15 research outputs found
Observation of the nonlinear Hall effect under time reversal symmetric conditions
The electrical Hall effect is the production of a transverse voltage under an
out-of-plane magnetic field. Historically, studies of the Hall effect have led
to major breakthroughs including the discoveries of Berry curvature and the
topological Chern invariants. In magnets, the internal magnetization allows
Hall conductivity in the absence of external magnetic field. This anomalous
Hall effect (AHE) has become an important tool to study quantum magnets. In
nonmagnetic materials without external magnetic fields, the electrical Hall
effect is rarely explored because of the constraint by time-reversal symmetry.
However, strictly speaking, only the Hall effect in the linear response regime,
i.e., the Hall voltage linearly proportional to the external electric field,
identically vanishes due to time-reversal symmetry. The Hall effect in the
nonlinear response regime, on the other hand, may not be subject to such
symmetry constraints. Here, we report the observation of the nonlinear Hall
effect (NLHE) in the electrical transport of the nonmagnetic 2D quantum
material, bilayer WTe2. Specifically, flowing an electrical current in bilayer
WTe2 leads to a nonlinear Hall voltage in the absence of magnetic field. The
NLHE exhibits unusual properties sharply distinct from the AHE in metals: The
NLHE shows a quadratic I-V characteristic; It strongly dominates the nonlinear
longitudinal response, leading to a Hall angle of about 90 degree. We further
show that the NLHE directly measures the "dipole moment" of the Berry
curvature, which arises from layer-polarized Dirac fermions in bilayer WTe2.
Our results demonstrate a new Hall effect and provide a powerful methodology to
detect Berry curvature in a wide range of nonmagnetic quantum materials in an
energy-resolved way
The Mayer-Rokitansky-Küster-Hauser syndrome (congenital absence of uterus and vagina) – phenotypic manifestations and genetic approaches
The Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome affects at least 1 out of 4500 women and has for a long time been considered as a sporadic anomaly. Congenital absence of upper vagina and uterus is the prime feature of the disease which, in addition, is often found associated with unilateral renal agenesis or adysplasia as well as skeletal malformations (MURCS association). The phenotypic manifestations of MRKH overlap various other syndromes or associations and thus require accurate delineation. Since MRKH manifests itself in males, the term GRES syndrome (Genital, Renal, Ear, Skeletal) might be more appropriate when applied to both sexes. The MRKH syndrome, when described in familial aggregates, seems to be transmitted as an autosomal dominant trait with an incomplete degree of penetrance and variable expressivity. This suggests the involvement of either mutations in a major developmental gene or a limited chromosomal deletion. Until recently progress in understanding the genetics of MRKH syndrome has been slow, however, now HOX genes have been shown to play key roles in body patterning and organogenesis, and in particular during genital tract development. Expression and/or function defects of one or several HOX genes may account for this syndrome