Abstract:In this research, the hafnium titanate oxide thin films, TixHf1–xO2, with titanium contents of x = 0, 0.25, 0.9, and 1 were deposited on germanium substrates by atomic layer deposition (ALD) at 300 °C. The approximate deposition rates of 0.2 Å and 0.17 Å per cycle were obtained for titanium oxide and hafnium oxide, respectively. X-ray Photoelectron Spectroscopy (XPS) indicates the formation of GeOx and germanate at the interface. X-ray diffraction (XRD) indicates that all the thin films remain amorphous for th… Show more
“…The prompt SET and gradual RESET in the multilayered systems can explain the rejuvenation of CFs. Analogous to this design, several studies have suggested partial rupture and formation of CFs in multilayered NVBRS devices. ,− This design helps in making the device reproducible and technologically feasible. The log I –log V for the performing device follows a Ohmic and SCLC as shown in Figure S32a,b.…”
Section: Resultsmentioning
confidence: 98%
“…Additionally, the incorporation of hafnium oxide into the TiO 2 layer increases the defect concentration and decreases the formation energy of V O , thus increasing the memory window and decreasing the operating voltage range, − , which can directly be observed from the device performance. Herein, the metal oxide base layers not only ameliorate the interfacial anomalies by posing as interlayers but also are originally reservoirs of supplementary oxygen ions, thereby influencing the operating voltage of the device while preventing leakage of current and penetration of electrode materials. − The distribution of operating voltage for nearly 25 devices is taken to test the reliability of the device (Figure S29c). The multibit storage levels are obtained by different LRS levels corresponding to the size of the filament obtained by controlling the CC (Figures S29d and S30a).…”
Herein, we report intriguing observations of an extremely stable nonvolatile bipolar resistive switching (NVBRS) memory device fabricated using HfO 2 −TiO 2 topologically protected by Al 2 O 3 as a stacked base layer for a CH 3 NH 3 PbI 3 (MAPI) electrolyte layer sandwiched between Ag and fluorine-doped tin oxide (FTO) electrodes. MAPI has been successfully synthesized by a rapid microwave−solvothermal (MW-ST) method within 10 min at 120 °C without requiring any inert gas atmosphere using lowcost precursors and solvents. Subsequently, MAPI powders are dissolved in aprotic solvents (DMF/DMSO = 8:2), and a spin-coated thin film is allowed to recrystallize upon annealing at 120 °C via a solution-based nanoscale self-assembly process. The fabricated memory device with the Ag/MAPI/Al 2 O 3 /TiO 2 -HfO 2 /FTO configuration shows an enhanced resistance ratio of 10 5 for >10 4 s at an extremely lower operating voltage (SET +0.2 V, RESET −0.2 V) when compared to that of the pristine MAPI device (±1 V, 10 2 , 10 4 s). We show that the memory device also exhibits a remarkable endurance of ≥3500 cycles due to the Al 2 O 3 robust coating on the HfO 2 −TiO 2 layer, facilitating prompt heterojunction formation. Thus, the adopted innovative strategies to prepare structurally and optically stable (∼1.5 years) MAPI under high-humid conditions could offer enhanced performance of NVBRS memory devices for medical, security, internet of things (IoT), and artificial intelligence (AI) applications.
“…The prompt SET and gradual RESET in the multilayered systems can explain the rejuvenation of CFs. Analogous to this design, several studies have suggested partial rupture and formation of CFs in multilayered NVBRS devices. ,− This design helps in making the device reproducible and technologically feasible. The log I –log V for the performing device follows a Ohmic and SCLC as shown in Figure S32a,b.…”
Section: Resultsmentioning
confidence: 98%
“…Additionally, the incorporation of hafnium oxide into the TiO 2 layer increases the defect concentration and decreases the formation energy of V O , thus increasing the memory window and decreasing the operating voltage range, − , which can directly be observed from the device performance. Herein, the metal oxide base layers not only ameliorate the interfacial anomalies by posing as interlayers but also are originally reservoirs of supplementary oxygen ions, thereby influencing the operating voltage of the device while preventing leakage of current and penetration of electrode materials. − The distribution of operating voltage for nearly 25 devices is taken to test the reliability of the device (Figure S29c). The multibit storage levels are obtained by different LRS levels corresponding to the size of the filament obtained by controlling the CC (Figures S29d and S30a).…”
Herein, we report intriguing observations of an extremely stable nonvolatile bipolar resistive switching (NVBRS) memory device fabricated using HfO 2 −TiO 2 topologically protected by Al 2 O 3 as a stacked base layer for a CH 3 NH 3 PbI 3 (MAPI) electrolyte layer sandwiched between Ag and fluorine-doped tin oxide (FTO) electrodes. MAPI has been successfully synthesized by a rapid microwave−solvothermal (MW-ST) method within 10 min at 120 °C without requiring any inert gas atmosphere using lowcost precursors and solvents. Subsequently, MAPI powders are dissolved in aprotic solvents (DMF/DMSO = 8:2), and a spin-coated thin film is allowed to recrystallize upon annealing at 120 °C via a solution-based nanoscale self-assembly process. The fabricated memory device with the Ag/MAPI/Al 2 O 3 /TiO 2 -HfO 2 /FTO configuration shows an enhanced resistance ratio of 10 5 for >10 4 s at an extremely lower operating voltage (SET +0.2 V, RESET −0.2 V) when compared to that of the pristine MAPI device (±1 V, 10 2 , 10 4 s). We show that the memory device also exhibits a remarkable endurance of ≥3500 cycles due to the Al 2 O 3 robust coating on the HfO 2 −TiO 2 layer, facilitating prompt heterojunction formation. Thus, the adopted innovative strategies to prepare structurally and optically stable (∼1.5 years) MAPI under high-humid conditions could offer enhanced performance of NVBRS memory devices for medical, security, internet of things (IoT), and artificial intelligence (AI) applications.
“…[18][19][20] The hydroxide peak also overlaps with the Ge 2 III O 3 and the peak at 532.5 eV is in accordance with Ge IV O 2 . 17 To this point, the Fe 6 Ge 5 characterisation uncovers a highly active OER catalyst consisting of a conductive Fe 6 Ge 5 core and an in situ formed amorphous shell. The stoichiometry of the newly formed shell is K x FeO 2 H y .…”
Section: 2184mentioning
confidence: 92%
“…S6b, ESI †). 17 For OER investigations of Fe 6 Ge 5 , we deposited 0.4 mg cm À2 on fluorine doped tin oxide (FTO) glass plates using a binder-free method (electrophoretic deposition (EPD), see ESI † for details and Fig. S7 and S8 for SEM/EDX data of the thin film).…”
After 1 h alkaline oxygen evolution reaction (OER), intermetallic Fe6Ge5 forms a core–shell structure that collapses under continuous OER revealing that core–shell structures can be only snapshots on a pathway to full precatalyst transformation.
“…The horizontal red lines represent the conduction edges, and the horizontal blue lines represent the valence band edges. The right-hand y -axis also represents the redox potential of different chemical species involved in common photocatalytic reactions. ,− …”
Metal oxide semiconductors with a bandgap between 2 and 4 eV are an important class of compounds in the electronics industry and for photocatalysis. With the demand for these materials expanding rapidly, especially in the field of photocatalysis, the fabrication of nanoscale metal oxide particles, which increases the surface-to-volume ratio and thereby reduces the materials costs, is an emphasis of current research. For the purpose of photocatalysis, another important quality is the ability to absorb light efficiently. However, due to the wide bandgap of metal oxide semiconductors, the absorptions are limited to the UV region. Conveniently, a wider range of wavelengths and physical properties can be enabled by doping these metal oxide nanoparticles. Furthermore, the synthesis of doped metal oxides in nanoparticle form offers utility in an expansive array of systems, substrates, and dispersion media. However, the reliable synthesis of nanosized colloidal particles of doped metal oxides remains an ongoing challenge for materials researchers. This manuscript gives a concise overview of research conducted regarding the synthesis of visible-light-active doped metal oxide nanoparticles (NPs) and analyzes how doping impacts the optical properties, making them active in the visible to near-infrared regions. The effects of doping on applications are also summarized. Given that the most commonly doped metal oxide materials are TiO 2 and ZnO, this review highlights both anion-and cation-doped TiO 2 and ZnO nanoparticles. In addition, doped perovskite nanoparticles (e.g., BaTiO 3 and SrTiO 3 ) as well as some of the lesser studied doped metal oxide nanoparticle systems are covered. This work is intended to provide not only a broad overview of existing doped metal oxide nanoparticles but also a foundation for the development of semiconducting nanoparticle architectures for next-generation applications.
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