Bimetallic Effect of Single Nanocatalysts Visualized by Super-Resolution Catalysis Imaging.

Compared with their monometallic counterparts, bimetallic nanoparticles often show enhanced catalytic activity associated with the bimetallic interface. Direct quantitation of catalytic activity at the bimetallic interface is important for understanding the enhancement mechanism, but challenging experimentally. Here using single-molecule super-resolution catalysis imaging in correlation with electron microscopy, we report the first quantitative visualization of enhanced bimetallic activity within single bimetallic nanoparticles. We focus on heteronuclear bimetallic PdAu nanoparticles that present a well-defined Pd-Au bimetallic interface in catalyzing a photodriven fluorogenic disproportionation reaction. Our approach also enables a direct comparison between the bimetallic and monometallic regions within the same nanoparticle. Theoretical calculations further provide insights into the electronic nature of N-O bond activation of the reactant (resazurin) adsorbed on bimetallic sites. Subparticle activity correlation between bimetallic enhancement and monometallic activity suggests that the favorable locations to construct bimetallic sites are those monometallic sites with higher activity, leading to a strategy for making effective bimetallic nanocatalysts. The results highlight the power of super-resolution catalysis imaging in gaining insights that could help improve nanocatalysts.

Introduction

Bimetallic nanoparticles are an important class of nanoscale catalysts in heterogeneous catalysis; they are widely used in industry due to the enhanced catalytic properties (i.e., activity, selectivity, and stability) compared with their monometallic counterparts.[1−3] Many experimental and theoretical efforts have been spent in understanding the catalytic enhancements from the bimetallic effects.[2,4,5] Two general mechanisms are often found to operate: (1) electronic (a.k.a. ligand) effect, in which the electronic properties of the catalytically active metal could be tuned by the other metal, leading to enhancement in activity;[6] (2) geometric (a.k.a. ensemble) effect, where two metals together could form highly active surface sites made by an ensemble of atoms in some specific atomic arrangement.[7,8] It is often challenging to deconvolute completely these two effects. Nevertheless the catalytic enhancement, in both cases, is a result of direct metal–metal interactions at the atomic scale, i.e., involving interfacing two types of metal components directly.

A majority of the scientific insights into bimetallic effects of nanoparticle catalysts came from studies at the ensemble level, where a large number of nanoparticles are measured simultaneously.[2,4−14] By varying the composition of the bimetallic nanoparticles (typically alloy), the location, or the geometry of bimetallic sites, one could optimize the bimetallic catalysts for the largest activity enhancement. For such ensemble-averaged measurements, bimetallic nanocatalysts present particular challenges, however. First, these nanocatalysts are highly heterogeneous; their differences in catalytic activity are masked by the ensemble averaging. Second, even on a single bimetallic nanoparticle, there are both bimetallic and monometallic surface sites; the latter could contribute significantly to the measured activity. Spatially resolved activity measurements within a single catalyst particle are thus desirable. A recent tip-enhanced Raman spectroscopy (TERS) imaging study showed that, on a bimetallic PdAu surface, the Pd edge atoms better activate the reactant than the Pd terrace atoms on a Au(111) surface.[15] Although with high spatial resolution (∼several nanometers), no quantitation of catalytic activity was available in such TERS imaging.

Single-molecule super-resolution fluorescence microscopy has emerged recently as an effective and complementary approach to study catalysis on nanoscale particles,[16−29] including thermal catalysis,[19−22,29] photocatalysis,[23,24,28] electrocatalysis,[25] and photoelectrocatalysis.[26] Individual nanocatalysts can be interrogated at nanometer spatial resolution and single-turnover temporal resolution in real time under operando conditions, where the activity differences among different nanoparticles or even among different surface sites on the same nanoparticle can be directly quantified.

Here we report the first single-molecule super-resolution imaging of the bimetallic effects within single nanoparticle catalysts, in particular single heteronuclear PdAu nanoparticles in catalyzing a photodriven fluorogenic disproportionation reaction. The heteronuclear architecture allows for a clear definition of an interfacial region between the two metal components and a concurrent comparison with monometallic regions on the same particle. We directly visualize the enhanced activity at the bimetallic regions within individual PdAu nanoparticles. DFT calculations further provide insights into the mechanism of the enhanced activation of the reactant molecule at bimetallic vs monometallic surface sites. The correlation between the catalytic activity of bimetallic and monometallic regions within the same particle reveals the desirable locations to form bimetallic sites, which could potentially guide the design of effective bimetallic nanocatalysts.

Results and Discussions

PdAu Nanoparticles Can Catalyze the Photodriven Fluorogenic Disproportionation Reaction of Resazurin

We chose a heteronuclear PdAu bimetallic nanoparticle as a model bimetallic catalyst. Each PdAu nanoparticle consists of a pentatwinned crystalline Pd nanorod (∼500–4000 nm in length and 25.5 ± 2.8 nm in diameter) with a pseudospherical Au nanoparticle (∼60–140 nm in diameter) grown on one or both of its tips (Figure A,B and Figure S1).[30] The heteronuclear architecture and the geometries of the two respective components enable ready identification of the interface between the two metals in each PdAu nanoparticle in scanning electron microscopy (SEM) characterizations. Elemental line profiling via energy dispersive spectroscopy confirms the heteronuclear nature with a clearly defined bimetallic junction between the Pd nanorod and the Au particle (Figure B, lower).

Figure 1

PdAu heteronuclear nanoparticles can catalyze the photodriven disproportionation reaction of resazurin to generate resorufin. (A) TEM image of heteronuclear bimetallic PdAu nanoparticles; structural measurements in Figure S1. (B) Upper: cartoon of PdAu nanoparticle. Lower: elemental line profile on a PdAu nanoparticle. Cyan, Pd; red, Au. Yellow line: the position of line scanning. (C) TEM image of mesoporous silica coated PdAu nanoparticles. (D) Proposed chemical equation of photodriven disproportionation reaction of resazurin (Rz–) to resorufin (Rf–) and a one-electron-oxidized radical species (Rz•) catalyzed by Pd or Au catalysts. (E) Fluorescence spectra of reaction solution containing 30.7 μM Rz– in 0.2 M pH 7.2 phosphate buffer in the presence of mesoporous silica coated PdAu nanoparticles under 50 mW 532 nm laser illumination; the increase of fluorescence at 583 nm indicates the formation of Rf–. Inset: the fluorescence intensity at 583 nm vs time profile of the reaction solution with catalysts under 50 mW 532 nm illumination (black), under 50 mW 488 nm illumination (red), without catalyst under 50 mW 532 nm excitation (blue), or with catalyst but no light illumination (green).

We further coated the PdAu nanoparticles with a mesoporous silica shell of 114 ± 11 nm thickness (Figure C), which allowed us to use UV-ozone to remove the organic ligands (e.g., polyvinylpyrrolidone (PVP)) on PdAu nanoparticles while maintaining their morphologies (especially the Pd–Au interface) and the accessibility of the metal surface to the reactant molecules via the mesopores.[31,32] NaBH4 was then used to reduce the oxide layer on the metal to activate the surface for catalysis after UV-ozone treatment. In the subsequent imaging experiment (see section ), the mesoporous silica shell also facilitates the fluorescence detection of the catalytic product molecules. These fluorescent product molecules desorb rapidly from the metal surface after catalytic formation, but temporarily adsorb onto the walls of the silica mesopores to be imaged, where the possible fluorescence quenching associated with direct detection on metal surfaces can also be circumvented (more discussions in Supporting Information section 2.2). (Note: for simplicity, we use “PdAu nanoparticles” to refer to these mesoporous silica coated nanoparticles in the writing below unless specified otherwise.)

Past studies have shown that the nonfluorescent molecule resazurin (Rz–), upon illumination with 532 nm light, can disproportionate to a one-electron reduced (Rz2–•) and a one-electron oxidized (Rz•) radical species,[33] and the former one (Rz2–•) can further disproportionate to generate the highly fluorescent molecule resorufin (Rf–) (two-electron reduced from Rz–) and resazurin (Rz–).[34]Figure D gives the expected overall reaction equation. We have independently confirmed this photodriven disproportionation reaction, and further determined its 3:1 reaction stoichiometry for Rz:Rf (Supporting Information sections 3.1 and 3.2). We found that the PdAu nanoparticles, as well as their monometallic components, can catalyze this photodriven fluorogenic reaction (Figure E, and black line in inset, Supporting Information sections 3.1 and 3.2). Control experiments show that, without the PdAu nanoparticle catalyst or light, the reaction is insignificant (Figure E inset, blue and green lines). Moreover, 488 nm light, which Rz– does not absorb but which can excite the conduction band electrons of the metal (Figure S4E), cannot drive this reaction (Figure E inset, red line), indicating that the photoexcitation of the reactant Rz–, rather than that of the metal, is a key step in the disproportionation reaction.

Single-Molecule Super-Resolution Catalysis Imaging of Single PdAu Nanoparticles

The fluorogenic nature of the photodriven resazurin disproportionation allowed us to use single-molecule super-resolution fluorescence microscopy to image this reaction on individual PdAu nanoparticles, an approach we developed previously.[31,32] In this approach, the particles were dispersed on a quartz slide within a microfluidic reactor. A continuous flow of a reactant solution and a constant 532 nm laser illumination led to a steady-state catalytic kinetics. Using wide-field total internal reflection fluorescence (TIRF) microscopy, we imaged the fluorescence of the product resorufin at the single-molecule level and localized their positions individually with ∼30–40 nm precision. The product molecules reside on the nanoparticle (i.e., adsorbed within the mesoporous silica shell) for ∼20 ms on average (i.e., ∼1 image frame) (Figure S7E) and do not show significant lateral diffusion (Supporting Information section 4.2.1) before desorbing and disappearing into the surrounding solution. We further confirmed the identity of the product resorufin by measuring the fluorescence spectrum on single PdAu nanoparticles (Figure S6B).

Figure A shows an exemplary map of thousands of product molecules imaged and localized on a single PdAu nanoparticle; its rod shape is apparent. Subsequent imaging through SEM independently confirmed the heteronuclear bimetallic morphology of each particle (Figure B), in which the Au particle is clearly visible at the tip of the Pd nanorod. Moreover, many product molecules are detected clearly in the mesoporous shell region, at distances of greater than ∼40 nm (our localization precision) away from the long-axis of the PdAu nanoparticle core; these detections directly support that the products adsorb onto silica-based sites within the mesopores.

Figure 2

Super-resolution catalysis imaging and single-to-sub particle level analysis of reaction kinetics of PdAu nanoparticles. (A) Positions of ∼2900 products detected on a single mesoporous silica coated PdAu nanoparticle. (B) SEM image of the nanoparticle in A. (C) Two-dimensional histogram of product positions on the nanoparticle in panels A and B in 50 × 50 nm2 bins. The nanoparticle has been reoriented to align horizontally. Outer white line, structural contour; white circle, the contour of the Au particle; both determined from the SEM image in panel B. (D) Segmentation of a typical PdAu nanoparticle: regions of monometallic Pd (Pd), Au-doped Pd next to the Pd–Au interface (PdAu), monometallic Au (Au), and Pd-doped Au next to the Pd–Au interface (AuPd). The end segment (Pdend) is described in section . (E) Proposed kinetic mechanism of the catalytic disproportionation. M–Rz–*: a metal-surface-adsorbed excited-state resazurin; n is the number of electrons on the metal; the changes in electron counts on the metal particle are denoted. (F) Reactant concentration [Rz–] (black) and 532 nm laser power density I (red) dependences of the turnover rate (TOR) per PdAu nanoparticle. Solid symbols: the single particle in panels A–C. Open symbols: results averaged over 53 nanoparticles. Error bars: SEM for y and SD for x. Solid and dashed lines: global fits of eq . (G, H) [Rz–] and I dependences of specific turnover rates of the segments (Pd, PdAu, Au, AuPd) for the nanoparticle in panels A–C.

We titrated the reactant concentration [Rz–] and the incident 532 nm laser power density I, and examined how the catalytic activity of individual PdAu nanoparticles depends on them. Over the course of these titrations, the catalytic activity of the particles showed no significant deactivation for ∼6 h (Figure S12A). We further accounted for potential changes in fluorescence detection efficiency due to changes in background noises during these titrations (Supporting Information section 4.2.2).

With increasing [Rz–], the turnover rates of PdAu nanoparticles follow the classic Langmuir saturation kinetics for heterogeneous catalysis, both at the single-particle level and after ensemble averaging (Figure F), further supporting that the catalysis here is mediated on metal surfaces, in which the mass transport through the silica mesopores does not limit reaction kinetics (otherwise a linear dependence on [Rz–] is expected). With increasing I, the turnover rates of individual particles increase linearly (Figure F), in contrast to the quadratic power dependence of the uncatalyzed photodriven disproportionation reaction (Figure S4F). This linear power dependence suggests that the rate-limiting step of the catalytic reaction merely involves one photoexcited reactant molecule, resazurin (Rz–*).

Taking together all above results, we formulated a working kinetic mechanism of the catalytic disproportionation (Figure E; details in Supporting Information section 4.4). The reduction part of disproportionation is imaged directly in our experiments, in which a surface-adsorbed photoexcited resazurin (M–Rz–*, n is the number of electrons on the metal catalyst particle) obtained two electrons from the catalyst to generate resorufin (Rf–). For the oxidation part, which is not directly measured, we proposed that it is a surface-adsorbed excited-state resazurin that donates one electron to the metal catalyst generating a neutral radical (Rz•), giving the overall reaction as that in Figure D. This mechanism gives the catalytic turnover rate v as (derivation in Supporting Information section 4.4)Here k is a catalytic rate constant and K is a reactant adsorption equilibrium constant on the metal surface. This equation predicts the saturating kinetics on [Rz–] and the linear dependence on I, as observed experimentally (Figure F). By globally fitting both [Rz–] and I dependences of v, we extracted k and K of PdAu nanoparticles at both the single-particle and the ensemble-averaged level.

Subparticle Analysis Reveals Enhanced Catalytic Activity around the Pd–Au Interface

The unique patterns of nanoparticles allowed us to overlay their super-resolution catalysis images onto their respective SEM images with ∼40 nm precision (Figure C; and Figure S10), on which the Pd–Au interface of the heteronuclear particle can be readily located in reference to the Au particle position. A higher catalytic activity (i.e., more reaction products) is apparent around the interfacial region (Figure C), suggesting a direct, and first-of-its-kind, visualization of bimetallic effect of catalytic enhancement.

We then dissected each heteronuclear PdAu nanoparticle into four different regions (Figure D): (1) a 100 nm long segment of the Pd nanorod adjacent to the interface, i.e., PdAu region, corresponding to a bimetallic component that is dominantly Pd with minor Au doping on the surface from the attached Au particle (Figure B, lower); (2) the rest of Pd nanorod away from the interface (excluding the other end of the Pd nanorod), representing the monometallic Pd component; (3) the Au hemisphere adjacent to the interface, i.e., AuPd region, corresponding to the other bimetallic component that is dominantly Au with minor Pd doping (Figure B, lower); and (4) the other hemisphere of Au, representing the monometallic Au component. The dimensions of all four regions are significantly larger than our spatial resolution (30–40 nm) to make these subparticle dissections physically meaningful. The specific catalytic rates of all four regions show saturation kinetics with increasing reactant concentration [Rz–] and a linear dependence on the light power density I (Figure G,H), as observed for the whole particle (Figure F). Fitting these results with eq gave the catalytic rate constant k and the reactant adsorption equilibrium constant K of each region for each PdAu nanoparticle.

Pooling results from 53 PdAu nanoparticles, the catalytic rate constants k of the bimetallic PdAu and AuPd regions are ∼50% more active on average than their monometallic Pd and Au counterparts (Figure A and Figure S12B), directly reporting bimetallic catalytic enhancement. On the other hand, the reactant adsorption equilibrium constant K shows an opposite trend: the K of bimetallic regions are ∼30% smaller on average than their monometallic counterparts (Figure B). Furthermore, for each type of region, the k and K of individual PdAu nanoparticles are anticorrelated (Figure C,D). Therefore, the enhanced catalytic activity at bimetallic regions is associated with weakened reactant adsorption, rationalizable by transition state theory, in which a less stable reactant is closer in energy to the transition state resulting in a lower activation barrier.

Figure 3

Subparticle catalytic properties of bimetallic vs monometallic regions. (A, B) The catalytic rate constant k (A) and reactant adsorption equilibrium constant K (B) of the bimetallic regions (PdAu, AuPd) vs monometallic regions (Pd, Au). Upper: results of individual nanoparticles; each dot is one PdAu nanoparticle. Lower: ensemble averages; error bars are SEM. (C, D) Scatter plots of k vs K for each type of region of individual PdAu nanoparticles; each dot is one region from one PdAu nanoparticle. ρ is Pearson’s cross correlation coefficient.

Control measurements and analyses show that (1) the mesoporous silica shells of the bimetallic and monometallic regions present equal accessibility to the reactant molecules (Figure S12E); (2) the fluorescence intensities and dwell times of the reaction products at the bimetallic regions are indistinguishable from those at the monometallic regions, and therefore the products are equally detected at different regions on the same nanoparticle (Figure S12D, F); and (3) the plasmonic enhancement effect is insignificant at the bimetallic regions (Supporting Information section 5). Altogether, these results support that the observed higher product detection rates at interfacial regions are indeed due to the bimetallic catalytic enhancement there.

Breaking the Metal–Metal Junction Abolishes the Enhanced Catalytic Activity at Bimetallic Regions

To further support that the enhanced catalytic activity is indeed related to the Pd–Au interface in the heteronuclear PdAu nanoparticle, we broke the Pd–Au junction by heating the PdAu nanoparticles at 450 °C for 1 h. A nanoscale gap appears between the Pd nanorod and the Au nanoparticle within the mesoporous silica shell (Figure A; more examples in Figure S3).

Figure 4

Super-resolution catalysis imaging of PdAu nanoparticles with nanoscale gaps (gap-PdAu nanoparticles). (A) TEM image of gap-PdAu nanoparticles coated with mesoporous silica. Inset: a zoom in. (B) Box plot of the catalytic rate constant k of the proximal (Aup) and distant (Aud) Au hemispheres with regard to the Pd nanorods in the gap-PdAu nanoparticles. (C) Two-dimensional histogram of ∼2500 product locations on a gap-PdAu nanoparticle. White line: structural contours of the outer shell and the spherical Au particle. (D) SEM image of the gap-PdAu nanoparticle in C. Inset: zoom in of the nanogap.

We then imaged these PdAu nanoparticles with nanoscale gaps (i.e., gap-PdAu nanoparticles) in catalyzing the same reaction (Figure C and Figure S14A), and with SEM, in which the gaps are visible (Figure D and Figure S14B). Strikingly, the enhanced catalytic activity originally around the Pd–Au interface vanished, supporting that the enhanced catalytic activity is specific to the heteronuclear bimetallic structure with direct Pd–Au contact.

Since the spherical Au particles are easily identifiable in the SEM images of these gap-PdAu nanoparticles, onto which the super-resolution catalysis images were mapped (Figure C,D), we compared the catalytic kinetics of the Au hemisphere proximal to the Pd nanorod (i.e., Aup) with the other hemisphere distant from the nanorod (i.e., Aud). (We could not reliably dissect out a Pd nanorod segment proximal to the Au particle because the nanorod end at the gap cannot be clearly located in the SEM image.) No significant differences in the catalytic rate constants were observed between the two hemispheres (Figure B) (nor in the reactant adsorption equilibrium constant K; Figure S14C), further supporting that the enhanced catalytic activity originally around the interface region is specific to the intact heteronuclear PdAu bimetallic structure.

It is worth noting that heat-breaking the Pd–Au junction should have left some Pd atoms on the Au particle, and therefore the proximal Au hemisphere should still behave like a AuPd region. However, the heating could have homogenized the structural and compositional differences between the two hemispheres. In any case, the abolishment of observable catalytic enhancement after breaking the junction supports that the enhancement is associated with the particular geometry with direct Pd–Au contact.

Electronic Structure Elucidation of Reactant Activation on Monometallic and Bimetallic Surfaces

Resazurin Interaction with Pd and PdAu Surfaces

We performed DFT calculations using the VASP package[35] to gain more insights into the activation on Pd, Au, or bimetallic surface sites of resazurin’s N–O bond, which is cleaved to become resorufin (Figure D; calculation details in Supporting Information sections 6.1–6.3). Although the photodriven disproportionation of resazurin involves its excited state (Figure E), these ground-state DFT calculations could still inform on how resazurin’s N–O bond gets activated upon interaction with metal surfaces. We first examined resazurin interaction with a Pd(100) surface, the dominant facets on the sides of Pd nanorods.[30] Note that the actual Pd nanorod side surface might not be the same as the perfect facet structure because there are always defects, edges, etc. and the sample preparation procedures such as NaBH4 reduction might also alter the surface structure. We chose Pd(100) (and Au(111) later) as a reasonable model surface for calculation purposes. The optimized adsorption geometry has resazurin lying flat on the surface (Figure A). The N–O fragment of resazurin is tilted away from the surface, in which the O atom sits approximately above the center of four Pd atoms and the N atom is above an edge bridging two Pd atoms. Importantly, compared with that in the free resazurin molecule, the N–O bond is elongated by 0.007 Å (Table S2), reflecting its weakening and thus activation for cleavage, consistent with Pd’s being a catalyst for the observed reaction.

Figure 5

Electronic interactions of resazurin with Pd and Au surfaces. (A, B) Optimized adsorption geometries of resazurin on Pd(100) and Au(111). The Pd or Au atoms to be substituted for evaluating bimetallic effects are numbered. (C, D) COHP analyses for the interactions between the N–O fragment of resazurin and the closest metal atoms on Pd(100) and Au(111), respectively. The horizontal lines represent the Fermi level (EF), referenced to the vacuum (E = 0). (E, F) The molecular orbitals of resazurin that are dominantly πN–O (doubly occupied) and πN–O* (unoccupied) in nature. (G, H) Schematics of the forward-donation and back-donation on Pd(100). (I, J) Schematics of the forward-donation and back-donation on Au(111). Only the N–O fragment of resazurin is drawn. We use to represent d orbitals of metal since they are pointed toward N–O. The solid black circles and triangles mark the projected positions of O and N on the metal surface, respectively.

We performed crystal orbital Hamiltonian population (COHP) analysis[36] to examine the interactions between the N–O fragment of resazurin and the Pd surface. COHP analysis allows for an energy-resolved visualization of bonding and antibonding orbital interactions between specific atoms (Figure C). The interactions mainly come from two types of Pd–O bonding interactions (Figure C, red shades below the Fermi level). One type involves N–O bonding orbitals (Figure C, blue line), located energetically below the Pd d band (at about −14 to −11.5 eV); this type of interaction is referred to as forward-donation.[37] The other type involves N–O antibonding orbitals, located energetically within the Pd d band (at about −7.6 to −6.6 eV); this type is referred to as back-donation.[37]

We further performed DFT calculations using the Gaussian package[38] to visualize the molecular orbitals of resazurin (Supporting Information section 6.6). Two N–O fragment based orbitals are identified to be likely involved in the forward- and back-donations between the N–O fragment and the Pd surface (Supporting Information section 6.6): one a doubly occupied π bonding orbital, denoted as πN–O (Figure E); the other an unoccupied π* orbital, denoted as πN–O* (Figure F). Both πN–O and πN–O* have orbital lobes on the O atom pointing toward the Pd surface for bonding interactions.

Combining the adsorption geometry, the COHP analysis, and the resazurin MOs, we schematically depicted the forward-donation and back-donation interactions between Pd and the O atom of resazurin, labeled as πN–O + d and d + πN–O*, respectively (Figure G,H). Both types of interactions weaken the N–O bond of resazurin, consistent with the elongated N–O bond of resazurin adsorbed on the Pd(100) surface. But these two interactions have opposite charge transfer directions: the forward-donation takes away charge density from a N–O π bonding orbital, whereas the back-donation injects charge density into a N–O π* antibonding orbital; the net charge transfer is from Pd to the N–O fragment (Table S2), indicating that the back-donation is a more dominant bonding interaction here.

To computationally evaluate how bimetallic sites can possibly enhance the activation of resazurin’s N–O bond for cleavage, we substituted by Au the eight surface Pd atoms (numbered in Figure A) that directly interact with the carbon atoms of resazurin. The substitution was done one atom at a time to dissect the effect of each substitution in forming bimetallic Au@Pd(100) surface sites, on which resazurin adsorption was further geometry optimized. No significant change of the resazurin adsorption geometry is observed on these model bimetallic surfaces (Supporting Information section 6.3.1). Among the eight structures on these Au@Pd(100) surfaces, one of the most stable structures is a Au substitution at the Pd atom no. 2 (Figure A), which is far from the N–O fragment of the resazurin. Here the O of N–O is closer to the metal surface and N–O is further elongated compared to that on Pd(111) (Table S2), indicating a more weakened N–O bond and likely a bimetallic effect of enhancing the activation of the N–O bond for cleavage, even though the second metal (i.e., Au here) is not directly bonded to the N–O fragment. COHP analysis identified the same forward- and back-donation interactions between Pd and O atoms (Figure S22A). More important, both interactions increase in magnitude compared with those on monometallic Pd(100) (Table S4), consistent with the further weakening and thus enhanced activation of the N–O bond for cleavage on bimetallic PdAu surfaces.

Resazurin Interactions with Au and AuPd Surfaces

We performed similar calculations of resazurin adsorption on a Au(111) surface. Au(111) surface was chosen as a model because the capping ligands PVP and iodide, used in the synthesis, prefer Au(111) facet sites in growing Au nanoparticles.[39,40] The optimized adsorption geometry has resazurin lying flat on the surface with 4 of its carbons and the O atom of the N–O fragment sitting on top of Au atoms (Figure B). Moreover, the N–O fragment is tilted toward the Au surface, suggesting strong interactions between Au and the N–O fragment; this is in contrast to that of resazurin–Pd(100) interactions where the N–O fragment is not directly on top of any Pd atom and is tilted away from the surface (Figure A). The N–O bond is also elongated (by 0.006 Å) on Au(111) compared with that in the free resazurin (Table S3), indicating a weakening of the N–O bond and thus activation toward cleavage.

Similarly, we did single Pd atom substitutions for the five Au atoms sitting directly below the resazurin atoms (Figure B) to evaluate the bimetallic effect. All five substitutions lead to shorter metal–O bonds (by ∼0.1 Å) compared with that on the Au(111) surface (Table S3), indicating even stronger interactions between the bimetallic surface and the N–O fragment. All of them also have a further elongated N–O bond (Table S3), indicating its enhanced activation via the bimetallic effect.

COHP analysis of resazurin on Au(111) identified forward- and back-donation interactions between Au and the O atom of the N–O fragment (Figure D), as in resazurin–Pd(100) interactions. The orbital overlap pattern here is different, as the O atom here sits directly on top of a Au atom (Figure I,J). The local net charge transfer is from Au to the N–O fragment, indicating that the back-donation is also more important here (Table S3). For the bimetallic surface Pd@Au(111), the COHP analysis also shows that both forward- and back-donation interactions increase between the metal and the N–O fragment (Table S4), leading to further activation of N–O.

Altogether, DFT calculations show that both substituting Pd by Au on Pd(100) and substituting Au by Pd on Au(111) could give a more lengthened N–O bond, from increases in both forward- and back-donation interactions, leading to the enhanced activation of the N–O bond for cleavage on the bimetallic surfaces.

Activity Correlation within Single Particle Reveals Optimal Locations for Bimetallic Sites

Our subparticle level activity quantitation also allowed us to examine how the activity enhancements of the bimetallic regions are related to the activity of the corresponding monometallic regions within the same particle (Figure A,B, black and red points); the latter would represent the original “monometallic” activity of the bimetallic region before the second metal was introduced. Strikingly, positive correlations are clearly observed. For the particles whose monometallic Pd region has higher catalytic rate constant k, their bimetallic activity enhancement ΔkBI (defined as k(PdAu) – k(Pd)) of the bimetallic PdAu region is also larger (Figure A). The same trend applies to the bimetallic AuPd region (Figure B). These trends indicate that when the particle, Pd or Au, is more active, the bimetallic enhancement is larger.

Figure 6

Rational strategy for generating more active bimetallic PdAu nanocatalysts. (A) Correlation between the catalytic activity enhancement of the bimetallic PdAu region and the monometallic Pd region on the same heteronuclear PdAu nanoparticle. Each black dot is a single PdAu nanoparticle. Hollow red squares are binned and averaged results. The pure single Pd nanorods (pink) serve as the control. ρ is Pearson’s correlation coefficient for the individual particles. (B) Same as panel A, but for the bimetallic AuPd vs the monometallic Au regions with pure Au nanoparticles (pink) as the control. (C) The catalytic rate constant k of the side and end regions of Pd nanorods (average from 46 nanoparticles). (D) Schematic of the proposed strategy to deposit the second metal onto the ends of nanorods of the first metal. Error bars are SEM for all y-axes and SD for all x-axes.

As a control, we also analyzed the corresponding subparticle regions of pure single Pd nanorods and single Au particles, which are minor components in the sample and imaged together with PdAu bimetallic nanoparticles. For each Pd nanorod, we compared the activity of the end regions adjacent to the two tips (which are at the same location as the bimetallic PdAu region in a PdAu nanoparticle) with the side activity (excluding the ends), which corresponds to the monometallic Pd region in a PdAu nanoparticle. For each Au nanoparticle, we arbitrarily dissected it into two hemispheres vertically and compared the left vs right hemisphere. Neither of the two controls shows any significant correlation (Figure A,B, pink points), indicating that possible intraparticle activity heterogeneity would not give the observed positive correlations between the bimetallic activity enhancement and the original monometallic activity.

These positive correlations suggest that, to obtain larger bimetallic activity enhancement, one should deposit the second metal onto originally more active monometallic surface sites of Pd or Au, constituting a possible rationalized strategy in making more active bimetallic nanoparticle catalysts. Implementing this strategy would require one to (1) identify what types of surface sites are more active on the initial monometallic particle and (2) selectively deposit the second metal onto the more active sites of the first metal.

Structurally anisotropic nanoparticles, such as 1-dimensional nanorods, offer opportunities to fulfill these two requirements. Regarding requirement 1, our previous study has identified that, for Au nanorods, their two ends are generally more active than their side facets in catalyzing an oxidative deacetylation reaction, possibly due to the higher activity of low coordination surface sites abundant at the ends.[31] Here we found the same phenomenon on Pd nanorods: their free end segment Pdend (Figure D) in the heteronuclear PdAu bimetallic particle is more active than their side facets (Figure C). Regarding requirement 2, one could utilize appropriate capping ligands that could selectively bind to the side facets of the first metal nanorods, leaving the two ends preferentially for the deposition of the second metal (Figure D). (Note that, for generating just bimetallic PdAu sites, the deposition of Au would certainly need to be much less in quantity to not grow a big Au particle.) Subsequent removal of the capping ligands would result in a bimetallic system where the second metal is at the desired higher activity sites of the first metal. Interestingly, this scheme is what underlies the synthesis of the heteronuclear bimetallic PdAu nanorod–nanoparticle in the current study, in which the Au particle grew selectively at the ends of Pd nanorods and the side facets of Pd nanorods were preferentially blocked by the PVP and iodide ligands.[30] Similar strategies have been reported in synthesizing Pd-tipped Au nanorods[41] and Pd-edged Ag nanocubes[42] for detecting catalytic products via surface-enhanced Raman scattering, and Pt-tipped Au nanorods for surface-plasmon-enhanced catalysis.[43] With appropriate ligands, one could expect this synthesis strategy to be applicable to particles that are less structurally anisotropic (e.g., pseudospheres) for generating bimetallic sites at desired locations.

Conclusions

In summary, using single-molecule super-resolution catalysis imaging in correlation with SEM, we have directly visualized and quantified the bimetallic activity enhancement on heteronuclear PdAu nanoparticles at the subparticle level in catalyzing the photodriven disproportionation of resazurin. DFT calculations provide insights into the electronic nature of the activation of the resazurin N–O bond on the metal surfaces via synergistic forward- and back-donation interactions. The results further suggest that higher activity monometallic sites are the optimal locations to form bimetallic sites for larger activity enhancement, demonstrating the effectiveness of the super-resolution catalysis imaging approach in deriving knowledge for guiding the development of better nanocatalysts.