1 / 8

MODULE 22 (701)

MODULE 22 (701). S 1  S n. T 1  T n. T 3. S 1. T 2. T 1. S 0. Absorption Spectrophotometry of Excited States. MODULE 22 (701). The underpinning of all absorption measurements, time-resolved or not, is the Beer-Lambert law.

Download Presentation

MODULE 22 (701)

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. MODULE 22 (701) S1  Sn T1  Tn T3 S1 T2 T1 S0 Absorption Spectrophotometry of Excited States

  2. MODULE 22 (701) The underpinning of all absorption measurements, time-resolved or not, is the Beer-Lambert law l is the molar decadic extinction coefficient (units of M-1 cm-1) at the wavelength l, and ℓ is the optical path length of the sample. When the species concentration changes with time, then Hence the time profile of the change in Alis directly related to the time profile of the absorber concentration.

  3. MODULE 22 (701) Al(t) is obtained by monitoring the time dependence of the change in the transmitted light intensity, I(t), at a constant value of I0. When I0 cannot be kept constant, its value must be determined for every I(t) value. I(t) is a light fluence quantity which is converted to electrical charge by a photosensitive detector (e.g. PMT). The measurement we make is a voltage time profile, V(t), which is referenced to V0, derived from I0. Thus From the time dependence of V, thence of Al and eventually of c, the rate parameters being sought can be determined.

  4. MODULE 22 (701) There are two ways of obtaining absorptiometric information. 1: Continuous photoelectric method: A photo-detector (e.g. PMT) monitors the intensity of the transmitted light through the sample at particular wavelength (l) in a continuous manner, before, during, and after the initiating light pulse is absorbed. The detector output is fed to the input amplifier of a waveform-recording device such as a digital oscilloscope (ADC). In this way recording of the V(t) profile is done in real time. Repeating the process over a series of wavelengths allows the investigator to build up the dynamic surface (A(l,t)) of the photo-induced transient.

  5. MODULE 22 (701) Schematic of nanosecond laser flash photolysis instrument

  6. MODULE 22 (701) An A(l,t) surface Time / ns Wavelength / nm

  7. MODULE 22 (701)

  8. MODULE 22 (701) A major limitation of photoelectric recording is the nanosecond barrier. From the intrinsic time response of the electronic devices that are used to process the output current of the detector. All such devices have impedance and even the best-designed circuitry has stray capacitance of typically 20 pF. Combining this with the 50  industry-standard of high bandwidth electronic amplifiers, yields a RC time constant of 1 ns. Hence instruments that are built from conventional electronic units will have waveform rise times in the ns region and therefore absorption changes having lifetimes in this time regime will be severely deformed. We need to find ways around this problem.

More Related