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Related Concept Videos

Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
Thin-Walled Hollow Shafts01:15

Thin-Walled Hollow Shafts

In analyzing a thin-walled hollow shaft subjected to torsional loading, a segment with width dx is isolated for examination. Despite its equilibrium state, this segment faces torsional shearing forces at its ends. These forces are quantitatively described by the product of the longitudinal shearing stress on the segment's minor surface and the area of this surface, leading to the concept of shear flow. This shear flow is consistent throughout the structure, indicating a uniform distribution of...
Steel Fastening Techniques01:17

Steel Fastening Techniques

Steel sections can be joined together through various fastening techniques including riveting, bolting, and welding, each suitable for different structural requirements and conditions.
Rivets are cylindrical steel fasteners with a specially designed head. During application, rivets are heated until white-hot and then inserted through pre-drilled holes in the steel sections. A pneumatic hammer is used to shape the exposed end into a second head, securing the sections together.
Bolting is another...

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Sputter Growth and Characterization of Metamagnetic B2-ordered FeRh Epilayers
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Mesoporous High-Entropy Alloys With Diverse Compositions via a Versatile Kinetic-Controlled Co-Growth Approach.

Jiaxin Rui1, Guangshu Zhou1, Tingting Wu1

  • 1State Key Laboratory of Flexible Electronics (LoFE) & Institute of Advanced Materials (IAM), Nanjing University of Posts & Telecommunications, Nanjing, China.

Small Methods
|March 10, 2026
PubMed
Summary

Synthesizing mesoporous high-entropy alloys (MHEAs) is now controllable. This new method creates MHEAs with tunable pore sizes, showing enhanced catalytic activity for applications.

Keywords:
high‐entropy alloyskinetic‐controlledmesoporesperoxidase‐like catalytictriblock copolymer

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Area of Science:

  • Materials Science
  • Nanotechnology
  • Catalysis

Background:

  • Mesoporous high-entropy alloys (MHEAs) offer unique properties due to accessible pores and multicomponent synergy.
  • Controlled synthesis of MHEAs with specific compositions, high entropy, and defined mesoporous structures is challenging.

Purpose of the Study:

  • To develop a versatile kinetic-controlled co-growth approach for synthesizing MHEAs.
  • To demonstrate the synthesis of MHEAs with tunable compositions and controlled mesopore sizes.

Main Methods:

  • Utilized a kinetic-controlled co-growth strategy for MHEA synthesis.
  • Extended the approach to various compositions including PtPdRhAgCu, PtPdRhAgRu, and others.
  • Adjusted mesoporous diameters (5.5–11.0 nm) using different triblock copolymers.

Main Results:

  • Achieved PtPdRhAgCu MHEAs with high mix configurational entropy (ΔSmix = 1.600 R) and uniform morphology (~58 nm).
  • Demonstrated tunable mesoporous diameters from 5.5 nm to 11.0 nm.
  • Observed significantly enhanced catalytic activity and peroxidase-like performance in MHEAs with ~11 nm mesopores.

Conclusions:

  • The kinetic-controlled co-growth approach enables controlled synthesis of MHEAs with tunable compositions and pore sizes.
  • MHEAs with optimized mesoporous structures exhibit superior catalytic performance.
  • This method provides a pathway for designing advanced MHEAs for catalytic applications.