Electrochemical migration is a critical factor contributing to failures in electronics due to humidity. When moisture accumulates on conductor-dielectric-conductor systems under bias voltage, electrochemical processes can be triggered, leading to the growth of metallic dendrites that may ultimately result in system failure. Despite its significance, many aspects of electrochemical migration remain unresolved, particularly regarding the physical characteristics of liquid buildup that facilitate dendrite growth and short circuit currents. While there are a few techniques that can measure water adsorption on the nanoscale, most conventional methods focus on water droplets within the size range of visible light wavelengths. In this study, we implemented a combined electrical-optical-ellipsometric measurement on FR-4 printed circuit boards featuring Sn surface finishes. Our experimental setup allowed for the measurement of water condensation across a wide range of thicknesses, while simultaneously monitoring the solder mask and metal electrodes during cooling. The ambient temperature of 25 C and a relative humidity of 60% were constant during the measurement. By employing this approach, we elucidated the mechanisms of dendrite formation and short circuit currents, demonstrating that the water film remains continuous between droplets on the solder mask surface. Compared to Sn the nucleation was delayed on the solder mask with a larger surface coverage at smaller thicknesses. This comprehensive methodology provides crucial insights into the electrochemical migration process, enhancing our understanding of the underlying phenomena that contribute to electronic failures due to humidity. Our work highlighted the complementary nature of ellipsometry and optical imaging.
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http://dx.doi.org/10.1016/j.heliyon.2025.e42117 | DOI Listing |
ACS Nano
March 2025
Hefei National Research Center for Physical Sciences at the Microscale, Department of Materials Science and Engineering, CAS Key Laboratory of Materials for Energy Conversion, University of Science and Technology of China. Hefei, Anhui 230026, China.
P2-type layered oxides, such as NaNiMnO, represent a promising class of cathode materials for Sodium-ion batteries (SIBs) due to their high theoretical energy density. However, their cycling stability is often compromised by severe phase transitions and irreversible lattice oxygen redox reactions at high voltages. In this work, we develop a Zn and Al codoping approach to design a NaNiZnMnAlO (ZA-NNMO) cathode for stable SIBs.
View Article and Find Full Text PDFNano Lett
March 2025
College of Physics and Energy, Fujian Normal University, Fuzhou 350117, China.
Combined solid electrolytes address cathode-anode compatibility in all-solid-state Li-ion batteries (ASSLBs), yet interface stability and ion transport mechanisms between different electrolytes remain unclear. Herein, we investigate LiPSCl (LPSC), LiInCl (LIC), and LiZrOCl (LZOC) composite electrolytes through electrochemical analysis and operando X-ray photoelectron spectroscopy. Our results reveal that the electrostatic potential difference between LPSC and LIC inhibits Li migration, leading to the decomposition of LIC into InCl and LiCl, causing battery failure.
View Article and Find Full Text PDFNat Commun
March 2025
School of Environmental Science and Engineering, Southern University of Science and Technology, Shenzhen, 518055, China.
To address the dual challenges of freshwater scarcity and energy storage demands, battery deionization has emerged as a promising technology for simultaneous salt removal and energy recovery. Compared to the significant research advancement in cation-storage electrodes, anion-storage counterparts remain a critical bottleneck thus limiting the industrialization of battery deionization technique. Here, we employ CuO as a Cl storage electrode material, by engineering the electrochemical-driven reversible synthesis-decomposition process between CuO and Cu(OH)Cl, the CuO electrode delivers the state-of-the-art high charge capacity of 286.
View Article and Find Full Text PDFACS Nano
March 2025
Department of Materials Science and Engineering, and Centre for Functional Photonics (CFP), City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong S.A.R. 999077, P.R. China.
Light-emitting colloidal lead halide perovskite nanocrystals (PeNCs) are considered promising candidates for next-generation vivid displays. However, the operational stability of light-emitting diodes (LEDs) based on PeNCs is still lower than those based on polycrystalline perovskite films, which requires an understanding of defect formation in PeNCs, both inside the crystal lattice ("bulk") and at the surface. Meanwhile, uncontrollable ion redistribution and electrochemical reactions under LED operation can be severe, which is also related to the bulk and surface quality of PeNCs, and a well-designed device architecture can boost carrier injection and balance radiative recombination.
View Article and Find Full Text PDFJ Colloid Interface Sci
March 2025
National-Local Joint Engineering Laboratory for Energy Conservation in Chemical Process Integration and Resources Utilization, School of Chemical Engineering, Hebei University of Technology, Xiping Road 5340, Beichen District, Tianjin 300130, PR China. Electronic address:
Solid-state electrolytes (SSEs) can replace the diaphragm and electrolyte in the traditional battery to solve safety perils such as electrolyte leakage and combustion, while their practical application is greatly hindered by their low ionic conductivity and poor ability to inhibit lithium dendrites. Herein, a laponite (LAP)/zeolitic imidazolate framework-8 (ZIF-8) hybrid material modified polyvinylidene fluoride (PVDF)-based composite polymer electrolytes (CPE) is reported. The in-situ modification of ZIF-8 induced by electrostatic interactions between LAP layers not only improves the dispersion of LAP, but also acts as an external bridge through hydrogen bonding with PVDF to construct a stable conductive network.
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