Single-particle Catalysis Research Articles

Label-Free Imaging of Catalytic H2O2 Decomposition on Single Colloidal Pt Nanoparticles Using Nanofluidic Scattering Microscopy.

Single-particle catalysis aims at determining factors that dictate the nanoparticle activity and selectivity. Existing methods often use fluorescent model reactions at low reactant concentrations, operate at low pressures, or rely on plasmonic enhancement effects. Hence, methods to measure single-nanoparticle activity under technically relevant conditions and without fluorescence or other enhancement mechanisms are still lacking. Here, we introduce nanofluidic scattering microscopy of catalytic reactions on single colloidal nanoparticles trapped inside nanofluidic channels to fill this gap. By detecting minuscule refractive index changes in a liquid flushed trough a nanochannel, we demonstrate that local H2O2 concentration changes in water can be accurately measured. Applying this principle, we analyze the H2O2 concentration profiles adjacent to single colloidal Pt nanoparticles during catalytic H2O2 decomposition into O2 and H2O and derive the particles' individual turnover frequencies from the growth rate of the O2 gas bubbles formed in their respective nanochannel during reaction.

Nanofluidic Trapping of Faceted Colloidal Nanocrystals for Parallel Single-Particle Catalysis.

Catalyst activity can depend distinctly on nanoparticle size and shape. Therefore, understanding the structure sensitivity of catalytic reactions is of fundamental and technical importance. Experiments with single-particle resolution, where ensemble-averaging is eliminated, are required to study it. Here, we implement the selective trapping of individual spherical, cubic, and octahedral colloidal Au nanocrystals in 100 parallel nanofluidic channels to determine their activity for fluorescein reduction by sodium borohydride using fluorescence microscopy. As the main result, we identify distinct structure sensitivity of the rate-limiting borohydride oxidation step originating from different edge site abundance on the three particle types, as confirmed by first-principles calculations. This advertises nanofluidic reactors for the study of structure–function correlations in catalysis and identifies nanoparticle shape as a key factor in borohydride-mediated catalytic reactions.

High-quality rapid laser drilling of transparent hard materials.

In this study, a hybrid method for high-quality rapid drilling of transparent hard materials which combines femtosecond laser (fs-laser) Bessel beam modifying materials and selective wet etching is presented. Using this method, micro-holes with no taper of different sizes (from 10 to 35 μm) and shapes (square, triangle, circular, and pentagram) are fabricated. Bessel beams of different lengths can be generated flexibly by loading different computer-generated holograms (CGHs) into the spatial light modulator (SLM) and the maximum length of light interacting with materials can reach 320 μm, leading to a reduction of the laser scanning time by two orders of magnitude. Moreover, a set of three-dimensional multi-layer submicron through-holes in crystal materials is also realized, with an aspect ratio of more than 1000 for each hole. These results indicate that this method has broad application potential in chip packaging, aviation manufacturing, single particle catalysis, and other fields.

Resolving multifrequential oscillations and nanoscale interfacet communication in single-particle catalysis.

In heterogeneous catalysis research, the reactivity of individual nanofacets of single particles is typically not resolved. We applied in situ field electron microscopy to the apex of a curved rhodium crystal (radius of 650 nanometers), providing high spatial (~2 nanometers) and time resolution (~2 milliseconds) of oscillatory catalytic hydrogen oxidation, to image adsorbed species and reaction fronts on the individual facets. Using ionized water as the imaging species, the active sites were directly imaged with field ion microscopy. The catalytic behavior of differently structured nanofacets and the extent of coupling between them were monitored individually. We observed limited interfacet coupling, entrainment, frequency locking, and reconstruction-induced collapse of spatial coupling. The experimental results are backed up by microkinetic modeling of time-dependent oxygen species coverages and oscillation frequencies.

Photomodulated Spatially Confined Chemical Reactivity in a Single Silver Nanoprism

Single-atom and single-particle catalysis is an area of considerable topical interest due to their potential in explaining important fundamental processes and applications across several areas. An interesting avenue in single-particle catalysis is spatial control of chemical reactivity within the particle by employing light as an external stimulus. To demonstrate this concept, we report galvanic replacement reactions (GRRs) as a spatial marker of subparticle chemical reactivity of a silver nanoprism with AuCl4- ions under optical excitation. The location of a GRR within a single Ag nanoprism can be spatially controlled depending on the plasmon mode excited. This leads to chemomorphological transformation of Ag nanoprisms into interesting Ag-Au structures. This spatial biasing effect is attributed to localized hot electron injection from the tips and edges of the silver nanoprisms to the adjacent reactants that correlate with excitation of different surface plasmon modes. The study also employs low-energy-loss EELS mapping to additionally probe the spatially confined redox reaction within a silver nanoprism. The findings presented here allow the visualization of a plasmon-driven subparticle chemical transformation with high resolution. The selective optical excitation of surface plasmon eigenmodes of anisotropic nanoparticles offers opportunities to spatially modulate chemical transformations mediated by hot electron transfer.

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

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.

A nanofluidic device for parallel single nanoparticle catalysis in solution

Studying single catalyst nanoparticles, during reaction, eliminates averaging effects that are an inherent limitation of ensemble experiments. It enables establishing structure–function correlations beyond averaged properties by including particle-specific descriptors such as defects, chemical heterogeneity and microstructure. Driven by these prospects, several single particle catalysis concepts have been implemented. However, they all have limitations such as low throughput, or that they require very low reactant concentrations and/or reaction rates. In response, we present a nanofluidic device for highly parallelized single nanoparticle catalysis in solution, based on fluorescence microscopy. Our device enables parallel scrutiny of tens of single nanoparticles, each isolated inside its own nanofluidic channel, and at tunable reaction conditions, ranging from the fully mass transport limited regime to the surface reaction limited regime. In a wider perspective, our concept provides a versatile platform for highly parallelized single particle catalysis in solution and constitutes a promising application area for nanofluidics.

Single Particle Plasmonics for Materials Science and Single Particle Catalysis

Single particle nanoplasmonic sensing and spectroscopy is a powerful and at the same time relatively easy-to-implement research method that allows monitoring of changes in the structure and properties of metal nanoparticles in real time and with only few restrictions in terms of surrounding medium, temperature and pressure. Consequently, it has been successfully used in materials science applications to, for instance, reveal the impact of size and shape of single metal nanoparticles on the thermodynamics of metal hydride formation and decomposition. In this Perspective, we review and discuss the research efforts that have spurred key advances in the development of single particle nanoplasmonic sensing and spectroscopy as a research tool in materials science. On this background we then assess the prospects and challenges toward its application in single particle catalysis, with the aim to enable operando studies of the relationship between metal nanoparticle structure or oxidation state and catalytic perfo...

Recent advances of single molecule/particle imaging with optical microscopic methods

Single-molecule and -particle imaging with optical microscopic methods have been widely used in various fields with the advantages of high resolution, high throughput and excellent sensitivity. This review summarized recent progresses of optical microscopic imaging of single-molecule and -particle in the areas of molecular detection, super-resolution imaging and single-particle catalysis. At last, we outlined the challenges and prospect of optical microscopic imaging techniques for single-molecule and -particle assay in biomedical applications.

DNA-directed assembly of gold nanohalo for quantitative plasmonic imaging of single-particle catalysis.

Plasmonic imaging under a dark-field microscope (DFM) holds great promise for single-particle analysis in bioimaging, nanophotonics, and nanocatalysis. Here, we designed a DNA-directed programmable assembly strategy to fabricate a halo-like Au nanostructure (nanohalo) that couples plasmonic large gold nanoparticles (L-AuNPs) with catalytically active small AuNPs (S-AuNPs) in a single nanoarchitecture. Catalytic reaction occurring on S-AuNPs changes its permittivity, which results in a significant variation of the plasmonic resonance of the nanohalo. Hence, we can indirectly monitor catalytic reactions on a single nanohalo under DFM, on the basis of which we have obtained quantitative information on both nanocatalysis and catalyst poisoning. Our study thus provides a cost-effective means to quantitatively study metal NP-based catalysis at single-particle level.

Geometry‐Assisted Three‐Dimensional Superlocalization Imaging of Single‐Molecule Catalysis on Modular Multilayer Nanocatalysts

To establish the structure-catalytic property relationships of heterogeneous catalysts, a detailed characterization of the three-dimensional (3D) distribution of active sites on a single catalyst is essential. Single-particle catalysis of a modular multilayer catalytic platform that consists of a solid silica core, a mesoporous silica shell, and uniformly distributed Pt nanoparticles sandwiched in between these layers is presented. The first 3D high-resolution super-localization imaging of single fluorescent molecules produced at active sites on the core-shell model nanocatalysts is demonstrated. The 3D mapping is aided by the well-defined geometry and a correlation study in scanning electron microscopy and total internal reflection fluorescence and scattering microscopy. This approach can be generalized to study other nano- and mesoscale structures.

Optical approaches in study of nanocatalysis with single-molecule and single-particle resolution

Studying the activity of individual nanocata- lysts, especially with high spatiotemporal resolution of single-molecule and single-turnover scale, is essential for the understanding of catalytic mechanism and the design- ing of effective catalysts. Several approaches have been developed to monitor the catalytic reaction on single catalysts. In this review, we summarized the updated progresses of several new spectroscopic and microscopic approaches, including single-molecule fluorescence micro- scopy, surface-enhanced Raman spectroscopy, surface plasmon resonance microscopy and X-ray microscopy, for the study of single-molecule and single-particle catalysis.