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The enhancement of ultrashort pulse excited two-photon fluorescence (TPF) based on resonant double grating waveguide structures (DGWS) was studied systematically.
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The transient voltage pulse excites mechanical resonance through the piezoelectric effect.
With a 3D sequence, a radiofrequency pulse excites a thick volume of tissue rather than a thin 2D section, with increased spatial resolution.
In essence, the first pulse excites the chemical system from its original potential energy surface onto another surface, thus bypassing a bottleneck in the original pathway because the reaction leaps onto another pathway at just the right time.
It is found that the fast electron pulse excites a strong electric field perpendicular to the tube axis in conductive CNT array that guides these ultra-hot electrons to propagate along the CNT and collimates the divergent fast electron beam into a tight beam.
The pump and Stokes pulses excite multiple Raman transitions within the bandwidth of the Stokes pulses.
Therefore, it is possible that the dilatational infrasonic pulse is excited by such subsidence.
By irradiating this so called axicon from the back with short laser pulses, focused broadband ultrasonic pulses are excited.
In pulse-train excited longitudinally detected EPR (PT-LOD EPR), a train of microwave pulses that periodically inverts the magnetization is applied.
For the first 90° selective excitation pulse we used a 60 ms Eburp2 pulse, which excites a frequency range of approximately 80 Hz.
The researchers have perfected a measurement technique in which they use an extremely short voltage pulse to excite an individual atom and then follow with a lower voltage to read the atom's magnetic state, or spin, shortly afterward.
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