@article {342,
	title = {Transient Struvite Formation during Stoichiometric (1:1) NH4+ and PO43{\textendash} Adsorption/Reaction on Magnesium Oxide (MgO) Particles},
	journal = {ACS Sustainable Chemistry \& Engineering},
	volume = {7},
	year = {2019},
	note = {doi: 10.1021/acssuschemeng.8b05318},
	month = {2019/01/07},
	pages = {1545 - 1556},
	publisher = {American Chemical Society},
	url = {https://doi.org/10.1021/acssuschemeng.8b05318},
	author = {Kiani, Daniyal and Sheng, Yiying and Lu, Baoying and Barauskas, Dovydas and Honer, Kenneth and Jiang, Zhe and Baltrusaitis, Jonas}
}
@article {122,
	title = {Transition Metal Sulfide Hydrogen Evolution Catalysts for Hydrobromic Acid Electrolysis.},
	journal = {Langmuir},
	volume = {29},
	year = {2013},
	note = {CAPLUS AN 2012:1776190(Journal; Online Computer File)},
	pages = {480 - 492},
	publisher = {American Chemical Society},
	abstract = {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 <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)]},
	keywords = {transition metal sulfide hydrogen catalyst hydrobromic acid electrolysis},
	isbn = {0743-7463},
	author = {Ivanovskaya, Anna and Singh, Nirala and Liu, Ru-Fen and Kreutzer, Haley and Baltrusaitis, Jonas and Van Nguyen, Trung and Metiu, Horia and McFarland, Eric.}
}
@article {161,
	title = {Thixotropic Hydrogel Derived from a Product of an Organic Solid-State Synthesis: Properties and Densities of Metal-Organic Nanoparticles.},
	journal = {Journal of the American Chemical Society},
	volume = {133},
	year = {2011},
	note = {CAPLUS AN 2011:232592(Journal; Online Computer File)},
	month = {2011///},
	pages = {3365 - 3371},
	publisher = {American Chemical Society},
	abstract = {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{\textquoteright}-tpcb to self-assemble with Cu(II) ions in [Cu2(hfac)4(3,4{\textquoteright}-tpcb)]$\infty$ (hfac is hexafluoroacetylacetonate) to form a solvated 1-dimensional coordination polymer. [on SciFinder(R)]},
	keywords = {nanoparticle hydrogel thixotropy copper coordination polymer crystal},
	isbn = {0002-7863},
	author = {Hamilton, Tamara D. and Bucar, Dejan-Kresimir and Baltrusaitis, Jonas and Flanagan, Douglas R. and Li, Yingjian and Ghorai, Suman and Tivanski, Alexei V. and MacGillivray, Leonard R.}
}
@article {163,
	title = {A template-free, thermal decomposition method to synthesize mesoporous MgO with a nanocrystalline framework and its application in carbon dioxide adsorption.},
	journal = {Journal of Materials Chemistry},
	volume = {20},
	year = {2010},
	note = {CAPLUS AN 2010:1212416(Journal)},
	month = {2010///},
	pages = {8705 - 8710},
	publisher = {Royal Society of Chemistry},
	abstract = {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)]},
	keywords = {air purifn carbon dioxide adsorption mesoporous magnesia, template free thermal decompn synthesis magnesia sorbent},
	isbn = {0959-9428},
	author = {Bian, Shao-Wei and Baltrusaitis, Jonas and Galhotra, Pragati and Grassian, Vicki H.}
}
