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Liang T. Chu, Ph.D.

  • Liang T. Chu

    Liang T. Chu, Ph.D.

    • Nuclear Chemistry Laboratory
    • Associate Professor, School of Public Health, Environmental Health Sciences

    • Ph.D., Physical Chemistry, Princeton University (1990)
    • Postdoctoral training: Jet Propulsion Laboratory, California Institute of Technology (1993)
    (518) 474-6340
    Fax: (518) 473-2895

Research Interests

The current research focus in Dr. Chu's laboratory involves the studies of the heterogeneous chemical reactions on ice-cloud and particle surfaces. These reactions occur in both the troposphere and lower stratosphere and can be very important to understand ozone depletion. The key chemical process of polar ozone depletion is the heterogeneous chlorine and bromine activation on Polar Stratospheric Cloud (PSC) surfaces.

We have demonstrated that the uptake of HBr on ice films, which are used to mimic type II PSCs, is about 1013 molecules/cm3 at PHBr~10-8 Torr and 188 K. This implies that HBr surface coverage is sub-monolayer on a PSC surface. Hydrobromic acid hydrates (both tri- and dihydrates) were formed at higher PHBr and identified in the laboratory. This is the major reason to account for the higher HBr uptake on ice in our study. If all HBr molecules are converted into active bromine and providing that bromine is about 100 times more efficient to deplete ozone on the per atom basis than chlorine in the lower stratosphere, this implies that the heterogeneous bromine reactions are an important factor contributing to ozone depletion. The process is even more significant when the chlorine and bromine species are coupled together.

The study was carried out in a fast-flow reactor and the HBr molecule was detected by a differentially-pumped mass spectrometer in the ultra-high vacuum condition. This ultra-sensitive instrument also allows us to study numerous chemical reactions. For example, we have investigated the reaction mechanism of HOCl+HBr(ad) arrowBrCl+H2O(ad). This reaction activates both the photochemical inactive chlorine and bromine on the ice-cloud surface, simultaneously. The study provides us not only the reaction probability, γ, but also the reaction mechanism in which we can show how HOCl and HBr molecules come together near the ice surface and to produce BrCl.

Some current research projects include: the effect of HOBr and HOCl on the SO2 oxidation at the boundary layer conditions, as well as halogen activation rates at the same conditions and the uptake rate and mechanism of Br2 on oxalic acid-ice surfaces.

A combination of FT-IR absorption and temperature programmed desorption (TPD) technique is used to determine molecular structures of both gas-phase and adsorbed species in Dr. Chu's laboratory. We employ the specular reflective FT-IR absorption technique to probe the adsorption of oxalic acid on ice surfaces, and desorbed species are probed by mass spectrometer in a TPD experiment.

Combined with theoretical chemistry calculations such as molecular dynamics simulations, the detailed knowledge as to how and where oxalic acid is adsorbed on the ice and possibly the hydration mechanism can be revealed. We will be able to shed light on the chemical binding nature of some atmospherically important species on ice-cloud surfaces and understand the halogen activation on molecular crystal ice surfaces at a molecular level. This will provide a better understanding of ozone loss mechanism in the atmosphere.

Select Publications

Zhu L, Sangwan M, Huang L, Du J, Chu LT.
Photolysis of Nitric Acid at 308 nm in the Absence and in the Presence of Water Vapor.
Journal of Physical Chemistry A.
Zhu CZ, Xiang B, Chu LT, Zhu L.
Reply to "Comment on '308 nm Photolysis of Nitric Acid in the Gas Phase, on Aluminum Surfaces, and on Ice Films".
Journal of Physical Chemistry A.
Hui Y, Chu LT.
Interaction of oxalic acid and ice on Cu surface.