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William J. Scheideler

Publications and source records attributed to William J. Scheideler.

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Probing the Dynamics of Two-Level System Defect Ensembles via Broadband Cryogenic Transient Dielectric Spectroscopy

Two-level system (TLS) defects in dielectrics are a major source of decoherence in superconducting circuits, yet their microscopic origin and distribution remain poorly understood. Existing circuit-QED probes access limited frequency ranges and mode volumes, restricting studies of isolated materials and interfaces. Here, we present Broadband Cryogenic Transient Dielectric Spectroscopy (BCTDS), a technique for probing TLS-hosting materials over a broad frequency range at cryogenic temperatures. Under strong finite-duration microwave excitation, the transient homodyne I-Q response exhibits coherent phase dynamics after the drive is turned off. Fourier analysis of the transient phase reveals characteristic V-shaped structures that move between cooldowns, consistent with thermocycling-induced changes in the local TLS defect environment that shift defect resonance frequencies. The transient response of BCTDS further enables estimation of susceptibility and two-time correlation functions of the TLS defect ensemble. The observed phase dynamics are qualitatively captured by a driven standard tunneling model containing only a few representative TLS defects. Despite its simplicity relative to the full experimental ensemble, the model reproduces the essential Floquet-dressed dynamics during the drive and generates post-pulse V-shaped structures and interference fringes consistent with the experimental data. The observed BCTDS response may reflect a crossover from localized TLS defect dynamics to a delocalized regime under strong driving, before being quenched into a transient regime that reflects the TLS defect resonance frequencies. Overall, BCTDS represents a potentially useful broadband, time-resolved wafer-level approach for probing TLS defects relevant to quantum technologies.

quant-ph

Eliminating the Perovskite Solar Cell Manufacturing Bottleneck via High-Speed Flexography

Perovskite solar cells have potential to deliver terawatt-scale power via low-cost manufacturing. However, scaling is limited by slow, high-temperature annealing of the inorganic transport layers and the lack of reliable, large-area methods for depositing thin (< 30 nm) charge transport layers (CTLs). We present a method for scaling ultrathin NiOx hole transport layers (HTLs) by pairing high-speed (60 m/min) flexographic printing with rapidly annealed sol-gel inks to achieve the fastest reported process for fabrication of inorganic CTLs for perovskites. By engineering precursor rheology for rapid film-leveling, NiOx HTLs were printed with high uniformity and ultralow pinhole densities resulting in photovoltaic performance exceeding that of spin-coated devices. Integrating these printed transport layers in planar inverted PSCs allows rapid fabrication of high efficiency (PCE > 15%) Cs(x)FA(1-x)PbI solar cells with improved short circuit currents (Jsc) of 22.4 mA/cm2. Rapid annealing of the HTL accelerates total processing time by 60X, while maintaining the required balance of optoelectronic properties and the chemical composition for effective hole collection. These results build an improved understanding of ultrathin NiOx and reveal opportunities to enhance device performance via scalable manufacturing of inorganic CTLs.

cond-mat.mtrl-sci