Martin Head-Gordon
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Research Interests
Martin Head-Gordon has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
- Alexis T. Bell
University of California
3 shared publications Joseph Gomes
Energy Bioscience Institute & Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA‐94720 (USA)
2 shared publicationsAdam Grippo
Energy Bioscience Institute and Department of Chemistry, University of California, Berkeley, CA‐94720 (USA)
1 shared publicationChristian G. Canlas
Department of Chemistry, University of California, Berkeley, CA 94720 (USA)
1 shared publicationDavid Hanna
Department of Chemical and Biomolecular Engineering, University of California, Berkeley, CA 94720 (USA)
1 shared publication- Francisco Dean Toste
Department of Chemistry, University of California, Berkeley, CA, 94720, USA
1 shared publication
Latest Publications
- Open Access
The Conundrum of Diffuse Basis Sets: A Blessing for Accuracy yet a Curse for Sparsity
Diffuse atomic orbital basis sets have proven to be essential to obtain accurate interaction energies, especially in regard to non-covalent interactions. However, they also have a detrimental impact on the sparsity of the one-particle density matrix (1-PDM), to a degree stronger than the spatial extent of the basis functions alone could explain. This is despite the fact that the matrix elements of the 1-PDM of insulators (systems with significant HOMO-LUMO gaps) are expected to decay exponentially with increasing real-space distance from the diagonal and the asymptotic decay rate is expected to have a well-defined basis set limit. The observed low sparsity of the 1-PDM appears to be independent of representation and even persists after projecting the 1-PDM onto a real-space grid, leading to the conclusion that this "curse of sparsity" is solely a basis set artifact, which, counterintuitively, becomes worse for larger basis sets, seemingly contradicting the notion of a well-defined basis set limit. We show that this is a consequence of the low locality of the contra-variant basis functions as quantified by the inverse overlap matrix $\mathbf{S}^{-1}$ being significantly less sparse than its covariant dual. Introducing the model system of an infinite non-interacting chain of helium atoms, we are able to quantify the exponential decay rate to be proportional to the diffuseness as well as local incompleteness of the basis set, meaning small and diffuse basis sets are affected the most. Finally, we propose one solution to the conundrum in the form of the complementary auxiliary basis set (CABS) singles correction in combination with compact, low l-quantum-number basis sets, showing promising results for non-covalent interactions.Open AccessThe Conundrum of Diffuse Basis Sets: A Blessing for Accuracy yet a Curse for Sparsity
Diffuse atomic orbital basis sets have proven to be essential to obtain accurate interaction energies, especially in regard to non-covalent interactions. However, they also have a detrimental impact on the sparsity of the one-particle density matrix (1-PDM), to a degree stronger than the spatial extent of the basis functions alone could explain. This is despite the fact that the matrix elements of the 1-PDM of insulators (systems with significant HOMO-LUMO gaps) are expected to decay exponentially with increasing real-space distance from the diagonal and the asymptotic decay rate is expected to have a well-defined basis set limit. The observed low sparsity of the 1-PDM appears to be independent of representation and even persists after projecting the 1-PDM onto a real-space grid, leading to the conclusion that this "curse of sparsity" is solely a basis set artifact, which, counterintuitively, becomes worse for larger basis sets, seemingly contradicting the notion of a well-defined basis set limit. We show that this is a consequence of the low locality of the contra-variant basis functions as quantified by the inverse overlap matrix $\mathbf{S}^{-1}$ being significantly less sparse than its covariant dual. Introducing the model system of an infinite non-interacting chain of helium atoms, we are able to quantify the exponential decay rate to be proportional to the diffuseness as well as local incompleteness of the basis set, meaning small and diffuse basis sets are affected the most. Finally, we propose one solution to the conundrum in the form of the complementary auxiliary basis set (CABS) singles correction in combination with compact, low l-quantum-number basis sets, showing promising results for non-covalent interactions. - 20 February 2015
- Published by Wiley in Angewandte Chemie
- Vol. 127 (15) , 4756-4760
Catalytic Upgrading of Biomass-Derived Methyl Ketones to Liquid Transportation Fuel Precursors by an Organocatalytic Approach
- 20 February 2015
- Published by Wiley in Angewandte Chemie
- Vol. 127 (15) , 4756-4760
Catalytic Upgrading of Biomass-Derived Methyl Ketones to Liquid Transportation Fuel Precursors by an Organocatalytic Approach
- Open Access
- 27 May 2014
- Published by Wiley in ChemSusChem
- Vol. 8 (3) , 568
Back Cover: The Role of Hydroxyl Group Acidity on the Activity of Silica-Supported Secondary Amines for the Self-Condensation ofn-Butanal (ChemSusChem 3/2015)
- 27 May 2014
- Published by Wiley in ChemSusChem
- Vol. 8 (3) , 568
Open AccessBack Cover: The Role of Hydroxyl Group Acidity on the Activity of Silica-Supported Secondary Amines for the Self-Condensation ofn-Butanal (ChemSusChem 3/2015)
- 23 May 2006
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 124 (20) , 204105
An efficient self-consistent field method for large systems of weakly interacting components
An efficient method for removing the self-consistent field (SCF) diagonalization bottleneck is proposed for systems of weakly interacting components. The method is based on the equations of the locally projected SCF for molecular interactions (SCF MI) which utilize absolutely localized nonorthogonal molecular orbitals expanded in local subsets of the atomic basis set. A generalization of direct inversion in the iterative subspace for nonorthogonal molecular orbitals is formulated to increase the rate of convergence of the SCF MI equations. Single Roothaan step perturbative corrections are developed to improve the accuracy of the SCF MI energies. The resulting energies closely reproduce the conventional SCF energy. Extensive test calculations are performed on water clusters up to several hundred molecules. Compared to conventional SCF, speedups of the order of (N∕O)2 have been achieved for the diagonalization step, where N is the size of the atomic orbital basis, and O is the number of occupied molecular orbitals.
- 23 May 2006
- Published by AIP Publishing in The Journal of Chemical Physics
- Vol. 124 (20) , 204105
An efficient self-consistent field method for large systems of weakly interacting components
An efficient method for removing the self-consistent field (SCF) diagonalization bottleneck is proposed for systems of weakly interacting components. The method is based on the equations of the locally projected SCF for molecular interactions (SCF MI) which utilize absolutely localized nonorthogonal molecular orbitals expanded in local subsets of the atomic basis set. A generalization of direct inversion in the iterative subspace for nonorthogonal molecular orbitals is formulated to increase the rate of convergence of the SCF MI equations. Single Roothaan step perturbative corrections are developed to improve the accuracy of the SCF MI energies. The resulting energies closely reproduce the conventional SCF energy. Extensive test calculations are performed on water clusters up to several hundred molecules. Compared to conventional SCF, speedups of the order of (N∕O)2 have been achieved for the diagonalization step, where N is the size of the atomic orbital basis, and O is the number of occupied molecular orbitals.