Picosecond broadband cars probe using the picosecond continuum

Claim 2

A coherent anti-Stokes Raman spectroscopy (CARS) method for producing a picosecond broadband CARS vibrational spectrum of a sample comprising the steps of: generating a probe pulse of coherent monochromatic radiation having a frequency ω 1 , said probe pulse having a duration on the order of picoseconds; generating a continuum pulse of broadband radiation, said continuum pulse having a range of frequencies ω WL and a duration on the order of picoseconds, said range of frequencies ω WL of said continuum pulse being related to said frequency ω 1 of said probe pulse such that the difference ω 1 -ω WL corresponds to a range of Raman active vibrational resonances in said sample; spatially and temporally combining said probe pulse and said continuum pulse; directing said combined probe pulse and continuum pulse into said sample to excite the Raman active vibrational resonances in said sample; and detecting a beam of radiation emitted by said sample, said beam of radiation including an anti-Stokes spectrum of energy characteristic of said sample.

Claim 3

The method recited in claim 1, wherein the said step of generating said continuum pulse comprises the steps of: providing a fundamental pulse of coherent monochromatic radiation having a fundamental frequency ω, said pulse having a duration on the order of picoseconds; focusing said fundamental pulse into a liquid cell containing a continuum generating medium, said continuum generating medium producing an output pulse of broadband radiation having a range of frequencies ω WL and a duration on the order of picoseconds; and filtering said output pulse to remove remanants of said fundamental pulse at said frequency ω to produce said continuum pulse.

Claim 4

The method recited in claim 2, wherein said step of focusing said pulse into said liquid cell further comprises the step of: focusing said pulse into said liquid cell containing D 2 O liquid acting as said continuum generating medium.

Claim 5

The method recited in claim 2, wherein said step of focusing said pulse into said liquid cell further comprises the step of: focusing said pulse into said liquid cell containing a 50 percent mixture of D 3 PO 4 in D 2 O liquid acting as said continuum generating medium.

Claim 6

The method recited in claim 1, wherein said step of generating said continuum pulse comprises the steps of: providing a first pulse of coherent monochromatic radiation having a frequency of 1/2ω, said first pulse having a duration on the order of picoseconds; passing said first pulse through a first second-harmonic generator to form a second pulse, said second pulse containing a first component at a frequency 1/2ω and a second component at a frequency ω; spatially dividing said first and second components of said second pulse into a first component pulse at said frequency 1/2ω and a second component pulse at said frequency ω; delaying said first component pulse by a first variable amount of time relative to said second component pulse; and generating said continuum pulse from said delayed first component pulse.

Claim 7

The method recited in claim 5, wherein said step of generating said continuum pulse further comprises the steps of: focusing said delayed first component pulse into a liquid cell containing a continuum generating medium, said continuum generating medium producing an output pulse of broadband radiation having a range of frequencies ω WL and a duration in the order of picoseconds; and filtering said output pulse to remove remanants of said delayed first component pulse at said frequency 1/2ω to produce said continuum pulse.

Claim 8

The method recited in claim 6, wherein said step of focusing said delayed first component pulse into said liquid cell further comprises the step of: focusing said delayed first component pulse into said liquid cell containing D 2 O liquid acting as said continuum generating medium.

Claim 9

The method recited in claim 6, wherein said step of focusing said delayed first component pulse into said liquid cell further comprises the step of: focusing said delayed first component pulse into said liquid cell containing a 50 percent mixture of D 3 PO 4 in D 2 O liquid acting as said continuum generating medium.

Claim 10

The method recited in claim 5, wherein said step of spatially and temporally combining said probe and continuum pulses further comprises the step of: adjusting said first variable amount of time to temporally align said continuum pulse with said probe pulse.

Claim 11

The method recited in claim 5, wherein said step of generating said probe pulse comprises the step of: providing said first pulse of radiation such that said frequency 1/2ω equals a frequency 1/2ω 1 , said second component pulse forming said probe pulse.

Claim 12

The method recited in claim 5, wherein said step of generating said probe pulse comprises the step of: passing said second component pulse through a frequency shifter to convert said second component pulse at said frequency ω to said probe pulse at said frequency ω 1 .

Claim 13

The method recited in claim 5 which further comprises the steps of: passing said second component pulse through a second second-harmonic generator to form a third pulse, said third pulse containing a third component pulse at a frequency 2ω and a fourth component at said frequency ω; spatially dividing said third and fourth components of said third pulse into a third component pulse at said frequency 2ω and a fourth component pulse at said frequency ω; delaying said third component pulse by a second variable amount of time relative to said fourth component pulse; spatially combining said delayed third component pulse with said combined probe and continuum pulses: directing said combined delayed third component pulse and said probe and continuum pulses into said sample, said delayed third component pulse acting as an excitation pulse to raise said sample to an excited state.

Claim 14

The method as recited in claim 12, wherein said step of generating said probe pulse comprises the step of: providing said first pulse of radiation such that said frequency 1/2ω equals a frequency 1/2ω 1 , said fourth component pulse forming said probe pulse.

Claim 15

The method recited in claim 12, wherein said step of generating said probe pulse comprises the step of: passing said fourth component pulse through a frequency shifter to convert said fourth component pulse at said frequency ω to said probe pulse at said frequency ω 1 .

Claim 16

The method recited in claim 1, wherein said step of detecting said beam of radiation emitted by said sample comprises the steps of: filtering said beam of radiation to remove remanants of said probe and continuum pulses; focusing said filtered beam into a spectrograph to develope said anti-Stokes spectrum; and detecting said anti-Stokes spectrum.

Claim 17

A coherant anti-Stokes Raman spectroscopy (CARS) apparatus for producing a picosecond broadband CARS vibrational spectrum of a sample comprising: means for generating a probe pulse of coherent monochromatic radiation having a frequency ω 1 , said probe pulse having a duration on the order of picoseconds; means for generating a continuum pulse of broadband radiation having a range of frequencies ω WL and a duration in the order of picoseconds, said range of frequencies ω WL of said continuum pulse being related to said frequency ω 1 of said probe pulse such that the difference ω 1 -ω WL corresponds to a range of Raman active vibrational resonances in said sample; means coupled to receive said probe pulse and said continuum pulse for spatially and temporally combining said pulses; means coupled to receive said combined probe and continuum pulses for directing said combined pulses into said sample to excite the vibrational resonances in said sample; and means coupled to receive a beam of radiation emitted by said sample in response to said excitation by said combined pulses for detecting an anti-Stokes spectrum of energy characteristic of said sample contained in said beam.

Claim 18

A coherant anti-Stokes Raman spectroscopy (CARS) apparatus for producing a picosecond broadband CARS vibrational spectrum of a sample comprising: means for generating a probe pulse of coherent monochromatic radiation having a frequency ω 1 , said probe pulse having a duration on the order of picoseconds; means for generating a continuum pulse of broadband radiation having a range of frequencies ω WL and a duration in the order of picoseconds, said range of frequencies ω WL of said continuum pulse being related to said frequency ω 1 of said probe pulse such that the difference ω 1 -ω WL corresponds to a range of Raman active vibrational resonances in said sample; means coupled to receive said probe pulse and said continuum pulse for spatially and temporally combining said pulses; means coupled to receive said combined probe and continuum pulses for directing said combined pulses into said sample to excite the vibrational resonances in said sample; and means coupled to receive a beam of radiation emitted by said sample in response to said excitation by said combined pulses for detecting an anti-Stokes spectrum of energy characteristic of said sample contained in said beam.

Claim 19

The apparatus as recited in claim 16, wherein said means for generating said probe pulse comprises: first second-harmonic generator means coupled to receive a first pulse at a frequency 1/2ω 1 for producing a second pulse including components at said frequency 1/2ω 1 and at said frequency ω 1 , said first and second pulses having durations on the order of picoseconds; and means coupled to receive said second pulse for spatially dividing said second pulse into a first component pulse at said frequency 1/2ω 1 and a second component pulse at said frequency ω 1 , said second component pulse forming said probe pulse.

Claim 20

The apparatus as recited in claim 16, wherein said means for generating said probe pulse comprises: first second-harmonic generator means coupled to receive a first pulse at a frequency 1/2ω for producing a second pulse including components at said frequency 1/2ω and at a frequency ω, said first and second pulses having durations on the order of picoseconds; means coupled to receive said second pulse for spatially dividing said second pulse into a first component pulse at said frequency 1/2ω and a second component pulse at said frequency ω; and frequency shift means coupled to receive said second component pulse for shifting the frequency of said second component pulse to said frequency ω 1 and for forming said probe pulse.

Claim 21

The apparatus as recited in claim 17, wherein said means for generating said continuum pulse comprises: a liquid cell containing a continuum generating medium, said first component pulse being focused into said cell, said cell producing said continuum pulse.

Claim 22

The apparatus as recited in claim 19, wherein said continuum generating medium comprises D 2 O liquid.

Claim 23

The apparatus as recited in claim 19, wherein said continuum generating medium comprises a 50 percent mixture of D 3 PO 4 in D 2 O liquid.

Claim 24

The apparatus as recited in claim 16, wherein said means for spatially and temporally combining said probe and continuum pulses comprises: delay means for delaying the generation of said continuum pulse relative to said probe pulse for temporally aligning said continuum pulse with said probe pulse.

Claim 25

The apparatus as recited in claim 19, wherein said means for spatially and temporally combining said probe and continuum pulses comprises: delay means coupled between said means for spatially dividing said second pulse and said liquid cell for delaying said first component pulse relative to said probe pulse.

Claim 26

The apparatus as recited in claim 16, which further comprises: means for generating an excitation pulse of coherent monochromatic radiation, said excitation pulse having a duration on the order of picoseconds; and means coupled between said means for combining said probe and continuum pulses and said means for directing said combined probe and continuum pulses for receiving said excitation pulse and said combined probe and continuum pulses and for combining said excitation pulse with said combined probe and continuum pulses, said excitation pulse being directed into said sample along with said combined probe and continuum pulses to raise said sample to an excited state.

Claim 27

The apparatus as recited in claim 24, wherein said means for generating said probe pulse comprises: first second-harmonic generator means coupled to receive a first pulse at a frequency 1/2ω for producing a second pulse including components at said frequency 1/2ω and at a frequency ω, said first and second pulses having durations on the order of picoseconds; means coupled to receive said second pulse for spatially dividing said second pulse into a first component pulse at said frequency 1/2ω and a second component pulse at said frequency ω; second second-harmonic generator means coupled to receive said second component pulse at said said frequency ω for producing a third pulse including components at said frequency ω and at a frequency 2ω; and means coupled to receive said third pulse for spatially dividing said third pulse into a third component pulse at said frequency ω and a fourth component pulse at said frequency 2ω, said third component pulse forming said probe pulse.

Claim 28

The apparatus as recited in claim 24, wherein said means for generating said probe pulse comprises: first second-harmonic generator means coupled to receive a first pulse at a frequency 1/2ω for producing a second pulse including components at said frequency 1/2ω and at a frequency ω, said first and second pulses having durations on the order of picoseconds; means coupled to receive said second pulse for spatially dividing said second pulse into a first component pulse at said frequency 1/2ω and a second component pulse at said frequency ω; second second-harmonic generator means coupled to receive said second component pulse at said said frequency ω for producing a third pulse including components at said frequency ω and at a frequency 2ω; means coupled to receive said third pulse for spatially dividing said third pulse into a third component pulse at said frequency ω and a fourth component pulse at said frequency 2ω; and frequency shift means coupled to receive said third component pulse for shifting the frequency of said third component pulse to said frequency ω 1 and for forming said probe pulse.

Claim 29

The apparatus as recited in claim 25, wherein said means for generating said excitation pulse comprises: means coupled to receive said fourth component pulse for delaying said fourth component pulse by a variable amount of time relative to said probe pulse and for producing said excitation pulse.

Claim 30

The apparatus as recited in claim 16, wherein said means for detecting said anti-Stokes spectrum comprises: means coupled to receive said beam of radiation from said sample for filtering said beam to remove remanants of said probe and continuum pulses to produce a filtered beam; and spectrograph means coupled to receive said filtered beam for developing said anti-Stokes spectrum from said beam.