Yun Yu, Wu Liyan, Behrendt Drew, Musavigharavi Pariasadat, Pradhan Dhiren K, He Yunfei, Guo Yichen, Rai Rajeev Kumar, Zhou Songsong, Johnson Craig L, Stach Eric, Agar Joshua C, Hanrahan Brendan M, Jariwala Deep, Olsson Roy H, Rappe Andrew M, Spanier Jonathan E
Department of Mechanical Engineering & Mechanics, Drexel University, Philadelphia, PA, 19104-2875, USA.
Department of Chemistry, University of Pennsylvania, Philadelphia, PA, 19104-6323, USA.
Adv Mater. 2025 Aug;37(33):e2501931. doi: 10.1002/adma.202501931. Epub 2025 Jun 9.
Ferroelectric nitrides attract immense attention due to their excellent electrical, mechanical, and thermal properties as well as for their compatibility with scalable semiconductor technology. The availability of high-quality nitride films possessing tailorable coercive voltage and field, however, remains challenging, and is a key for deeper exploration of switching dynamics and practical applications in low-power devices. 2D growth of epitaxial thin (≲20 nm) c-axis-oriented ScAlN films is reported on AlO (0001) and on electrically conductive 4H-SiC (0001), obtained by reflection high-energy electron diffraction-monitored layer-by-layer physical vapor deposition growth. Films exhibit high quality, as evidenced by rocking curve full-width at half-maximum (FWHM) as narrow as ≈0.02°, and an atomically abrupt film-substrate interface with low dislocation density. The coercive field of ScAlN/4H-SiC (0001) heterostructures is as low as 2.75 MV cm. Moreover, a high endurance of >10 cycles at saturation polarization is achieved. Density functional theory calculations of a model system reveal that an improved crystal quality, including atomically abrupt ferroelectric nitride-metal interface, facilitates the reduction in the switching barriers, and leads to reduced coercivity. These findings demonstrate the feasibility of obtaining high-quality epitaxial ferroelectric nitride films on highly scalable and radiation-resistant substrates, and their potential for energy-efficient electronic devices.
铁电氮化物因其优异的电学、力学和热学性能以及与可扩展半导体技术的兼容性而备受关注。然而,获得具有可定制矫顽电压和电场的高质量氮化物薄膜仍然具有挑战性,这是深入探索开关动力学以及在低功耗器件中的实际应用的关键。本文报道了通过反射高能电子衍射监测的逐层物理气相沉积生长,在AlO(0001)和导电的4H-SiC(0001)上外延生长的厚度小于20nm的c轴取向ScAlN薄膜。薄膜表现出高质量,半高宽摇摆曲线(FWHM)窄至约0.02°,且薄膜-衬底界面原子级陡峭,位错密度低,这证明了薄膜的高质量。ScAlN/4H-SiC(0001)异质结构的矫顽场低至2.75 MV/cm。此外,在饱和极化下实现了大于10次循环的高耐久性。对模型系统的密度泛函理论计算表明,包括原子级陡峭的铁电氮化物-金属界面在内的晶体质量的改善,有助于降低开关势垒,并导致矫顽力降低。这些发现证明了在高度可扩展且抗辐射的衬底上获得高质量外延铁电氮化物薄膜的可行性,以及它们在节能电子器件中的潜力。