Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/8769
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPathak, Biswarupen_US
dc.contributor.authorKumar, Sourabhen_US
dc.date.accessioned2022-03-17T01:00:00Z-
dc.date.accessioned2022-03-21T11:29:45Z-
dc.date.available2022-03-17T01:00:00Z-
dc.date.available2022-03-21T11:29:45Z-
dc.date.issued2020-
dc.identifier.citationPathak, B., Senapati, D., De, S. K., Kumar, S., Ray, S., Mondal, S., . . . Roy, A. (2020). Au-seeded ag-nanorod networks for electrocatalytic sensing. ACS Applied Nano Materials, 3(10), 9969-9983. doi:10.1021/acsanm.0c01976en_US
dc.identifier.issn2574-0970-
dc.identifier.otherEID(2-s2.0-85096610395)-
dc.identifier.urihttps://doi.org/10.1021/acsanm.0c01976-
dc.identifier.urihttps://dspace.iiti.ac.in/handle/123456789/8769-
dc.description.abstractSpherical gold nanoseed (∼5−6 nm)-induced (but not seed-mediated) silver nanorods (Hy-Au@AgNRs) of variable lengths have been synthesized by a new methodology that shows enhancement in catalytic activity as a function of nanorod length. Detailed characterization by atomic-scale resolution spectroscopy, precision scattering measurements, high-resolution microscopy, and theoretical modeling through the density functional theory (DFT) quantifies the presence of an enhanced number of multiple coaxial twin boundaries for longer Hy-Au@AgNRs, which ultimately results in an increased mechanical strain. By considering greater mechanical strain within Hy-Au@ AgNRs, the density of states (DOS) calculation shows a prominent shift in electron density toward the Fermi level to assist in the tremendous catalytic activity of the longest nanorod (NR) (Hy-Au@AgNR840). Further assembling of these inherently active Hy-Au@AgNR840s by thiol click chemistry not only efficiently creates multiple low-coordinated crystal sites to improve their catalytic activity but also the resultant uniform two-dimensional (2D) platform shows better adsorptivity and easy moldability on the electrode surface for increased shelf life, a uniform porous structure to trap a large extent of redox systems, enhanced stability in a broad pH and solvent range to increase the applicability, and long-term stability under ambient conditions for safe storing, making this material a unique nonenzymatic scalable universal electrocatalytic platform. The ability of this material to act as a nonenzymatic universal catalytic platform has been verified by applying it for highly specific and ultrasensitive detection of a series of human metabolites, which include different important vitamins, potent endogenous antioxidants, essential amino acids for the biosynthesis of proteins, simple monosaccharides, and essential trace-metal ions. Our study for the first time mechanistically explores the combined role of anisometric seeding to create an intermetallic twin boundary along with its size to control the strain-induced catalytic activity to offer us a universal 2D electrocatalytic sensing platform by a combined approach of experiment and theory. © 2020 American Chemical Societyen_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.sourceACS Applied Nano Materialsen_US
dc.subjectBiochemistryen_US
dc.subjectCrystal structureen_US
dc.subjectDensity functional theoryen_US
dc.subjectGold metallographyen_US
dc.subjectMetabolitesen_US
dc.subjectMetal ionsen_US
dc.subjectMetalsen_US
dc.subjectNanorodsen_US
dc.subjectRedox reactionsen_US
dc.subjectTrace elementsen_US
dc.subjectAtomic-scale resolutionen_US
dc.subjectEssential amino acidsen_US
dc.subjectHigh-resolution microscopyen_US
dc.subjectLong term stabilityen_US
dc.subjectScattering measurementsen_US
dc.subjectTheoretical modelingen_US
dc.subjectTwo Dimensional (2 D)en_US
dc.subjectUltrasensitive detectionen_US
dc.subjectCatalyst activityen_US
dc.titleAu-seeded Ag-nanorod networks for electrocatalytic sensingen_US
dc.typeJournal Articleen_US
Appears in Collections:Department of Chemistry

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetric Badge: