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Instruments / Technical Area	Publication Details	Published
B18-Core EXAFS	Exact stoichiometry high surface area mesoporous AlPO4 glass for efficient catalysis Jin He , Wei Guo , Peixi Cong , Jeff Armstrong , Rihong Li , Shuaipeng Wang , Da Shi , Andrew M. Beale , Raed Abu-Reziq , David Avnir Journal Of Materials Science 42 DOI: 10.1007/s10853-022-07577-y Diamond Proposal Number(s): [18835] Show Abstract ▼ Abstract: Mesoporous AlPO4 materials have attracted much attention in catalysis due to their high thermal and chemical stability. Of particular interest for catalysis is the pure stoichiometry high surface area (> 500 m2/g) mesoporous AlPO4 (mAlPO4) glass prepared via a template-free aqueous sol–gel synthetic route. Toward the application of this material for catalysis, we have developed methods for loading it with nanoparticles (NPs) of catalytic metals—Pd and Rh—and carried out a detailed characterization study of the resulting doped materials by a wide array of analytical methods, including synchrotron X-ray absorption spectroscopy, inelastic neutron scattering and more. The applicability of this material for catalysis, both by itself and as a support for catalytic NPs, was then evaluated. The pure mAlPO4 exhibited excellent acid-catalyzed [3 + 2] cycloaddition of nitriles and sodium azide. mAlPO4 loaded with the Pd NPs catalyzed very efficiently deoxygenation reactions of benzyl alcohols. mAlPO4 loaded with Rh NPs catalyzed with high selectivity, the hydrogenation of phenols and cresols and full conversion the hydrogenation of the industrially very high-volume toluene to methylcyclohexane. The materials-science aspects of these successful catalysts were studied in detail, leading, for instance, to the understanding of the important role of the interfacial Rh/Pd–O-P bonds.	Sep 2022
B18-Core EXAFS	Affecting an ultra-high work function of silver David Avnir , Jin He , Jeff Armstrong , Peixi Cong , Barak Menagen , Lior Igaher , Andrew M. Beale , Lioz Etgar Angewandte Chemie International Edition DOI: 10.1002/anie.201912293 Diamond Proposal Number(s): [18835] Show Abstract ▼ Abstract: Efficient control of the work function (WF) of metals and their increase to ultra‐high values are crucial for their applications in functional devices applying interfacial charge transport processes. We report an ultra‐high increase in the WF of silver, from 4.26 to 7.42 eV, that is, an increase of up to ~3.1 eV. This, apparently, highest WF on record for metals supports and is supported by recent computational studies which predict the potential ability to affect an increase of the WF of metals by more than 4 eV. We achieved the ultra‐high increase by a new approach: Rather than using the common method of 2D adsorption of polar molecules layers on the metal surface, we have incorporated WF modifying components ‐ L‐cysteine and Zn(OH) 2 ‐ within the metal, resulting in a 3D architecture. Detailed material characterization by a large array of analytical methods was carried out (XRD, SEM, EDS mapping, TGA/MS, synchrotron X‐ray absorption, inelastic neutron scattering, Raman spectroscopy) the combination of which points to a WF enhancement mechanism which is based on affecting directly the charge transfer ability of the metal separately by cysteine and hydrolyzed zinc(II), and synergistically by the combination of the two components through the known Zn‐cysteine finger redox trap effect. Some additional properties include the ability to fine‐tune the WF from the pure silver values and up; the conductivity of the doped silver remains practically unaffected; the WF is stable beyond 3 months of storage; and it is heat resistant up to 150 o C. The ability to tailor WF changes from the standard value of silver and up over a wide range, will certainly find its applications wherever tuning of the WF is needed for the design of charge transport devices.	Jan 2020
B18-Core EXAFS	Composite materials with combined electronic and ionic properties Noam Ralbag , Meirav Mann-Lahav , Elena S. Davydova , Uri Ash , Reuven Galed , Michael Handl , Renate Hiesgen , Emanuele Magliocca , William Mustain , Jin He , Peixi Cong , Andrew Beale , Gideon S. Grader , David Avnir , Dario R. Dekel Matter DOI: 10.1016/j.matt.2019.04.007 Diamond Proposal Number(s): [18835] Show Abstract ▼ Abstract: In this work, we develop a new type of composite material that combines both electrocatalytic and ionic properties, by doping a silver metal catalyst with an anion-conducting ionomer at the molecular level. We show that ionomer entrapment into the silver metallic structure is possible, imparting unique properties to the catalytic character of the metallic silver. The novel composite material is tested as the cathode electrode of fuel cells, showing significant improvement in cell performance as compared with the undoped counterpart. This new type of material may then replace the current design of electrodes in advanced fuel cells or other electrochemical devices. The possibility to merge different properties into one composite material by molecular entrapment in metals can open the way to new materials, leading to unexplored fields and applications.	Aug 2019

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