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We present a direct observation of carbon-atom tunneling in the flipping reaction of formaldehyde between its two mirror-reflected states on a Cu(110) surface using low-temperature scanning tunneling microscopy (STM). The flipping reaction was monitored in real time, and the reaction rate was found to be temperature independent below 10 K. This indicates that this reaction is governed by quantum mechanical tunneling, albeit involving a substantial motion of the carbon atom (∼1 Å). In addition, deuteration of the formaldehyde molecule resulted in a significant kinetic isotope effect (RCH2O/RCD2O ≈ 10). The adsorption structure, reaction pathway, and tunneling probability were examined by density functional theory calculations, which corroborate the experimental observations.

Ag nanowire with the receiving and transmitting Ag bow tie antenna pairs at its incident and emission ends was patterned on the SiO(2) substrate to realize an enhanced surface plasmon emission with a factor of 45 compared to the single Ag nanowire without antenna pairs. The receiving and transmitting bow tie antenna pairs enhanced the plasmon coupling and emission efficiencies of the Ag nanowire. And the maximum plasmon emission sensitively depended on the length of Ag nanowire, the arm length of bow tie antennas, and the incident angle of optical excitation. This enhanced plasmon emission was confirmed by finite-difference time-domain simulations and explored with analytical calculations using the impedance matching theory at optical frequency.