The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Oct. 06, 2020

Filed:

Sep. 01, 2017
Applicant:

Robert Neil Campbell, Corrales, NM (US);

Inventor:

Robert Neil Campbell, Corrales, NM (US);

Assignee:

Other;

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
H01S 3/0943 (2006.01); H01S 3/16 (2006.01); H01S 3/223 (2006.01); H01S 3/067 (2006.01); H01S 3/22 (2006.01); H01S 3/00 (2006.01); H01S 3/10 (2006.01); H01S 3/13 (2006.01); H01S 5/40 (2006.01); H01S 3/094 (2006.01); H01S 3/0941 (2006.01); H01S 3/23 (2006.01);
U.S. Cl.
CPC ...
H01S 3/1616 (2013.01); H01S 3/1643 (2013.01); H01S 3/2232 (2013.01); H01S 3/005 (2013.01); H01S 3/06754 (2013.01); H01S 3/0941 (2013.01); H01S 3/0943 (2013.01); H01S 3/094096 (2013.01); H01S 3/10084 (2013.01); H01S 3/13 (2013.01); H01S 3/22 (2013.01); H01S 3/223 (2013.01); H01S 3/2207 (2013.01); H01S 3/2308 (2013.01); H01S 3/2391 (2013.01); H01S 5/4012 (2013.01);
Abstract

Efficient laser diode excited Thulium (Tm) doped solid state systems, directly matched to a combination band pump transition of Carbon Dioxide (CO), have matured to the point that utilization of such in combination with COadmits effectively a laser diode pumped COlaser. The laser diode excited Tm solid state pump permits Continuous Wave (CW) or pulsed energy application. Appropriate optical pumping admits catalyzer free near indefinite gas lifetime courtesy of the absence of significant discharge driven dissociation and contamination. As a direct consequence of the preceding arbitrary multi isotopologue CO, symmetric and asymmetric, gas mixes may be utilized without significant degradation or departure from initial mix specifications. This would admit, at raised pressure, a system continuously tunable from approximately 9 μm to approximately 11.5 μm, or sub picosecond amplification. This method offers advantages in regards scalability, pulse energy and power, over alternative non linear conversion techniques in access to this spectral region.


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