Welcome to the new version of CaltechAUTHORS. Login is currently restricted to library staff. If you notice any issues, please email coda@library.caltech.edu
Published March 10, 2010 | Supplemental Material + Accepted Version
Journal Article Open

Evolution of catalysts directed by genetic algorithms in a plug-based microfluidic device tested with oxidation of methane by oxygen

Abstract

This paper uses microfluidics to implement genetic algorithms (GA) to discover new homogeneous catalysts using the oxidation of methane by molecular oxygen as a model system. The parameters of the GA were the catalyst, a cocatalyst capable of using molecular oxygen as the terminal oxidant, and ligands that could tune the catalytic system. The GA required running hundreds of reactions to discover and optimize catalyst systems of high fitness, and microfluidics enabled these numerous reactions to be run in parallel. The small scale and volumes of microfluidics offer significant safety benefits. The microfluidic system included methods to form diverse arrays of plugs containing catalysts, introduce gaseous reagents at high pressure, run reactions in parallel, and detect catalyst activity using an in situ indicator system. Platinum(II) was identified as an active catalyst, and iron(II) and the polyoxometalate H5PMo10V2O40 (POM-V2) were identified as active cocatalysts. The Pt/Fe system was further optimized and characterized using NMR experiments. After optimization, turnover numbers of approximately 50 were achieved with approximately equal production of methanol and formic acid. The Pt/Fe system demonstrated the compatibility of iron with the entire catalytic cycle. This approach of GA-guided evolution has the potential to accelerate discovery in catalysis and other areas where exploration of chemical space is essential, including optimization of materials for hydrogen storage and CO2 capture and modifications.

Additional Information

© 2010 American Chemical Society. Published In Issue: March 10, 2010. Article ASAP: February 11, 2010. Received: November 20, 2009. This work was supported by NIH T32 GM008720 (J.E.K.), the NSF CRC CHE-0526693, and the Camille Dreyfus Teacher-Scholar Awards Program (S.D.). O.D. is grateful to the Welch Foundation (Grant No. E-1571), A.P. Sloan Foundation, and Camille and Henry Dreyfus foundation for supporting this research. We thank Elizabeth B. Haney and Heidi Park for contributions to writing and editing this manuscript.

Attached Files

Accepted Version - nihms178778.pdf

Supplemental Material - Ismagilov_JACS_2010_catalysis_GA_132_3128_3132_JEK_supp_info.pdf

Supplemental Material - ja909853x_si_002.mpg

Files

Ismagilov_JACS_2010_catalysis_GA_132_3128_3132_JEK_supp_info.pdf
Files (17.2 MB)
Name Size Download all
md5:4e620282e3234a20335a8280a84583fc
811.9 kB Preview Download
md5:5cdbd2fff629f50f49ec93a75bfd8dc6
13.2 MB Download
md5:e6cef334dc1d7f09b54cbae864a711e4
3.1 MB Preview Download

Additional details

Created:
August 19, 2023
Modified:
October 24, 2023