Grain tailoring helps ultrathin ferroelectric memories take the heat
Peer-Reviewed Publication
Updates every hour. Last Updated: 1-Nov-2026 18:16 ET (1-Nov-2026 23:16 GMT/UTC)
Hafnia-based ferroelectric memories are emerging as promising candidates for next-generation nonvolatile memory because they combine excellent scalability with compatibility with CMOS technology. Further reducing the thickness of ferroelectric films can lower operating voltage and increase storage density, but maintaining reliability at high temperatures becomes increasingly challenging. Researchers at Fudan University have now shown that tailoring the size and orientation of ferroelectric grains can help address this challenge. Their ultrathin devices remain highly stable at 225 °C, pointing to a route toward dense and reliable ferroelectric memories for harsh thermal environments. The study was published in Science Bulletin.
Researchers have engineered a symmetry-mismatched van der Waals interface by stacking twofold-symmetric black arsenic (b-As) with threefold-symmetric 2H transition-metal dichalcogenides (2H-TMDs). The interface creates directional in-plane polarization and a strong bulk photovoltaic effect (BPVE), allowing devices to generate photocurrent without external bias while distinguishing light polarization. Optimized b-As/WSe2 devices respond across 405–1064 nm and reach 946 mA/W responsivity, 9.28 x 109 Jones detectivity, a 0.95 V−1 BPV coefficient, and a dichroic ratio of 10.82 at 638 nm.
New study shows that catastrophic fractures begin not with an explosive crack, but with tiny two-dimensional patches that creep almost imperceptibly before suddenly racing through a material. The findings offer a new picture of material failure, with implications ranging from detecting fractures to understanding how earthquakes begin.
Soft X-ray absorption spectroscopy (XAS) was adopted to measure organic molecules that contain sp2-hybridized carbons in organic solvents (Soft-XAS-OS) for applying the Hiyama cross-coupling reaction, a carbon-carbon bond-forming reaction. The C=C π* peaks of phenyl groups of an arylsilane and silicates in organic solvents were observed using the C K-edge XAS. Combining the XAS spectra with the inner-shell quantum chemical calculations, the energy shifts of the C=C π* peaks were related to the C‒Si bond lengths of an arylsilane and silicates, which are key factors for the reactivities in the Hiyama cross-coupling reaction.
Photocatalytic reactions can be driven by both photochemical and photothermal processes. However, their individual contributions and synergistic effect remain to be clarified. Herein, we investigated the respective roles of these effects using a Cu–TiO2/Ti model catalyst that integrated photochemical and photothermal functionalities within a single photocatalytic system. Employing photocatalytic methanol decomposition as a model reaction, the Cu–TiO2/Ti catalyst achieved a high H2 yield rate of 0.511 mmol h−1 with selectivity of 96.6% toward HCHO among oxidation products, attributed to the cooperative action of photochemical and photothermal processes. In situ resonant Auger electron spectroscopy (RAS), together with in situ Cu K-edge X-ray absorption fine structure and excited-state density functional theory calculations, revealed the accumulation of photogenerated electrons at Cu sites from TiO2, suggests the possible formation of an electron transfer pathway from TiO2 to Cu, which promotes stepwise methanol dehydrogenation to HCHO and H2. Simultaneously, the photothermal contribution from Ti enhanced catalytic activity by accelerating reaction kinetics and promoting the desorption of HCHO, thereby suppressing its overoxidation to CO.