We have measured the temperature dependent thermoelectric power (TEP)
of doped polyacetylene (PA) under the high magnetic field up to 20 tes
la. The dopants are I-2, FeCl3, AuCl3 and NbCl5. The overall temperatu
re dependence is characteristic to that of the diffusive metals, i.e.
the TEP is positive and it decreases quasi-linearly upon cooling. Howe
ver, the zero field TEP, S(T, H=0T), shows significant differences bet
ween the iodine doped PA and the other metal-halide doped ones at low
temperature. While the S(T, H=0T) for iodine doped PA is quasi-linear
in temperature down to 4.2 K, the S(T, H=0T) of metal-halide doped sam
ples become temperature independent below T congruent to 20 K and some
of them show even negative TEP with a broad minimum peak at low tempe
rature. At H=20T, both iodine and metal halide doped PA shows an abrup
t decrease of 1 similar to 2 mu V/K in TEP at T similar to 70K, except
the most heavily doped [CH(AuCl4)(y)](x) where no such drop appears.
In the low temperature region, the Delta S(T)=S(T,H=20T)-S(T,H=0T) of
metal-halide doped PA becomes more negative and the minimum peak of TE
P shifts slightly to higher temperature. Similar tendency is observed
at zero field TEP of [CH(AuCl4)(y)](x) as we increase the doping conce
ntration y. For the iodine doped Pq the low temperature Delta S(T)=S(T
,H=20T)-S(T,H=0T) is more or less the same as that of T similar to 70K
where the abrupt jump occurred, i.e., the S(T,H=20T) of iodine doped
PA remains quasi-linear as a function of temperature down to 4.2 K. Th
e magneto resistance rho(T,H) of these samples is also measured and th
e results are compared with the above S(T,H) data. Since no appreciabl
e amount of anisotropy of the stretch oriented PA with respect to the
applied magnetic field direction is observed in S(T,H) and rho(T,H) an
d furthermore, because of the significant difference of S(T,H) between
the iodine doped PA and the metal-halide doped ones, the spin-spin in
teraction between the conduction electron spin in the metallic PA chai
n and the localized spin in the metal-halide dopant located nearby the
polymer chain could be the prime origin of the observed magneto TEP p
henomena.