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Julien Roul

Publications and source records attributed to Julien Roul.

2 recordsLinked to original sources

Enhancing dissipative cat qubit protection by squeezing

Dissipative cat-qubits are a promising architecture for quantum processors due to their built-in quantum error correction. By leveraging two-photon stabilization, they achieve an exponentially suppressed bit-flip error rate as the distance in phase-space between their basis states increases, incurring only a linear increase in phase-flip rate. This property substantially reduces the number of qubits required for fault-tolerant quantum computation. Here, we implement a squeezing deformation of the cat qubit basis states, further extending the bit-flip time while minimally affecting the phase-flip rate. We demonstrate a steep reduction in the bit-flip error rate with increasing mean photon number, characterized by a scaling exponent $\gamma=4.3$, rising by a factor of 74 per added photon. Specifically, we measure bit-flip times of 22 seconds for a phase-flip time of 1.3 $\mu$s in a squeezed cat qubit with an average photon number $\bar{n}=4.1$, a 160-fold improvement in bit-flip time compared to a standard cat. Moreover, we demonstrate a two-fold reduction in $Z$-gate infidelity, with an estimated phase-flip probability of $\epsilon_X = 0.085$ and a bit-flip probability of $\epsilon_Z = 2.65 \cdot 10^{-9}$ which confirms the gate bias-preserving property. This simple yet effective technique enhances cat qubit performances without requiring design modification, moving multi-cat architectures closer to fault-tolerant quantum computation.

quant-ph

Dynein dynamics at the microtubule plus-ends and cortex during division in the C. $\textit{elegans}$ zygote

During asymmetric cell division, dynein generates forces, which position the spindle to reflect polarity and ensure correct daughter cell fates. The transient cortical localization of dynein raises the question of its targeting. We found that it accumulates at the microtubule plus-ends like in budding yeast, indirectly hitch-hiking on $\text{EBP-2}^{\text{EB1}}$ likely via dynactin. Importantly, this mechanism, which modestly accounts for cortical forces, does not transport dynein, which displays the same binding/unbinding dynamics as $\text{EBP-2}^{\text{EB1}}$. At the cortex, dynein tracks can be classified as having either directed or diffusive-like motion. Diffusive-like tracks reveal force-generating dyneins. Their densities are higher on the posterior tip of the embryos, where $\text{GPR-1/2}^{\text{LGN}}$ concentrate, but their durations are symmetric. Since dynein flows to the cortex are non-polarized, we suggest that this posterior enrichment increases dynein binding, thus accounts for the force imbalance reflecting polarity, and supplements the regulation of mitotic progression via the non-polarized detachment rate.

q-bio.SC