With the current trend of device miniaturization, the measurement and control of interfacial adhesion forces are increasingly important in fields such as biomechanics and cell biology. However, conventional fiber optic force sensors with high Young’s modulus (>70 GPa) are usually unable to measure adhesion forces on the micro- or nano-Newton level on the surface of micro/nanoscale structures. Here, we demonstrate a method for interfacial adhesion force measurement in micro/nanoscale structures using a fiber-tip microforce sensor (FTMS). The FTMS, with microforce sensitivity of 1.05 nm/μN and force resolution of up to 19 nN, is fabricated using femtosecond laser two-photon polymerization nanolithography to program a clamped-beam probe on the end face of a single-mode fiber. As a typical verification test, the micronewton-level contact and noncontact adhesion forces on the surfaces of hydrogels were measured by FTMS. In addition, the noncontact adhesion of human hair was successfully measured with the sensor.
The non-adiabatic relaxation processes and the fragmentation dynamics of Rydberg-excited N,N,N′,N′-tetramethylmethylenediamine (TMMDA) are investigated using femtosecond time-resolved photoelectron imaging and time-resolved mass spectroscopy. Excitation at 208 nm populates TMMDA in a charge-localized 3p state. Rapid internal conversion (IC) to 3s produces two charge-delocalized conformers with independent time constants and distinct population ratios. As the system explores the 3s potential surface, the structural evolution continues on a 1.55 ps timescale, followed by a slower (12.1 ps) relaxation to the ground state. A thorough comparison of the time-dependent mass and photoelectron spectra suggests that ionization out of the 3p state ends up with the parent ion, the vibrational energy of which is insufficient for the bond cleavage. On the contrary, by virtue of the additional energy acquired by IC from 3p, the internal energy deposited in 3s is available to break the C–N bond, leading to the fragment ion. The fragmentation is found to occur on the ion surface instead of the Rydberg surface.
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