Cu-Ag alloy interconnect is promising for ultra-large-scale integration (ULSI) microelectronic system of which device dimension keeps shrinking. In this study, seedless electrodeposition of Cu-Ag alloy directly on W diffusion barrier as interconnect technology is presented in respect of nano-nucleation control. Chemical equilibrium state of electrolyte was fundamentally investigated according to the pH of electrolyte because direct nano-nucleation of Cu-Ag alloy on W surface is challenging. Chelation behavior of Cu2+ and Ag+ ions with citrate (Cit) and ammonia ligands was dependent on the pH of electrolyte. The amount and kind of Cu- and Ag-based complexes determine the deposition rate, size, elemental composition, and surface morphology of Cu-Ag alloy nano-nuclei formed on W surface.
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http://dx.doi.org/10.1166/jnn.2016.12263 | DOI Listing |
Angew Chem Int Ed Engl
September 2024
Institute of New Energy Materials, School of Materials Science and Engineering, Tianjin University, Tianjin, 300072, China.
The prerequisite for electrocatalytic hydrogenation reactions (EHRs) is HO splitting to form surface hydrogen species (*H), which occupy catalytic sites and lead to mismatched coverage of *H and reactants, resulting in unsatisfactory activity and selectivity. Thus, modulating the splitting pathway of HO is significant for optimizing the EHR process. Herein, a Cu-Ag alloy with a superlattice structure of staggered-ordered Cu and Ag is theoretically predicted and experimentally proven to undergo a pathway for HO splitting called the hydrogen transfer reaction (HTR) in the water layer, which involves the formation of *H, the capture of *H by a water cluster to form H*(HO) and subsequent hydrogenation reactions by H*(HO).
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September 2024
College of Engineering, Hebei Provincial Key Laboratory of Information Fusion and Intelligent Control, Hebei Normal University, Shijiazhuang, 050024, China.
Small
November 2024
Department of Energy Science and Engineering, Daegu Gyeongbuk Institute of Science and Technology (DGIST), 333 Techno jungang-daero, Daegu, 42988, Republic of Korea.
Zero-excess Li-metal batteries (ZE-LMBs) have emerged as the ultimate battery platform, offering an exceptionally high energy density. However, the absence of Li-hosting materials results in uncontrolled dendritic Li deposition on the Cu current collector, leading to chronic loss of Li inventory and severe electrolyte decomposition, limiting its full utilization upon cycling. This study presents the application of ultrathin (≈50 nm) coatings comprising six metallic layers (Cu, Ag, Au, Pt, W, and Fe) on Cu substrates in order to provide insights into the design of Li-depositing current collectors for stable ZE-LMB operation.
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May 2024
School of Materials Science and Engineering, Jiangsu University, Zhenjiang 212013, China.
Due to the lower cost compared to screen-printed silver contacts, the Ni/Cu/Ag contacts formed by plating have been continuously studied as a potential metallization technology for solar cells. To address the adhesion issue of backside grid lines in electroplated n-Tunnel Oxide Passivating Contacts (n-TOPCon) solar cells and reduce ohmic contact, we propose a novel approach of adding a Ni/Si alloy seed layer between the Ni and Si layers. The metal nickel layer is deposited on the backside of the solar cells using electron beam evaporation, and excess nickel is removed by HSO:HO etchant under annealing conditions of 300-425 °C to form a seed layer.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2024
Institutes of Physical Science and Information Technology, Department of Materials Science and Engineering, Centre for Atomic Engineering of Advanced Materials, Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education, Department of Chemistry and Anhui Province Key Laboratory of Chemistry for Inorganic/Organic Hybrid Functionalized Materials, Anhui University, Hefei, Anhui, 230601, PR China.
Owing to the significant attention directed toward alloy metal nanoclusters, it is crucial to explore the relationship between their structures and their performance during the electrocatalytic CO reduction reaction (eCORR) and discover potential synergistic effects for the design of novel functional nanoclusters. However, a lack of suitable analogs makes this investigation challenging. In this study, we synthesized a well-defined pair of structural analogs, [AuCu(SAdm)(Dppm)Cl] and [AuAg(SAdm)(Dppm)Cl] (AuCu and AuAg, respectively), and characterized them.
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