The rate of nuclear fusion in the
molecule is of the order of
1012 s-1, hence it is too fast to measure experimentally. The
reaction is strongly dominated by the resonance 5He
,
which lies about 55 keV above
threshold. Because of
the centrifugal barrier of the J=1 states of the molecule, fusion is
expected to take place mainly from J=0 states, i.e.,
(J,v)=(0,1) and (0,0),
into which the initial state (1,1) is quickly converted via fast E1Auger transitions.
For ,
on the other hand, the transition from
is
strongly suppressed (since it requires spin flip, analogous to the
ortho-para transitions in the homonuclear hydrogen molecule), and fusion
takes place mainly from the J=1 states, if the molecule is resonantly formed in
the (1,1) state. This in fact offers a unique opportunity to study the
p wave fusion reaction at very low energy, which is difficult to do in a
beam experiment. An interesting feature of this reaction is that the fusion
width ratio of the (n+ 3He) channel to the (p + t) channel is about
1.4, apparently violating charge symmetry.
In a simple approach, the fusion rate is calculated by treating three-body
Coulomb physics (molecular wave functions) and nuclear physics
separately [54], a method known as factorization. For ,
we have
More accurate approaches treat the nuclear force dynamically by directly incorporating it as a complex potential in the three-body Hamiltonian (optical potential method) [55,56], or as complex boundary conditions at the nuclear surface (R-matrix method) [57,58,59]. These elaborate approaches agree rather well with each other, as well as with the simple factorization approach.
In
collisions, fusion ``in flight'', i.e., without forming a
bound
molecule, is also possible, and its rates have been
calculated by various methods including, most recently, Faddeev
equations (see [26] and references therein). The reactions are
enhanced, compared to bare nuclear collisions, especially if virtual
states exist, due to the increased overlap of the nuclear wave functions.