Metal–Organic Framework Thin Films on High-Curvature Nanostructures Toward Tandem Electrocatalysis
AuthorsDe Luna, Phil
García de Arquer, F. Pelayo
Proppe, Andrew H.
Kelley, Shana O.
Sargent, Edward H.
KAUST DepartmentAdvanced Membranes and Porous Materials Research Center
Chemical Science Program
Functional Materials Design, Discovery and Development (FMD3)
Physical Science and Engineering (PSE) Division
Online Publication Date2018-08-21
Print Publication Date2018-09-19
Permanent link to this recordhttp://hdl.handle.net/10754/630519
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AbstractIn tandem catalysis, two distinct catalytic materials are interfaced to feed the product of one reaction into the next one. This approach, analogous to enzyme cascades, can potentially be used to upgrade small molecules such as CO2 to more valuable hydrocarbons. Here, we investigate the materials chemistry of metal-organic framework (MOF) thin films grown on gold nanostructured microelectrodes (AuNMEs), focusing on the key materials chemistry challenges necessary to enable the applications of these MOF/AuNME composites in tandem catalysis. We applied two growth methods-layer-by-layer and solvothermal-to grow a variety of MOF thin films on AuNMEs and then characterized them using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The MOF@AuNME materials were then evaluated for electrocatalytic CO2 reduction. The morphology and crystallinity of the MOF thin films were examined, and it was found that MOF thin films were capable of dramatically suppressing CO production on AuNMEs and producing further-reduced carbon products such as CH4 and C2H4. This work illustrates the use of MOF thin films to tune the activity of an underlying CO2RR catalyst to produce further-reduced products.
CitationDe Luna P, Liang W, Mallick A, Shekhah O, García de Arquer FP, et al. (2018) Metal–Organic Framework Thin Films on High-Curvature Nanostructures Toward Tandem Electrocatalysis. ACS Applied Materials & Interfaces 10: 31225–31232. Available: http://dx.doi.org/10.1021/acsami.8b04848.
SponsorsThis publication is based in part on work supported by the Center Partnership Funds Program, made by King Abdullah University of Science and Technology (KAUST), by the Ontario Research Fund Research Excellence Program, and by the Natural Sciences and Engineering Research Council (NSERC) of Canada. P.D.L. wishes to thank the Natural Sciences and Engineering Research Council (NSERC) of Canada for support in the form of the Canadian Graduate Scholarship—Doctoral award.
PublisherAmerican Chemical Society (ACS)