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The origin and function of chirality in DNA, proteins, and other building blocks of life represent a central question in biology. Observations of spin polarization and magnetization associated with electron transport through chiral molecules, known collectively as the chiral induced spin selectivity effect, suggest that chirality improves electron transfer. Using reconfigurable nanoscale control over conductivity at the LaAlO₃/SrTiO₃interface, we create chiral electron potentials that explicitly lack mirror symmetry. Quantum transport measurements on these chiral nanowires reveal enhanced electron pairing persisting to high magnetic fields (up to 18 tesla) and oscillatory transmission resonances as functions of both magnetic field and chemical potential. We interpret these resonances as arising from an engineered axial spin-orbit interaction within the chiral region. The ability to create one-dimensional electron waveguides with this specificity creates opportunities to test, via analog quantum simulation, theories about chirality and spin-polarized electron transport in one-dimensional geometries. 

The thermoelectric properties of quasi‐1D electron waveguides at the LaAlO₃/SrTiO₃interface at millikelvin temperatures are investigated. A highly enhanced and oscillating thermopower is found for these electron waveguides, with values exceeding 100 μV K⁻¹at 0.1 K in the electron‐depletion regime. The Mott relation, which governs the band‐term thermopower of noninteracting electrons, agrees well with the experimental findings in and around regimes where strongly attractive electron–electron interactions lead to a previously reported Pascal series of conductance explained by bound states of electrons. These results pave the way for quantized thermal transport studies of emergent electron liquid phases in which transport is governed by quasiparticles with charges that are integer multiples or fractions of an electron.