{"title":"Binder-assisted electroplating of porous copper: formation of an interconnected network with enhanced electrolyte-accessible interfacial area","authors":"Isao Shitanda, Natsumi Fujiwara, Tomoharu Shiozawa, Michiko Tagaya, Masahiro Yoshino, Hikari Watanabe, Masayuki Itagaki","doi":"10.1007/s10008-026-06662-5","DOIUrl":null,"url":null,"abstract":"<div><p>A binder-assisted electroplating process is reported for the fabrication of porous copper electrodes in a room-temperature aqueous sulfate bath. A precursor layer composed of copper powder and a sodium alginate binder was deposited on an electroless-Cu-coated substrate, and electrolytic copper plating was carried out at room temperature in a sulfate bath. Cross-sectional scanning electron microscopy revealed that, in the early stage of plating, electrodeposited copper formed bridges at interparticle contact points, producing an interconnected three-dimensional network <sub>dl</sub>) obtained from cyclic voltammetry in the non-Faradaic region in 0.1 mol L<sup>− 1</sup> Na<sub>2</sub>SO<sub>4</sub> (pH 4). The C<sub>dl</sub> values were 1.09 × 10<sup>− 2</sup>, 2.32, and 1.94 mF cm<sup>− 2</sup> for a flat Cu plate, the 5 min porous Cu, and the 30 min porous Cu, respectively, corresponding to relative increases of approximately 213-fold and 178-fold over the flat reference. These results are consistent with the formation of an electrolyte-accessible porous Cu network by binder-assisted electroplating; quantitative comparison with other porous Cu fabrication routes is beyond the scope of this communication. Linear sweep voltammetry and impedance measurements in 0.1 mol L<sup>− 1</sup> Na<sub>2</sub>SO<sub>4</sub> (pH 4) showed a negatively shifted anodic dissolution onset for the porous electrode and a distributed, porous-electrode impedance response. </p><h3>Graphical Abstract</h3><div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":665,"journal":{"name":"Journal of Solid State Electrochemistry","volume":"30 10","pages":"3623 - 3631"},"PeriodicalIF":3.1000,"publicationDate":"2026-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Solid State Electrochemistry","FirstCategoryId":"5","ListUrlMain":"https://link.springer.com/article/10.1007/s10008-026-06662-5","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ELECTROCHEMISTRY","Score":null,"Total":0}
引用次数: 0
Abstract
A binder-assisted electroplating process is reported for the fabrication of porous copper electrodes in a room-temperature aqueous sulfate bath. A precursor layer composed of copper powder and a sodium alginate binder was deposited on an electroless-Cu-coated substrate, and electrolytic copper plating was carried out at room temperature in a sulfate bath. Cross-sectional scanning electron microscopy revealed that, in the early stage of plating, electrodeposited copper formed bridges at interparticle contact points, producing an interconnected three-dimensional network dl) obtained from cyclic voltammetry in the non-Faradaic region in 0.1 mol L− 1 Na2SO4 (pH 4). The Cdl values were 1.09 × 10− 2, 2.32, and 1.94 mF cm− 2 for a flat Cu plate, the 5 min porous Cu, and the 30 min porous Cu, respectively, corresponding to relative increases of approximately 213-fold and 178-fold over the flat reference. These results are consistent with the formation of an electrolyte-accessible porous Cu network by binder-assisted electroplating; quantitative comparison with other porous Cu fabrication routes is beyond the scope of this communication. Linear sweep voltammetry and impedance measurements in 0.1 mol L− 1 Na2SO4 (pH 4) showed a negatively shifted anodic dissolution onset for the porous electrode and a distributed, porous-electrode impedance response.
期刊介绍:
The Journal of Solid State Electrochemistry is devoted to all aspects of solid-state chemistry and solid-state physics in electrochemistry.
The Journal of Solid State Electrochemistry publishes papers on all aspects of electrochemistry of solid compounds, including experimental and theoretical, basic and applied work. It equally publishes papers on the thermodynamics and kinetics of electrochemical reactions if at least one actively participating phase is solid. Also of interest are articles on the transport of ions and electrons in solids whenever these processes are relevant to electrochemical reactions and on the use of solid-state electrochemical reactions in the analysis of solids and their surfaces.
The journal covers solid-state electrochemistry and focusses on the following fields: mechanisms of solid-state electrochemical reactions, semiconductor electrochemistry, electrochemical batteries, accumulators and fuel cells, electrochemical mineral leaching, galvanic metal plating, electrochemical potential memory devices, solid-state electrochemical sensors, ion and electron transport in solid materials and polymers, electrocatalysis, photoelectrochemistry, corrosion of solid materials, solid-state electroanalysis, electrochemical machining of materials, electrochromism and electrochromic devices, new electrochemical solid-state synthesis.
The Journal of Solid State Electrochemistry makes the professional in research and industry aware of this swift progress and its importance for future developments and success in the above-mentioned fields.