Skip to main content Accessibility help
×
Hostname: page-component-cd9895bd7-jn8rn Total loading time: 0 Render date: 2024-12-26T07:35:46.480Z Has data issue: false hasContentIssue false

10 - The crystal field engineered

Published online by Cambridge University Press:  24 September 2009

Brian Henderson
Affiliation:
University of Cambridge
Ralph H. Bartram
Affiliation:
Mansfield Center
Get access

Summary

The successful launch of the alexandrite laser by Allied Chemicals Inc. and the elucidation of essential design parameters [Walling et al. (1979), (1980)] spawned rapid growth of research into Cr3+-based lasers [Caird and Payne (1991)]. Possible alternative gain media to alexandrite included the Cr3+-doped garnets [Struve and Huber (1985)]. However, the development of Cr3+ : colquiriite lasers at Lawrence Livermore National Laboratory [Payne et al. (1988a), (1989a)] deflected attention away from the Cr3+ garnets, these mixed fluoride gain media being as efficient as alexandrite and almost as broadband as Ti-sapphire. Two distractions from the dominance of Cr3+ ion broadband tunable lasers were the inventions of the Ti-sapphire (Ti3+ : Al2O3) [Moulton (1982a,b)] and the Cr4+ : forsterite [Petricevic et al. (1988)] lasers. At present Ti3+ : Al2O3 and Nd3+ : YAG are the market leaders in solid state laser production against which new developments are assessed. Their pre-eminence derives in part from the quality and quantity of laser rods that can be produced at modest cost. Both materials have excellent photothermal and thermomechanical properties, and are robust components under laser operating conditions. However, despite much spectroscopic research Ti-sapphire is still the only usable Ti3+-activated solid state laser. In contrast, operation of several 3d2-ion doped lasers have been reported giving broadband tunability at near-infrared wavelengths (1.0–1.7 μm) which have potential applications in optical communications, medical sciences and on remote sensing LIDAR platforms.

Type
Chapter
Information
Publisher: Cambridge University Press
Print publication year: 2000

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Save book to Kindle

To save this book to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×