With the view towards future non-volatile random access memories that can be integrated at a large scale, extensive study on resistive switching (RS) devices arranged in a crossbar array is currently underway. Although the crossbar array architecture offers relatively simple and acceptable scalability, the presence of sneak current is recognized as a critical issue that needs to be resolved at device level. In addressing this issue, we demonstrate a new type of RS device fabricated by combining graphene oxide (G-O) and zinc oxide (ZnO) with highly asymmetric current-voltage (I-V) characteristics depending on the polarity of bias voltage. The distinctive highly asymmetric I-V characteristics result from the presence of a hetero-junction interface formed between the G-O and ZnO layers. This hetero-junction manifests resistance in the range of GΩ under both forward and reverse bias voltage when the device is in the OFF state, in contrast, when the device is in the ON state, it exhibits resistance in the range of MΩ or kΩ under forward bias and GΩ under reverse bias. We propose to employ demonstrated RS devices with highly asymmetric I-V characteristics to mitigate adverse effects of the sneak current.
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http://dx.doi.org/10.1088/1361-6528/aadd6f | DOI Listing |
Adv Mater
December 2024
School of Chemistry and Chemical Engineering and State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai, 200240, China.
Asymmetric catalysis is essential for addressing the increasing demand for enantiopure compounds. Recent advances in reticular chemistry have demonstrated that metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) possess highly regular porous architectures, exceptional tunability, and the ability to incorporate chiral functionalities through their open channels or cavities. These characteristics make them highly effective and enantioselective catalysts for a wide range of asymmetric transformations.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Tianjin University, School of Materials Science and Engineering, Bldg 31, Tianjin, CHINA.
Single-atom catalysts (SACs) with nonplanar configurations possess unique capabilities for tailoring the oxygen reduction reaction (ORR) catalytic performance compared with the ones with planar configurations, owing to the additional orbital rearrangement arising from the asymmetric coordination atoms. However, the systematic investigation of these nonplanar SACs has long been hindered by the difficulty in screening feasible nonplanar configurations and precisely controlling the coordination structures. Herein, we demonstrate a combined high-throughput screening and experimental verification of nonplanar SACs (ppy-MN3) for highly active and selective 2e- ORR electrocatalysis.
View Article and Find Full Text PDFNat Commun
December 2024
Key Laboratory for Quantum Materials of Zhejiang Province, Department of Physics, School of Science, Westlake University, 18 Shilongshan Road, Hangzhou, 310024, Zhejiang Province, China.
Extending ferroelectric materials to two-dimensional limit provides versatile applications for the development of next-generation nonvolatile devices. Conventional ferroelectricity requires materials consisting of at least two constituent elements associated with polar crystalline structures. Monolayer graphene as an elementary two-dimensional material unlikely exhibits ferroelectric order due to its highly centrosymmetric hexagonal lattices.
View Article and Find Full Text PDFAdv Mater
December 2024
State Key Lab of High Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai, 200050, P. R. China.
Nickel-iron layered double hydroxides (NiFe LDHs) are considered as promising substitutes for precious metals in oxygen evolution reaction (OER). However, most of the reported NiFe LDHs suffer from poor long-term stability because of the Fe loss during OER resulting in severe inactivation. Herein, a dynamically stable chelating interface through in situ transformation of asymmetric aldehyde-ligand (THB, 1,3,5-Tris(3'-hydroxy-4'-formylphenyl)-benzene) modified NiFe LDHs to anchor Fe and significantly enhance the OER stability is reported.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Faculty of Chemistry and Chemical Engineering, Yunnan Normal University, Kunming 650500, PR China; Key Laboratory of Photochemical Conversion and Optoelectronic Materials, CAS-HKU Joint Laboratory on New Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, University of Chinese Academy of Sciences, Beijing 100049, PR China.
In this work, Pt single atoms (SAs) were engineered on the surface of CdInS (CIS) to trigger abundant generation and stable existence of sulfur vacancies (S). Through quasi in situ X-ray photoelectron spectroscopy (XPS) and work function analysis, the photogenerated electrons are first captured by Pt SAs and S, and then transferred from Pt SAs to S, ultimately increasing the electron density of S. Meanwhile, S have significant advantages in adsorbing CO molecules.
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