期刊
NANO LETTERS
卷 17, 期 11, 页码 6569-6574出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.7b02235
关键词
Time-resolved photoemission microscopy; plasmoemission; surface plasmon polariton; photoemission; above-threshold photoemission
类别
资金
- Deutsche Forschungsgemeinschaft [SFB 616, SPP 1391, CRC 1242]
- ERC (Complexplas)
- BMBF
- Zeiss-Stiftung
- BW Stiftung
- University of Stuttgart
- Max-Planck-Institute for Solid State Research
We use subcycle time-resolved photoemission microscopy to unambiguously distinguish optically triggered electron emission (photoemission) from effects caused purely by the plasmonic field (termed plasmoemission). We find from time-resolved imaging that nonlinear plasmoemission is dominated by the transverse plasmon field component by utilizing a transient standing wave from two counter-propagating plasmon pulses of opposite transverse spin. From plasmonic foci on flat metal surfaces, we observe highly nonlinear plasmoemission up to the fifth power of intensity and quantized energy transfer, which reflects the quantum-mechanical nature of surface plasmons. Our work constitutes the basis for novel plasmonic devices such as nanometer-confined ultrafast electron sources as well as applications in time-resolved electron microscopy.
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