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High-harmonic generation (HHG) is a non-linear process during which a target (gas, plasma, solid or liquid sample) is illuminated by an intense laser pulse.Under such conditions, the sample will emit the high order harmonics of the generation beam (above the fifth harmonic).
Similarly, in Indium, there exists a strong transition 4d 10 5s 2 → 4d 9 5s 2 5p at 19.92 eV with a high gf value of 1.11. [10] The energy of this transition corresponds to 13th harmonic with 800 nm excitation wavelength. This enhancement in a particular harmonic order is most commonly known as Resonant High Harmonic Generation (RH).
High harmonic generation (HHG) is a nonlinear process where intense laser radiation is converted from one fixed frequency to high harmonics of that frequency by ionization and recollision of an electron. It was first observed in 1987 by McPherson et al. who successfully generated harmonic emission up to the 17th order at 248 nm in neon gas. [3]
The heat content of an ideal gas is independent of pressure (or volume), but the heat content of real gases varies with pressure, hence the need to define the state for the gas (real or ideal) and the pressure. Note that for some thermodynamic databases such as for steam, the reference temperature is 273.15 K (0 °C).
In surface second harmonic generation, the second harmonic signal is proportional to the square of the electric field. The electric field is stronger at the interface because of the surface plasmon resulting in a non-linear optical effect. This larger signal is often exploited to produce a stronger second harmonic signal. [14]
For gases, departure from 3 R per mole of atoms is generally due to two factors: (1) failure of the higher quantum-energy-spaced vibration modes in gas molecules to be excited at room temperature, and (2) loss of potential energy degree of freedom for small gas molecules, simply because most of their atoms are not bonded maximally in space to ...
J.A. Dean (ed), Lange's Handbook of Chemistry (15th Edition), McGraw-Hill, 1999; Section 6, Thermodynamic Properties; Table 6.3, Enthalpies and Gibbs Energies of Formation, Entropies, and Heat Capacities of the Elements and Inorganic Compounds
The technique was developed in 1987 by Yuen-Ron Shen and his students as an extension of second harmonic generation spectroscopy and rapidly applied to deduce the composition, orientation distributions, and structural information of molecules at gas–solid, gas–liquid and liquid–solid interfaces.