CoPt纳米空心球甲醇电催化氧化和原位电化学傅里叶变换红外光谱研究

采用化学还原和电位置换法制备了CoPt 纳米空心球, 该催化剂对甲醇氧化表现出较好的电催化活性.透射电镜(TEM)、能量散射光谱(EDS)和电化学循环伏安实验结果表明, 在0.1 mol·L^-1 H₂SO₄+0.1 mol·L^-1CH₃OH中进行测试时, CoPt 纳米空心球发生了去合金化过程, 催化剂表面Co元素溶解, 形成了富Pt 表面, 表现出更好的电催化活性, 同时表现出较好的结构稳定性. 采用原位电化学红外光谱在分子水平研究了CoPt 纳米空心球上甲醇氧化过程, 发现甲醇在CoPt 纳米空心球氧化中间产物主要为CO, 且CO表现出异常红外效应, 与CO为探针分子在CoPt纳米空心球上得到的红外光谱结果一致. 研究结果表明, 去合金化方法是一种有效调节催化剂表面组成和性能的手段, 原位电化学红外光谱是潜在的原位研究有机小分子氧化机理的方法, 在燃料电池中将得到广泛的应用.     

Characterization of superparamagnetic "core-shell" nanoparticles and monitoring their anisotropic phase transition to ferromagnetic "solid solution" nanoalloys

The structure, magnetism, and phase transition of core-shell type CoPt nanoparticles en route to solid solution alloy nanostructures are systematically investigated. The characterization of Co(core)Pt(shell) nanoparticles obtained by a "redox transmetalation" process by transmission electron microscopy (TEM) and, in particular, X-ray absorption spectroscopy (XAS) provides clear evidence for the existence of a core-shell type bimetallic interfacial structure. Nanoscale phase transitions of the Co(core)Pt(shell) structures toward c-axis compressed face-centered tetragonal (fct) solid solution alloy CoPt nanoparticles are monitored at various stages of a thermally induced annealing process and the obtained fct nanoalloys show a large enhancement of their magnetic properties with ferromagnetism. The relationship between the nanostructures and their magnetic properties is in part elucidated through the use of XAS as a critical analytical tool.     

Electroplating of metal nanotubes and nanowires in a high aspect-ratio nanotemplate

Ordered metal (Co, Pt, and CoPt alloy) nanotube and nanowire structures were fabricated by a simple electroplating method in high aspect-ratio anodic aluminum oxide (AAO) membrane. The growth rate in pulse mode is always larger than that in constant-current mode, which represents that diffusion limitation exists in this electroplating condition. It is also found that the sputtered Au layer structure could influence the electroplating. Traditional nanowires could be fabricated in the template with a uniform Au layer as conducting contact. In case of unblocked AAO membrane, metal electroplating begins from the Au particles which were attached inside the holes during the sputtering step and produces metal nanotubes. Pt and CoPt nanotubes could be easily prepared by this method and might be applied as catalyst and magnetic material.     

CoPt nanoparticles and their catalytic properties in electrooxidation of CO and CH(3)OH studied by in situ FTIRS

CoPt nanoparticles supported on a glassy carbon electrode (denoted as CoPt/GC) were prepared by galvanic replacement reaction between electrodeposited Co nanoparticles and K(2)PtCl(6) solution. Scanning electron microscope (SEM) and transmission electron microscope (TEM) were both employed to characterize the CoPt nanoparticles. It was shown that the CoPt nanoparticles have irregular shapes and most of them exhibit a core-shell structure with a porous Co core and a shell of Pt tiny particles. The composition of the CoPt nanoparticles was analyzed by energy-dispersive X-ray spectroscopy (EDX), which depicts a Co : Pt ratio of ca. 21 : 79. Studies of cyclic voltammetry (CV) demonstrated that CoPt/GC possesses a much higher catalytic activity towards CO and methanol electrooxidation than a nanoscale Pt thin film electrode. In situ FTIR spectroscopic studies have revealed for the first time, that a CoPt nanoparticles electrode exhibits abnormal IR effects (AIREs) for IR absorption of CO adsorbed on it. In comparison with the IR features of CO adsorbed on a bulk Pt electrode, the direction of the IR bands of CO adsorbed on the CoPt/GC electrode is inverted completely, and the intensity of the IR bands has been enhanced up to 15.4 times. The AIREs is significant in detecting the adsorbed intermediate species involved in electrocatalytic reactions. The results demonstrated a reaction mechanism of CH(3)OH oxidation on CoPt/GC in alkaline solutions through evidencing CO(L), CO(M), HCOO(-), CO(3)(2-), HCO(3)(-) and CO(2) as intermediate and product species by in situ FTIRS.     

氢原子在Pt及Pt系双金属催化表面吸附的密度泛函理论研究

采用密度泛函理论(dFT)考察了Pt(100)、(110)、(111)三种表面氢原子的吸附行为, 计算了覆盖度为0.25 ML时氢原子在Pt 三种表面和M-Pt(111)双金属(M=Al, Fe, Co, Ni, Cu, Pd)上的最稳定吸附位、表面能以及吸附前后金属表面原子层间弛豫情况. 分析了氢原子在不同双金属表面吸附前后的局域态密度变化以及双金属表面d 带中心偏离费米能级的程度并与氢吸附能进行了关联. 计算结果表明, 在Pt(100), Pt(110)和Pt(111)表面, 氢原子的稳定吸附位分别为桥位、短桥位和fcc 穴位. 三种表面中以Pt(111)的表面能最低, 结构最稳定. 氢原子在不同M-Pt(111)双金属表面上的最稳定吸附位均为fcc 穴位, 其中在Ni-Pt 双金属表面的吸附能最低, Co-Pt 次之. 表明氢原子在Ni-Pt 和Co-Pt 双金属表面的吸附最稳定. 通过对氢原子在M-Pt(111)双金属表面吸附前后的局域态密度变化的分析, 验证了氢原子吸附能计算结果的准确性. 掺杂金属Ni、Co、Fe 的3d-Pt(111)双金属表面在吸附氢原子后发生弛豫, 第一层和第二层金属原子均不同程度地向外膨胀. 此外, 3d金属的掺入使得其对应的M-Pt(111)双金属表面d带中心与Pt 相比更靠近费米能级, 吸附氢原子能力增强, 表明3d-Pt系双金属表面有可能比Pt具有更好的脱氢活性.     

Study of nucleation and growth in the organometallic synthesis of magnetic alloy nanocrystals: the role of nucleation rate in size control of CoPt3 nanocrystals

High quality CoPt(3) nanocrystals were synthesized via simultaneous reduction of platinum acetylacetonate and thermodecomposition of cobalt carbonyl in the presence of 1-adamantanecarboxylic acid and hexadecylamine as stabilizing agents. The high flexibility and reproducibility of the synthesis allows us to consider CoPt(3) nanocrystals as a model system for the hot organometallic synthesis of metal nanoparticles. Different experimental conditions (reaction temperature, concentration of stabilizing agents, ratio between cobalt and platinum precursors, etc.) have been investigated to reveal the processes governing the formation of the metal alloy nanocrystals. It was found that CoPt(3) nanocrystals nucleate and grow up to their final size at an early stage of the synthesis with no Ostwald ripening observed upon further heating. In this case, the nanocrystal size can be controlled only via proper balance between the rates for nucleation and for growth from the molecular precursors. Thus, the size of CoPt(3) nanocrystals can be precisely tuned from approximately 3 nm up to approximately 18 nm in a predictable and reproducible way. The mechanism of homogeneous nucleation, evolution of the nanocrystal ensemble in the absence of Ostwald ripening, nanocrystal faceting, and size-dependent magnetic properties are investigated and discussed on the example of CoPt(3) magnetic alloy nanocrystals. The developed approach was found to be applicable to other systems, e.g., FePt and CoPd(2) magnetic alloy nanocrystals.     

A general method for the rapid synthesis of hollow metallic or bimetallic nanoelectrocatalysts with urchinlike morphology

We have reported a facile and general method for the rapid synthesis of hollow nanostructures with urchinlike morphology. In-situ produced Ag nanoparticles can be used as sacrificial templates to rapidly synthesize diverse hollow urchinlike metallic or bimetallic (such as Au/Pt) nanostructures. It has been found that heating the solution at 100 degrees C during the galvanic replacement is very necessary for obtaining urchinlike nanostructures. Through changing the molar ratios of Ag to Pt, the wall thickness of hollow nanospheres can be easily controlled; through changing the diameter of Ag nanoparticles, the size of cavity of hollow nanospheres can be facilely controlled; through changing the morphologies of Ag nanostructures from nanoparticle to nanowire, hollow Pt nanotubes can be easily designed. This one-pot approach can be extended to synthesize other hollow nanospheres such as Pd, Pd/Pt, Au/Pd, and Au/Pt. The features of this technique are that it is facile, quick, economical, and versatile. Most importantly, the hollow bimetallic nanospheres (Au/Pt and Pd/Pt) obtained here exhibit an area of greater electrochemical activity than other Pt hollow or solid nanospheres. In addition, the approximately 6 nm hollow urchinlike Pt nanospheres can achieve a potential of up to 0.57 V for oxygen reduction, which is about 200 mV more positive than that obtained by using a approximately 6 nm Pt nanoparticle modified glassy carbon (GC) electrode. Rotating ring-disk electrode (RRDE) voltammetry demonstrates that approximately 6 nm hollow Pt nanospheres can catalyze an almost four-electron reduction of O(2) to H(2)O in air-saturated H(2)SO(4) (0.5 M). Finally, compared to the approximately 6 nm Pt nanoparticle catalyst, the approximately 6 nm hollow urchinlike Pt nanosphere catalyst exhibits a superior electrocatalytic activity toward the methanol oxidation reaction at the same Pt loadings.     

Co-Pt alloy nanoparticles produced using a template of nanoparticle array

A monolayer of Co-Pt alloy nanoparticles in the nanometer-size regime was fabricated using a nanotemplate approach. 1.7-nm-thick Co46Pt54 film was deposited onto a preexisting array of Ni seed particles embedded in a polyimide film. During subsequent annealing, the deposited Co46Pt54 film coalesced onto the seed particles to produce a monolayer of Co-Pt alloy particles. Deposition and annealing were repeated to increase both average particle size and volume fraction of the alloy particles. It was also shown that the annealing temperature was critical in controlling the particle size distribution and the final composition of the nanoparticles. This method of forming a single layer of vertically aligned nanoparticles can be easily extended to a large area as well as to produce a different combination of alloy particles on a polymer film.     

Synthesis of "solid solution" and "core-shell" type cobalt--platinum magnetic nanoparticles via transmetalation reactions

In this article, we report the synthesis of "solid solution" and "core-shell" types of well-defined Co--Pt nanoalloys smaller than 10 nm. The formation of these alloys is driven by redox transmetalation reactions between the reagents without the need for any additional reductants. Also the reaction proceeds selectively as long as the redox potential between the two metals is favorable. The reaction between Co(2)(CO)(8) and Pt(hfac)(2) (hfac = hexafluoroacetylacetonate) results in the formation of "solid solution" type alloys such as CoPt(3) nanoparticles. On the other hand, the reaction of Co nanoparticles with Pt(hfac)(2) in solution results in "Co(core)Pt(shell)" type nanoalloys. Nanoparticles synthesized by both reactions are moderately monodispersed (sigma < 10%) without any further size selection processes. The composition of the alloys can also be tuned by adjusting the ratio of reactants. The magnetic and structural properties of the obtained nanoparticles and reaction byproducts are characterized by TEM, SQUID, UV/vis, IR, EDAX, and XRD.     

Dissolution of oxygen reduction electrocatalysts in an acidic environment: density functional theory study

Density functional theory is employed to determine the reaction thermodynamics of a group of chemical and electrochemical reactions chosen to investigate the dissolution of metal atoms from oxygen reduction reaction catalysts in an acid medium. Once a set of thermodynamically allowed reactions is established, those reactions are selected to investigate the relative stabilities of Pt atoms and of other transition metal atoms (Ir, Pd, Rh, Ni, and Co) toward the dissolution reactions. The dissolution reactions that are found thermodynamically favorable are electrochemical and involve adsorbed oxygenated compounds that are intermediate species of the oxygen reduction reaction. Iridium is found to be the most stable among the various pure metals in comparison to Pt. Most of the metals alloyed with Pt cause a decrease of the Pt stability against dissolution, except for Ni, which does not affect it. On the other hand, the influence of Pt on the stability of the second metal in the alloy follows the same trend as in pure metal catalysts, with Ir being the most stable. When both atoms in a PtM alloy are involved in dissolution reactions, alloyed Ir is also found more stable than Pt in a given dissolution reaction, and the same behavior is found in alloyed Co for most of the reactions studied.     

钴铂合金薄膜的循环伏安电沉积及其异常红外性能研究

运用循环伏安电沉积在玻碳基底上制得纳米结构钴铂合金薄膜,扫描电子显微镜和X-射线能量散射谱研究表明,钴铂薄膜主要由平均粒经为139 nm的纳米粒子组成,钴和铂的原子比为3:5. 以CO为探针分子,电化学原位FTIR反射光谱研究发现钴铂薄膜具有异常红外效应. 吸附态CO发生异常红外吸收,谱峰比本体钴和铂分别增强了34和43倍.     

Magnetic properties of nanocrystalline CoPt electrodeposited films. Influence of P incorporation

Platinum-rich CoPt films have been electrodeposited with the aim of preparing hard magnetic films on silicon-based substrates without the need for subsequent annealing. Electrodeposition conditions have permitted the crystalline structure of the films to be controlled. Pt percentages of up to 60–65 wt.% have been attained while maintaining the hexagonal Co phase, leading to CoPt films with moderate coercivity and good corrosion resistance. However, when low deposition potentials were used, CoPt films with higher Pt percentages were obtained, but in this case, the films exhibited an fcc structure, having lower coercivity and less corrosion resistance. The presence of hypophosphite in the solution limited the platinum percentage in the deposited CoPtP films, but an hexagonal close-packed (hcp) structure was always observed in this case. The incorporation of P into the deposits led to increases in both the coercivity of the films and the corrosion resistance of the coatings, with respect to pure CoPt. The highest coercivity was obtained for hcp CoPtP deposits with 40 wt.% of Pt.     

片状碳载金属纳米颗粒复合物的制备及其氧还原电活性

将双氰胺、蔗糖与酞菁铁(钴)的混合物通过简单热解法,制备出Co/C-N、Fe/C-N和Fe-Co/C-N纳米复合物。随后利用热还原法,将少量铂沉积于Co/C-N上得到片状碳负载的Co-Pt纳米颗粒Co-Pt/C-N。对样品进行了详细表征,并研究了其在全域pH范围内(酸性、中性与碱性溶液)中的氧还原反应(ORR)活性。结果表明,Co/C-N具有比Fe/C-N和Fe-Co/C-N更高的ORR起始电位和半波电位,并且在碱性和中性溶液中,Co/C-N表现出比Pt/C更强的ORR电活性;在酸性溶液中,铂负载量(质量分数)8.1%的Co-Pt/C-N表现出与Pt/C相近的ORR起始与半波电位。催化剂优异的电活性主要归因于片状碳形成的三维结构、金属纳米颗粒的均匀分布以及丰富的吡啶氮。     

Synthesis of Hollow Platinum–Palladium Nanospheres with a Dendritic Shell as Efficient Electrocatalysts for Methanol Oxidation

Engineering the size, composition, and morphology of platinum‐based nanomaterials can provide a great opportunity to improve the utilization efficiency of electrocatalysts and reinforce their electrochemical performances. Herein, three‐dimensional platinum–palladium hollow nanospheres with a dendritic shell (PtPd‐HNSs) are successfully fabricated through a facile and economic route, during which SiO₂ microspheres act as the hard template for the globular cavity, whereas the triblock copolymer F127 contributes to the formation of the dendritic shell. In contrast with platinum hollow nanospheres (Pt‐HNSs) and commercial platinum on carbon (Pt/C) catalyst, the novel architecture shows a remarkable activity and durability toward the methanol oxidation reaction (MOR) owing to the coupled merits of bimetallic nanodendrites and a hollow interior. As a proof of concept, this strategy is also extended to trimetallic gold–palladium–platinum hollow nanospheres (AuPdPt‐HNSs), which paves the way towards the controlled synthesis of other bi‐ or multimetallic platinum‐based hollow electrocatalysts.     

Fabrication of Efficient Hydrogenation Nanoreactors by Modifying the Freedom of Ultrasmall Platinum Nanoparticles within Yolk–Shell Nanospheres

The synthesis of silica‐based yolk–shell nanospheres confined with ultrasmall platinum nanoparticles (Pt NPs) stabilized with poly(amidoamine), in which the interaction strength between Pt NPs and the support could be facilely tuned, is reported. By ingenious utilization of silica cores with different surface wettability (hydrophilic vs. ‐phobic) as the adsorbent, Pt NPs could be confined in different locations of the yolk–shell nanoreactor (core vs. hollow shell), and thus, exhibit different interaction strengths with the nanoreactor (strong vs. weak). It is interesting to find that the adsorbed Pt NPs are released from the core to the hollow interiors of the yolk–shell nanospheres when a superhydrophobic inner core material (SiO₂?Ph) is employed, which results in the preparation of an immobilized catalyst (Pt@SiO₂?Ph); this possesses the weakest interaction strength with the support and shows the highest catalytic activity (88 500 and 7080 h^?1 for the hydrogenation of cyclohexene and nitrobenzene, respectively), due to its unaffected freedom of Pt NPs for retention of the intrinsic properties.     

High temperature selective growth of single-walled carbon nanotubes with a narrow chirality distribution from a CoPt bimetallic catalyst

Chirality-controlled synthesis of single-walled carbon nanotubes (SWCNTs) is a prerequisite for their practical applications in electronic and optoelectronic devices. We report here a novel bimetallic CoPt catalyst for the selective growth of high quality SWCNTs with a narrow chirality distribution at relatively high temperatures of 800 °C and 850 °C using atmospheric pressure alcohol chemical vapor deposition. The addition of Pt into a Co catalyst forms a CoPt alloy and significantly reduces the diameters of the as-grown SWCNTs and narrows their chirality distributions.     

Gold hollow nanospheres: tunable surface plasmon resonance controlled by interior-cavity sizes

Uniform gold hollow nanospheres with tunable interior-cavity sizes were fabricated by using Co nanoparticles as sacrificial templates and varying the stoichiometric ratio of starting material HAuCl4 over the reductants. The formation of these hollow nanostructures is attributed to two subsequent reduction reactions: the initial reduction of HAuCl4 by Co nanoparticles, followed by the reduction by NaBH4. In addition, a thick layer of silica was successfully coated onto the gold hollow nanospheres. These nanostructures are extensively characterized by TEM, XRD, HRTEM, SEM, electron diffraction, energy-dispersive X-ray analysis, and UV-visible absorption spectroscopy. It is evident that the SPR peak locations corresponding to these hollow nanospheres are shifted over a region of more than 100 nm wavelength due to changes of shell thickness, which make these optically active nanostructures of great interest in both fundamental research and practical applications.     

A novel amperometric biosensor based on NiO hollow nanospheres for biosensing glucose

NiO hollow nanospheres were synthesized by controlled precipitation of metal ions with urea using carbon microspheres as templates, which were for the first time adopted to construct a novel amperometric glucose biosensor. Glucose oxidase was immobilized on the surface of hollow nanospheres through chitosan-assisted cross-linking technique. Due to the high specific active sites and high electrocatalytic activity of NiO hollow nanospheres, the constructed glucose biosensors exhibited a high sensitivity of 3.43 μA/mM. The low detection limit was estimated to be 47 μM (S/N = 3), and the Michaelis-Menten constant was found to be 7.76 mM, indicating the high affinity of enzyme on NiO hollow nanospheres to glucose. These results show that the NiO hollow nanospheres are a promising material to construct enzyme biosensors.     

Synthesis of hollow CaCO3 nanospheres templated by micelles of poly(styrene-b-acrylic acid-b-ethylene glycol) in aqueous solutions

An asymmetric triblock copolymer, poly(styrene-b-acrylic acid-b-ethylene glycol) (PS-b-PAA-b-PEG), was synthesized via reversible addition-fragmentation chain transfer controlled radical polymerization. Micelles of PS-b-PAA-b-PEG with PS core, PAA shell, and PEG corona were then prepared in aqueous solutions, followed by extensive characterization based on dynamic light scattering, zeta-potential, and transmission electron microscopy (TEM) measurements. The well-characterized micelles were used to fabricate hollow nanospheres of CaCO(3) as a template. It was elucidated from TEM measurements that the hollow nanospheres have a uniform size with cavity diameters of ca. 20 nm. The X-ray diffraction analysis revealed a high purity and crystallinity of the hollow nanospheres. The hollow CaCO(3) nanospheres thus obtained have been used for the controlled release of an anti-inflammatory drug, naproxen. The significance of this study is that we have overcome a previous difficulty in the synthesis of hollow CaCO(3) nanospheres. After mixing of Ca(2+) and CO(3)(2-) ions, the growth of CaCO(3) is generally quite rapid to induce large crystal, which prevented us from obtaining hollow CaCO(3) nanospheres with controlled structure. However, we could solve this issue by using micelles of PS-b-PAA-b-PEG as a template. The PS core acts as a template that can be removed to form a cavity of hollow CaCO(3) nanospheres, the PAA shell is beneficial for arresting Ca(2+) ions to produce CaCO(3), and the PEG corona stabilizes the CaCO(3)/micelle nanocomposite to prevent secondary aggregate formation.     

One-step synthesis of SnO2 and TiO2 hollow nanostructures with various shapes and their enhanced lithium storage properties

A versatile one-step method for the general synthesis of metal oxide hollow nanostructures is demonstrated. This method involves the controlled deposition of metal oxides on shaped α-Fe(2)O(3) crystals which are simultaneously dissolved. A variety of uniform SnO(2) hollow nanostructures, such as nanococoons, nanoboxes, hollow nanorings, and nanospheres, can be readily generated. The method is also applicable to the synthesis of shaped TiO(2) hollow nanostructures. As a demonstration of the potential applications of these hollow nanostructures, the lithium storage capability of SnO(2) hollow structures is investigated. The results show that such derived SnO(2) hollow structures exhibit stable capacity retention of 600-700?mA h g(-1) for 50?cycles at a 0.2?C rate and good rate capability at 0.5-1?C, perhaps benefiting from the unique structural characteristics.