Related Experiment Video
Updated: Feb 7, 2026

07:32
Synthesis of Graphene Nanofluids with Controllable Flake Size Distributions
Published on: July 17, 2019
7.1K
Structural superlubricity in graphite flakes assembled under ambient conditions
He Deng1, Ming Ma, Yiming Song
1School of Mechanical Engineering, Southwest Jiaotong University, Chengdu 610031, PR China.
Nanoscale
|July 19, 2018
Summary
Structural superlubricity was achieved in ambient conditions using graphite flakes. A novel running-in process removes contaminants, reducing friction without altering surface structure, enabling practical applications.
Area of Science:
- Materials Science
- Tribology
- Nanotechnology
Background:
- Microscale structural superlubricity typically requires ultra-clean interfaces, limiting practical use.
- Previous studies focused on in-situ cleaved graphite or vacuum-assembled friction pairs.
- Ambient assembly conditions introduce unavoidable contaminants at interfaces.
Purpose of the Study:
- To investigate microscale structural superlubricity in graphite flake pairs assembled under ambient conditions.
- To understand the mechanism behind friction reduction in the presence of contaminants.
- To explore the potential for practical applications of superlubricity.
Main Methods:
- Assembled graphite flake friction pairs under ambient conditions.
- Observed friction behavior during reciprocating motion.
- Analyzed surface morphology and chemical composition before and after testing.
Main Results:
- Achieved microscale structural superlubricity in graphite flake pairs assembled under ambient conditions.
- Observed a novel running-in phenomenon where friction decreased with motion.
- Identified the removal of confined third bodies as the mechanism for friction reduction, with no observed morphological or chemical changes.
Conclusions:
- Microscale structural superlubricity is achievable in graphite flake pairs under ambient conditions.
- A new running-in mechanism involving third-body removal facilitates superlubricity.
- Findings enhance understanding of superlubricity and pave the way for broader practical applications.
Related Concept Videos
Assembly of Complex Microtubule Structures
2.5K
Complex microtubule structures are present in resting cells and in dividing cells. In resting cells, they are responsible for maintaining the cellular architecture, tracks for intracellular transport, positioning of organelles, assembly of cilia and flagella. They mediate the bipolar spindle assembly for chromosomal segregation and positioning of the cell division plate in dividing cells. The formation of microtubule complex structures depends on the cell type, cell stage, and cell function.
2.5K
Protein Complex Assembly
16.8K
Proteins can form homomeric complexes with another unit of the same protein or heteromeric complexes with different types. Most protein complexes self-assemble spontaneously via ordered pathways, while some proteins need assembly factors that guide their proper assembly. Despite the crowded intracellular environment, proteins usually interact with their correct partners and form functional complexes.
Many viruses self-assemble into a fully functional unit using the infected host cell to...
Many viruses self-assemble into a fully functional unit using the infected host cell to...
16.8K
Additional Subnuclear Structures
5.4K
The eukaryotic nucleus is a double membrane-bound organelle that contains nearly all of the cell’s genetic material in the form of chromosomes. It is rightly called the “brain” of the cell as it shoulders the responsibility of responding to various physiological processes, stress, altered metabolic conditions, and other cellular signals.
The nucleus contains many membrane-less subnuclear organelles or nuclear bodies, such as nucleoli, Cajal bodies, speckles,...
The nucleus contains many membrane-less subnuclear organelles or nuclear bodies, such as nucleoli, Cajal bodies, speckles,...
5.4K
Structural Protein Function
30.0K
Structural proteins are a category of proteins responsible for functions ranging from cell shape and movement to providing support to major structures such as bones, cartilage, hair, and muscles. This group includes proteins such as collagen, actin, myosin, and keratin.
Collagen, the most abundant protein in mammals, is found throughout the body. In connective tissue, such as skin, ligaments, and tendons, it provides tensile strength and elasticity. In bones and teeth, it mineralizes to...
Collagen, the most abundant protein in mammals, is found throughout the body. In connective tissue, such as skin, ligaments, and tendons, it provides tensile strength and elasticity. In bones and teeth, it mineralizes to...
30.0K
Protein and Protein Structure
88.2K
Proteins are one of the most abundant organic molecules in living systems and have the most diverse range of functions of all macromolecules. Proteins may be structural, regulatory, contractile, or protective. They may serve in transport, storage, or membranes; or they may be toxins or enzymes. Their structures, like their functions, vary greatly. They are all, however, amino acid polymers arranged in a linear sequence.
A protein's shape is critical to its function. For example, an enzyme...
A protein's shape is critical to its function. For example, an enzyme...
88.2K
Spindle Assembly
4.3K
Spindle assembly occurs through three, often coexisting, pathways – the centrosome-mediated pathway, the chromatin-mediated pathway, and the microtubule-mediated pathway – collectively contributing to form a robust spindle apparatus.
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
In most cells, centrosomes are the primary microtubule nucleation centers. In the centrosome-mediated pathway, the G2-prophase transition triggers centrosome maturation and increased microtubule nucleation. Progressive nucleation results in a...
4.3K

