Add like
Add dislike
Add to saved papers

Molecular high-order harmonic spectra and its application to the generation of the isolated attosecond pulse.

Molecular high-order harmonic generation (HHG) spectra from H2 + and its application to the generation of the isolated attosecond pulses (IAPs) have been numerically investigated. Results show that (i) the 7th harmonic order is enhanced with the nuclei around the equilibrium internuclear, and as the internuclear distance increased, this enhanced harmonic produces a red-shift (even disappearance). Theoretical analyses show that the electronic transition between the ground and the 1st excited states is responsible for the red-shift enhanced harmonic. (ii) The harmonic spectra exhibit several maxima and minima, and a red-shift of these points is predicted as the internuclear distance increased. (iii) By properly choosing the internuclear distance, the harmonic yield is enhanced, and there is only the single quantum path contributing to the harmonic spectra. (iv) Further, by properly adding the half-cycle pulse as well as the spatial inhomogeneous effect, a 375 eV supercontinuum with a pulse enhancement of 3.9 dB and some attosecond X-ray pulses shorter than 60as can be produced.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app