Single Atom Level Research Articles

Isolated Pd atoms in a silver matrix: Spectroscopic and chemical properties.

Over the past decade, single-atom alloys (SAAs) have been a lively topic of research due to their potential for achieving novel catalytic properties and circumventing some known limitations of heterogeneous catalysts, such as scaling relationships. In researching SAAs, it is important to recognize experimental evidence of peculiarities in their electronic structure. When an isolated atom is embedded in a matrix of foreign atoms, it exhibits spectroscopic signatures that reflect its surrounding chemical environment. In the present work, using photoemission spectroscopy and computational chemistry, we discuss the experimental evidence from Ag0.98Pd0.02 SAAs that show free-atom-like characteristics in their electronic structure. In particular, the broad Pd4d valence band states of the bulk Pd metal become a narrow band in the alloy. The measured photoemission spectra were compared with the calculated photoemission signal of a free Pd atom in the gas phase with very good agreement, suggesting that the Pd4d states in the alloy exhibit very weak hybridization with their surroundings and are therefore electronically isolated. Since AgPd alloys are known for their superior performance in the industrially relevant semi-hydrogenation of acetylene, we considered whether it is worthwhile to drive the dilution of Pd in the inert Ag host to the single-atom level. We conclude that although site-isolation provides beneficial electronic structure changes to the Pd centers due to the difficulty in activating H2 on Ag, utilizing such SAAs in acetylene semi-hydrogenation would require either a higher Pd concentration to bring isolated sites sufficiently close together or an H2-activating support.

Spatially Confined Formation of Single Atoms in Highly Porous Carbon Nitride Nanoreactors

Reducing the size of a catalyst to a single atom (SA) level can dramatically change its physicochemical properties and significantly boost its catalytic activity. However, the massive synthesis of SA catalysts still remains a grand challenge mainly because of the aggregation and nucleation of the generated atoms during the reaction. Here, we design and implement a spatially confined synthetic strategy based on a porous-hollow carbon nitride (p-CN) coordinated with 1-butyl-3-methylimidazole hexafluorophosphate, which can act as a nanoreactor and allow us to obtain metal SA catalysts (p-CN@M SAs). This relatively easy and highly effective method provides a way to massively synthesize single/multiple atoms (p-CN@M SAs, M = Pt, Pd, Cu, Fe, etc.). Moreover, the amorphous NiB-coated p-CN@Pt SAs can further increase the loading amount of Pt SAs to 3.7 wt %. The synthesized p-CN@Pt&NiB electrocatalyst exhibits an extraordinary hydrogen evolution reaction activity with the overpotential of 40.6 mV@10 mA/cm-2 and the Tofel slope of 29.26 mV/dec.

Single-atom level symmetry breaking visualized with STEM

Researchers use scanning transmission electron microscope data with principal component analysis to observe symmetry breaking at the single-atom level.

Single-atom level determination of 3-dimensional surface atomic structure via neural network-assisted atomic electron tomography

Functional properties of nanomaterials strongly depend on their surface atomic structures, but they often become largely different from their bulk structures, exhibiting surface reconstructions and relaxations. However, most of the surface characterization methods are either limited to 2D measurements or not reaching to true 3D atomic-scale resolution, and single-atom level determination of the 3D surface atomic structure for general 3D nanomaterials still remains elusive. Here we demonstrate the measurement of 3D atomic structure at 15 pm precision using a Pt nanoparticle as a model system. Aided by a deep learning-based missing data retrieval combined with atomic electron tomography, the surface atomic structure was reliably measured. We found that <100> and <111> facets contribute differently to the surface strain, resulting in anisotropic strain distribution as well as compressive support boundary effect. The capability of single-atom level surface characterization will not only deepen our understanding of the functional properties of nanomaterials but also open a new door for fine tailoring of their performance.

Probing precipitation properties.

Superheavy elements are short-lived and only available on a single-atom level, making their chemical properties very challenging to study. Now, through their co-precipitation with samarium, single atoms of rutherfordium have been shown to form hydroxide complexes but not ammine ones.

Single-atom control of electrical conductance and thermopower through single-cluster junctions.

The control of single atoms offers fundamental insight into understanding the charge transport through single clusters, and the atomic precision of the clusters provides the opportunity to manipulate the charge transport even at the single-atom level. Herein, we designed and investigated the electrical conductance and thermopower of Anderson-type polyoxometalate (POM) clusters with single-atom variation using the scanning tunneling microscopy break-junction (STM-BJ) technique. Our results show the electrical conductance of single clusters can be changed by an order of magnitude by substituting different center-metal atoms, and the electrical conductance of clusters shows different bias-dependence. Furthermore, the Seebeck coefficients of the POM clusters also can be significantly changed by the center-metal atoms. The non-equilibrium quantum transport calculations reveal that the electrostatic potential profile is non-uniformly dependent on the center-metal atoms. This leads to gating of electrical conductance by bias voltage. This supports the tuning of thermopower and bias dependent transmission spectra. This work provides the fundamental understanding of single-atom control of charge transport in POM single-cluster junctions.

Porphyrin for possessing low valence state of metal center

We discovered that metal center confined in the porphyrin structure can process lower valence state (LV) via reversible photoinduced electron transfer in both singlet and triplet states, which are confirmed by X-ray photoelectron spectroscopy (XPS), X-ray absorption fine structure (XAFS), electron spin resonance (ESR) and density functional theory (DFT) calculations. More importantly, this controlling strategy was hardly influenced by the electronegative properties of surrounding porphyrin structures, at the same time, it can be widely applied to various metal elements such as Zn, Cu, Ni, Co, Fe. This work provides a new vision to fabricate and deeply understand the metal center with lower valence state from single atom level.

Second-harmonic generation divergence-a method for domain size evaluation of 2D materials.

Single-atomic-layered materials are important for future electronics. They allow optoelectronic devices to be fabricated at the single-atomic layer level. A single-atomic-layered two-dimensional (2D) transition metal dichalcogenide (TMD) film is usually composed of randomly orientated single-crystalline domains, and the size distribution of the domains on a large-area film has a significant impact on the applications of the film, but the impact is difficult to characterize. We report an approach to evaluate the size of the single-crystalline domains by measuring the second-harmonic generation divergence caused by the domains of different orientations. Using this method, domain size mapping on an 8×8mm2 region of a continuous MoS2 film is achieved. This method provides a fast and efficient way of domain size characterization across a large area in a non-destructive and transfer-free manner for single-atomic-layered TMD films.

Atom-by-Atom Evolution of the Same Ligand-Protected Au21, Au22, Au22Cd1, and Au24 Nanocluster Series.

Atom-by-atom manipulation on metal nanoclusters (NCs) has long been desired, as the resulting series of NCs can provide insightful understanding of how a single atom affects the structure and properties as well as the evolution with size. Here, we report crystallizations of Au22(SAdm)16 and Au22Cd1(SAdm)16 (SAdm = adamantanethiolate) which link up with Au21(SAdm)15 and Au24(SAdm)16 NCs and form an atom-by-atom evolving series protected by the same ligand. Structurally, Au22(SAdm)16 has an Au3(SAdm)4 surface motif which is longer than the Au2(SAdm)3 on Au21(SAdm)15, whereas Au22Cd1(SAdm)16 lacks one staple Au atom compared to Au24(SAdm)16 and thus the surface structure is reconstructed. A single Cd atom triggers the structural transition from Au22 with a 10-atom bioctahedral kernel to Au22Cd1 with a 13-atom cuboctahedral kernel, and correspondingly, the optical properties are dramatically changed. The photoexcited carrier lifetime demonstrates that the optical properties and excited state relaxation are highly sensitive at the single atom level. By contrast, little change in both ionization potential and electron affinity is found in this series of NCs by theoretical calculations, indicating the electronic properties are independent of adding a single atom in this series. The work provides a paradigm that the NCs with continuous metal atom numbers are accessible and crystallizable when meticulously designed, and the optical properties are more affected at the single atom level than the electronic properties.

Single-Atom Cu Catalysts for Enhanced Electrocatalytic Nitrate Reduction with Significant Alleviation of Nitrite Production.

Metallic Cu is a well-known electrocatalyst for nitrate reduction reaction (NO3 RR), but it suffers from relatively low activity, poor stability, and inducing nitrite accumulation during the long-term operation. Herein, it is found that Cu catalysts minimized at the single-atom level can overcome the limitations of bulk materials in NO3 RR. A metal-nitrogen-carbon (M-N-C) electrocatalyst composed of carbon nanosheets embedding isolated copper atoms coordinated with N, Cu-N-C-800, is synthesized by pyrolysis of a Cu-based metal-organic framework at 800°C. In comparison with Cu nanoparticles and Cu plate-800, kinetic measurements show that the Cu-N-C-800 electrocatalyst is more active and stable and distinctly suppresses the release of nitrite intermediate into the solution. The combined results of experimental data and density functional theory calculations indicate that Cu bound with N (particularly Cu-N2 ) is the key to favorable adsorption of NO3 - and NO2 - . This strong binding is responsible for the enhanced rate of nitrate conversion to the end products of ammonia and nitrogen. These findings highlight the promise of single-atom Cu electrocatalysts for nitrate reduction with desirable performance.

Atom-by-atom analysis of sintering dynamics and stability of Pt nanoparticle catalysts in chemical reactions.

Supported Pt nanoparticles are used extensively in chemical processes, including for fuel cells, fuels, pollution control and hydrogenation reactions. Atomic-level deactivation mechanisms play a critical role in the loss of performance. In this original research paper, we introduce real-time in-situ visualization and quantitative analysis of dynamic atom-by-atom sintering and stability of model Pt nanoparticles on a carbon support, under controlled chemical reaction conditions of temperature and continuously flowing gas. We use a novel environmental scanning transmission electron microscope with single-atom resolution, to understand the mechanisms. Our results track the areal density of dynamic single atoms on the support between nanoparticles and attached to them; both as migrating species in performance degradation and as potential new independent active species. We demonstrate that the decay of smaller nanoparticles is initiated by a local lack of single atoms; while a post decay increase in single-atom density suggests anchoring sites on the substrate before aggregation to larger particles. The analyses reveal a relationship between the density and mobility of single atoms, particle sizes and their nature in the immediate neighbourhood. The results are combined with practical catalysts important in technological processes. The findings illustrate the complex nature of sintering and deactivation. They are used to generate new fundamental insights into nanoparticle sintering dynamics at the single-atom level, important in the development of efficient supported nanoparticle systems for improved chemical processes and novel single-atom catalysis.This article is part of a discussion meeting issue ‘Dynamic in situ microscopy relating structure and function’.

Visualizing single atom dynamics in heterogeneous catalysis using analytical in situ environmental scanning transmission electron microscopy.

Progress is reported in analytical in situ environmental scanning transmission electron microscopy (ESTEM) for visualizing and analysing in real-time dynamic gas-solid catalyst reactions at the single-atom level under controlled reaction conditions of gas environment and temperature. The recent development of the ESTEM advances the capability of the established ETEM with the detection of fundamental single atoms, and the associated atomic structure of selected solid-state heterogeneous catalysts, in catalytic reactions in their working state. The new data provide improved understanding of dynamic atomic processes and reaction mechanisms, in activity and deactivation, at the fundamental level; and in the chemistry underpinning important technological processes. The benefits of atomic resolution-E(S)TEM to science and technology include new knowledge leading to improved technological processes, reductions in energy requirements and better management of environmental waste. This article is part of a discussion meeting issue 'Dynamic in situ microscopy relating structure and function'.

Photon-recoil imaging: Expanding the view of nonlinear x-ray physics.

Addressing the ultrafast coherent evolution of electronic wave functions has long been a goal of nonlinear x-ray physics. A first step toward this goal is the investigation of stimulated x-ray Raman scattering (SXRS) using intense pulses from an x-ray free-electron laser. Earlier SXRS experiments relied on signal amplification during pulse propagation through dense resonant media. By contrast, our method reveals the fundamental process in which photons from the primary radiation source directly interact with a single atom. We introduce an experimental protocol in which scattered neutral atoms rather than scattered photons are detected. We present SXRS measurements at the neon K edge and a quantitative theoretical analysis. The method should become a powerful tool in the exploration of nonlinear x-ray physics.

Nonlinear x-ray spectroscopy

Spectroscopy The extension of nonlinear optics to the x-ray spectral domain is a promising direction in the development of x-ray spectroscopy. Although theoretical concepts of nonlinear x-ray spectroscopy were developed decades ago, scientists still struggle to implement them because of the elusive nature of nonlinear effects. Eichmann et al. now present atomic momentum spectroscopy (AMS), which is based on the detection of the scattered atom after momentum transfer from x-ray photons (see the Perspective by Pfeifer). The authors show how AMS can observe stimulated x-ray Raman scattering signals at the neon K edge on a single-atom level and distinguish them from other competing processes. These results pave the way for future nonlinear x-ray spectroscopy methods for the study of x-ray–matter interactions. Science , this issue p. [1630][1]; see also p. [1568][2] [1]: /lookup/doi/10.1126/science.abc2622 [2]: /lookup/doi/10.1126/science.abd6168

Visualization of atomic scale reaction dynamics of supported nanocatalysts during oxidation and ammonia synthesis using in-situ environmental (scanning) transmission electron microscopy

Visualization of atomic scale reaction dynamics of supported nanocatalysts during oxidation and ammonia synthesis using in-situ environmental (scanning) TEM. Reaction dynamics in gases at operating temperatures at the atomic level are the basis of heterogeneous gas–solid catalyst reactions and are crucial to the catalyst function. Supported noble metal nanocatalysts such as platinum are of interest in fuel cells and as diesel oxidation catalysts for pollution control, and practical ruthenium nanocatalysts are explored for ammonia synthesis. Graphite and graphitic carbons are of interest as supports for the nanocatalysts. Despite considerable literature on the catalytic processes on graphite and graphitic supports, reaction dynamics of the nanocatalysts on the supports in different reactive gas environments and operating temperatures at the single atom level are not well understood. Here we present real time in-situ observations and analyses of reaction dynamics of Pt in oxidation, and practical Ru nanocatalysts in ammonia synthesis, on graphite and related supports under controlled reaction environments using a novel in-situ environmental (scanning) transmission electron microscope with single atom resolution. By recording snapshots of the reaction dynamics, the behaviour of the catalysts is imaged. The images reveal single metal atoms, clusters of a few atoms on the graphitic supports and the support function. These all play key roles in the mobility, sintering and growth of the catalysts. The experimental findings provide new structural insights into atomic scale reaction dynamics, morphology and stability of the nanocatalysts.

Elliptical isolated attosecond-pulse generation from an atom in a linear laser field

We theoretically demonstrate a scheme to produce elliptically polarized isolated attosecond pulses, based on the high-order harmonic generation from the current-carrying state of an atom exposed in linearly polarized laser fields. It is shown that the nonzero ellipticity of the attosecond pulse generated at the single-atom level is attributed to the nonvanishing angular momentum of the state, which is further elucidated by the strong-field approximation model. With specific carrier envelope phases (CEPs), isolated attosecond pulses with large ellipticity can be obtained. Moreover, the ellipticity of high-order harmonics remains almost invariable versus the CEP of the few-cycle driving field. Hence, the temporal profile and ellipticity of the attosecond-pulse radiation can be manipulated separately, which is beneficial to shape the attosecond-pulse radiation without compromising the ellipticity. The obtained elliptical attosecond pulse may serve as a potential tool to explore and manipulate the ultrafast dynamics in magnetic materials and chiral media.

Revealing the Correlation between Catalytic Selectivity and the Local Coordination Environment of Pt Single Atom

Single atom catalysts (SACs) have recently attracted great attention in heterogeneous catalysis and have been regarded as ideal models for investigating the strong interaction between metal and support. Despite the huge progress over the past decade, the deep understanding on the structure-performance correlation of SACs at a single atom level still remains to be a great challenge. In this study, we demonstrate that the variation in the coordination number of the Pt single atom can significantly promote the propylene selectivity during propyne semihydrogenation (PSH) for the first time. Specifically, the propylene selectivity greatly increases from 65.4% to 94.1% as the coordination number of Pt-O increases from ∼3.4 to ∼5, whereas the variation in the coordination number of Pt-O slightly influences the turnover frequency values of SACs. We anticipate that the present work may deepen the understanding on the structure-performance of SACs and also promote the fundamental research in single atom catalysis.

Parametric attosecond pulse amplification far from the ionization threshold from high order harmonic generation in He.

Parametric amplification of attosecond coherent pulses around 100 eV at the single-atom level is demonstrated for the first time by using the 3D time-dependent Schrödinger equation in high-harmonic generation processes from excited states of He+. We present the attosecond dynamics of the amplification process far from the ionization threshold and resolve the physics behind it. The amplification of a particular central photon energy requires the seed XUV pulses to be perfectly synchronized in time with the driving laser field for stimulated recombination to the He+ ground state and is only produced in a few specific laser cycles in agreement with the experimental measurements. Our simulations show that the amplified photon energy region can be controlled by varying the peak intensity of the laser field. Our results pave the way to the realization of compact attosecond pulse intense XUV lasers with broad applications.

Imaging Nucleation, Growth and Disorder at the Single-atom Level by Atomic Electron Tomography (AET)

Imaging Nucleation, Growth and Disorder at the Single-atom Level by Atomic Electron Tomography (AET)

A Single-Atom Manipulation Approach for Synthesis of Atomically Mixed Nanoalloys as Efficient Catalysts.

Synthesis of well-defined atomically mixed alloy nanoparticles on desired substrates is an ultimate goal for their practical application. Herein we report a general approach for preparing atomically mixed AuPt, AuPd, PtPd, AuPtPd NAs(nanoalloys) through single-atom level manipulation. By utilizing the ubiquitous tendency of aggregation of single atoms into nanoparticles at elevated temperatures, we have synthesized nanoalloys on a solid solvent with CeO2 as a carrier and transition-metal single atoms as an intermediate state. The supported nanoalloys/CeO2 with ultra-low noble metal content (containing 0.2 wt % Au and 0.2 wt % Pt) exhibit enhanced catalytic performance towards complete CO oxidation at room temperature and remarkable thermostability. This work provides a general strategy for facile and rapid synthesis of well-defined atomically mixed nanoalloys that can be applied for a range of emerging techniques.