|CCL 08.09.28 IMA Mathematical and Algorithmic Challenges in Electronic Structure Theory, Minneapolis, MN|
From: chemistry-request at ccl.net
To: chemistry-request at ccl.net
Date: Fri Oct 12 21:42:19 2007
Subject: 08.09.28 IMA Mathematical and Algorithmic Challenges in Electronic Structure Theory, Minneapolis, MN
IMA Mathematical and Algorithmic Challenges in Electronic Structure Theory http://www.ima.umn.edu/2008-2009/W9.29-10.3.08/ University of Minnessota, Minneapolis, MN September 29-October 3, 2008 Organizers: Eric Cances CERMICS, Ecole Nationale des Ponts et Chausses Anna I. Krylov Chemistry, University of Southern California Juan C. Meza Lawrence Berkeley National Laboratory John P. Perdew Physics, Tulane University Description: Electronic structure calculations are the very core of quantum chemistry and play an increasingly important role in nano-technologies, molecular biology and materials science. This workshop will focus on two topics: * the mathematical challenges in developing accurate, efficient, and robust algorithms for electronic structure calculations of large systems; * the latest methodological developments and the remaining open problems in Density Functional Theory. Algorithms for electronic structure calculations: Density functional theory (DFT) is the most widely used ab initio method in material simulations. DFT can be used to calculate the electronic structure, the charge density, the total energy and the atomic forces of a material system, and with the advance of new algorithms and supercomputers, DFT can now be used to study thousand-atom systems. But there are many problems that either require much larger systems (more than 100,000 atoms), or many total energy calculation steps (molecular dynamics or atomic relaxations). Some possible applications include the study of nanostructures and the design of novel materials. Unfortunately, conventional DFT algorithms scale as O(N3), where N is the size of the system (e.g., the number of atoms) putting many problems beyond the reach of even planned petascale computers. Therefore understanding the electronic structures of larger systems will require new mathematical advancements and algorithms. Some areas that will be addressed in this workshop include linear-scaling methods that reduce the order of complexity for DFT algorithms, large-scale nonlinear eigenvalue problems, and optimization techniques for solving the Schrdinger equation. In addition, we will discuss the implementation and parallelization of these methods for large supercomputer systems. Contrarily to DFT, wavefunction theory provides us with a series of increasingly refined systematic approximations to the exact solution of the electronic Schrdinger equation. Wave function based electronic structure methods, which are implemented in a variety of packaged programs, can now be routinely employed to predict structures, spectra, properties and reactivity of molecules, sometimes with accuracy rivaling that of the experiment. However, due to the steep computational scaling, mathematical and algorithmic complexity, the following challenges remain: * properties calculation for correlated wave functions; * extending efficient and predictive methods and algorithms for open-shell and electronically excited species; * reducing the computational cost and scaling. The workshop will discuss the mathematical and algorithmic aspects of the above in the context of coupled-cluster (including equation-of-motion) and multi-reference methods. The density functional theory (DFT) of Hohenberg, Kohn and Sham is a way to find the ground-state density n(r) and energy E of a many-electron system (atom, molecule, condensed material) by solving a constrained minimization problem whose first order optimality conditions (the Kohn-Sham equations) can be written as a nonlinear eigenvalue problem. It resembles the Hartree-Fock theory, but is formally exact because it includes the effects of electron correlation as well as exchange in the density functional for the exchange-correlation energy Exc[n] and in its functional derivative, the exchange-correlation potential vxc([n],r). Time-dependent properties and excited states are also accessible through a time-dependent version of DFT. Density functional theory is much more computationally efficient than correlated-wavefunction theory, especially for large systems, but has the disadvantage that in practice Exc[n] and vxc([n],r) must be approximated (usually through a nonsytematic "educated guess"), leading in many cases to moderate but useful accuracy. Used almost exclusively in condensed matter physics since the 1970's, DFT became popular in quantum chemistry in the 1990's due to the development of more accurate approximations. Besides the algorithmic challenges discussed above, the principal challenges facing DFT are (a) better understanding of the exact theory itself and derivation of further exact properties of Exc[n] and vxc([n],r), and (b) improved approximations that satisfy known exact constraints and sometimes are also fitted to known data.NOTE THAT E-MAIL ADDRESSES HAVE BEEN MODIFIED!!!
All @ signs were changed to ~~ to fight spam. Before you send e-mail, you need to change ~~ to @
For example: change joe~~big123comp.com to firstname.lastname@example.org
Please let colleagues know about conference listingts at Computational Chemistry List Conference Page at http://www.ccl.net/chemistry/a/conferences/.
Please help: If you find this conference list useful but you noticed some conference missing, please consider including it here by using the Conference Submission Page. It is free but your support is welcome. You will help others!!!
|Modified: Sat Oct 13 01:42:19 2007 GMT|
|Page accessed 3901 times since Sat Oct 13 01:42:19 2007 GMT|
Please help maintain CCL: If you found that your conference is listed here, please consider supporting CCL as a Supporting Member or use other Paid Services of CCL to ensure the continuation of this useful service. We cannot do it without your help.