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Near-infrared Zeeman spectroscopy for the spatially resolved measurement of helium emission spectra in Heliotron J

DOI:10.1088/1361-6587/aaebdf 期刊:Plasma Physics and Controlled Fusion 出版年份:2019 更新时间:2025-09-04 15:30:14
摘要: A passive spectroscopic method that can measure spatially resolved emission spectra only by observing from a single diagnostic port without assuming plasma symmetry was applied to the stellarator-heliotron device Heliotron J. The emission spectra from the inboard and outboard sides were separated using the difference in their Zeeman effects. On the basis of the fact that in a spectrum as a function of the wavelength, the magnitude of the wavelength splitting by the Zeeman effect relative to the Doppler broadening increases with the wavelength, the method was applied to a near-infrared helium emission line (He I 1s2s 3S?1s2p 3P, 1083 nm), and it was confirmed that the uncertainty in the separated spectra was reduced compared with that in the application to visible emission lines. From the emissivity of the separated spectra, the local recycling flux was evaluated using the inverse photon efficiency method.
作者: Taiichi Shikama,Shinichiro Kado,Hiroyuki Okada,Satoshi Yamamoto,Leo Matsuoka,Shinji Kobayashi,Kazunobu Nagasaki,Yuji Nakamura,Akihiro Ishizawa,Masahiro Hasuo
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Quantification of the neutral recycling flux in fusion-related toroidal devices is an important issue for achieving a high-performance steady-state discharge, improving the energy confinement time by preventing edge plasma cooling, and assessing numerical simulation results to specify the designs of next-generation devices.

The study demonstrated that the accuracy of measuring local atomic spectra using the Zeeman effect can be improved by adopting an emission line at a longer wavelength. The method proved effective for evaluating the local recycling flux and has potential applications in measuring toroidal and poloidal distributions of the recycling flux with multiple viewing chords.

The approximation that atomic emission is radially localized may not fully account for the actual extended emission, leading to apparent broadening of the separated spectra. The study also notes that adopting a spectrometer with better wavelength resolution could further reduce uncertainty in the fitting results.

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