Decay modes and lifetimes of hydrogen metastable states

In summary, the Protium atom has two low-lying excited states with long lifetimes. The 2s state has a decay energy of 121 nm but is forbidden due to no angular momentum difference, so the fastest allowed decay is through two-photon emission with a lifetime of 0.15 s. The Triplet 1s state has a decay energy of 211 mm and predominantly decays through single photon emission with a lifetime of 10 million years. The diprotium molecule also has low-lying excited states that lack dipole moments and are therefore forbidden to decay. The first vibrational excited state has a decay energy of 2.12 μm and decays through non-radiative processes with a very
  • #1
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Protium atom has two low lying excited states with long lifetimes.
These are:
  1. 2s. Decay energy would be 121 nm, but forbidden (no angular momentum difference). Fastest allowed decay is two-photon emission, lifetime 0,15 s
  2. Triplet 1s. Decay energy 211 mm. Prevalent decay single photon emission, lifetime 10 million years.
But diprotium molecule also has a lot of low lying excited states which lack dipole moments and whose decay is therefore forbidden. Which are their prevalent decay paths and lifetimes in vacuum, excluding collision-induced dipoles? The lower states being:
  1. First vibrational excited state - decay energy 2,12 μm
  2. Parahydrogen first rotational excited state, J=2 (due to Pauli principle, J=1 state cannot exist for parahydrogen) - decay energy 28,22 μm
  3. Spontaneous decay of orthohydrogen - decay energy about 85 μm, but rather strongly forbidden. How strongly exactly - what´s fastest allowed decay mode, and the lifetime?
 
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  • #2
The first vibrational excited state of the diprotium molecule has no dipole moment and is therefore forbidden to decay. The predominant decay path is through non-radiative processes such as collisional quenching. The lifetime in this case is very short, on the order of nanoseconds.The parahydrogen first rotational excited state (J=2) is also forbidden to decay, but the predominant decay path is through intersystem crossing via photon-induced spin-orbit coupling, with a lifetime of approximately 10-15 microseconds.Finally, the spontaneous decay of orthohydrogen is very strongly forbidden due to its large energy gap. The fastest allowed decay path is likely through Auger electron emission, with a lifetime of approximately 5-10 picoseconds.
 

1. What are hydrogen metastable states?

Hydrogen metastable states are excited states of the hydrogen atom where the electron is in a higher energy level than its ground state. These states have longer lifetimes than the ground state and can emit light when the electron transitions back to the ground state.

2. How do hydrogen metastable states decay?

Hydrogen metastable states can decay through a process called spontaneous emission, where the electron transitions back to the ground state and emits a photon. They can also decay through collisions with other particles, such as electrons or atoms, which can cause the electron to lose energy and transition back to the ground state.

3. What is the lifetime of a hydrogen metastable state?

The lifetime of a hydrogen metastable state can vary depending on the specific state and the environment it is in. Generally, the lifetime can range from a few milliseconds to a few seconds. However, some highly excited states can have lifetimes on the order of minutes.

4. How are hydrogen metastable states important in research and technology?

Hydrogen metastable states have many applications in research and technology. They are used in spectroscopy to study the structure and properties of atoms and molecules. They also play a role in plasma physics and are important in the development of technologies such as lasers and atomic clocks.

5. Can hydrogen metastable states be manipulated or controlled?

Yes, hydrogen metastable states can be manipulated and controlled through the use of external electric and magnetic fields. This can change the energy levels of the electron and affect the lifetime of the state. This manipulation is important in many research and technological applications.

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