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High Pressure Studies of Ultra-Incom...

Xie, Miao.

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High Pressure Studies of Ultra-Incompressible, Superhard Metal Borides.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	High Pressure Studies of Ultra-Incompressible, Superhard Metal Borides./
作者:	Xie, Miao.
面頁冊數:	145 p.
附註:	Source: Dissertation Abstracts International, Volume: 75-03(E), Section: B.
Contained By:	Dissertation Abstracts International75-03B(E).
標題:	Chemistry, Inorganic. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3604143
ISBN:	9781303595097

High Pressure Studies of Ultra-Incompressible, Superhard Metal Borides.
Xie, Miao.

High Pressure Studies of Ultra-Incompressible, Superhard Metal Borides. - 145 p.

Source: Dissertation Abstracts International, Volume: 75-03(E), Section: B.

Thesis (Ph.D.)--University of California, Los Angeles, 2013.

Superhard, ultra-incompressible transition-metal borides are exciting candidate materials for applications in cutting, forming, grinding, polishing and wear-protecting coatings. The existence of a network of directional, covalent bonds, together with a high electron density has been suggested as the key to their remarkable mechanical properties. The goal of this work is to examine how variations in bonding changes the mechanical properties of transition-metal borides. To achieve this, high-pressure diamond anvil cell (DAC) techniques are used to correlate mechanical properties with the electronic and atomic structure of these materials in an effort to understand their intrinsic hardness.

ISBN: 9781303595097Subjects--Topical Terms:

517253
Chemistry, Inorganic.

High Pressure Studies of Ultra-Incompressible, Superhard Metal Borides.
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245 1 0 $a High Pressure Studies of Ultra-Incompressible, Superhard Metal Borides.
300 $a 145 p.
500 $a Source: Dissertation Abstracts International, Volume: 75-03(E), Section: B.
500 $a Advisers: Sarah H. Tolbert; Richard B. Kaner.
502 $a Thesis (Ph.D.)--University of California, Los Angeles, 2013.
520 $a Superhard, ultra-incompressible transition-metal borides are exciting candidate materials for applications in cutting, forming, grinding, polishing and wear-protecting coatings. The existence of a network of directional, covalent bonds, together with a high electron density has been suggested as the key to their remarkable mechanical properties. The goal of this work is to examine how variations in bonding changes the mechanical properties of transition-metal borides. To achieve this, high-pressure diamond anvil cell (DAC) techniques are used to correlate mechanical properties with the electronic and atomic structure of these materials in an effort to understand their intrinsic hardness.
520 $a This work is divided into two parts: the first uses high-pressure Raman spectroscopy to probe the microscopic bonding structure of rhenium diboride (ReB2), one of the hardest transition-metal boride; the second investigates both elastic and plastic deformations in the inexpensive but still superhard material tungsten tetraboride (WB4) and its solid solutions using synchrotron-based in situ high-pressure X-ray diffractions.
520 $a In the first part, we aim to gain an understanding of the correlation between microscopic bonding and macroscopic properties of superhard ReB 2. Pressure-dependent Raman spectroscopy and DFT calculations are used to explore lattice vibrations in ReB2. We interpret the results in terms of bond directionality and stiffness to connect hardness with bond character.
520 $a In the second part, we focus on a less expensive boride, WB4 and its solid solutions, using in situ high-pressure diffraction techniques. Two types of measurements are described. First, axial X-ray diffraction, where the X-ray beam is parallel to the compression direction and the sample is compressed hydrostatically; second, radial X-ray diffraction, where the incoming X-ray beam is perpendicular to the compression direction and the sample is confined under non-hydrostatic stress. By combining axial- and radial-diffraction measurements, we explore how the atomic network in metal borides evolves elastically and plastically under hydrostatic and non-hydrostatic pressures. With this information, we can understand how the intrinsic bonding in WB4 produces high hardness. More importantly, we can explore how changes to the electronic and physical structure arising from solid solutions formation can result in the remarkable hardness values observed for many complex WB4 based solid solutions.
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650 4 $a Chemistry, Inorganic. $3 517253
650 4 $a Chemistry, Physical. $3 560527
650 4 $a Engineering, Materials Science. $3 1017759
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710 2 $a University of California, Los Angeles. $b Chemistry 0153. $3 2096181
773 0 $t Dissertation Abstracts International $g 75-03B(E).
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791 $a Ph.D.
792 $a 2013
793 $a English
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