東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁 到查詢結果 [ subject:"Physics, Molecular." ]

切換: 標籤 | MARC模式 | ISBD

A density-functional theory includin...

Johnson, Erin R.

FindBook

Google Book

Amazon

博客來

A density-functional theory including dispersion interactions.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	A density-functional theory including dispersion interactions./
作者:	Johnson, Erin R.
面頁冊數:	233 p.
附註:	Source: Dissertation Abstracts International, Volume: 69-03, Section: B, page: 1709.
Contained By:	Dissertation Abstracts International69-03B.
標題:	Physics, Molecular. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=NR37078
ISBN:	9780494370780

A density-functional theory including dispersion interactions.
Johnson, Erin R.

A density-functional theory including dispersion interactions. - 233 p.

Source: Dissertation Abstracts International, Volume: 69-03, Section: B, page: 1709.

Thesis (Ph.D.)--Queen's University (Canada), 2008.

The London dispersion interaction is responsible for attraction between non-polar molecules and is of great importance in describing structure and reactivity in many areas of chemistry. Dispersion is difficult to model accurately. Density Functional Theory (DFT) methods, widely used in computational chemistry today, do not include the necessary physics. This often leads to qualitatively incorrect predictions when DFT is applied to dispersion-bound systems. A novel DFT method has been developed which is capable of accurately modeling dispersion. Dispersion attraction between molecules arises when an instantaneous dipole moment in one molecule induces a dipole moment in a second molecule. Our approach proposes that the source of these instantaneous dipole moments is the position-dependent dipole moment of the exchange hole. The model is no more computationally expensive than existing DFTs and gives remarkably accurate dispersion coefficients, intermolecular separations, intermolecular binding energies, and intermolecular conformational energies. Our dispersion theory is also combined with previous post-exact-exchange models of dynamical and nondynamical correlation, yielding a unified exact-exchange-based energy functional called DF07. DF07 overcomes many of the outstanding problems in DFT arising from local exchange approximations. The DF07 model is shown to provide highly accurate results for thermochemistry, kinetics, and van der Waals interactions.

ISBN: 9780494370780Subjects--Topical Terms:

1018648
Physics, Molecular.

A density-functional theory including dispersion interactions.
LDR:02239nam 2200241 a 45 001 962524
005 20110830
008 110831s2008 ||||||||||||||||| ||eng d
020 $a 9780494370780
035 $a (UMI)AAINR37078
035 $a AAINR37078
040 $a UMI $c UMI
100 1 $a Johnson, Erin R. $3 1285583
245 1 2 $a A density-functional theory including dispersion interactions.
300 $a 233 p.
500 $a Source: Dissertation Abstracts International, Volume: 69-03, Section: B, page: 1709.
502 $a Thesis (Ph.D.)--Queen's University (Canada), 2008.
520 $a The London dispersion interaction is responsible for attraction between non-polar molecules and is of great importance in describing structure and reactivity in many areas of chemistry. Dispersion is difficult to model accurately. Density Functional Theory (DFT) methods, widely used in computational chemistry today, do not include the necessary physics. This often leads to qualitatively incorrect predictions when DFT is applied to dispersion-bound systems. A novel DFT method has been developed which is capable of accurately modeling dispersion. Dispersion attraction between molecules arises when an instantaneous dipole moment in one molecule induces a dipole moment in a second molecule. Our approach proposes that the source of these instantaneous dipole moments is the position-dependent dipole moment of the exchange hole. The model is no more computationally expensive than existing DFTs and gives remarkably accurate dispersion coefficients, intermolecular separations, intermolecular binding energies, and intermolecular conformational energies. Our dispersion theory is also combined with previous post-exact-exchange models of dynamical and nondynamical correlation, yielding a unified exact-exchange-based energy functional called DF07. DF07 overcomes many of the outstanding problems in DFT arising from local exchange approximations. The DF07 model is shown to provide highly accurate results for thermochemistry, kinetics, and van der Waals interactions.
590 $a School code: 0283.
650 4 $a Physics, Molecular. $3 1018648
690 $a 0609
710 2 $a Queen's University (Canada). $3 1017786
773 0 $t Dissertation Abstracts International $g 69-03B.
790 $a 0283
791 $a Ph.D.
792 $a 2008
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=NR37078