Nonadiabatic coupling and vector correlation in dissociation of triatomic hydrogen.

نویسندگان

  • U Galster
  • U Müller
  • M Jungen
  • H Helm
چکیده

We determine experimentally the vector correlation among the three neutral ground state hydrogen atoms which appear in dissociation of neutral H3* molecules. The sum of the kinetic energies of the three H-atoms is fixed by selecting the energy of the H3* molecule by laser excitation in the range between 0.85 and 3.60 eV. The highly structured maps of correlation in the motion of the three atoms provide a direct view of the internal molecular couplings which initiate dissociation. We discuss this feature in a model calculation and in terms of a new quantum chemical calculations of the potential energy surfaces of H3*.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Stark field control of nonadiabatic dynamics in triatomic hydrogen.

We show experimentally that an external electric field can be used to control the amplitudes of nonadiabatic paths taken by a dissociating molecule. In the example presented here, this control is achieved by Stark-field mixing in H(3) Rydberg states with different decay paths. The final state continuum is in each path formed by three-particle wave packets of slow neutral hydrogen atoms in their...

متن کامل

Precision measurements and computations of transition energies in rotationally cold triatomic hydrogen ions up to the midvisible spectral range.

First-principles computations and experimental measurements of transition energies are carried out for vibrational overtone lines of the triatomic hydrogen ion H(3)(+) corresponding to floppy vibrations high above the barrier to linearity. Action spectroscopy is improved to detect extremely weak visible-light spectral lines on cold trapped H(3)(+) ions. A highly accurate potential surface is ob...

متن کامل

Vibrationally and rotationally nonadiabatic calculations on H3+ using coordinate-dependent vibrational and rotational masses

Using the core-mass approach, we have generated a vibrational-mass surface for the triatomic H3+. The coordinate-dependent masses account for the off-resonance nonadiabatic coupling and permit a very accurate determination of the rovibrational states using a single potential energy surface. The new, high-precision measurements of 12 rovibrational transitions in the ν2 bending fundamental of H3+...

متن کامل

Two- and three-body kinematical correlation in the dissociative recombination of H(3)(+).

Fragmentation patterns for dissociative recombination of the triatomic hydrogen molecular ion H(3)(+) in the vibrational ground state have been measured using the storage ring technique and molecular fragment imaging. A broad distribution of vibrational states in the H(2) fragment after two-body dissociation and a large predominance of nearly linear momentum geometries after three-body dissocia...

متن کامل

Extremely narrow peaks in predissociation of sodium dimer due to rovibronic coupling.

In sodium dimer the 2 (3)Pi(g), 3 (3)Pi(g), and 4 (3)Sigma(g) (+) electronic states are coupled; the coupling of the two (3)Pi(g) states is due to vibrational motion while the nonadiabatic interaction between the (3)Sigma(g) (+) and the (3)Pi(g) states-in particular, the 3 (3)Pi(g) state-is mediated by rotational interaction. The resulting vibronic problem is studied in some detail. The bound v...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Faraday discussions

دوره 127  شماره 

صفحات  -

تاریخ انتشار 2004