METHODS, COMPOSITIONS AND DEVICES FOR PERFORMING IONIZATION DESORPTION ON SILICON DERIVATIVES
Embodiments of the present invention are directed to a substrate for performing ionization desorption on porous silicon, methods for performing such ionization desorption and methods of making substrates. One embodiment directed to a substrate for performing ionization desorption on silicon comprises a substrate having a surface having a formula of: As used above, X is H or Y, where at least at least twenty five mole percent of X is Y and Y is hydroxyl, or —O—R 1 , or O—SiR 1 , R 2 , R 3 wherein R 1 , R 2 , and R 3 are selected from the group consisting of alkyl, alkenyl, alkynyl, aromatic, amino alkyl, amino alkenyl, amino alkynyl, pyridinyl, pyrridonyl, and carbonyl, alcohol and carboxylic acid derivatives thereof having one to twenty five atoms, and hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives. The letter “n” represents an integer from 1 to infinity and any vacant valences are silicon atoms, hydrogen or impurities.
1 . A substrate for performing ionization desorption on silicon comprising a substrate having a formula of:
wherein X is H or Y, where at least at least twenty five mole percent of X is Y and Y is hydroxyl, or —O—R 1 or O—SiR 1 , R 2 , R 3 wherein R 1 , R 2 , and R 3 are selected from the group consisting of alkyl, alkenyl, alkynyl, aromatic, amino alkyl, amino alkenyl, amino alkynyl, pyridinyl, pyrridonyl, and carbonyl, alcohol and carboxylic acid derivatives thereof having one to twenty five atoms, and hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives.
2 . The article of manufacture of claim 1 wherein Y is hydroxyl.
3 . The article of manufacture of claim 1 wherein said mole percent is twenty-five to fifty.
4 . The article of manufacture of claim 1 wherein at least a portion of Y is represented by the Formula II below:
wherein R 1 , R 2 , and R 3 are methyl or alkyl carbon chains of less than or equal to eighteen carbons or single and poly-aromatic hydrocarbons and their hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives.
5 . The article of manufacture of claim 4 wherein R 1 , R 2 , and R 3 are methyl or alkyl carbon chains of less than or equal to eighteen carbons.
6 . A method of making a substrate for performing ionization desorption on silicon, comprising the steps of providing a surface comprising silicon hydride on said substrate, reacting at least five mole percent of the silicon hydride with oxygen to form a silicon oxide.
7 . The method of claim 6 further comprising reacting said silicon oxide with a compound represented by the formula WY, wherein W is selected from the group consisting of halogens, methoxy, or ethoxy, and Y is represented by formula:
wherein R 1 , R 2 , and R 3 are methyl or alkyl carbon chains of less than or equal to eighteen carbons or single and poly-aromatic hydrocarbons and their hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives.
8 . The method of claim 7 wherein said compound represented by the formula WY is trimethylchlorosilane.
9 . The method of claim 7 wherein said compound represented by the formula WY is amino propyldimethylethoxysilane.
10 . A method of performing laser desorption ionization on silicon comprising the steps of providing a sample on a porous silicon surface having a formula of:
wherein X is H or Y, where at least at least twenty five mole percent of X is Y and Y is hydroxyl, or —O—R 1 or O—SiR 1 , R 2 , R 3 wherein R 1 , R 2 , and R 3 are selected from the group consisting of alkyl, alkenyl, alkynyl, aromatic, amino alkyl, amino alkenyl, amino alkynyl, pyridinyl, pyrridonyl, and carbonyl, alcohol and carboxylic acid derivatives thereof having one to twenty five atoms, and hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives, ionizing at least a portion of said sample by means of a laser to form an ionized sample, placing said ionized sample in mass spectrometer means for a determination of a mass charge relationship.
12 . The method of claim 11 wherein said sample is provided on said substrate and withdrawn to leave a residue having compounds of interest laser ionization.
13 . The article of manufacture of claim 10 wherein Y is hydroxyl.
14 . The article of manufacture of claim 10 wherein said mole percent is twenty five to fifty.
15 . The article of manufacture of claim 10 wherein at least a portion of Y is represented by the Formula II below:
wherein R 1 , R 2 , and R 3 are methyl or alkyl carbon chains of less than or equal to eighteen carbons or single and poly-aromatic hydrocarbons and their hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives.
16 . The article of manufacture of claim 13 wherein R 1 , R 2 , and R 3 are methyl or alkyl carbon chains of less than or equal to eighteen carbons.
17 . An apparatus for performing laser desorption ionization mass analysis comprising:
a substrate having a porous silicon surface having a formula of:
wherein X is H or Y, where at least at least twenty five mole percent of X is Y and Y is hydroxyl, or —O—R 1 or O—SiR 1 , R 2 , R 3 wherein R 1 , R 2 , and R 3 are selected from the group consisting of alkyl, alkenyl, alkynyl, aromatic, amino alkyl, amino alkenyl, amino alkynyl, pyridinyl, pyrridonyl, and carbonyl, alcohol and carboxylic acid derivatives thereof having one to twenty five atoms, and hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives,
a laser aligned with said substrate to pulse light energy on said sample to ionize and vaporize a portion of said sample, to form a ionized sample, and
a mass analyser for receiving said ionized sample for a determination of a mass charge relationship.
18 . The apparatus of claim 14 wherein said Y is represented by the Formula II below:
wherein R 1 , R 2 , and R 3 are methyl or alkyl carbon chains of less than or equal to eighteen carbons or single and poly-aromatic hydrocarbons and their hydroxyl, amino, amide, carboxyl, ester, carbonyl, sulfhydryl, sulfonyl, phosphoral, bromo, iodo, chloro and fluoro derivatives and, Y represented by Formula II has a mole percent of two to ten.