Author
Listed:
- Khadga J. Karki
(Lund University)
- Julia R. Widom
(University of Oregon
Present address: Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA)
- Joachim Seibt
(Lund University)
- Ian Moody
(University of Oregon)
- Mark C. Lonergan
(University of Oregon)
- Tõnu Pullerits
(Lund University)
- Andrew H. Marcus
(University of Oregon)
Abstract
Recently there has been growing interest in the role of coherence in electronic dynamics. Coherent multidimensional spectroscopy has been used to reveal coherent phenomena in numerous material systems. Here we utilize a recent implementation of coherent multidimensional spectroscopy—two-dimensional photocurrent spectroscopy—in which we detect the photocurrent from a PbS quantum dot photocell resulting from its interactions with a sequence of four ultrafast laser pulses. We observe sub-picosecond evolution of two-dimensional spectra consistent with multiple exciton generation. Moreover, a comparison with two-dimensional fluorescence spectra of the quantum dots demonstrates the potential of two-dimensional photocurrent spectroscopy to elucidate detailed origins of photocurrent generating electronic state coherence pathways. Since the measurement is based on detecting the photocell current in situ, the method is well suited to study the fundamental ultrafast processes that affect the function of the device. This opens new avenues to investigate and implement coherent optimization strategies directly within devices.
Suggested Citation
Khadga J. Karki & Julia R. Widom & Joachim Seibt & Ian Moody & Mark C. Lonergan & Tõnu Pullerits & Andrew H. Marcus, 2014.
"Coherent two-dimensional photocurrent spectroscopy in a PbS quantum dot photocell,"
Nature Communications, Nature, vol. 5(1), pages 1-7, December.
Handle:
RePEc:nat:natcom:v:5:y:2014:i:1:d:10.1038_ncomms6869
DOI: 10.1038/ncomms6869
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