Pd Monolayer Research Articles

Design rules for catalysis in single-particle plasmonic nanogap reactors with precisely aligned molecular monolayers

Plasmonic nanostructures can both drive and interrogate light-driven catalytic reactions. Sensitive detection of reaction pathways is achieved by confining optical fields near the active surface. However, effective control of the reaction kinetics remains a challenge to utilize nanostructure constructs as efficient chemical reactors. Here we present a nanoreactor construct exhibiting high catalytic and optical efficiencies, based on a nanoparticle-on-mirror (NPoM) platform. We observe and track pathways of the Pd-catalysed C-C coupling reaction of molecules within a set of nanogaps presenting different chemical surfaces. Atomic monolayer coatings of Pd on the different Au facets enable tuning of the reaction kinetics of surface-bound molecules. Systematic analysis shows the catalytic efficiency of NPoM-based nanoreactors greatly improves on platforms based on aggregated nanoparticles. More importantly, we show Pd monolayers on the nanoparticle or on the mirror play significantly different roles in the surface reaction kinetics. Our data provides clear evidence for catalytic dependencies on molecular configuration in well-defined nanostructures. Such nanoreactor constructs therefore yield clearer design rules for plasmonic catalysis.

Tailoring the Spin Reorientation Transition of Co Films by Pd Monolayer Capping.

We have characterized the magnetization easy-axis of ultra-thin Co films (2-5 atomic layers, AL) grown on Ru(0001) when they are capped with a monolayer of Pd. The addition of a Pd monolayer turns the magnetization of 3 and 4 AL-thick Co films from an in-plane to an out-of-plane alignment, but not that of a 5 AL-thick film. These observations are explained in terms of an enhancement of the surface anisotropy. The exposure of the sample to hydrogen, CO or a combination of both gases does not overcome this effect.

Tunable interfacial properties of monolayer GeSb2Te4 on metal surfaces

Abstract Atomically thin monolayer (ML) GeSb 2 Te 4 (GST) holds promising prospects in non-volatile memory applications because of its high non-homogeneous crystallization rate. In GST-based devices, the interaction between GST and metals is crucial, as it affects the electronic properties. Herein, based on first-principles calculations, we investigate the interaction and Schottky barrier height of contacts formed by the combination of ML GST with various metals. It is found that the interfaces of GST with Pt, Pd, Ir and W exhibit strong interaction, characterized by large binding energies ranging from 1.394 to 1.015 eV , and the interfaces between GST and Cu, Ag and Au display weak interaction. For the seven contacts, Ag and W form Ohmic contacts with ML GST, while Cu, Au, Pd, Ir, and Pt form n-type Schottky contacts, with Schottky barrier heights ranging from 0.029 to 0.353 eV . The strong Fermi level pinning at GST-metal interface is observed with a pinning factor of 0.378. Additionally, altering the interfacial distance and optimizing the layers of GST enable a transition from Ohmic contact to Schottky contact. These findings provide crucial guidance for the design and optimization of electronic devices based on phase change materials like GST.

Designing nanoporous Pd catalyst with dual enhancement of thermodynamics and kinetics for formic acid oxidation reaction

Conventional strategies for developing highly efficient electrocatalysts involve enhancing thermodynamics to minimize overpotential and improving kinetics to maximize reaction current. However, current research on Pd-based catalysts for formic acid oxidation reaction (FAOR) mainly focuses on accelerating its kinetics to increase the peak current. This study proposes a catalyst design that can simultaneously improve the kinetics and thermodynamics of FAOR. Specifically, the home-made catalyst (NPG-Pt1-Pd1) is obtained by sequentially depositing monolayer Pt and Pd shells on the surface of nanoporous gold (NPG) substrate. Compared with commercial Pd/C, this electrocatalyst exhibits a noticeable negative shift in onset potential (∼100 mV) and a significantly improved peak current (∼6 times). Experimental data and theoretical calculations demonstrate that NPG-Pt1-Pd1 exhibits a comparatively suitable adsorption energy for small molecules, not only reducing the overpotential but also accelerating the reaction rate of FAOR. Moreover, when applied in direct formic acid fuel cells (DFAFC), the NPG-Pt1-Pd1 anode with an exceptionally low Pd loading of 8.5 μg cm−2, achieves a remarkable power density of 141 mW cm−2. The power efficiency of Pd is 230 times that of Pd/C (1 mg cm−2, 73 mW cm−2). Therefore, this work provides a new methodology for developing efficient Pd-based FAOR electrocatalysts.

Effect of loading different transition metals W, Pt and Pd monolayers on quinoline hydrogenation and C–N bond cleavage over Mo2C(001)

Nitrogen-containing compounds such as quinoline in coal-based crude oils cause environmental pollution in the course of application. Consequently, dealing with the nitrogen-containing compounds from coal-based crude oil is of paramount importance. The hydrogenation and CN bond cleavage mechanisms of quinoline on the active Mo-terminated over Mo2C(001) surface, as well as on surfaces doped with W, Pt and Pd monolayers, were examined employing the density functional theory (DFT) method. The Pd and Pt-doped catalysts exhibited higher hydrogenation activity. The catalytic efficiency is enhanced by the loading of different metals, particularly with d-band center further away from the Fermi energy level. Additionally, a novel CN bond cleavage mechanism for quinoline has been proposed. The new proposed mechanism is more conducive for the CN bond cleavage. After a thorough comparison, the Pd-loaded catalyst was identified as the most effective for quinoline hydrogenation and CN bond cleavage.

Theoretically predicted innovative palladium stripe dopingcobalt(1 1 1) surface with excellent catalytic performance for carbon monoxide oxidative coupling to dimethyl oxalate

Pd-based catalysts are extensively employed to catalyze CO oxidative coupling to generate DMO, while the expensive price and high usage of Pd hinder its massive application in industrial production. Designing Pd-based catalysts with high efficiency and low Pd usage as well as expounding the catalytic mechanisms are significant for the reaction. In this study, we theoretically predict that Pd stripe doping Co(1 1 1) surface exhibits excellent performance than pure Pd(1 1 1), Pd monolayer supporting on Co(1 1 1) and Pd single atom doping Co(1 1 1) surface, and clearly expound the catalytic mechanisms through the density functional theory (DFT) calculation and micro-reaction kinetic model analysis. It is obtained that the favorable reaction pathway is COOCH3–COOCH3 coupling pathway over these four catalysts, while the rate-controlling step is COOCH3+CO+OCH3→2COOCH3 on Pd stripe doping Co(1 1 1) surface, which is different from the case (2COOCH3→DMO) on pure Pd(1 1 1), Pd monolayer supporting on Co(1 1 1) and Pd single atom doping Co(1 1 1) surface. This study can contribute a certain reference value for developing Pd-based catalysts with high efficiency and low Pd usage for CO oxidative coupling to DMO.

Molecule Saturation Boosts Acetylene Semihydrogenation Activity and Selectivity on a Core‐Shell Ruthenium@Palladium Catalyst

AbstractIncreasing selectivity without the expense of activity is desired but challenging in heterogeneous catalysis. By revealing the molecule saturation and adsorption sensitivity on overlayer thickness, strain, and coordination of Pd‐based catalysts from first‐principles calculations, we designed a stable Pd monolayer (ML) catalyst on a Ru terrace to boost both activity and selectivity of acetylene semihydrogenation. The least saturated molecule is most sensitive to the change in catalyst electronic and geometric properties. By simultaneously compressing the Pd ML and exposing the high coordination sites, the adsorption of more saturated ethylene is considerably weakened to facilitate the desorption for high selectivity. The even stronger weakening to the least saturated acetylene drives its hydrogenation such that it is more exothermic, thereby boosting the activity. Tailoring the molecule saturation and its sensitivity to structure and composition provides a tool for rational design of efficient catalysts.

Molecule Saturation Boosts Acetylene Semihydrogenation Activity and Selectivity on a Core-Shell Ruthenium@Palladium Catalyst.

Increasing selectivity without the expense of activity is desired but challenging in heterogeneous catalysis. By revealing the molecule saturation and adsorption sensitivity on overlayer thickness, strain, and coordination of Pd-based catalysts from first-principles calculations, we designed a stable Pd monolayer (ML) catalyst on a Ru terrace to boost both activity and selectivity of acetylene semihydrogenation. The least saturated molecule is most sensitive to the change in catalyst electronic and geometric properties. By simultaneously compressing the Pd ML and exposing the high coordination sites, the adsorption of more saturated ethylene is considerably weakened to facilitate the desorption for high selectivity. The even stronger weakening to the least saturated acetylene drives its hydrogenation such that it is more exothermic, thereby boosting the activity. Tailoring the molecule saturation and its sensitivity to structure and composition provides a tool for rational design of efficient catalysts.

Computational Screening of Two-Dimensional Metal-Organic Frameworks as Efficient Single-Atom Catalysts for Oxygen Reduction Reaction.

The development of efficient and inexpensive oxygen reduction reaction (ORR) catalysts is crucial for renewable energy technologies. Herein, using density functional theory (DFT) methods and microkinetic simulations, we systematically investigated the ORR catalytic performance of a series of 2D metal-organic frameworks M3 (HADQ)2 (HADQ=2,3,6,7,10,11-hexaamine dipyrazino quinoxaline). It shows that all 2D M3 (HADQ)2 (M=Cr, Mn, Fe, Co, Ni, Cu, Ru, Rh and Pd) monolayers are metallic, due to π-conjugated crystal orbitals centered on the central metals and ligand N atoms. The catalytic activity of M3 (HADQ)2 depends on the binding strength between ORR intermediates and metal species, and can be tuned via changing the central metals. Among these candidates, Rh3 (HADQ)2 and Co3 (HADQ)2 show superior ORR performance to Pt (111) with high half-wave potentials of 0.99 and 0.93 V, respectively. Moreover, the screened two catalysts have excellent intermediate-tolerance ability for dynamic coverage of oxygenated species on the active sites. Our work provides a new path towards developing efficient ORR electrocatalysts.

AuFe3@Pd/γ-Fe2O3 Nanosheets as an In Situ Regenerable and Highly Efficient Hydrogenation Catalyst

Heterogenous Pd catalysts play a pivotal role in the chemical industry; however, it is plagued by S2- or other strong adsorbates inducing surface poisoning long term. Herein, we report the development of AuFe3@Pd/γ-Fe2O3 nanosheets (NSs) as an in situ regenerable and highly active hydrogenation catalyst. Upon poisoning, the Pd monolayer sites could be fully and oxidatively regenerated under ambient conditions, which is initiated by •OH radicals from surface defect/FeTetra vacancy-rich γ-Fe2O3 NSs via the Fenton-like pathway. Both experimental and theoretical analyses demonstrate that for the electronic and geometric effect, the 2-3 nm AuFe3 intermetallic nanocluster core promotes the adsorption of reactant onto Pd sites; in addition, it lowers Pd's affinity for •OH radicals to enhance their stability during oxidative regeneration. When packed into a quartz sand fixed-bed catalyst column, the AuFe3@Pd/γ-Fe2O3 NSs are highly active in hydrogenating the carbon-halogen bond, which comprises a crucial step for the removal of micropollutants in drinking water and recovery of resources from heavily polluted wastewater, and withstand ten rounds of regeneration. By maximizing the use of ultrathin metal oxide NSs and intermetallic nanocluster and monolayer Pd, the current study demonstrates a comprehensive strategy for developing sustainable Pd catalysts for liquid catalysis.

Fabrication and catalytic performance of a new diaminopyridine Pd(II) monolayer supported on graphene oxide for catalyzing Suzuki coupling reaction

A new “Chanel like” diaminopyridine Pd(II) catalytic monolayer supported on Graphene Oxide (called GO@DAP-Pd) was prepared by self-assembly (SA) and characterized by XRD, Raman, FT-IR, SEM, TEM and XPS. Catalytic property of GO@DAP-Pd prepared use different Pd source in Suzuki coupling reaction was explored, in which the catalytic activity can be influenced with different palladium sources due to the different size of Pd nanoparticles formed. GO@DAP-Pd1 fabricated with (C6H5CN)2PdCl2 as Pd source, exhibited a higher catalytic activity and could be reused at least 7 times. The deactivation of catalyst was mainly due to the aggregation of active Pd and the loss of a small amount of active Pd, resulting in the deactivation of the catalyst. The catalytic mechanism was detail explored by hot filtration, poisoning experiments, XRD, Raman, XPS and React IR, and the results showed that catalytic process occurred at the interface, including substrates adsorption, intermediate formation and product desorption. The structure and synergy in active sites containing PdO(110), Pd(200, 111) and Pd(111)/PdO(002) are crucial to enhance the catalytic activity. The method to form the multi-active sites in situ on the surface of organometallic monolayer can supply an efficient way to design and prepare the high active catalytic monolayer.

Quadrupole topological insulators in Ta2M3Te5 (M = Ni, Pd) monolayers

Higher-order topological insulators have been introduced in the precursory Benalcazar-Bernevig-Hughes quadrupole model, but no electronic compound has been proposed to be a quadrupole topological insulator (QTI) yet. In this work, we predict that Ta2M3Te5 (M = Pd, Ni) monolayers can be 2D QTIs with second-order topology due to the double-band inversion. A time-reversal-invariant system with two mirror reflections (Mx and My) can be classified by Stiefel-Whitney numbers (w1, w2) due to the combined symmetry TC2z. Using the Wilson loop method, we compute w1 = 0 and w2 = 1 for Ta2Ni3Te5, indicating a QTI with qxy = e/2. Thus, gapped edge states and localized corner states are obtained. By analyzing atomic band representations, we demonstrate that its unconventional nature with an essential band representation at an empty site, i.e., Ag@4e, is due to the remarkable double-band inversion on Y–Γ. Then, we construct an eight-band quadrupole model with Mx and My successfully for electronic materials. These transition-metal compounds of A2M1,3X5 (A = Ta, Nb; M = Pd, Ni; X = Se, Te) family provide a good platform for realizing the QTI and exploring the interplay between topology and interactions.

Ultrasensitive Sub-monolayer Palladium Induced Chirality Switching and Topological Evolution of Skyrmions.

Chiral spin textures are fundamentally interesting, with promise for device applications. Stabilizing chirality is conventionally achieved by introducing Dzyaloshinskii-Moriya interaction (DMI) in asymmetric multilayers, where the thickness of each layer is at least a few monolayers. Here we report an ultrasensitive chirality switching in (Ni/Co)n multilayer induced by capping with only 0.22 monolayer of Pd. Using spin-polarized low-energy electron microscopy, we monitor the gradual evolution of domain walls from left-handed to right-handed Néel walls and quantify the DMI induced by the Pd capping layer. We also observe the chiral evolution of a skyrmion during the DMI switching, where no significant topological protection is found as the skyrmion winding number varies. This corresponds to a minimum energy cost of <1 attojoule during the skyrmion chirality switching. Our results demonstrate the detailed chirality evolution within skyrmions during the DMI sign switching, which is relevant to practical applications of skyrmionic devices.

(Invited) Pd Monolayer Catalyst As Transformative Concept for Electrolytic Hydrogen Isotope Separation

The effect of strain in Pd monolayer catalyst is explored for electrolytic hydrogen isotope separation. Positive/negative strain increases/decreases strength of adsorbed hydrogen bond in overpotential region where recombination of hydrogen atoms is the rate determining step in hydrogen evolution reaction. As a result, the increased/decreased hydrogen isotope separation efficiency of Pd monolayers is expected as compared to bulk Pd. The positive/negative strain rises/lowers diffusion barrier for adsorbed hydrogen atoms. This effect favors/retards recombination of isotopes with smaller mass. As the surface is stretched/compressed, the neighboring adsorption sites separate/approach each other which affects heavier hydrogen isotopes more/less and result in their lower/higher probability for recombination. All these fundamental consideration indicate that Pd monolayers with different level of strain should have much different separation factors than corresponding bulk electrodes. To study described effects, Pd monolayers we synthesized electrochemically on Au(111) and Ru(0001) electrodes each yielding qualitatively different strain levels (Au-positive, Ru-negative). The adsorption strength of hydrogen isotopes is studied by infra-red spectroscopy. These results are input in classical models for isotope separation[1] T calculations. The calculated ratio between the rates of hydrogen and deuterium recombination and separation factors for Pd monolayers and corresponding bulk electrodes are compared to experimentally measured ones. The following discussion focuses on understanding and quantification of strain effects on separation efficiency of Pd monolayers. [1] B. E. Conway, Proceedings of The Royal Society of London, A. Mathematical and Physical Sciences, 247, 400 (1958).

Which Is Better for Hydrogen Evolution on Metal@MoS2 Heterostructures from a Theoretical Perspective: Single Atom or Monolayer?

Single atom (SA)- and monolayer (ML)-supported catalysts are two main technical routines to increase electrochemical catalytic performance and reduce cost. To date, it is still a debate which one is better for catalysis in experiments as both routines face a puzzling problem of searching for balance between stability and catalytic activity. Here, hydrogen evolution on two-dimensional 2H-MoS2 with SA- and ML-adsorbed metal atoms (23 kinds in total) is taken as an example to solve this question by first-principles calculations. The thermodynamic stability during synthesis, in vacuum, and in electrochemical reaction conditions is determined to access the stability of MoS2 loaded with single (MS@MoS2) and monolayer metal atoms (MM@MoS2). The realistic catalytic surfaces determined by surface Pourbaix diagrams, the free energy changes of hydrogen atoms at different coverages, and the exchange current densities are applied to determine hydrogen evolution reaction (HER) activity. The results show that all MM@MoS2 are much more stable than the corresponding MS@MoS2 as the metal-metal interaction in MLs could make the former structures more stable. In general, MM@MoS2 show higher hydrogen evolution activities than those of MS@MoS2. In detail, the exchange current densities of MoS2 loaded by Pd ML and Au ML are 6.208, and 1.109 mA/cm-2, respectively, which are comparable to Pt(111). Combining with small binding energies, the Pd and Au MLs are the most promising catalysts for hydrogen evolution. The purpose of this work is to highlight the advantages and disadvantages of SA- and ML-supported surfaces as HER catalysts and provide a fundamental standard for studying them.

Pd Monolayer on the 3D-Hollow-Porous Au Microsphere as an Advanced Electrocatalyst for the Ethanol Oxidation Reaction

Pd is a highly active non-Pt anode in direct ethanol fuel cells, and its morphology and structural composition heavily influence its electrocatalytic efficiency. In this study, three-dimensional (3D)-hollow Au microspheres (HNPs-Au) as a support for the Pd monolayer (HNPs-Au@Pd) were synthesized using a simple template method and galvanic replacement reaction. The experimental results and theoretical calculations show that the presence of HNPs-Au enhances the catalytic activity of ethanol oxidation in alkaline media, improving the electroactivity of metallic Pd. Benefiting from the 3D-hollow-porous structure and the significant synergistic impact between Au and Pd (balancing the adsorption energy of the intermediate and reactant molecules), HNPs-Au@Pd achieves a 10.8-fold mass activity and a 3.3-fold enhancement of the specific activity for the ethanol oxidation reaction when compared to commercial Pd/C. The present work not only enriches the preparation strategy of porous metal materials but also opens up a sector for the construction of anodic electrocatalysts with a wide range of applications.

Pt- and Pd-modified transition metal nitride catalysts for the hydrogen evolution reaction.

Hydrogen production via electrochemical splitting of water using renewable electricity represents a promising strategy. Currently, platinum group metals (PGMs) are the best performing hydrogen evolution reaction (HER) catalysts. Thus, the design of non-PGM catalysts or low-loading PGM catalysts is essential for the commercial development of hydrogen generation technologies via electrochemical splitting of water. Here, we employed density functional theory (DFT) calculations to explore Pt and Pd modified transition metal nitrides (TMNs) as low-cost HER catalysts. Our calculations show that Pt/Pd binds strongly with TMs on TMN(111) surfaces, leading to the formation of stable Pt and Pd-monolayer (ML)-TMN(111) structures. Furthermore, our calculated hydrogen binding energy (HBE) demonstrates that Pt/MnN, Pt/TiN, Pt/FeN, Pt/VN, Pt/HfN, Pd/FeN, Pd/TaN, Pd/NbN, Pd/TiN, Pd/HfN, Pd/MnN, Pd/ScN, Pd/VN, and Pd/ZrN are promising candidates for the HER with a low value of limiting potential (UL) similar to that calculated on Pt(111).

Adsorption of CO and H2S on pristine and metal (Ni, Pd, Pt, Cu, Ag, and Au)-mediated SnS monolayers: a first-principles study.

A SnS monolayer is a new two-dimensional material with a black phosphorous structure, with high carrier mobility and a large surface-to-volume ratio, and is an ideal candidate material for gas sensors. The adsorption and sensing behaviors between the SnS monolayer and gas molecules are enhanced under the action of TM atoms with high catalytic performance. The adsorption behavior of CO and H2S on intrinsic and transition metal atom modified SnS monolayers is investigated based on the first principles calculations. The adsorption structure, adsorption energy, electron transfer, density of states, electron local density, work function, and desorption properties are discussed to evaluate the potential applications of SnS monolayers as scavengers and gas sensors for CO and H2S molecules. The results show that Ni, Pd, Pt and Cu atoms tend to be adsorbed on TH sites, while Ag and Au atoms are more easily captured by TS sites. Further studies have shown that all TM atoms can significantly enhance the sensing behavior between the SnS monolayer and the gas molecules. The adsorption performance of the CO molecule on the TM-mediated SnS (TM-SnS) monolayer is obviously better than that of the H2S molecule. Furthermore, the effects of electric field and biaxial strain on the sensing properties of gas molecules on Ni-SnS monolayers are also investigated. Finally, the desorption time of gas molecules from the TM-SnS monolayer is estimated. This will provide experimenters with theoretical guidance for the application of SnS-based sensing materials, and our work is of great significance for predicting new monochalcogenide sensing materials.

Magnetic properties of 3d, 4d, and 5d transition-metal atomic monolayers in Fe/TM/Fe sandwiches: Systematic first-principles study

Previous studies have accurately determined the effect of transition metal point defects on the properties of bcc iron. The magnetic properties of transition metal monolayers on the iron surfaces have been studied equally intensively. In this work, we investigated the magnetic properties of the 3d, 4d, and 5d transition-metal (TM) atomic monolayers in Fe/TM/Fe sandwiches using the full-potential local-orbital (FPLO) scheme of density functional theory. We prepared models of Fe/TM/Fe structures using the supercell method. We selected the total thickness of our system so that the Fe atomic layers furthest from the TM layer exhibit bulk iron-bcc properties. Along the direction perpendicular to the TM layer, we observe oscillations of spin and charge density. For Pt and W we obtained the largest values of perpendicular magnetocrystalline anisotropy and for Lu and Ir the largest values of in-plane magnetocrystalline anisotropy. All TM layers, except Co and Ni, reduce the total spin magnetic moment in the generated models, which is in good agreement with the Slater-Pauling curve. Density of states calculations showed that for Ag, Pd, Ir, and Au monolayers, a distinct van Hove singularity associated with TM/Fe interface can be observed at the Fermi level.

CO oxidative coupling to dimethyl oxalate over Pd monolayer supported on SiC substrate: insight into the effects of different exposed terminals

Developing supported Pd-based catalysts with the low Pd amount and excellent catalytic performance is essential for CO oxidative coupling to dimethyl oxalate (DMO), where elucidating the effects of different exposed terminals of substrate materials on catalytic performance is crucial to the design of supported catalysts. Herein, Pd monolayer was supported on SiC with different exposed terminals, constructing the models of PdML/SiC(111)-Si and PdML/SiC(111)-C terminal, which was used to investigate the effects of different exposed terminals of substrate materials on DMO synthesis from CO and OCH3. The density functional theory (DFT) calculations illustrated there existed no difference in the optimum path to generate DMO, which was COOCH3-COOCH3 coupling path on two catalysts. However, the rate control steps of the optimum path were different, with 2COOCH3 → DMO on the PdML/SiC(111)-Si terminal and COOCH3 + (CO + OCH3) → 2COOCH3 on the PdML/SiC(111)-C terminal. The micro-reaction kinetic model analysis further showed that the catalytic performance of PdML/SiC(111)-Si terminal was favorable than that of PdML/SiC(111)-C terminal, mainly attributing to that the difference in the exposed terminals of substrate materials led to the different electrons transfer directions of the Pd monolayer, then changed the adsorption energy of reactants (CO, OCH3) and key intermediates (COOCH3, OCCOOCH3), and further changed rate control step of the optimum path. This work offers the insights in rational design of supported Pd-based catalyst for heterogeneous catalytic reaction.