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It is well established that causal linear response functions can be found by computing the much simpler imaginary time-ordered Matsubara functions and performing an analytic continuation. This principle is the basis for much of our understanding of linear response for interacting and disordered systems, via diagrammatic perturbation theory. Similar imaginary-time approaches have recently been introduced for computing nonlinear response functions as well, for example in [Annalen der Physik 536, 2300504 (2024); Physical Review X 11, 041006 (2021)], where the authors analytically continue the Matsubara functions to obtain the Keldysh response functions. In this work, we provide a proof of this connection to all orders in perturbation theory using an equation of motion based approach. We show by induction that causal nonlinear response functions at every order can be obtained from an analytic continuation of an appropriate time-ordered Matsubara function. We demonstrate this connection explicitly for second order response functions in the Lehmann representation. As a byproduct of our approach, we derive an explicit expression for the Lehmann representation of $$n$$-th order response functions by solving the equations of motion. We also use our result to find an analytic spectral density representation for both causal response functions and Matsubara functions. As an example, we apply our method to derive the non-linear $A^3$ term in the $SU(2)$ spin Hall response of an insulator with spin rotation symmetry. Finally, we show how our results lead to a family of generalized sum rules, focusing explicitly on the asymptotic expression for $$n$$-th harmonic generation rate. Our work opens the door to using imaginary time approaches to study nonlinear response functions in general condensed matter systems.more » « lessFree, publicly-accessible full text available June 29, 2027
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We introduce stable real-space invariants (SRSIs), topological invariants defined from adiabatic deformations between Wannier states, generalizing previously discovered local and composite real-space invariants. SRSIs are Z- and Zn-valued (n=2,4) linear combinations of Wannier state multiplicities characterizing the stable equivalence of atomic insulators. We enumerate all SRSIs in nonmagnetic space groups with and without spin-orbit coupling. ZSRSIs are in one-to-one correspondence with momentum-space symmetry data and thus determine symmetry indicators of topology (SIs). ZnSRSIs capture real-space information beyond momentum-space symmetry data and SIs. Applying SRSIs to split elementary band representations (EBRs) whose symmetry data decomposes into positive sums of other EBR symmetry data, we diagnose the topology of all 211 cases across 51 space groups except for 8 exceptions in 5 space groups. Our results solidify Topological Quantum Chemistry beyond SIs and momentum-space symmetry data. Finally, we use SRSIs to diagnose an obstructed atomic insulator in a realistic material.more » « lessFree, publicly-accessible full text available June 29, 2027
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Recent work on Abelian topological phases with rotational symmetry has raised the question of whether rotational symmetry can protect gapless propagating edge modes. Here we address this issue by considering the coupling of topological phases to the extrinsic geometry of the background. First, we analyze an effective hydrodynamic theory for an Abelian topological phase with vanishing Hall conductance. After integrating out the bulk hydrodynamic degrees of freedom, we identify charge neutral, rotationally invariant-mass terms by coupling the propagating boundary modes to the extrinsic geometry. This allows us to integrate out the edge modes and we find a gapped theory described by a local induced action that depends on the extrinsic geometry of the boundary, regardless of the shift. Finally, we apply these ideas to a microscopic theory and find the explicit bulk terms which respect gauge and rotational symmetry and open a gap in the edge spectrum.more » « lessFree, publicly-accessible full text available October 1, 2026
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Free, publicly-accessible full text available December 1, 2026
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