Completeness of non-normalizable modes

We establish the completeness of some characteristic sets of non-normalizable modes by constructing fully localized square steps out of them, with each such construction expressly displaying the Gibbs phenomenon associated with trying to use a complete basis of modes to fit functions with discontinuous edges. As well as being of interest in and of itself, our study is also of interest to the recently introduced large extra dimension brane-localized gravity program of Randall and Sundrum, since the particular non-normalizable mode bases that we consider (specifically the irregular Bessel functions and the associated Legendre functions of the second kind) are associated with the tensor gravitational fluctuations which occur in those specific brane worlds in which the embedding of a maximally four-symmetric brane in a five-dimensional anti-de Sitter bulk leads to a warp factor which is divergent. Since the brane-world massless four-dimensional graviton has a divergent wave function in these particular cases, its resulting lack of normalizability is thus not seen to be any impediment to its belonging to a complete basis of modes, and consequently its lack of normalizability should not be seen as a criterion for not including it in the spectrum of observable modes. Moreover, because the divergent modes we consider form complete bases, we can even construct propagators out of them in which these modes appear as poles with residues which are expressly finite. Thus even though normalizable modes appear in propagators with residues which are given as their finite normalization constants, non-normalizable modes can just as equally appear in propagators with finite residues too -- it is just that such residues will not be associated with bilinear integrals of the modes.Comment: 34 pages, 6 figures. Revte

Reaction blockading in charged-neutral excited-state chemistry at low collision energy

We study an excited atom-polar molecular ion chemical reaction (Ca$^*$ + BaCl$^+$) at low temperature by utilizing a hybrid atom-ion trapping system. The reaction rate and product branching fractions are measured and compared to model calculations as a function of both atomic quantum state and collision energy. At the lowest collision energy we find that the chemical dynamics dramatically differ from capture theory predictions and are primarily dictated by the radiative lifetime of the atomic quantum state instead of the underlying excited-state interaction potential. We provide a simple rule for calculating at what temperature this regime, where the collision complex lifetime is longer than the radiative lifetime of the quantum state, is reached. This effect, which greatly suppresses the reactivity of short-lived excited states, provides a means for directly probing reaction range. It also naturally suppresses unwanted chemical reactions in hybrid trapping experiments, allowing longer molecular ion coherence and interrogation times.Comment: 13 pages, 5 figure

Macrodimers: ultralong range Rydberg molecules

We study long range interactions between two Rydberg atoms and predict the existence of ultralong range Rydberg dimers with equilibrium distances of many thousand Bohr radii. We calculate the dispersion coefficients $C_{5}$, $C_{6}$ and $C_{8}$ for two rubidium atoms in the same excited level $np$, and find that they scale like $n^{8}$, $n^{11}$ and $n^{15}$, respectively. We show that for certain molecular symmetries, these coefficients lead to long range potential wells that can support molecular bound levels. Such macrodimers would be very sensitive to their environment, and could probe weak interactions. We suggest experiments to detect these macrodimers.Comment: 4 pages, submitted to PR

Ultracold collisions for atom--diatom systems with a reaction barrier

Theoretical results for ultracold atom-molecule collisions involving exoergic reactions are presented. Systems with a reaction barrier are considered; specifically, we report the results of extensive computations for D + H 2 and Cl + H2. We analyzed the extreme situation of translationally cold collisions between an atom and an internally hot molecule; namely, for D + H2 we explored the role played by the internal vibrational excitation of the diatomic target for initial states H2(υ) with υ = 0,1,2,…, 8. The υ-dependence of the zero-temperature limit of the reaction rate coefficient shows two distinct regimes: a barrier dominated regime for υ \u3c 4, and a barrierless regime for υ \u3e 4. Also, for highly excited initial states, the distribution over the final states of the products shows an approximate conservation of the internal vibrational energy. For Cl + H2 we studied in detail the isotopic effect by varying continuously the mass of H, which allowed us to find resonance effects in the threshold behavior of cross sections. These resonances are caused by long-lived van der Waals complexes (Cl···H2) which have vanishingly small binding energy, or by virtual states of the Cl···H 2 complex.

Ultracold collisions for atom--diatom systems with a reaction barrier

Theoretical results for ultracold atom-molecule collisions involving exoergic reactions are presented. Systems with a reaction barrier are considered; specifically, we report the results of extensive computations for D + H 2 and Cl + H2. We analyzed the extreme situation of translationally cold collisions between an atom and an internally hot molecule; namely, for D + H2 we explored the role played by the internal vibrational excitation of the diatomic target for initial states H2(υ) with υ = 0,1,2,…, 8. The υ-dependence of the zero-temperature limit of the reaction rate coefficient shows two distinct regimes: a barrier dominated regime for υ \u3c 4, and a barrierless regime for υ \u3e 4. Also, for highly excited initial states, the distribution over the final states of the products shows an approximate conservation of the internal vibrational energy. For Cl + H2 we studied in detail the isotopic effect by varying continuously the mass of H, which allowed us to find resonance effects in the threshold behavior of cross sections. These resonances are caused by long-lived van der Waals complexes (Cl···H2) which have vanishingly small binding energy, or by virtual states of the Cl···H 2 complex.