Wet-Chemical Synthesis of Concave Hexoctahedral Pd and Pd@Pt Nanocrystals for Methanol Electrooxidation.

Nanocrystals (NCs) exposed with high-index facets usually show enhanced electrocatalytic performances. However, it is a great challenge to persevere with high-index facets against their high surface energy during the synthesis. Herein, we successfully synthesize concave hexoctahedral (c-HOH) Pd NCs exposed with 48 high-index {741} facets using a facile one-pot wet-chemical protocol. Control experiments illustrate that l-ascorbic acid plays a critical role in the formation of the c-HOH morphology, acting as both reducing and capping agents. Moreover, we can extend the synthesis for fabricating c-HOH Pd@Pt core-shell NCs by simply introducing a Pt precursor into the reaction solution, attaining remarkably boosted electrocatalysis for methanol electrooxidation reaction (MOR). Integrating the merits of {741} facets, concave structure, and ligand and strain effect of the core-shell structure, c-HOH Pd4@Pt1 core-shell NCs showed an excellent MOR mass activity of 1.18 A mgPGM-1 or 3.60 A mgPt-1, which is 3.80 or 11.61 times higher than that of commercial Pt/C, respectively.

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.

Breaking Surface Atomic Monogeneity of Rh2 P Nanocatalysts by Defect-Derived Phosphorus Vacancies for Efficient Alkaline Hydrogen Oxidation.

Breaking atomic monogeneity of catalyst surfaces is promising for constructing synergistic active centers to cope with complex multi-step catalytic reactions. Here, we report a defect-derived strategy for creating surface phosphorous vacancies (P-vacancies) on nanometric Rh2 P electrocatalysts toward drastically boosted electrocatalysis for alkaline hydrogen oxidation reaction (HOR). This strategy disrupts the monogeneity and atomic regularity of the thermodynamically stable P-terminated surfaces. Density functional theory calculations initially verify that the competitive adsorption behavior of Had and OHad on perfect P-terminated Rh2 P{200} facets (p-Rh2 P) can be bypassed on defective Rh2 P{200} surfaces (d-Rh2 P). The P-vacancies enable the exposure of sub-surface Rh atoms to act as exclusive H adsorption sites. Therein, the Had cooperates with the OHad on the peripheral P-sites to effectively accelerate the alkaline HOR. Defective Rh2 P nanowires (d-Rh2 P NWs) and perfect Rh2 P nanocubes (p-Rh2 P NCs) are then elaborately synthesized to experimentally represent the d-Rh2 P and p-Rh2 P catalytic surfaces. As expected, the P-vacancy-enriched d-Rh2 P NWs catalyst exhibits extremely high catalytic activity and outstanding CO tolerance for alkaline HOR electrocatalysis, attaining 5.7 and 14.3 times mass activity that of p-Rh2 P NCs and commercial Pt/C, respectively. This work sheds light on breaking the surface atomic monogeneity for the development of efficient heterogeneous catalysts.

Two-dimensional template-directed synthesis of one-dimensional kink-rich Pd3Pb nanowires for efficient oxygen reduction.

Developing facile synthetic strategies toward ultrafine one-dimensional (1D) nanowires (NWs) with rich catalytic hot spots is pivotal for exploring effective heterogeneous catalysts. Herein, we demonstrate a two-dimensional (2D) template-directed strategy for synthesizing 1D kink-rich Pd3Pb NWs with abundant grain boundaries to serve as high-efficiency electrocatalysts toward oxygen reduction reaction (ORR). In this one-pot synthesis, ultrathin Pd nanosheets were initially generated, which then served as self-sacrificial 2D nano-templates. A dynamic equilibrium growth was subsequently established on the 2D Pd nanosheets through the center-selected etching of Pd atoms and edge-preferred co-deposition of Pd/Pb atoms. This was followed by the oriented attachment of the generated Pd/Pb alloy nanograins and fragments. Thus, kink-rich Pd3Pb NWs with rich grain boundary defects were obtained in high yield, and these NWs were used as electrocatalytic active catalysts. The surface electronic interaction between Pd and Pb atoms effectively decreased the surface d-band center to weaken the binding of oxygen-containing intermediates toward improved ORR kinetics. Specifically, the kink-rich Pd3Pb NWs/C catalyst delivered outstanding ORR mass activity and specific activity (2.26 A⋅mgPd-1 and 2.59 mA⋅cm-2, respectively) in an alkaline solution. These values were respectively 13.3 and 10.8 times those of state-of-the-art commercial Pt/C catalyst. This study provides an innovative strategy for fabricating defect-rich low-dimensional nanocatalysts for efficient energy conversion catalysis.

Equilibrated PtIr/IrOx Atomic Heterojunctions on Ultrafine 1D Nanowires Enable Superior Dual-Electrocatalysis for Overall Water Splitting.

Dual-active-sites atomically coupled on ultrafine 1D nanowires (NWs) can offer synergic atomic heterojunctions (AHJs) and high atomic-utilization toward multipurpose and superior catalysis. Here, ≈2-nm-thick PtIr/IrOx hybrid NWs are elaborately synthesized with equilibrated Pt/IrOx AHJs as high-efficiency bifunctional electrocatalysts for overall water splitting. Mechanism studies reveal the atomically coupled Pt-IrOx dual-sites are favorable for facilitating water dissociation, alleviating the binding of H* on Pt sites and inversely regulating the *OH adsorption and oxidation on bridge Ir-Ir sites. By simply equilibrating the Pt-IrOx ratio, the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) can be substantially accelerated. In particular, Pt-rich PtIr/IrOx -30 NWs attain 11-fold enhancements for HER compared to Pt/C in 1.0 m KOH, while IrOx -rich PtIr/IrOx -50 NWs express about five times mass activity referring to Ir/C for OER. Remarkably, the ratio-optimized PtIr/IrOx NWs electrode couple achieves a durably continuous H2 production under a substantially low cell voltage.

Concave nano-octahedral alloys: wet chemical synthesis of bimetallic Pt-Pd nanocrystals with high-index {hhl} Facets.

Concave morphologies provide noble metal nanocrystals (NCs) with unique performances due to large specific surface areas, high curves, hot spots, and elevated energy facets. As a result, concave morphologies have attracted considerable attention in many areas. However, most NCs with concave shapes are currently made of a single metal, leaving plenty of room for easy wet chemical synthesis and structural analysis of unique concave structures, especially bimetallic compounds. In this work, concave octahedral Pt-Pd alloy NCs with high-index {hhl} faces were synthesized using glycine as a coordination molecule and polyvinylpyrrolidone as the surfactant and reducing agent. The high-index facets coupled with the synergistic and electronic effects between Pt and Pd provided concave octahedral Pt-Pd alloy NCs with excellent activity and stability toward the electrooxidation of formic acid when compared to their convex counterparts and commercial Pt black.

Amplified Interfacial Effect in an Atomically Dispersed RuOx -on-Pd 2D Inverse Nanocatalyst for High-Performance Oxygen Reduction.

Atomically dispersed oxide-on-metal inverse nanocatalysts provide a blueprint to amplify the strong oxide-metal interactions for heterocatalysis but remain a grand challenge in fabrication. Here we report a 2D inverse nanocatalyst, RuOx -on-Pd nanosheets, by in situ creating atomically dispersed RuOx /Pd interfaces densely on ultrathin Pd nanosheets via a one-pot synthesis. The product displays unexpected performance toward the oxygen reduction reaction (ORR) in alkaline medium, which represents 8.0- and 22.4-fold enhancement in mass activity compared to the state-of-the-art Pt/C and Pd/C catalysts, respectively, showcasing an excellent Pt-alternative cathode electrocatalyst for fuel cells and metal-air batteries. Density functional theory calculations validate that the RuOx /Pd interface can accumulate partial charge from the 2D Pd host and subtly change the adsorption configuration of O2 to facilitate the O-O bond cleavage. Meanwhile, the d-band center of Pd nanosubstrates is effectively downshifted, realizing weakened oxygen binding strength.

Structure-intensified PtCoRh spiral nanowires as highly active and durable electrocatalysts for methanol oxidation.

Platinum (Pt)-based nanocatalysts with a high density of surface atomic steps hold great prospects in electrocatalysis. However, the structural instability under harsh redox conditions is still a rigorous challenge. Here, we demonstrate that ternary PtCoRh alloyed spiral nanowires (SNWs), which have the advantages of one-dimensional nanowires, alloy synergy, surface atomic steps, and anti-corrosive Rh incorporation, can serve as active and robust MOR electrocatalysts in acidic media. The results showed that the Pt77Co11Rh12 SNWs delivered the highest mass activity (1.48 A mg-1) and specific activity (4.76 mA cm-2), as well as the best durability in the long-term MOR test, compared with the Pt85Co10Rh5 and Pt85Co15 SNWs and Pt black. Further inspections of the morphology, composition, and electronic structure revealed that the incorporated Rh atoms not only stabilized the highly rugged SNWs and the easily leaching Co atoms but also delicately tuned the electron transfer among the three metallic elements, leading to the enhancement of MOR activity, structural stability and anti-CO-poisoning ability. Our work provides a rational strategy for the development of highly efficient and durable alcohol oxidation electrocatalysts.

Kinetically Manipulating the Nucleus Attachment to Create Atypical Defective Rh-Pt Alloyed Nanostructures as Active Electrocatalysts.

Defective metal nanostructures have attracted great attention due to the striking catalytic behavior of the defect sites. Atypical metal nanocrystals generated from attached nuclei can accommodate abundant grain boundaries (GBs) and twin boundaries (TBs). However, the understanding of their growth-mechanism and precisely synthetic control over such defective nanocrystals are still scarce. Herein, using the Rh-Pt nanoalloy as a model system, we systematically demonstrate that a prudent control of the reaction kinetics can manipulate the metal nucleation and nucleus attachment to create atypical nanocrystals, including small isolated nanoparticles (NPs), defect-rich wavy nanowires (WNWs), and {100} facet-bounded spliced nanocubes (SNCs). In the ethanol oxidation electrocatalysis, the Rh47 Pt53 WNWs featured with abundant TBs and GBs show the greatest mass activity (0.655 A ⋅ mg-1 Pt , 2.9 times to the commercial Pt/C) and durability. Our work captures the core of reaction kinetics on regulating the nucleus attachment and enables the rational control over the nanocrystal morphology and defect.

Edge Enrichment of Ultrathin 2D PdPtCu Trimetallic Nanostructures Effectuates Top-Ranked Ethanol Electrooxidation.

Atomic edge sites on two-dimensional (2D) nanomaterials display striking catalytic behavior, whereas edge engineering for 2D metal nanocatalysts remains an insurmountable challenge. Here we advance a one-pot synthesis of ultrathin 2D PdPtCu trimetallic nanosheets and nanorings with escalating low-coordinated edge proportions from 11.74% and 23.11% to 45.85% as cutting-edge ethanol oxidation reaction (EOR) electrocatalysts. This in situ edge enrichment hinges on a competitive surface capping and etching strategy with integrated manipulation of the reaction kinetics. Electrocatalysis tests demystify an edge-relied EOR performance, where the edge-richest 9.0 nm-Pd61Pt22Cu17 nanorings attain an exceptional activity (12.42 A mg-1Pt+Pd, 20.2 times that of commercial Pt/C) with substantially improved durability. Molecularly mechanistic studies certify that the unsaturated edge sites on these 2D catalysts prevail, triggering the C-C bond scission and succeeding CO removal to facilitate a 12-electron-transferring EOR process. This study introduces the "metal-edge-driven" concept and enables the "edge sites on 2D multimetallic nanocatalysts" technique to design versatile heterocatalysts.

One-pot synthesis of Pd@Pt3Ni core-shell nanobranches with ultrathin Pt3Ni{111} skins for efficient ethanol electrooxidation.

Coating an ultrathin platinum-rich skin on nanosubstrates made of other cheaper metals is an effective strategy for fabricating active electrocatalysts with low Pt-content. We developed a facile one-pot synthesis of Pd@Pt3Ni core-shell nanobranches with ultrathin Pt3Ni{111} skins that have active and durable catalytic performances for ethanol electrooxidation.

Shape-Controlled Synthesis of Colloidal Metal Nanocrystals by Replicating the Surface Atomic Structure on the Seed.

Controlling the surface structure of metal nanocrystals while maximizing the utilization efficiency of the atoms is a subject of great importance. An emerging strategy that has captured the attention of many research groups involves the conformal deposition of one metal as an ultrathin shell (typically 1-6 atomic layers) onto the surface of a seed made of another metal and covered by a set of well-defined facets. This approach forces the deposited metal to faithfully replicate the surface atomic structure of the seed while at the same time serving to minimize the usage of the deposited metal. Here, the recent progress in this area is discussed and analyzed by focusing on the synthetic and mechanistic requisites necessary for achieving surface atomic replication of precious metals. Other related methods are discussed, including the one-pot synthesis, electrochemical deposition, and skin-layer formation through thermal annealing. To close, some of the synergies that arise when the thickness of the deposited shell is decreased controllably down to a few atomic layers are highlighted, along with how the control of thickness can be used to uncover the optimal physicochemical properties necessary for boosting the performance toward a range of catalytic reactions.

Ligand-Assisted, One-Pot Synthesis of Rh-on-Cu Nanoscale Sea Urchins with High-Density Interfaces for Boosting CO Oxidation.

Predictable synthesis of bimetallic nanocrystals with spatially controlled metal distributions offers a versatile route to the development of highly efficient nanocatalysts. Here we report a one-pot synthesis of super branched Rh-on-Cu nanoscale sea urchins (Rh-Cu NSUrs) with a high density of Cu-Rh interfaces by manipulating the ligand coordination chemistry. Structural analysis and UV-vis spectra reveal that ascorbic acid can serve as a Rh-selective coordination ligand in the nonaqueous synthesis to reverse the reduction potentials of Rh3+ and Cu2+ cations. The sequential reduction of Cu2+ and then Rh3+ cations, as well as the island epitaxial growth of Rh atoms on Cu cores, leads to the formation of Rh-on-Cu nanostructures mimicking sea urchin. The size of the Cu cores and the density of Rh branches can both be facilely regulated by tuning the mole ratio of Cu to Rh. The Cu-Rh NSUrs show enhanced activity and stability in catalyzing CO oxidation, as the intrinsic Cu-Rh interfaces can act as catalytic hot spots through a bifunctional mechanism. The Cu-Rh two-component system can separate the adsorption and activation of CO and O2 on the Rh and Cu surfaces, respectively, accelerating the generation of CO2 at the interfaces.

Well-faceted noble-metal nanocrystals with nonconvex polyhedral shapes.

Precise engineering of noble-metal nanocrystals (NCs) is not only an important fundamental research topic, but also has great realistic significance in improving their performances required by the poor reserve and high cost of noble metals. Well-faceted noble-metal NCs with nonconvex polyhedral shapes could be promising candidates to optimize their performance and thus minimize their usage, as they may integrate a well-defined surface structure and a large surface area together, enabling them to have outstanding performance and high efficiency of atomic utilization. Moreover, undesirable aggregation and ripening phenomena could be avoided. This review provides a comprehensive summary of the unique characteristics and corresponding models of well-faceted nonconvex polyhedral noble-metal NCs by classifying the cases into four distinct types, namely the concave polyhedral structure, excavated polyhedral structure, branched structure and nanocage structure, respectively. Due to the complexity of nonconvex morphologies and the thermodynamic antipathy for the growth of nonconvex shaped NCs, we firstly demonstrate the structure characterization and synthetic methodology in detail. Subsequently, typical applications in electrocatalysis and plasmonic fields are presented to demonstrate the unique surface and morphological effects generated from the well-faceted nonconvex NCs. To promote further development in this field, the perspectives and challenges concerning well-faceted noble-metal NCs with nonconvex shapes are put forward in the end.

Rational design and synthesis of excavated trioctahedral Au nanocrystals.

Excavated polyhedral nanostructures, possessing the features of high surface area and well-defined surface structure with a specific crystal facet and avoidance of aggregation, could be one of the best choices for the purpose of reducing consumption and improving performance of noble metals in many application fields. However, the formation of the excavated structures is thermodynamically unfavourable and its rational synthesis is far beyond our knowledge. In this work, taking overgrowth of Pd onto trioctahedral Au nanocrystals as a model, we present a deep insight study for synthesizing an excavated structure relying on the protection role of surfactants under suitable crystal growth kinetics. Based on the abovementioned understanding, we designed a simple and effective strategy to synthesize Au nanocrystals with excavated trioctahedral structure in one step. Due to the novel feature of the excavated structure and exposed high energy {110} facets, excavated trioctahedral Au NCs exhibited optical extinction at the near-infrared region and showed high catalytic activity towards the reduction of p-nitrophenol. Moreover, the synthetic strategy can be extended to the synthesis of excavated Au-Pd alloys.

Atomic layer-by-layer deposition of platinum on palladium octahedra for enhanced catalysts toward the oxygen reduction reaction.

We systematically evaluated two different approaches to the syntheses of Pd@PtnL (n = 2-5) core-shell octahedra. We initially prepared the core-shell octahedra using a polyol-based route by titrating a Pt(IV) precursor into the growth solution containing Pd octahedral seeds at 200 °C through the use of a syringe pump. The number of Pt atomic layers could be precisely controlled from two to five by increasing the volume of the precursor solution while fixing the amount of seeds. We then demonstrated the synthesis of Pd@PtnL octahedra using a water-based route at 95 °C through the one-shot injection of a Pt(II) precursor. Due to the large difference in reaction temperature, the Pd@PtnL octahedra obtained via the water-based route showed sharper corners than their counterparts obtained through the polyol-based route. When compared to a commercial Pt/C catalyst based upon 3.2 nm Pt particles, the Pd@PtnL octahedra prepared using both methods showed similar remarkable enhancement in terms of activity (both specific and mass) and durability toward the oxygen reduction reaction. Calculations based upon periodic, self-consistent density functional theory suggested that the enhancement in specific activity for the Pd@PtnL octahedra could be attributed to the destabilization of OH on their PtnL*/Pd(111) surface relative to the {111} and {100} facets exposed on the surface of Pt/C. The destabilization of OH facilitates its hydrogenation, which was found to be the rate-limiting step of the oxygen reduction reaction on all these surfaces.

Atomic layer-by-layer deposition of Pt on Pd nanocubes for catalysts with enhanced activity and durability toward oxygen reduction.

An effective strategy for reducing the Pt content while retaining the activity of a Pt-based catalyst is to deposit the Pt atoms as ultrathin skins of only a few atomic layers thick on nanoscale substrates made of another metal. During deposition, however, the Pt atoms often take an island growth mode because of a strong bonding between Pt atoms. Here we report a versatile route to the conformal deposition of Pt as uniform, ultrathin shells on Pd nanocubes in a solution phase. The introduction of the Pt precursor at a relatively slow rate and high temperature allowed the deposited Pt atoms to spread across the entire surface of a Pd nanocube to generate a uniform shell. The thickness of the Pt shell could be controlled from one to six atomic layers by varying the amount of Pt precursor added into the system. Compared to a commercial Pt/C catalyst, the Pd@PtnL (n = 1-6) core-shell nanocubes showed enhancements in specific activity and durability toward the oxygen reduction reaction (ORR). Density functional theory (DFT) calculations on model (100) surfaces suggest that the enhancement in specific activity can be attributed to the weakening of OH binding through ligand and strain effects, which, in turn, increases the rate of OH hydrogenation. A volcano-type relationship between the ORR specific activity and the number of Pt atomic layers was derived, in good agreement with the experimental results. Both theoretical and experimental studies indicate that the ORR specific activity was maximized for the catalysts based on Pd@Pt2-3L nanocubes. Because of the reduction in Pt content used and the enhancement in specific activity, the Pd@Pt1L nanocubes showed a Pt mass activity with almost three-fold enhancement relative to the Pt/C catalyst.

Controlling the size and composition of nanosized Pt-Ni octahedra to optimize their catalytic activities toward the oxygen reduction reaction.

Electrocatalysts based on Pt-Ni alloys have received considerable interest in recent years owing to their remarkable activities toward the oxygen reduction reaction (ORR). Here, we report the synthesis of nanosized Pt-Ni octahedra with a range of controlled sizes and compositions in an effort to optimize their ORR activities. If we employed benzyl ether as a solvent for the synthesis, we could readily control the edge lengths of the Pt-Ni octahedra in the range of 6-12 nm and keep the Pt/Ni atomic ratio at around 2.4 by varying the amount of oleylamine added into the reaction system. If we adjusted the amount of Ni precursor, the atomic ratio of Pt to Ni in the Pt-Ni octahedra could be controlled in the range of 1.4-3.7 and their edge lengths were kept at 9 nm. For the catalysts with a Pt/Ni atomic ratio around 2.4, their specific ORR activities (per unit surface area) increased monotonically as the edge length increased from 6 to 12 nm. However, the mass activities (per unit mass of Pt) of these Pt-Ni octahedra showed a maximum value at an edge length of 9 nm. The specific and mass activities for the Pt-Ni octahedra with an edge length of 9 nm but different compositions both showed peak values at a Pt/Ni atomic ratio of 2.4.

Organic-inorganic interface-induced multi-fluorescence of MgO nanocrystal clusters and their applications in cellular imaging.

Surface functionalization of inorganic nanomaterials through chemical binding of organic ligands on the surface unsaturated atoms, forming unique organic-inorganic interfaces, is a powerful approach for creating special functions for inorganic nanomaterials. Herein, we report the synthesis of hierarchical MgO nanocrystal clusters (NCs) with an organic-inorganic interface induced multi-fluorescence and their application as new alternative labels for cellular imaging. The synthetic method was established by a dissolution and regrowth process with the assistance of carboxylic acid, in which the as-prepared MgO NCs were modified with carboxylic groups at the coordinatively unsaturated atoms of the surface. By introducing acetic acid to partially replace oleic acid in the reaction, the optical absorption of the produced MgO NCs was progressively engineered from the UV to the visible region. Importantly, with wider and continuous absorption profile, those MgO NCs presented bright and tunable multicolor emissions from blue-violet to green and yellow, with the highest absolute quantum yield up to (33±1) %. The overlap for the energy levels of the inorganic-organic interface and low-coordinated states stimulated a unique fluorescence resonance energy transfer phenomenon. Considering the potential application in cellular imaging, such multi-fluorescent MgO NCs were further encapsulated with a silica shell to improve the water solubility and stability. As expected, the as-formed MgO@SiO2 NCs possessed great biocompatibility and high performance in cellular imaging.

Enhanced shape stability of Pd-Rh core-frame nanocubes at elevated temperature: in situ heating transmission electron microscopy.

Shape stability of Pd-Rh core-frame nanocubes was studied by in situ heating transmission electron microscopy. Pd-Rh nanocubes could maintain cubic shape at elevated temperature compared with pure Pd. The surface diffusion process of Rh onto {100} side surfaces is believed to postpone the degradation to higher temperature.