<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Kiani, Daniyal</style></author><author><style face="normal" font="default" size="100%">Sheng, Yiying</style></author><author><style face="normal" font="default" size="100%">Lu, Baoying</style></author><author><style face="normal" font="default" size="100%">Barauskas, Dovydas</style></author><author><style face="normal" font="default" size="100%">Honer, Kenneth</style></author><author><style face="normal" font="default" size="100%">Jiang, Zhe</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Transient Struvite Formation during Stoichiometric (1:1) NH4+ and PO43– Adsorption/Reaction on Magnesium Oxide (MgO) Particles</style></title><secondary-title><style face="normal" font="default" size="100%">ACS Sustainable Chemistry &amp; Engineering</style></secondary-title><short-title><style face="normal" font="default" size="100%">ACS Sustainable Chem. Eng.</style></short-title></titles><dates><year><style  face="normal" font="default" size="100%">2019</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2019/01/07</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://doi.org/10.1021/acssuschemeng.8b05318</style></url></web-urls></urls><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">7</style></volume><pages><style face="normal" font="default" size="100%">1545 - 1556</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">doi: 10.1021/acssuschemeng.8b05318</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Ivanovskaya, Anna</style></author><author><style face="normal" font="default" size="100%">Singh, Nirala</style></author><author><style face="normal" font="default" size="100%">Liu, Ru-Fen</style></author><author><style face="normal" font="default" size="100%">Kreutzer, Haley</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Van Nguyen, Trung</style></author><author><style face="normal" font="default" size="100%">Metiu, Horia</style></author><author><style face="normal" font="default" size="100%">McFarland, Eric.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Transition Metal Sulfide Hydrogen Evolution Catalysts for Hydrobromic Acid Electrolysis.</style></title><secondary-title><style face="normal" font="default" size="100%">Langmuir</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">transition metal sulfide hydrogen catalyst hydrobromic acid electrolysis</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2013</style></year></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">29</style></volume><pages><style face="normal" font="default" size="100%">480 - 492</style></pages><isbn><style face="normal" font="default" size="100%">0743-7463</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Mixed metal sulfides contg. combinations of W, Fe, Mo, Ni, and Ru were synthesized and screened for activity and stability for the H evolution reaction (HER) in aq. HBr.  Co- and Ni-substituted RuS2 were identified as potentially active HER electrocatalysts by high-throughput screening (HTS), and the specific compns. Co0.4Ru0.6S2 and Ni0.6Ru0.4S2 were identified by optimization.  H evolution activity of Co0.4Ru0.6S2 in HBr is greater than RuS2 or CoS2 and comparable to Pt and com. RhxSy.  Structural and morphol. characterizations of the Co-substituted RuS2 suggest that the nanoparticulate solids are a homogeneous solid soln. with a pyrite crystal structure.  No phase sepn. is detected for Co substitutions &lt;30% by x-ray diffraction.  In 0.5 M HBr electrolyte, the Co-Ru electrode material synthesized with 30% Co rapidly lost ∼34% of the initial loading of Co; thereafter, it was obsd. to exhibit stable activity for HER with no further loss of Co.  D. functional theory calcns. indicate that the S22- sites are the most important for HER and the presence of Co influences the S22- sites such that the H binding energy at sufficiently high H coverage is decreased compared to Ru sulfide.  Although showing high HER activity in a flow cell, the reverse reaction of H oxidn. is slow on the RuS2 catalysts tested when compared to Pt and Rh sulfide, leaving Rh sulfide as the only suitable tested material for a regenerative HBr cell due its stability compared to Pt. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">1</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2012:1776190(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Hamilton, Tamara D.</style></author><author><style face="normal" font="default" size="100%">Bucar, Dejan-Kresimir</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Flanagan, Douglas R.</style></author><author><style face="normal" font="default" size="100%">Li, Yingjian</style></author><author><style face="normal" font="default" size="100%">Ghorai, Suman</style></author><author><style face="normal" font="default" size="100%">Tivanski, Alexei V.</style></author><author><style face="normal" font="default" size="100%">MacGillivray, Leonard R.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Thixotropic Hydrogel Derived from a Product of an Organic Solid-State Synthesis: Properties and Densities of Metal-Organic Nanoparticles.</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of the American Chemical Society</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">nanoparticle hydrogel thixotropy copper coordination polymer crystal</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2011///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">American Chemical Society</style></publisher><volume><style face="normal" font="default" size="100%">133</style></volume><pages><style face="normal" font="default" size="100%">3365 - 3371</style></pages><isbn><style face="normal" font="default" size="100%">0002-7863</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Metallogels form from Cu(II) ions and tetratopic ligand rctt-1,2-bis(3-pyridyl)-3,4-bis(4-pyridyl)cyclobutane.  The tetrapyridyl cyclobutane was synthesized in the org. solid state.  The gel forms with a variety of counteranions and gels water.  The hydrogel is thixotropic and is composed of nanoscale metal-org. particles (NMOPs), a high surface area of which likely accounts for the gelation of the polar aq. medium.  A shear stress profile of the thixotropic hydrogel gave a yield value of 8.33 Pa.  A novel combination of at. force microscopy (AFM) and scanning transmission x-ray microscopy (STXM) is used to assess the densities of individual NMOPs.  A d. of 1.37 g/cm3 was detd.  A single-crystal x-ray diffraction study demonstrates the ability of the unsym. cyclobutane 3,4'-tpcb to self-assemble with Cu(II) ions in [Cu2(hfac)4(3,4'-tpcb)]∞ (hfac is hexafluoroacetylacetonate) to form a solvated 1-dimensional coordination polymer. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">10</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2011:232592(Journal; Online Computer File)</style></notes></record><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Bian, Shao-Wei</style></author><author><style face="normal" font="default" size="100%">Baltrusaitis, Jonas</style></author><author><style face="normal" font="default" size="100%">Galhotra, Pragati</style></author><author><style face="normal" font="default" size="100%">Grassian, Vicki H.</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">A template-free, thermal decomposition method to synthesize mesoporous MgO with a nanocrystalline framework and its application in carbon dioxide adsorption.</style></title><secondary-title><style face="normal" font="default" size="100%">Journal of Materials Chemistry</style></secondary-title></titles><keywords><keyword><style  face="normal" font="default" size="100%">air purifn carbon dioxide adsorption mesoporous magnesia</style></keyword><keyword><style  face="normal" font="default" size="100%">template free thermal decompn synthesis magnesia sorbent</style></keyword></keywords><dates><year><style  face="normal" font="default" size="100%">2010</style></year><pub-dates><date><style  face="normal" font="default" size="100%">2010///</style></date></pub-dates></dates><publisher><style face="normal" font="default" size="100%">Royal Society of Chemistry</style></publisher><volume><style face="normal" font="default" size="100%">20</style></volume><pages><style face="normal" font="default" size="100%">8705 - 8710</style></pages><isbn><style face="normal" font="default" size="100%">0959-9428</style></isbn><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">Alk. earth-based oxides are important materials for CO2 storage.  A template-free method to synthesize meso-porous MgO by thermal decompn. of anhyd. magnesium acetate is presented.  Characterization of cryst. phase, particle and pore sizes, and surface area for mesoporous MgO was done using a variety of techniques: SEM, high resoln. transmission electron microscopy, powder x-ray diffraction, and N2 adsorption anal.  Results showed meso-porous MgO synthesized from anhyd. magnesium acetate had a high surface area (120-136 m2/g) and a narrow pore size distribution (3-4 nm).  The pore was comprised of small, primary MgO nano-particle aggregates with inter-particle connections.  In-situ transmission Fourier transform IR spectroscopy assessed CO2 adsorption by meso-porous MgO.  This spectroscopic assessment showed meso-porous MgO exhibited enhanced CO2 adsorption capacity vs. com. available MgO nano-particles.  This difference was mainly attributed to increased surface area.  Differences in surface carbonate/bicarbonate speciation, obsd. between meso-porous and com. MgO, were related to structural differences of the smaller nano-particles. [on SciFinder(R)]</style></abstract><issue><style face="normal" font="default" size="100%">39</style></issue><notes><style face="normal" font="default" size="100%">CAPLUS AN 2010:1212416(Journal)</style></notes></record></records></xml>