Related Experiment Video
Updated: Jul 3, 2026

Ultrahigh Density Array of Vertically Aligned Small-molecular Organic Nanowires on Arbitrary Substrates
Published on: June 18, 2013
Enhanced Control of Single Crystalline Ag Dendritic Growth on Al Foil via Galvanic Displacement and Simultaneous
Lidija D Rafailović1,2, Stefan M Noisternig2,3, Jana Bischoff2
1Department of Materials Science Chair of Materials Physics Montanuniversität Leoben 8700 Leoben Austria.
Abstract:
A facile synthesis platform for the formation of stable single crystalline Ag dendrites is demonstrated. Using a porous electrospun polyacrylonitrile nanofiber network on Al foil as a template facilitates more uniform dendritic growth in the presence of D-glucose. In contrast, a denser polymer network restricts the nucleation site availability on the Al foil, highlighting the critical role of the substrate. The growth formation of silver dendrites is reduced in the solution when two simultaneous processes occur: The electroreduction of Ag+ in the D-glucose solution and galvanic displacement driven by the interaction of Ag+ with the aluminum substrate. High-resolution transmission electron microscopy analysis shows the single crystalline nature of Ag dendrites grown from the Al substrate, revealing atomic structures with closely packed layers forming highly faulted face-centered cubic and hexagonal close-packed structures. The remarkable long-term stability of Ag dendrites is primarily attributed to their single crystalline structure, with additional contributions from capping by D-gluconic acid, as confirmed by Raman analysis. This novel approach to the generation of highly stable Ag dendrites has significant potential for applications such as surface-enhanced Raman scattering, which has to date been considered to be very sensitive to environmental effects.
More Related Videos
10:27Simultaneous Multi-surface Anodizations and Stair-like Reverse Biases Detachment of Anodic Aluminum Oxides in Sulfuric and Oxalic Acid Electrolyte
Published on: October 5, 2017
05:02Growth of Gold Dendritic Nanoforests on Titanium Nitride-coated Silicon Substrates
Published on: June 3, 2019
Related Concept Videos
Preparation of Alcohols via Addition Reactions
The acid-catalyzed addition of water to the double bond of alkenes is a large-scale industrial method used to synthesize low-molecular-weight alcohols. An acidic atmosphere is required to allow the hydrogen in the water molecule to act as an electrophile and attack the double bond in an alkene. The addition of a proton to the double bond creates a carbocation intermediate. The proton preferentially bonds to the less substituted end of the double bond to create a more stable carbocation...
Alcohols from Carbonyl Compounds: Reduction
Catalytic hydrogenation is similar to the reduction of an alkene or alkyne by adding H2 across the pi bond in the presence of transition metal catalysts like Raney Ni, Pd–C, Pt, or Ru. Aldehydes and ketones can be reduced by this method, often under mild to moderate heat (25–100°C) and...
Alcohols from Carbonyl Compounds: Grignard Reaction
Magnesium from the reagent coordinates with carbonyl oxygen, further reducing the carbonyl carbon's electron density. Thus, the carbonyl carbon is a...
Oxidation of Alcohols
The process of oxidation in a chemical reaction is observed in any of the three forms:
Acid Halides to Alcohols: LiAlH4 Reduction
The mechanism proceeds in three steps. First, the nucleophilic hydride ion attacks the carbonyl carbon of the acid halide to form a tetrahedral intermediate. Next, the carbonyl group is re-formed, and the halide ion departs as a leaving group, generating an aldehyde. A second nucleophilic attack by the hydride yields an alkoxide ion, which, upon protonation, gives a primary alcohol as...
Aldol Condensation with β-Diesters: Knoevenagel Condensation