REVIEW 1 cited by
A new scheme for isomer pumping and depletion with high-power lasers
Not yet reviewed by Pith; the record is open.
This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.
SPECIMEN: schema-true, not a live event
T0 review · schema-true
One-sentence machine reading of the paper's core claim.
pith:XXXXXXXX · record.json · timestamp
Signed reviews
abstract
We propose a novel scheme for the population and depletion of nuclear isomers. The scheme combines the $\gamma$-photons with energies $\gtrsim 10$ keV emitted during the interaction of a contemporary high-intensity laser pulse with a plasma and one or multiple photon beams supplied by intense lasers. Due to nonlinear effects, two- or multi-photon absorption dominates over the conventional multi-step one-photon process for an optimized gamma flash. Moreover, this nonlinear effect can be greatly enhanced with the help of externally supplied low-energy photons coming from another laser. These low-energy photons act such that the effective cross-section experienced by the $\gamma$-photons becomes tunable, growing with the intensity $I_0$ of the beam. Assuming $I_{0}\sim 10^{18}$ Wcm$^{-2}$ for the photon beam, an effective cross-section as large as $10^{-21}$ cm$^2$ to $10^{-28}$ cm$^2$ for the $\gamma-$photon can be achieved. Thus, within state-of-the-art 10 PW laser facilities, the yields from two-photon absorption can reach $10^6$ to $10^9$ isomers per shot for selected states that are separated from their ground state by E2 transitions. Similar yields for transitions with higher multipolarities can be accommodated by multi-photon absorption with additional photons provided.
Forward citations
Cited by 1 Pith paper
-
Isomer production by multi-photon excitation
A numerical time-dependent Schrödinger study predicts that the n-photon excitation probability of the 8 eV 229mTh isomer scales as intensity^n times pulse width squared in the perturbative regime, with saturation at h...
Discussion (0). Continue with ORCID to comment.