9014-63-5 Purity
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Specification
N-Tetratetracontane (TTC), a long-chain alkane, was applied as a passivation layer to optimize the semiconductor/dielectric interface in flexible ferroelectric organic field-effect transistor (Fe-OFET) nonvolatile memory (NVM) devices. The TTC layer was thermally deposited onto spin-coated P(VDF-TrFE-CTFE) ferroelectric terpolymer films at a rate of 0.5-1 Å/s, with deposition thickness precisely monitored using a quartz crystal oscillator. Post-deposition annealing at 75 °C for 2 hours was employed to smooth the TTC layer. This treatment significantly influenced the growth behavior of the overlying pentacene semiconductor, inducing a layer-by-layer growth mode that yielded enlarged crystalline grains and improved interfacial morphology. Subsequently, a 40 nm thick pentacene layer was thermally evaporated onto the dielectric surfaces, followed by sequential thermal deposition of Cu (60 nm)/MoO₃ (5 nm) to define source and drain electrodes. Devices fabricated on PEN substrates exhibited enhanced mobility (~0.5 cm² V⁻¹ s⁻¹), low programming/erasing voltage (±15 V), and stable electrical performance under mechanical bending. This study demonstrates the critical role of TTC in modulating interfacial properties to achieve high-performance, low-voltage, and mechanically durable flexible Fe-OFET NVMs.
The adsorption behavior and electronic influence of n-Tetratetracontane (n-C₄₄H₉₀, TTC) on Au(111) surfaces was systematically studied using angle-resolved ultraviolet photoemission spectroscopy (ARUPS). A single molecular layer of TTC was deposited via resistance heating of high-purity TTC contained in a quartz crucible under ultrahigh vacuum (< 2 × 10⁻⁹ Pa). The Au(111) substrate was cleaned through repeated Ar⁺ sputtering (1 keV) and annealing cycles at ~600 °C until the Shockley surface state peak was distinctly observed in the ARUPS spectrum.
Using a He I resonance line (hν = 21.218 eV) as the excitation source, spectra were acquired with a hemispherical energy analyzer (Omicron EA-125 HR) offering ~70 meV resolution. The TTC monolayer, adopting a flat-on configuration, induced a measurable energy shift (~160 meV) of the Shockley surface state toward the Fermi level, indicating significant modulation of the quasi-two-dimensional surface electron system.This study demonstrates TTC's utility in tuning metallic surface electronic structures through non-covalent molecular adsorption, offering valuable insight for molecular electronics and organic-metal interface engineering.