusion models c
annot cope with high-field phenomena because they do not comprise energy as
a dynamical variable. Furthermore for many applications in optoelectronics
one needs to describe the transient interaction of electromagnetic radiati
on with carriers in complex semiconductor materials and since the character
istic times are of order of the electron momentum or energy flux relaxation
times, some higher moments of the distribution function must be necessaril
y involved. Therefore these phenomena cannot be described within the framew
ork of the drift-diffusion equations (which are valid only in the quasi-sta
tionary limit). Therefore generalizations of the drift-diffusion equations
have been sought which would incorporate energy as a dynamical variable and
also would not be restricted to quasi-stationary situations. These models
are loosely speaking called hydrodynamical models. One of the earliest hydr
odynamical models currently used in applications was originally put forward
by Blotekjaer [1] and subsequently investigated by Baccarani and Wordeman
[2] and by other authors [3]. Eventually other models have also been invest
igated, some including also non-parabolic effects [4-6, 8-20]. Most of the
implemented hydrodynamical models suffer from serious theoretical drawbacks
due to the ad hoc treatment of the closure problem (lacking a physically c
onvincing motivation) and the modeling of the production terms (usually ass
umed to be of the relaxation type and this, as we shall see, leads to serio
us inconsistencies with the Onsager reciprocity relations). In these lectur
es we present a general overview of the theory underlying hydrodynamical mo
dels. In particular we investigate in depth both the closure problem and th
e modeling of the production terms and present a recently introduced approa
ch based on the maximum entropy principle (physically set in the framework
of extended thermodynamics [21, 22]). The considerations and the results re
ported in the paper are exclusively concerned with silicon.