Bastian J. M. Etzold

Covalent Incorporation of Aminated Nanodiamond into an Epoxy Polymer Network

Outstanding mechanical and optical properties of diamond nanoparticles in combination with their biocompatibility have recently attracted much attention. Modification of the surface chemistry and incorporation into a polymer is required in many applications of the nanodiamond. Nanodiamond powder with reactive amino groups (∼20% of the number of surface carbon atoms in each 5 nm particle) was produced in this work by covalent linking of ethylenediamine to the surface carboxyl groups via amide bonds. The synthesized material was reacted with epoxy resin, yielding a composite, in which nanodiamond particles are covalently incorporated into the polymer matrix. The effect of amino groups grafted on the nanodiamond on the curing chemistry of the epoxy resin was analyzed and taken into consideration. Covalently bonded nanodiamond-epoxy composites showed a three times higher hardness, 50% higher Youngs modulus, and two times lower creep compared to the composites in which the nanodiamond was not chemically linked to the matrix. Aminated nanodiamond produced and characterized in the present study may also find applications beyond the composites, for example, as a drug, protein, and gene delivery platform in biology and medicine, as a solid support in chromatography and separation science, and in solid state peptide synthesis.

Photonic crystal fibres for chemical sensing and photochemistry

In this review, we introduce photonic crystal fibre as a novel optofluidic microdevice that can be employed as both a versatile chemical sensor and a highly efficient microreactor. We demonstrate that it provides an excellent platform in which light and chemical samples can strongly interact for quantitative spectroscopic analysis or photoactivation purposes. The use of photonic crystal fibre in photochemistry and sensing is discussed and recent results on gas and liquid sensing as well as on photochemical and catalytic reactions are reviewed. These developments demonstrate that the tight light confinement, enhanced light-matter interaction and reduced sample volume offered by photonic crystal fibre make it useful in a wide range of chemical applications.

Analysis of evaporation and thermal decomposition of ionic liquids by thermogravimetrical analysis at ambient pressure and high vacuum

Ionic liquids (ILs) are widely discussed as alternative green solvents not only because of their unique chemical properties, but also because of their extremely low vapour pressure and – at least in some cases – relatively high thermal stability. Two complementary methods are analyzed and compared to determine both the rate constant of decomposition and the vapour pressure of four ILs: (1) thermogravimetrical analysis at ambient pressure (TGap) with an overflow of inert gases, and (2) high vacuum (HV) experiments with a magnetic suspension balance (MSB). At ambient pressure, [EMIM][MeSO3] and [EMIM][CF3SO3] decompose without a significant contribution of evaporation, which leads to the rate constant of thermal degradation. For both ILs, the vapour pressure can only be determined at HV by the MSB, because the evaporation rate is then higher than the decomposition rate. For the relatively volatile ILs [EMIM][NTf2] and [BMIM][NTf2] the vapour pressure can be derived both by the MSB at HV as well as by TGap. General strategies to determine the volatility and stability of ILs and criteria for the maximum operation temperature with regard to decomposition and evaporation are presented.

Aqueous-phase reforming of xylitol over Pt/C and Pt/TiC-CDC catalysts: catalyst characterization and catalytic performance

The aqueous phase reforming (APR) of xylitol was studied over five Pt/C catalysts. The correlation between physico-chemical properties of the catalysts and catalytic performance was established. The Pt/C catalysts have different textural properties as well as different mean Pt cluster sizes and surface acidity. The average Pt cluster size was investigated by means of CO chemisorption as well as by TEM. The reaction was found to be structure sensitive and TOF linearly increases with increasing average Pt cluster size in the studied domain. The catalysts which possess higher surface acidity favoured higher rates of hydrocarbon production. On the contrary the Pt/C materials with lower acidities generated hydrogen with high selectivity and TOF.

Accelerating Oxygen-Reduction Catalysts through Preventing Poisoning with Non-Reactive Species by Using Hydrophobic Ionic Liquids

Developing cost-effective electrocatalysts for the oxygen reduction reaction (ORR) is a prerequisite for broad market penetration of low-temperature fuel cells. A major barrier stems from the poisoning of surface sites by nonreactive oxygenated species and the sluggish ORR kinetics on the Pt catalysts. Herein we report a facile approach to accelerating ORR kinetics by using a hydrophobic ionic liquid (IL), which protects Pt sites from surface oxidation, making the IL-modified Pt intrinsically more active than its unmodified counterpart. The mass activity of the catalyst is increased by three times to 1.01 A mg(-1) Pt @0.9 V, representing a new record for pure Pt catalysts. The enhanced performance of the IL-modified catalyst can be stabilized after 30 000 cycles. We anticipate these results will form the basis for an unprecedented perspective in the development of high-performing electrocatalysts for fuel-cell applications.

Chemical and (Photo)‐Catalytical Transformations in Photonic Crystal Fibers

The concept of employing photonic crystal fibers for chemical and (photo)‐catalytical transformations is presented. These optofluidic microdevices represent a versatile platform where light and fluids can interact for spectroscopic or photoactivation purposes. The use of photonic crystal fibers in chemistry and sensing is reviewed and recent applications as catalytic microreactors are presented. Results on homogeneous catalysis and the immobilization of homogeneous and heterogeneous catalysts in the fiber channels are discussed. The examples demonstrate that combining catalysis and the excellent light guidance of photonic crystal fibers provides unique features for example, for photocatalytic activation and quantitative photospectroscopic reaction analysis.

Boosting Performance of Low Temperature Fuel Cell Catalysts by Subtle Ionic Liquid Modification

High cost and poor stability of the oxygen reduction reaction (ORR) electrocatalysts are the major barriers for broad-based application of polymer electrolyte membrane fuel cells. Here we report a facile and scalable approach to improve Pt/C catalysts for ORR, by modification with small amounts of hydrophobic ionic liquid (IL). The ORR performance of these IL-modified catalysts can be readily manipulated by varying the degree of IL filling, leading to a 3.4 times increase in activity. Besides, the IL-modified catalysts exhibit substantially enhanced stability relative to Pt/C. The enhanced performance is attributed to the optimized microenvironment at the interface of Pt and electrolyte, where advantages stemming from an increased number of free sites, higher oxygen concentration in the IL and electrostatic stabilization of the nanoparticles develop fully, at the same time that the drawback of mass transfer limitation remains suppressed. These findings open a new avenue for catalyst optimization for next-generation fuel cells.

Vanadium pentoxide/carbide-derived carbon core–shell hybrid particles for high performance electrochemical energy storage

A novel, two step synthesis is presented combining the formation of carbide-derived carbon (CDC) and redox-active vanadium pentoxide (V2O5) in a core–shell manner using solely vanadium carbide (VC) as the precursor. In a first step, the outer part of VC particles is transformed to nanoporous CDC owing to the in situ formation of chlorine gas from NiCl2 at 700 °C. In a second step, the remaining VC core is calcined in synthetic air to obtain V2O5/CDC core–shell particles. Materials characterization by means of electron microscopy, Raman spectroscopy, and X-ray diffraction clearly demonstrates the partial transformation from VC to CDC, as well as the successive oxidation to V2O5/CDC core–shell particles. Electrochemical performance was tested in organic 1 M LiClO4 in acetonitrile using half- and asymmetric full-cell configuration. High specific capacities of 420 mA h g−1 (normalized to V2O5) and 310 mA h g−1 (normalized to V2O5/CDC) were achieved. The unique nanotextured core–shell architecture enables high power retention with ultrafast charging and discharging, achieving more than 100 mA h g−1 at 5 A g−1 (rate of 12C). Asymmetric cell design with CDC on the positive polarization side leads to a high specific energy of up to 80 W h kg−1 with a superior retention of more than 80% over 10 000 cycles and an overall energy efficiency of up to 80% at low rates.

Improved synthesis and hydrothermal stability of Pt/C catalysts based on size-controlled nanoparticles

A novel method for the preparation of stable Pt/C catalysts with size-controlled nanoparticles has been developed. The method is based on in situ synthesis of the nanoparticles (reduction with NaBH4 in the presence of a support and PVP). Compared to the conventional ex situ route (colloidal synthesis followed by impregnation), this in situ route yields smaller nanoparticles (2.5–3.9 nm) of narrower size distribution. The catalysts prepared by the in situ synthesis showed a higher stability in water at 80 °C, indicating a stronger interaction between the support and the metallic phase. Hydrothermal stability tests were also conducted under conditions equivalent to those of aqueous phase reforming (200 °C, 17 bar and water and diluted acetic acid). Hydrothermal treatment proved to be an excellent method to improve the resistance to leaching of the catalysts. Metal loss was negligible while PVP was almost completely removed from the catalyst; hence, most of the porosity was recovered and the dispersion measured by CO chemisorption increased from 5 to 34–75%. Water at 200 °C was more effective than diluted acetic acid for the removal of PVP. TEM images confirmed that the Pt nanoparticles did not undergo significant changes either in size or morphology upon the hydrothermal treatment, and XPS analysis showed a homogeneous distribution of Pt nanoparticles within the catalyst granules.

Dynamics of Bulk Oxygen in the Selective Oxidation of Acrolein

The gas‐phase oxidation of acrolein to acrylic acid on a hydrothermally prepared mixed oxide catalyst was investigated by steady‐state isotopic transient kinetic analysis (SSIKTA) as well as different types of concentration‐programmed techniques (CPR‐pulse, CPO) under in situ or process‐relevant conditions. Balancing the amounts of active oxygen gives an overview of the quantities of participating bulk oxygen species. The dynamics of bulk oxygen lead to re‐oxidation processes on the catalyst surface and thus influence the selectivity pattern of the network of acrolein oxidation. Furthermore, the bulk dynamics are activated by temperature.