We study theoretically and observe experimentally the evolution of periodic wave trains by utilizing surface gravity water wave packets. Our experimental system enables us to observe both the amplitude and the phase of these wave packets. For low steepness waves, the propagation dynamics is in the linear regime, and these waves unfold a Talbot carpet.
View Article and Find Full Text PDFWe show that in order to guide waves, it is sufficient to periodically truncate their edges. The modes supported by this type of wave guide propagate freely between the slits, and the propagation pattern repeats itself. We experimentally demonstrate this general wave phenomenon for two types of waves: (i) plasmonic waves propagating on a metal-air interface that are periodically blocked by nanometric metallic walls, and (ii) surface gravity water waves whose evolution is recorded, the packet is truncated, and generated again to show repeated patterns.
View Article and Find Full Text PDFWe study theoretically and observe experimentally the evolution of solitary surface gravity water wavepackets propagating in homogeneous and time-dependent flow created by a computer-controlled water pump, resulting in an effective linear potential. Unlike a potential free soliton, in this case the wavepacket envelope accelerates, while its phase is proportional to the cubic power of the position in the water tank. For increased wave steepness, we observe the emergence of asymmetry in the envelope, and hence it no longer retains its soliton shape.
View Article and Find Full Text PDFWe theoretically study and successfully observe the evolution of Gaussian and Airy surface gravity water wave packets propagating in an effective linear potential. This potential results from a homogeneous and time-dependent flow created by a computer-controlled water pump. For both wave packets we measure the amplitudes and the cubic phases appearing due to the linear potential.
View Article and Find Full Text PDFWe employed steady-state and time-resolved fluorescence techniques to study the rates of excited-state proton and deuteron transfer (ESPT) from an irreversible photoacid, 1-naphthol-4-sulfonate, to solvent mixtures of HO and DO. We found that the overall ESPT rate to the solvent mixture does not follow a linear relation with the HO mole ratio. We used a chemical kinetic model to explain the deviation of the ESPT rate constant from linear behavior with HO mole ratio.
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