Qiang Junjie, Zhou Lianrong, Peng Yigeng, Yu Chao, Lu Peifen, Pan Shengzhe, Lu Chenxu, Chen Gang, Lu Ruifeng, Zhang Wenbin, Wu Jian
State Key Laboratory of Precision Spectroscopy, East China Normal University, Shanghai 200241, China.
School of Physics and Microelectronics Key Laboratory of Materials Physics of Ministry of Education, Zhengzhou University, Zhengzhou 450001, China.
Phys Rev Lett. 2024 Mar 8;132(10):103201. doi: 10.1103/PhysRevLett.132.103201.
We explored the collision-induced vibrational decoherence of singly ionized D_{2} molecules inside a helium nanodroplet. By using the pump-probe reaction microscopy with few-cycle laser pulses, we captured in real time the collision-induced ultrafast dissipation of vibrational nuclear wave packet dynamics of D_{2}^{+} ion embedded in the droplet. Because of the strong coupling of excited molecular cations with the surrounding solvent, the vibrational coherence of D_{2}^{+} in the droplet interior only lasts for a few vibrational periods and completely collapses within 140 fs. The observed ultrafast coherence loss is distinct from that of isolated D_{2}^{+} in the gas phase, where the vibrational coherence persists for a long time with periodic quantum revivals. Our findings underscore the crucial role of ultrafast collisional dissipation in shaping the molecular decoherence and solvation dynamics during solution chemical reactions, particularly when the solute molecules are predominantly in ionic states.