H. Zhang

Electron Acceleration via Trapping inside Ion Mirror-mode Structures within A Large-scale Magnetic Flux Rope

Z. H. Zhong [1,2], H. Zhang [1,3], M. Zhou [1,2], D. B. Graham [4], R. X. Tang [1,2], X. H. Deng [1,2], Yu. V. Khotyaintsev [4]

Abstract

Fermi acceleration is believed as a crucial process for the acceleration of energetic electrons within flux ropes (FRs) during magnetic reconnection. However, in finite-length FRs with a large core field, the finite contracting and the escaping of electrons along the axis can significantly limit the efficiency of Fermi acceleration. Using observations from the Magnetospheric Multiscale mission in the magnetotail, we demonstrate that magnetic mirror structures inside the FR can effectively prevent the escape of energetic electrons and overcome the limitation of finite contraction. Energetic electrons were produced and formed a power-law energy distribution in these mirror structures. By evaluating the acceleration rates, we show that these energetic electrons can be continuously accelerated within the mirror structures near the central region of the FR. These results unveil a novel mechanism that is universally applicable to electron acceleration within FRs in space, laboratory, and astrophysical plasmas.

Optical Mass Spectrometry of Cold $\mathrm{RaOH}^+$ and ${\mathrm{RaOCH}_3}^+$

M. Fan [1,2], C. A. Holliman [1,2], X. Shi [1,2], H. Zhang [3], M. W. Straus [1,2], X. Li [4], S. W. Buechele [1,2], A. M. Jayich [1,2]

Abstract

We present an all-optical mass spectrometry technique to identify trapped ions. The new method uses laser-cooled ions to determine the mass of a cotrapped dark ion with a sub-dalton resolution within a few seconds. We apply the method to identify the first controlled synthesis of cold, trapped $\mathrm{RaOH}^+$ and ${\mathrm{RaOCH}_3}^+$. These molecules are promising for their sensitivity to time and parity violations that could constrain sources of new physics beyond the standard model. The nondestructive nature of the mass spectrometry technique may help identify molecular ions or highly charged ions prior to optical spectroscopy. Unlike previous mass spectrometry techniques for small ion crystals that rely on scanning, the method uses a Fourier transform which is inherently broadband and comparatively fast. The technique's speed provides new opportunities for studying state-resolved chemical reactions in ion traps.