Fig. 2: Evidence for nonreciprocal directional dichroism.
From: Visualizing rotation and reversal of the Néel vector through antiferromagnetic trichroism

a Absorption coefficient (A) spectra (kX > 0, Eω||Y) at 4.2 K. The blue- and the red-colored data were obtained after ME cooling procedure with EZ = +100 kV m−1 and −100 kV m−1, respectively, and μ0HY = +0.15 T. The inset shows an experimental geometry. b Difference absorption spectra, ΔA = A(+100 kV/m) − A(−100 kV/m), for kX > 0 (purple) and kX < 0 (dark yellow). c ΔA spectra at various temperatures above and below TN = 44 K. d The temperature dependence of ΔA at 1.65 eV, where ΔA takes the maximum in the spectra. In (a–d), the cooling electric and magnetic fields applied during the ME cooling were removed before each measurement. e Schematic hole-energy spectrum of Cu(3d)-O(2p) bonding molecular orbitals of the square-planar CuO46− unit partly reproduced from ref. [38]. a(z2) is omitted for clarity. An electric-dipole (magnetic-dipole) transition with a Y-(Z-)axis electric (magnetic) field of light, allowed in C4 symmetry, is denoted by a green (red) arrow. A spin–orbit coupling term lxsx + lysy hybridizes b(xy) and e(xz) [e(yz)].