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arxiv: 1004.4118 · v2 · pith:N4SYB5RWnew · submitted 2010-04-23 · 🪐 quant-ph · cond-mat.other· physics.ins-det

DC-powered Fe3+:sapphire Maser and its Sensitivity to Ultraviolet Light

classification 🪐 quant-ph cond-mat.otherphysics.ins-det
keywords sapphiremaseroscillatoranalysischemicalhemexhereless
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The zero-field Fe3+:sapphire whispering-gallery-mode maser oscillator exhibits several alluring features: Its output is many orders of magnitude brighter than that of an active hydrogen maser and thus far less degraded by spontaneous-emission (Schawlow-Townes) and/or receiving-amplifier noise. Its oscillator loop is confined to a piece of mono-crystalline rock bolted into a metal can. Its quiet amplification combined with high resonator Q provide the ingredients for exceptionally low phase noise. We here concentrate on novelties addressing the fundamental conundrums and technical challenges that impede progress. (1) Roasting: The "mase-ability" of sapphire depends significantly on the chemical conditions under which it is grown and heat-treated. We provide some fresh details and nuances here. (2) Simplification: This paper obviates the need for a Ka-band synthesizer: it describes how a 31.3 GHz loop oscillator, operating on the preferred WG pump mode, incorporating Pound locking, was built from low-cost components. (3) "Dark Matter": A Siegman-level analysis of the experimental data determines the substitutional concentration of Fe3+ in HEMEX to be less than a part per billion prior to roasting and up to a few hundred ppb afterwards. Chemical assays, using different techniques (incl. glow discharge mass spectra spectroscopy and neutron activation analysis) consistently indicate, however, that HEMEX contains iron at concentrations of a few parts per million. Drawing from several forgotten-about/under-appreciated papers, this substantial discrepancy is addressed. (4) Excitons: Towards providing a new means of controlling the Fe3+:sapph. system, a cryogenic sapphire ring was illuminated, whilst masing, with UV light at wavelengths corresponding to known electronic and charge-transfer (thus valence-altering) transitions. Preliminary experiments are reported.

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