Abstract
Most approaches for solving the electronic Schrödinger equation do not fully exploit the functional-analytic simplicity of the electronic wavefunction. Because of this, the cost of these methods explodes exponentially with increasing electron number, an effect that is often called the curse of dimension. Recent work in mathematics and computer science shows how, by exploiting the smoothness of molecular wavefunctions, one can design methods that achieve the same accuracy as full configuration interaction, but with polynomial cost. The mathematical background of this approach is presented, along with a detailed prescription for identifying the relevant Slater determinants and a demonstration of the method’s effectiveness for atomic systems. In the basis-set limit, this truncated configuration interaction method is size-consistent.
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