A nickel film electroplated onto a metal substrate can be used as a catalyst for water splitting and a magnetic material for spin valves. Although the nucleation and growth of Ni on Au(111) have already been examined with in situ scanning tunneling microscopy (STM), the current study provides new insights of the structure of the first layer of Ni on an ordered Au(111) electrode in 0.1 M KSO + 1 mM HSO + 10 mM NiSO (pH 3). Prolonged STM scanning of the Ni monolayer on a Au(111) electrode revealed interfacial mixing to produce a surface alloy, initially assuming segregated Ni domains and later transforming them to a homogeneous Ni/Au phase. The formation of the Ni/Au(111) surface alloy affected the structure of the subsequent bulk Ni deposition. The inclusion of 2-mercapto-1-methylimidazole (MMI) in the deposition bath incurred Ni deposition at a less negative potential and a faster rate, resulting in an overall 5.3 times more Ni deposited on the Au electrode in potentiodynamic experiments. MMI molecules were adsorbed on the Ni deposit to prevent Ni dissolution in the Au(111) electrode. MMI could catalyze the presumed rate-determining step from Ni to Ni en route to the metallic Ni. The resultant Ni film with MMI had a 3D texture without a preferred crystal orientation on the Au electrode, as opposed to a layer type growth of Ni on Au(111) without MMI.
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http://dx.doi.org/10.1021/acsomega.4c00154 | DOI Listing |
J Phys Chem C Nanomater Interfaces
November 2024
Leiden Institute of Chemistry, Leiden University, PO Box 9502, 2300 RA Leiden, The Netherlands.
Oxidation-reduction cycles (ORCs) on Au(111) in 0.1 M sulfuric acid solution change the electrode morphology due to the formation of many new nanosized islands. With increasing the cycle number, the roughness of the surface increases due to the formation of multiatomic-step adatom islands and pits.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Key Laboratory of the Ministry of Education for Advanced Catalysis Materials, Institute of Physical Chemistry, College of Chemistry and Materials Science, Zhejiang Normal University, 321004, Jinhua, P. R. China.
The recent discovery of frustrated Lewis pairs (FLPs) during the activation of small molecules has inspired extensive research across the full span of chemical science. Owing to the nature of weak interactions, it is experimentally challenging to directly observe and modulate FLP at the molecular scale. Here we design a boron cluster anion building block (BH ) and organic amine cations ([NR], R=-CH, -CH) as the FLP to prove the feasibility of controlling their interaction in the electric double layer (EDL) via an electrochemical strategy.
View Article and Find Full Text PDFACS Omega
September 2024
Department of Chemistry, National Central University, Chungli County, Taoyuan City 32049, Taiwan ROC.
11-acryloylamino undecanoic acid (AAUA) is a versatile polymerizable surfactant that has been applied to coat medical devices, and these applications can benefit from a fundamental understanding of its interaction with a metal substrate. Cyclic voltammetry and scanning tunneling microscopy (STM) were used to examine the adsorption configuration of AAUA molecules on an ordered Au(111) electrode and their mutual interactions, as AAUA was adsorbed from a methanol dosing solution. In addition to the van der Waals force between the aliphatic groups, the hydrogen bonding between the carboxylic acid and acrylamide groups was also important to guide the spatial arrangement of AAUA admolecules on the Au electrode.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Department of Chemistry-Ångström Laboratory, Uppsala University, Lägerhyddsvägen 1, BOX 538, 75121, Uppsala.
We have studied polarized Au(100) and Au(111) electrodes immersed in electrolyte solution by implementing finite-field methods in density functional theory-based molecular dynamics simulations. This allows us to directly compute the Helmholtz capacitance of electric double layer by including both electronic and ionic degrees of freedom, and the results turn out to be in excellent agreement with experiments. It is found that the electronic response of Au electrode makes a crucial contribution to the high Helmholtz capacitance and the instantaneous adsorption of Cl can lead to a charge inversion on the anodic polarized Au(100) surface.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2024
Jiangsu Key Laboratory for Carbon-Based Functional Materials and Devices , Institute of Functional Nano and Soft Materials (FUNSOM), Soochow University, 199 Ren'ai Road, Suzhou 215123, Jiangsu, P. R. China.
Metal-free carbon materials (MFCMs) have extensive applications in electrocatalysis because of their comparable catalytic activity to that of Pt/C in some cases. Understanding the structure-property relationship is crucial for the reasonable design of more efficient catalysts. To reveal the structure-property relationship of the hydrogen evolution reaction (HER), we prepared nanowire model catalysts on single-crystalline Au(111) electrodes through state-of-the-art on-surface synthesis.
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