Chemical models predict that the deuterated fraction (the column density ratio between a molecule containing D and its counterpart containing H) of N2H+, Dfrac(N2H+), is high in massive pre-protostellar cores and rapidly drops of an order of magnitud
e after the protostar birth, while that of HNC, Dfrac(HNC), remains constant for much longer. We tested these predictions by deriving Dfrac(HNC) in 22 high-mass star forming cores divided in three different evolutionary stages, from high-mass starless core candidates (HMSCs, 8) to high-mass protostellar objects (HMPOs, 7) to Ultracompact HII regions (UCHIIs, 7). For all of them, Dfrac (N2H+) was already determined through IRAM-30m Telescope observations, which confirmed the theoretical rapid decrease of Dfrac(N2H+) after protostar birth (Fontani et al. 2011). Therefore our comparative study is not affected by biases introduced by the source selection. We have found average Dfrac(HNC) of 0.012, 0.009 and 0.008 in HMSCs, HMPOs and UCHIIs, respectively, with no statistically significant differences among the three evolutionary groups. These findings confirm the predictions of the chemical models, and indicate that large values of Dfrac(N2H+) are more suitable than large values of Dfrac(HNC) to identify cores on the verge of forming high-mass stars, likewise what found in the low-mass regime.
We study the entangling power of a nanoelectromechanical system (NEMS) simultaneously interacting with two separately trapped ions. To highlight this entangling capability, we consider a special regime where the ion-ion coupling does not generate ent
anglement in the system, and any resulting entanglement will be the result of the NEMS acting as an entangling device. We study the dynamical behavior of the bipartite NEMS-induced ion-ion entanglement as well as the tripartite entanglement of the whole system (ions+NEMS). We found some quite remarkable phenomena in this hybrid system. For instance, the two trapped ions initially uncorrelated and prepared in coherent states can become entangled by interacting with a nanoelectromechanical resonator (also prepared in a coherent state) as soon as the ion-NEMS coupling achieve a certain value, and this can be controlled by external voltage gate on the NEMS device.
This paper is concerned with quantum dynamics of a system coupled to a critical reservoir. In this context, we employ the Dicke model which is known to exhibit a super radiant quantum phase transition (QPT) and we allow one of the mirrors to move und
er a linear restoring force. The electromagnetic field couples to the movable mirror though radiation pressure just like in typical optomechanical setups. We show that, in the thermodynamical limit, the super-radiant phase induces a classical driving force on the mirror without causing decoherence.
