New Calcium Hydrides with Mixed Atomic and Molecular Hydrogen
Two new polyhydrides of calcium have been synthesized at high pressures and high temperatures and characterized by Raman spectroscopy, infrared spectroscopy, and synchrotron X-ray diffraction. Above 20 GPa and 700 K, we synthesize a phase having a monoclinic (C2/m) structure with Ca2H5 composition,...
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Veröffentlicht in: | Journal of physical chemistry. C 2018-08, Vol.122 (34), p.19370-19378 |
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container_title | Journal of physical chemistry. C |
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creator | Mishra, Ajay K Muramatsu, Takaki Liu, Hanyu Geballe, Zachary M Somayazulu, Maddury Ahart, Muhtar Baldini, Maria Meng, Yue Zurek, Eva Hemley, Russell J |
description | Two new polyhydrides of calcium have been synthesized at high pressures and high temperatures and characterized by Raman spectroscopy, infrared spectroscopy, and synchrotron X-ray diffraction. Above 20 GPa and 700 K, we synthesize a phase having a monoclinic (C2/m) structure with Ca2H5 composition, which is characterized by a distinctive vibration at 3789 cm–1 at 25 GPa. The observed Raman spectrum is in close agreement with first-principles calculations of a Ca2H5 structure characterized by a lattice containing a central layer of H2 molecules oriented along the (100) direction. At higher pressures (e.g., 116 GPa and 1600 K), we synthesize another phase, which has the composition of CaH4 and a denser body-centered tetragonal structure. This weakly metallic phase also contains molecular-like H2 units, and its spectroscopic as well as diffraction signatures match closely with those predicted from first-principles calculations. This phase is observed to persist on decompression to 60 GPa at room temperature. The elongation of the H–H bond in these hydrides is a result of the Ca–H2 interaction, analogous to what occurs in molecular compounds, where H2 binds side-on to a d-element, such as in Kubas complex. |
doi_str_mv | 10.1021/acs.jpcc.8b05030 |
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This weakly metallic phase also contains molecular-like H2 units, and its spectroscopic as well as diffraction signatures match closely with those predicted from first-principles calculations. This phase is observed to persist on decompression to 60 GPa at room temperature. The elongation of the H–H bond in these hydrides is a result of the Ca–H2 interaction, analogous to what occurs in molecular compounds, where H2 binds side-on to a d-element, such as in Kubas complex.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/acs.jpcc.8b05030</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>08 HYDROGEN ; INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY</subject><ispartof>Journal of physical chemistry. 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The observed Raman spectrum is in close agreement with first-principles calculations of a Ca2H5 structure characterized by a lattice containing a central layer of H2 molecules oriented along the (100) direction. At higher pressures (e.g., 116 GPa and 1600 K), we synthesize another phase, which has the composition of CaH4 and a denser body-centered tetragonal structure. This weakly metallic phase also contains molecular-like H2 units, and its spectroscopic as well as diffraction signatures match closely with those predicted from first-principles calculations. This phase is observed to persist on decompression to 60 GPa at room temperature. 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(ANL), Argonne, IL (United States)</creatorcontrib><creatorcontrib>Carnegie Inst. of Washington, Washington, DC (United States)</creatorcontrib><creatorcontrib>Energy Frontier Research Centers (EFRC) (United States). Energy Frontier Research in Extreme Environments (EFree)</creatorcontrib><collection>CrossRef</collection><collection>OSTI.GOV - Hybrid</collection><collection>OSTI.GOV</collection><jtitle>Journal of physical chemistry. C</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mishra, Ajay K</au><au>Muramatsu, Takaki</au><au>Liu, Hanyu</au><au>Geballe, Zachary M</au><au>Somayazulu, Maddury</au><au>Ahart, Muhtar</au><au>Baldini, Maria</au><au>Meng, Yue</au><au>Zurek, Eva</au><au>Hemley, Russell J</au><aucorp>Argonne National Lab. (ANL), Argonne, IL (United States)</aucorp><aucorp>Carnegie Inst. of Washington, Washington, DC (United States)</aucorp><aucorp>Energy Frontier Research Centers (EFRC) (United States). Energy Frontier Research in Extreme Environments (EFree)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>New Calcium Hydrides with Mixed Atomic and Molecular Hydrogen</atitle><jtitle>Journal of physical chemistry. C</jtitle><addtitle>J. Phys. Chem. C</addtitle><date>2018-08-30</date><risdate>2018</risdate><volume>122</volume><issue>34</issue><spage>19370</spage><epage>19378</epage><pages>19370-19378</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>Two new polyhydrides of calcium have been synthesized at high pressures and high temperatures and characterized by Raman spectroscopy, infrared spectroscopy, and synchrotron X-ray diffraction. Above 20 GPa and 700 K, we synthesize a phase having a monoclinic (C2/m) structure with Ca2H5 composition, which is characterized by a distinctive vibration at 3789 cm–1 at 25 GPa. The observed Raman spectrum is in close agreement with first-principles calculations of a Ca2H5 structure characterized by a lattice containing a central layer of H2 molecules oriented along the (100) direction. At higher pressures (e.g., 116 GPa and 1600 K), we synthesize another phase, which has the composition of CaH4 and a denser body-centered tetragonal structure. This weakly metallic phase also contains molecular-like H2 units, and its spectroscopic as well as diffraction signatures match closely with those predicted from first-principles calculations. This phase is observed to persist on decompression to 60 GPa at room temperature. 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title | New Calcium Hydrides with Mixed Atomic and Molecular Hydrogen |
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