Abstract

An enhanced supersonic carbon source produces carbon atoms in their C(3Pj) electronic ground states via laser ablation of graphite at 266 nm. The 30 Hz (40±2) mJ output of a Nd-YAG laser is focused onto a rotating graphite rod with a 1000 mm focal length UV-grade fused silica plano-convex lens to a spot of (0.5±0.05) mm diameter. Ablated carbon atoms are subsequently seeded into helium or neon carrier gas yielding intensities up to 1013 C atoms cm−3 in the interaction region of a universal crossed beam apparatus. The greatly enhanced number density and duty cycle shift the limit of feasible crossed beam experiments down to rate constants as low as 10−11–10−12 cm3 s−1. Carbon beam velocities between 3300 and 1100 m s−1, with speed ratios ranging from 2.8 to 7.2, are continuously tunable on-line and in situ without changing carrier gases by varying the time delay between the laser pulse, the pulsed valve, and a chopper wheel located 40 mm after the laser ablation. Neither electronically excited carbon atoms nor ions could be detected within the error limits of a quadrupole-mass spectrometric detector. Carbon clusters are restricted to ∼10% C2 and C3 in helium, minimized by multiphoton dissociation, and eliminating the postablation nozzle region.

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