Related Experiment Video
Updated: Jan 12, 2026

Fabrication of Ti3C2 MXene Microelectrode Arrays for In Vivo Neural Recording
Published on: February 12, 2020
Amorphous Cu Intermediate Modification During Lewis Acid Etching of High-Entropy MAX to MXene Using CuCl2
Yingnan Yan1, Xinpeng Huang1, Xuehua Yan1,2
1School of Materials Science and Engineering, Jiangsu University, Zhenjiang, Jiangsu, 212013, China.
None:
High-entropy MXenes (HE-MXenes) represent a highly promising frontier in 2D materials, but their safe, fluorine-free synthesis remains a critical challenge. Recently, Lewis acidic molten salt etching has been emerged as a promising alternative due to its high operational safety and precise regulation of MXene surface terminal groups. This work reports a strategy utilizing anhydrous CuCl2 to etch the high-entropy MAX (HE-MAX) phase, (TiVNbMoW)3AlC2. The investigation reveals that the reaction is hindered by the formation of a previously unreported amorphous intermediate structure (M3C2-ClCux). However, this intermediate phase, trapped at a specific etchant concentration, degrades the material's electrochemical performance. By optimizing the etchant ratio, the adverse influence of the M3C2-ClCux on the electrochemical performance is effectively mitigated, enabling the successful synthesis of an accordion-like HE-MXene. The electrochemical energy storage performance of this HE-MXene is systematically evaluated in acidic and alkaline electrolytes. More importantly, this study not only presents a viable F-free synthetic route for HE-MXene but also reveals a novel reaction mechanism that is crucial for future process optimization and rational material design.
More Related Videos
10:15Solar-Driven Electrochemical Green Fuel Production from CO2 and Water Using Ti3C2Tx MXene-Supported CuZn and NiCo Catalysts
Published on: November 7, 2025
09:45Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
Published on: March 20, 2017
Related Concept Videos
Acid Halides to Ketones: Gilman Reagent
As shown below, the mechanism proceeds in two steps. First, one of the alkyl groups of the reagent acts as a nucleophile and attacks the acyl carbon of the acid chloride to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen...
Extraction: Advanced Methods
Acid Halides to Carboxylic Acids: Hydrolysis
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
Formation of Complex Ions
Electrophilic 1,2- and 1,4-Addition of HX to 1,3-Butadiene
Acid Halides to Amides: Aminolysis
In the first step of the aminolysis mechanism, the amine attacks the carbonyl carbon of the acyl chloride to form a tetrahedral intermediate. In the second step, the carbonyl group is re-formed with the elimination of a chloride...