scholarly journals Operando detection of single nanoparticle activity dynamics inside a model pore catalyst material

2020 ◽  
Vol 6 (25) ◽  
pp. eaba7678 ◽  
Author(s):  
David Albinsson ◽  
Stephan Bartling ◽  
Sara Nilsson ◽  
Henrik Ström ◽  
Joachim Fritzsche ◽  
...  

Nanoconfinement in porous catalysts may induce reactant concentration gradients inside the pores due to local conversion. This leads to inefficient active material use since parts of the catalyst may be trapped in an inactive state. Experimentally, these effects remain unstudied due to material complexity and required high spatial resolution. Here, we have nanofabricated quasi–two-dimensional mimics of porous catalysts, which combine the traits of nanofluidics with single particle plasmonics and online mass spectrometry readout. Enabled by single particle resolution at operando conditions during CO oxidation over a Cu model catalyst, we directly visualize reactant concentration gradient formation due to conversion on single Cu nanoparticles inside the “model pore” and how it dynamically controls oxidation state—and, thus, activity—of particles downstream. Our results provide a general framework for single particle catalysis in the gas phase and highlight the importance of single particle approaches for the understanding of complex catalyst materials.


Author(s):  
E. G. Rightor

Core edge spectroscopy methods are versatile tools for investigating a wide variety of materials. They can be used to probe the electronic states of materials in bulk solids, on surfaces, or in the gas phase. This family of methods involves promoting an inner shell (core) electron to an excited state and recording either the primary excitation or secondary decay of the excited state. The techniques are complimentary and have different strengths and limitations for studying challenging aspects of materials. The need to identify components in polymers or polymer blends at high spatial resolution has driven development, application, and integration of results from several of these methods.



2018 ◽  
Author(s):  
Alysia E. Herr ◽  
Ronald P. Kiene ◽  
John W. H. Dacey ◽  
Philippe D. Tortell

Abstract. The northeast subarctic Pacific (NESAP) is a globally important source of the climate-active gas dimethylsulfide (DMS), yet the processes driving DMS variability across this region are poorly understood. Here we examine the spatial distribution of DMS at various spatial scales across contrasting oceanographic regimes of the NESAP. We present a new data set of high spatial resolution DMS measurements across hydrographic frontal zones along the British Columbia continental shelf, together with key environmental variables and biological rate measurements. We combine these new data with existing observations to produce a revised summertime DMS climatology for the NESAP, yielding a broader context for our sub-mesoscale process studies. Our results demonstrate sharp DMS concentration gradients across hydrographic frontal zones, and suggest the presence of two distinct DMS cycling regimes corresponding to microphytoplankton-dominated waters along the continental shelf, and nanoplankton-dominated cross-shelf transitional waters. DMS concentrations across the continental shelf transition (range





2011 ◽  
Vol 1363 ◽  
Author(s):  
Muhammad Asri Idris ◽  
Janusz Nowotny ◽  
Sean S. Li

ABSTRACTThe present work reports surface segregation in polycrystalline yttria-stabilised zirconia (cubic) including 10 mol% Y2O3 (10YSZ). The 10YSZ specimen was annealed in the range 1073 K - 1673 K in the gas phase of controlled oxygen activity. The segregation-induced intensity profiles of 89Y, 40Ca, 28Si, 27Al, 133Cs, 197Au and 90Zr was measured using secondary ion mass spectrometry (SIMS). The data obtained show that (i) annealing of 10YSZ results in the formation of segregation-induced concentration gradients of 89Y, 40Ca, 28Si, 27Al and (ii) segregation-induced profiles depend on oxygen activity.



1978 ◽  
Vol 33 (7) ◽  
pp. 935-944 ◽  
Author(s):  
John W. Hamer ◽  
Donald E. Cormack




2003 ◽  
Vol 31 (6) ◽  
pp. 1453-1455 ◽  
Author(s):  
I. Karakikes ◽  
R.E. Barber ◽  
I.E.G. Morrison ◽  
N. Fernández ◽  
R.J. Cherry

Dual-wavelength single-particle fluorescence imaging has been used to quantify the co-localization of receptors and/or ligands on cells by widefield microscopy. Methods for correction of chromatic aberration and identification of submicroscopic artefacts are presented, with data for the lipopolysaccharide/CD14 and MHC class II/CD74 systems.





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