As a matter of fact, most of our technical electrochemical energy storage s
ystems opera re outside the limitations of thermodynamics. As in the case o
f rechargeable batteries with aqueous electrolytes (part I of this article)
, kinetics control the operation and safety also in batteries with nonaqueo
us electrolytes (this second and final part). A striking example is the lit
hium ion battery which possesses an operating voltage of >3,5 V and a very
high energy density. From a thermodynamic viewpoint such a cell is impossib
le because the used organic electrolyte is in contact with two lithium inse
rtion electrodes that operate at extreme reducing and oxidizing potentials,
respectively. However, a unique mechanism kinetically prevents the decompo
sition of the electrolyte due to the formation of electronically insulating
interphases between electrode and electrolyte that are still permeable to
the electrochemically active Li+ cations. Lithium ion batteries have alread
y made their break-through into the market as small format sq stems for por
table electronics. The only "kinetically shielded" high energy density howe
ver, might be a safety complication for large format batteries, which are a
ssembled for electric vehicle (EV) propulsion. Safety concerns are also val
id for high temperature (300 degrees C) batteries such as the sodium-sulfur
and sodium-nickel chloride systems. These systems are still in the stage o
f "experimental batteries", which may find future application in large unit
s fur EV's or uninterruptible power systems. The paper is concluded by a pe
rformance comparison of various rechargeable battery systems with aqueous a
nd nonaqueous electrolytes. (Possible) applications in consumer electronics
and EV's are discussed in more detail.