Physicists use lasers to capture first snapshots of rapid chemical bonds breaking
Lasers have successfully recorded a chemical reaction that happens as fast as a quadrillionth of a second, which could help scientists understand and control chemical reactions.
The idea for using a laser to record a few femtoseconds of a molecule's extremely fast vibrations as it breaks apart came from Kansas State University physicists. Chii-Dong Lin, university distinguished professor of physics, and Anh-Thu Le, research associate professor in James R. Macdonald Laboratory, are part of an international collaborative project published in the Oct. 21 issue of Science.
"If you want to see something that happens very, very fast, you need a tool that can measure a very, very tiny time period," Lin said. "The only light available in femtosecond measurements is a laser."
A femtosecond is one-millionth of a billionth of a second, which is a million times shorter than a nanosecond. Until recently, there was no way to measure what happens during a chemical reaction in that short of a period.
Lin's research group made its first molecular movie of an oxygen molecule using lasers in 2012, but to record a larger molecule -- such as the four-atom acetylene molecule -- they needed a more advanced laser. After five years of collaboration with Jens Biegert's group from ICFO-The Institute of Photonic Sciences, a member of The Barcelona Institute of Science and Technology, Lin's idea became reality.
The international team used the molecule's own electrons to scatter the molecule -- a process called mid-infrared laser-induced electron diffraction, or LIED -- and capture snapshots of acetylene as it is breaking apart. An intense laser is used to affectan acetylene molecule -- composed of two hydrogen atoms and two carbon atoms -- to strip out an electron and initiate the breakup of the molecule. After nine femtoseconds, the laser drives the free electron back to the elongated molecule to create an image.
"Scientists will eventually be able to apply this tool in chemistry, biology and other physical sciences to look at different types of molecules and processes," Lin said.
According to Lin, acetylene's four-atom chemical structure provides multiple possibilities where the bonds could break. Being able to measure where and when those breaks occur can help researchers better understand chemical reactions, which Lin said will lead to better control of a reaction and is applicable to multiple areas of science.
"In order to control something, you have to know where it is first," Lin said. "If you throw a ball over a house, you can't see what happens to it, so you can't control it anymore. But if you have a way to see each second of the ball in the air, you can figure out why it ends up where it does and potentially change the way you throw it to control the outcome or to influence it in real time."
Lin's research group started working with Kansas State University distinguished professor emeritus Lew Cocke's research group in 2008 to conduct the first LIED experiment, which led to the current development. The initial experiments enabled the researchers to apply their theory to decode signals from electrons that produce the image. By decoding the image, the researchers accurately measured the molecule's new bond distances, which are smaller than one hundred-millionth of a centimeter.
"Since the snapshots, which are taken by the electrons, occur in a very strong laser field, it was thought to be nearly impossible to decode the electron information and measure the small distances," said Le, who provided critical decoding of the molecule's structure in the snapshot from Barcelona. "This is the first real-time observation of the breakup of a molecule within nine femtoseconds."
Ultrafast electron diffraction imaging of bond breaking in di-ionized acetylene B. Wolter, M. G. Pullen, A.-T. Le, M. Baudisch, K. Doblhoff-Dier, A. Senftleben, M. Hemmer, C. D. Schröter, J. Ullrich, T. Pfeifer, R. Moshammer, S. Gräfe. Vendrell, C. D. Lin, J. Biegert Science 21 Oct 2016: Vol. 354, Issue 6310, pp. 308-312 DOI: 10.1126/science.aah3429