Low-coordinated Atoms Research Articles

Difference in the Catalytic Activity of Atoms in the Corners and at the Edges of Gold Nanoparticles: Hydrogen Isotope Exchange Reaction.

The goal of this work is to investigate the catalytic activities of low-coordination atoms located in gold nanoparticles. Gold nanoparticles with sizes from 0.7 to 40 nm deposited on γ-Al2O3 were used as a catalyst. Synthesized gold nanoparticles and prepared catalysts were characterized by HRTEM, SEM, XRD, DLS, and UV-Vis spectroscopy. The specific activity of gold nanoparticles towards the isotope exchange reaction at 77 K was studied as a function of nanoparticle size. The catalytic activity increases significantly when the particle size is less than 3 nm. The activities of low-coordination gold atoms located at the edges and in the corners are markedly different. Corner atoms (CN = 6) are more than 40 times more active in the reaction of hydrogen isotope exchange than edge atoms (CN = 7). TOF for atoms with coordination numbers CN = 6 and CN = 7 are 0.258 ± 0.020 and 0.006 ± 0.001 molecules site-1 s-1, respectively. An equation was proposed for the dependence of the catalytic activity of the reaction on the particle size, the number of atoms on the surface, and their activity.

Promotion of Single-Electron Transfer by Low-Coordinated Co Single Atoms to Facilitate Advanced Oxidation Processes in Wastewater Treatment.

Heterogeneous catalysts are fascinating for advanced oxidation processes (AOPs) in wastewater treatment to reduce cost, metal contamination, and pH operation limitations. However, they usually encounter low catalytic efficiency because of the difficult single-electron-transfer (SET) pathway during AOPs. Herein, an efficient heterogeneous catalyst for AOPs is realized through the rational regulation of N coordination around Co single-atom (SA) centers in favor of SET. As guided by calculations, low N coordination enables a high density of electronic states at the Fermi energy level of SA Co to facilitate SET activation of peroxomonosulfate (PMS). A special oxide-compounding method is further applied to decrease the N coordination of SA Co on the carbon carriers from common Co1-N3/4 to the desired Co1-N2. Co1-N2 shows a delightful activity for AOP degradation of various organic pollutants with kinetic rate and turnover frequency values up to 0.862 min-1 and 389 h-1, respectively, greatly outperforming those of Co1-N3/4. It is also superior in a wide pH operation range and has strong resistance to environmental disturbances. Detailed mechanistic investigations confirm the generation of singlet oxygen (1O2) instead of common radical O species from the SET between PMS and Co1-N2, corroborating the calculated results and accounting for the enhanced AOP activity.

Constructing Unsaturated Ru Atom Arrays Confined in Mn Oxides to Boost Neutral Water Reduction.

Recently, Ru single atoms supported on carbon nanomaterials have demonstrated ultrahigh activity for acid hydrogen evolution reaction (HER), however their neutral HER activity remains low due to the sluggish kinetics for both the water dissociation step to generate H* intermediates and subsequent H* recombination in neutral electrolytes. Here, we synthesize ordered low-coordinated Ru atom arrays confined in Mn oxides (i.e., Li4Mn5O12) for concurrently boosting the water dissociation and H* recombination, thus achieving a 6-fold HER activity enhancement than commercial Pt/C in neutral media. Control experiments indicate that low-coordinated Ru atoms with strong affinity to oxygen atoms of water molecules facilitate the water dissociation to rapidly generate H*. More importantly, both electrochemical and theoretic results uncover that the array-like structure allows the activation of two water molecules on two adjacent Ru atoms for enabling direct H*-H* recombination via the Tafel step, while isolated Ru atoms can only activate water one by one for recombining H* via the sluggish Heyrovsky step. Clearly, this work paves new avenues to boosting the electrocatalytic activity by constructing ordered metal atoms assembles with controllable coordination environments.

Nanocluster-agminated amorphous cobalt nanofilms for highly selective electroreduction of nitrate to ammonia

Developing highly-efficient electrocatalysts for the nitrate reduction reaction (NITRR) is a persistent challenge. Here, we present the successful synthesis of 14 amorphous/low crystallinity metal nanofilms on three-dimensional carbon fibers (M-NFs/CP), including Al, Ti, Mn, Fe, Co, Ni, Cu, Zn, Ag, In, Sn, Pb, Au, or Bi, using rapid thermal evaporation. Among these samples, our study identifies the amorphous Co nanofilm with fine agglomerated Co clusters as the optimal electrocatalyst for NITRR in a neutral medium. The resulting Co-NFs/CP exhibits a remarkable Faradaic efficiency (FENH3) of 91.15 % at − 0.9 V vs RHE, surpassing commercial Co foil (39 %) and Co powder (20 %), despite sharing the same metal composition. Furthermore, during the electrochemical NITRR, the key intermediates on the surface of the Co-NFs/CP catalyst were detected by in situ Fourier-transform infrared (FTIR) spectroscopy, and the possible reaction ways were probed by Density functional theory (DFT) calculations. Theoretical calculations illustrate that the abundant low-coordinate Co atoms of Co-NFs/CP could enhances the adsorption of *NO3 intermediates compared to crystalline Co. Additionally, the amorphous Co structure lowers the energy barrier for the rate-determining step (*NH2→*NH3). This work opens a new avenue for the controllable synthesis of amorphous/low crystallinity metal nano-catalysts for various electrocatalysis reaction applications.

Rapid synthesis of PdCu nanosheets with enhanced electrocatalytic activity toward polyalcohol oxidation reaction

Reasonable design of Pd-based catalysts with specific composition and morphology is of great importance for promoting the commercial application.of direct alcohol fuel cells (DAFCs). Recently, two-dimension (2D) with high density of defects and massive low-coordinated surface atom has become research highlights in the field of catalysis. Herein, we report a wet chemical method for synthesizing PdCu nanosheets with abundant wrinkles. The ultrathin two-dimensional structure endows catalysts plentiful catalytic active sites and large specific surface area, improving atomic utilization efficiency. The formation of bimetallic PdCu alloy structure leads to the adjustment of Pd electronic structure, resulting in lattice compression effect. Benefitting from the structural and compositional characteristics, PdCu nanosheets (NSs) exhibits excellent electrocatalytic performance for ethylene glycol oxidation reaction (EGOR) and glycerol oxidation reaction (GOR) with the mass activity of 7031 mA mg−1/5117 mA mg−1, which is 4.4/3.9 times higher than that of commercial Pd/C catalysts. Furthermore, the remained mass activity of PdCu NSs is 3991/3851 mA mg−1 after the durability measurement for EGOR/GOR, which confirm PdCu NSs possesses superior stability. We believe that our synthetic strategy could provide robust reference for the development of high-performance eletrocatalysts.

Engineering Internal and External Low-Coordination Atoms in Nickel-Organic Framework Nanoarrays to Promote the Electrochemical Oxygen Evolution Reaction.

Monometallic nickel-organic frameworks based on a carboxylated ligand [2,6-naphthalenedicarboxylic acid (Ni-NDC)] have abundant and uniformly distributed single-atom Ni sites, enabling superior oxygen evolution reaction (OER) activity. In theory, most of the Ni atoms inside Ni-NDC microcrystals are coordinatively saturated except for the surface. Therefore, there are no accessible low-coordination atoms (LCAs) as electrocatalytic sites for the OER. One effective way is to expose more LCAs by preparing self-supporting Ni-NDC nanoarrays (Ni-NDC NAs) with hierarchical secondary structural units. Another effective method is to create more internal LCAs by removing partial ligands or coordination atoms attached to the Ni atoms. Herein, by combining the two strategies, we engineered LCAs in the interior and exterior of Ni-NDC to synergistically accelerate the OER. In brief, ultrathick "brick-like" Ni-NDC NAs were first prepared with dissolution and coordination effects of NDC on self-sacrificial templates of "agaric-like" nickel hydroxide nanoarrays [Ni(OH)2 NAs]. Subsequently, dual-coordinated NDC was partially replaced by monocoordinated 2-naphthoic acid (NA). The Ni-NDC NAs were further tailed into ultrathin "liner leaf-like" nanoneedle arrays (LCAs-Ni-NDC NAs). As a consequence, the LCAs-Ni-NDC NAs have more internal and external LCAs, which can deliver an OER performance that is superior to that of Ni-NDC NAs.

A single Mn atom supported by a boron-vacancy in a BN monolayer: An encouraging catalyst for CO oxidation

Single-atom catalysts (SACs) are known for their exceptional activity, primarily attributed to the abundance of low-coordinated metal atoms, which enable efficient activation of robust chemical bonds, including CO bonds. In this work, we explore the prospective utilization of a specific SAC, isolated Mn atoms supported on Boron nitrogen (Mn/BN), for CO oxidation. By analyzing the adsorption/co-adsorption energies of CO, O2, O2+CO, and 2CO, we create a set of screening criteria and conduct a comparative analysis of the chemical processes involved in CO oxidation. The Langmuir-Hinshelwood (LH), Eley-Rideal (ER), termolecular Langmuir-Hinshelwood (TLH) and termolecular Eley-Rideal (TER) mechanisms are investigated. Results indicate the ER and LH mechanisms feature pronouncedly lower barrier of 0.33 and 0.41 eV, respectively, for the rate-limiting step, than those of the TLH (0.72 eV) and TER (3.00 eV) mechanisms, suggesting that the ER and LH mechanisms are favorable at normal temperature. This study offers valuable insights that can inform future developments in the design of low-temperature CO oxidation processes utilizing SACs.

Metal bond strength regulation enables large-scale synthesis of intermetallic nanocrystals for practical fuel cells.

Structurally ordered L10-PtM (M = Fe, Co, Ni and so on) intermetallic nanocrystals, benefiting from the chemically ordered structure and higher stability, are one of the best electrocatalysts used for fuel cells. However, their practical development is greatly plagued by the challenge that the high-temperature (>600 °C) annealing treatment necessary for realizing the ordered structure usually leads to severe particle sintering, morphology change and low ordering degree, which makes it very difficult for the gram-scale preparation of desirable PtM intermetallic nanocrystals with high Pt content for practical fuel cell applications. Here we report a new concept involving the low-melting-point-metal (M' = Sn, Ga, In)-induced bond strength weakening strategy to reduce Ea and promote the ordering process of PtM (M = Ni, Co, Fe, Cu and Zn) alloy catalysts for a higher ordering degree. We demonstrate that the introduction of M' can reduce the ordering temperature to extremely low temperatures (≤450 °C) and thus enable the preparation of high-Pt-content (≥40 wt%) L10-Pt-M-M' intermetallic nanocrystals as well as ten-gram-scale production. X-ray spectroscopy studies, in situ electron microscopy and theoretical calculations reveal the fundamental mechanism of the Sn-facilitated ordering process at low temperatures, which involves weakened bond strength and consequently reduced Ea via Sn doping, the formation and fast diffusion of low-coordinated surface free atoms, and subsequent L10 nucleation. The developed L10-Ga-PtNi/C catalysts display outstanding performance in H2-air fuel cells under both light- and heavy-duty vehicle conditions. Under the latter condition, the 40% L10-Pt50Ni35Ga15/C catalyst delivers a high current density of 1.67 A cm-2 at 0.7 V and retains 80% of the current density after extended 90,000 cycles, which exceeds the United States Department of Energy performance metrics and represents among the best cathodic electrocatalysts for practical proton-exchange membrane fuel cells.

Bicontinuous RuO2 nanoreactors for acidic water oxidation

Improving activity and stability of Ruthenium (Ru)-based catalysts in acidic environments is eager to replace more expensive Iridium (Ir)-based materials as practical anode catalyst for proton-exchange membrane water electrolyzers (PEMWEs). Here, a bicontinuous nanoreactor composed of multiscale defective RuO2 nanomonomers (MD-RuO2-BN) is conceived and confirmed by three-dimensional tomograph reconstruction technology. The unique bicontinuous nanoreactor structure provides abundant active sites and rapid mass transfer capability through a cavity confinement effect. Besides, existing vacancies and grain boundaries endow MD-RuO2-BN with generous low-coordination Ru atoms and weakened Ru-O interaction, inhibiting the oxidation of lattice oxygen and dissolution of high-valence Ru. Consequently, in acidic media, the electron- and micro-structure synchronously optimized MD-RuO2-BN achieves hyper water oxidation activity (196 mV @ 10 mA cm−2) and an ultralow degradation rate of 1.2 mV h−1. A homemade PEMWE using MD-RuO2-BN as anode also conveys high water splitting performance (1.64 V @ 1 A cm−2). Theoretical calculations and in-situ Raman spectra further unveil the electronic structure of MD-RuO2-BN and the mechanism of water oxidation processes, rationalizing the enhanced performance by the synergistic effect of multiscale defects and protected active Ru sites.

Biphase Pd Nanosheets with Atomic-Hybrid RhOx/Pd Amorphous Skins Disentangle the Activity-Stability Trade-Off in Oxygen Reduction Reaction.

The activity-stability trade-off relationship of oxygen reduction reaction (ORR) is a tricky issue that strikes the electrocatalyst population and hinders the widespread application of fuel cells. Here neoteric biphase Pd nanosheets that are structured with ultrathin two-dimensional crystalline Pd inner cores and ≈1 nm thin atomic-hybrid RhOx/Pd amorphous skins, named c/a-Pd@PdRh NSs, for disentangling this trade-off dilemma for alkaline ORR are developed. The superthin amorphous skins significantly amplify the quantity of flexibly low-coordinated atoms for electrocatalysis. An in situ selected oxidation of the top-surface Rh dopants creates atomically hybrid RhOx/Pd disorder surfaces. Detailed energy spectra and theoretical simulation confirm that these RhOx/Pd interfaces can arouse a surface charge redistribution, causing significant electron deficiency and lowered d-band center for surface Pd. Meanwhile, anticorrosive Rh/RhOx species can thermodynamically passivate the neighboring Pd atoms from oxidative dissolution. Thanks to these amplified interfacial effects, the biphase c/a-Pd@PdRh NSs simultaneously exhibit a superhigh ORR activity (5.92 A mg-1, 22.8 times that of Pt/C) and an outstanding long-lasting stability after 100k cycles of accelerated durability test, showcasing unprecedented electrocatalysts for breaking the activity-stability trade-off relationship of ORR. This work paves a bran-new strategy for designing high-performance electrocatalysts through creating modulated amorphous skins on low-dimensional nanomaterials.

Utilizing the oxygen-atom trapping effect of Co3O4 with oxygen vacancies to promote chlorite activation for water decontamination

Heterogeneous high-valent cobalt-oxo [≡Co(IV)=O] is a widely focused reactive species in oxidant activation; however, the relationship between the catalyst interfacial defects and ≡Co(IV)=O formation remains poorly understood. Herein, photoexcited oxygen vacancies (OVs) were introduced into Co3O4 (OV-Co3O4) by a UV-induced modification method to facilitate chlorite (ClO2-) activation. Density functional theory calculations indicate that OVs result in low-coordinated Co atom, which can directionally anchor chlorite under the oxygen-atom trapping effect. Chlorite first undergoes homolytic O-Cl cleavage and transfers the dissociated O atom to the low-coordinated Co atom to form reactive ≡Co(IV)=O with a higher spin state. The reactive ≡Co(IV)=O rapidly extracts one electron from ClO2- to form chlorine dioxide (ClO2), accompanied by the Co atom returning a lower spin state. As a result of the oxygen-atom trapping effect, the OV-Co3O4/chlorite system achieved a 3.5 times higher efficiency of sulfamethoxazole degradation (~0.1331 min-1) than the pristine Co3O4/chlorite system. Besides, the refiled OVs can be easily restored by re-exposure to UV light, indicating the sustainability of the oxygen atom trap. The OV-Co3O4 was further fabricated on a polyacrylonitrile membrane for back-end water purification, achieving continuous flow degradation of pollutants with low cobalt leakage. This work presents an enhancement strategy for constructing OV as an oxygen-atom trapping site in heterogeneous advanced oxidation processes and provides insight into modulating the formation of ≡Co(IV)=O via defect engineering.

Highly active single-layer 2H-MoS2 for CO2 hydrogenation to methanol

Few-layer MoS2 were recently discovered as promising catalyst for CO2 hydrogenation to methanol, despite extreme conditions proposed for its synthesis. Herein, we developed an exceptionally facile, safe, and scalable strategy to prepare single-layer MoS2 (s-MoS2) at ambient pressure using instantaneous self-assembled micelles of didodecyldimethylammonium (DA)−MoS4 complexes as precursor. During the pyrolysis, the presence and subsequent decomposition of coordinated DA inhibited the growth and sheet-stacking of MoS2 in c-direction, resulting in discrete s-MoS2 molecular sheets which maximize the exposure of in-plane S vacancies (Sv). Remarkably, s-MoS2 displayed 77% methanol selectivity and methanol space time yield of 1.54 g·gMoS2–1·h–1, representing the top levels among reported MoS2 catalysts under similar conditions. Density functional theory (DFT) simulations attribute high activity of s-MoS2 to its ability to stabilize in-plane low-coordinated Mo atoms in the vicinity of Sv on both sides of monolayer. The superior performance of s-MoS2 creates new prospects for technological applications beyond CO2 hydrogenation.

Twinning Engineering of Platinum/Iridium Nanonets as Turing-Type Catalysts for Efficient Water Splitting.

The twin boundary, a common lattice plane of mirror-symmetric crystals, may have high reactivity due to special atomic coordination. However, twinning platinum and iridium nanocatalysts are grand challenges due to the high stacking fault energies that are nearly 1 order of magnitude larger than those of easy-twinning gold and silver. Here, we demonstrate that Turing structuring, realized by selective etching of superthin metal film, provides 14.3 and 18.9 times increases in twin-boundary densities for platinum and iridium nanonets, comparable to the highly twinned silver nanocatalysts. The Turing configurations with abundant low-coordination atoms contribute to the formation of nanotwins and create a large active surface area. Theoretical calculations reveal that the specific atom arrangement on the twin boundary changes the electronic structure and reduces the energy barrier of water dissociation. The optimal Turing-type platinum nanonets demonstrated excellent hydrogen-evolution-reaction performance with a 25.6 mV overpotential at 10.0 mA·cm-2 and a 14.8-fold increase in mass activity. And the bifunctional Turing iridium catalysts integrated in the water electrolyzer had a mass activity 23.0 times that of commercial iridium catalysts. This work opens a new avenue for nanocrystal twinning as a facile paradigm for designing high-performance nanocatalysts.

Ultradurable Pt-Based Catalysts for Oxygen Reduction Electrocatalysis

An oxygen reduction reaction (ORR) is the key half reaction of proton exchange membrane fuel cells (PEMFCs), and is highly dependent on Pt-based nanocrystals as core electrocatalysts. Despite the exceptional ORR activity from adjusting the electronic structures of surface or near-surface atoms, several serious issues, including the corrosion of carbon supports, the preferential leaching of active metal elements, the instability of surface low-coordinated atoms and the sintering/agglomeration of nanocrystals, still exist, challenging the ORR durability of developed Pt-based ORR catalysts. From the point of view of the catalyst structure design, in this review, we summarized the state-of-the-art structural regulation strategies for improving the ORR durability of Pt-based catalysts. The current limitation of Pt-based binary catalysts for ORR electrocatalysis is firstly discussed, and the detailed strategies are further classified into the optimization of supports, metal-doped alloys, core/shell structures, intermetallics and high-entropy alloys, etc. The structure–performance relationship is detailedly explained, especially emphasizing the elimination of the above restrictions. Finally, the existing challenges and future research direction are further presented, aiming at practicing the PEMFC devices of the ultradurable Pt-based catalysts.

Prediction of superhard C1+xN1-x compounds with metal-free magnetism and narrow band gaps.

The scarcity of superhard materials with magnetism or a narrow band gap, despite their potential applications in various fields, makes it desirable to design such materials. Here, a series of C1+xN1-x compounds are theoretically designed by replacing different numbers of nitrogen atoms with carbon atoms in the synthesized C1N1 compound. The results indicate that the compounds C5N3 and C7N1 possess both superhardness and antiferromagnetic ordering due to the introduction of low-coordinated carbon atoms. The hardness of the two compounds is about 40.3 and 54.5 GPa, respectively. The magnetism in both compounds is attributed to the unpaired electrons in low-coordinated carbon atoms, and the magnetic moments are 0.42 and 0.39 μB, respectively. Interestingly, the magnetism in C5N3 remains unaffected by the external pressure used in this study, whereas C7N1 becomes nonmagnetic when the pressure exceeds ∼80 GPa. Electronic calculations reveal that both compounds behave as indirect band gap semiconductors, with narrow energy gaps of about 0.30 and 0.20 eV, respectively. Additionally, the other two compounds, C6N2-I and C6N2-III, exhibit nonmagnetic ordering and possess hardness values of 52.6 and 35.0 GPa, respectively. C6N2-I behaves as a semiconductor with an energy gap of 0.79 eV, and C6N2-III shows metallic behavior. Notably, the energy gaps of C5N3 and C6N2-I remain nearly constant under arbitrary pressure due to their porous and superhard structure. These compounds fill the gap in magnetic or narrow band gap superhard materials, and they can be used in the spintronic or optoelectronic fields where conventional superhard materials are not suitable.

Engineering low-coordination atoms on RhPt bimetallene for 12-electron ethanol electrooxidation

The three-dimensional perforated RhPt bimetallene achieves a high exposure ratio of low-coordinated RhPt diatomic sites, demonstrating excellent activity and remarkable selectivity for 12-electron ethanol oxidation to CO2.

Theoretical insights into the generation and reactivity of hydride on the ZnO(101̄0) surface.

ZnO is an important catalytic material for CO/CO2 hydrogenation. In this work, the pristine ZnO(101̄0) and the surfaces with Zn-O dimer vacancies (ZnO(101̄0)-(Zn-O)DiV) and oxygen vacancies are calculated. We find that the hydride (H-) species can be generated via heterolytic H2 dissociation on these surfaces, and that ZnO(101̄0)-(Zn-O)DiV only needs to overcome the energy barrier of ∼0.10 eV. This is because the ZnO system has flexible orbitals for electron storage and release and the low-coordinated Zn3c atoms at the defect sites can form stable Zn-H- covalent bonds with high symmetry. Flexible Zn orbitals also impart the unique feature of activating multiple electrophilic adsorbates simultaneously as excess electrons exist. Moreover, we show that the covalent Zn-H- species can regulate the catalytic activity and selectivity for CO2 hydrogenation by preferentially producing *HCOO intermediates at Zn-O dimer vacancies. These results may help in the design of efficient Zn-based hydrogenation catalysts.

Ultrathin two-dimensional photocatalysts for carbon dioxide reduction into fuels and chemicals

The extensive burning of fossil fuels has caused energy shortages and worsened the greenhouse effect, posing a significant threat to human survival and development. The use of solar energy as a renewable source to reduce CO2 emissions and produce green fuels and high-value chemicals is seen as a promising solution to the ongoing energy crisis. Ultrathin two-dimensional photocatalysts have large surface areas and numerous low-coordination surface atoms, giving them substantial potential for highly efficient photocatalytic performance. These materials can reduce carrier transmission distance, enhance reactant adsorption and activation (e.g., CO2 and H2O), lower energy barriers, facilitate specific reactions, inhibit competing reactions, and regulate catalytic efficiency and selectivity. This article provides a concise overview of ultrathin two-dimensional semiconductor synthesis, clarifies catalytic mechanisms, explores various photocatalytic applications, and outlines strategies to enhance photoconversion performance. It also emphasizes the primary challenges and opportunities faced by ultrathin photocatalysts. We anticipate that this review will offer valuable insights for further research in two-dimensional photocatalysis and encourage the practical application of these unique materials in energy conversion.

Low-Temperature Propane Activation and Mineralization over a Co3O4 Sub-nanometer Porous Sheet: Atomic-Level Insights.

Light alkanes make up a class of widespread volatile organic compounds (VOCs), bringing great environmental hazards and health concerns. However, the low-temperature catalytic destruction of light alkanes is still a great challenge to settle due to their high reaction inertness and weak polarity. Herein, a Co3O4 sub-nanometer porous sheet (Co3O4-SPS) was fabricated and comprehensively compared with its bulk counterparts in the catalytic oxidation of C3H8. Results demonstrated that abundant low-coordinated Co atoms on the Co3O4-SPS surface boost the activation of adsorbed oxygen and enhance the catalytic activity. Moreover, Co3O4-SPS has better surface metal properties, which is beneficial to electron transfer between the catalyst surface and the reactant molecules, promoting the interaction between C3H8 molecules and dissociated O atoms and facilitating the activation of C-H bonds. Due to these, Co3O4-SPS harvests a prominent performance for C3H8 destruction, 100% of which decomposed at 165 °C (apparent activation energy of 49.4 kJ mol-1), much better than the bulk Co3O4 (450 °C and 126.9 kJ mol-1) and typical noble metal catalysts. Moreover, Co3O4-SPS also has excellent thermal stability and water resistance. This study deepens the atomic-level insights into the catalytic capacity of Co3O4-SPS in light alkane purification and provides references for designing efficacious catalysts for thermocatalytic oxidation reactions.

In situ preparation and determination of CeO2 high-index surface atomic structures

Understanding the properties regarding the high-index surfaces of the oxide nanocrystals is of great importance, but it remains challenging to obtain atomic-level information due to the lack of efficient preparation methods for high-index surfaces. Herein, we presented a work to in situ prepare and determine the intrinsic atomic structures of nanocrystalline CeO2 high-index surfaces via in situ spherical aberration (Cs)-corrected scanning transmission electron microscopy (STEM). By utilizing a reshaping process driven by the Wulff reconstruction, high-index surfaces of CeO2 nanocrystals including {210} {311}, and {533} were successfully prepared. Combined STEM with the density functional theory calculations, these high-index surface structures were determined with atomic precision, and interestingly {533} exhibited a unique atomic pit feature with low-coordinated Ce atoms exposure and unique electrical properties. This work has revealed new information about CeO2 high-index surfaces through experiments, enhancing our understanding of these surfaces, and also providing a new route for preparing high-index surfaces.