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美国科学家发现玻璃表面的奇特性(附原文)

已有 3118 次阅读 2017-4-11 16:11 |个人分类:新观察|系统分类:论文交流|关键词:学者| glass, property, surfaces), Pennsylvania)

美国科学家发现玻璃表面的奇特性(附原文)

诸平

2017410来自美国宾夕法尼亚大学University of Pennsylvania)的消息,该大学的研究人员已经开发一种新技术,使用此项技术研究玻璃表面性质有令人惊讶的发现。图1是来自宾夕法尼亚大学的照片,此照片是处于玻璃表面病毒的3D图像。此项研究成果2016年12月12日,Alejandro Manjavacas等人就已经在预印本文库网站公布arXiv:1612.03733v1,2017年3月31日在《物理评论快报》(Phys. Rev. Lett.)网站发表。


Fig. 1 A 3D image of the virus on the glass surface. Credit: University of Pennsylvania

宾夕法尼亚大学的研究人员开发出此项新技术,用于研究不同类型的玻璃表面。使用这种技术,研究者发现了玻璃顶层的一种令人吃惊性质,为开发更好的玻璃材料铺平了道路。

这项研究是由宾夕法尼亚大学文理学院化学系研究生Yue Zhang音译和化学助理教授Zahra Fakhraai领导完成的。张悦因为此项研究获得美国物理学会(APSPadden,表明在聚合物物理研究方面的卓越成果得到认可

晶体和液体之间的区别就是晶体有序固体,液体无序可以充满任何容器。但如果使液体得到充分冷却,即使变成固体,其分子仍将是处于无序运动状态,只不过是运动速度会慢下来像玻璃这样的材料形成非晶态材料。例如,蜂蜜在常温下是一种液体,但遇到冷时其属性变得更像一固体。宾夕法尼亚大学的研究人员正在研究界面或表面究竟怎样影响玻璃的属性。根据Fakhraai的解释,对玻璃材料引入种自由表面,运动再次加速乃至传播到此薄膜虽然蜂蜜看上去似乎固体,但是分子充其量也不过是5 nm10 nm而已,仍将保持液体和运动。如果一根针放在蜂蜜表面,,形成一个弯液面,允许分子在周围运动,而同样的针如果放在固体表面就形成如此效应。更多信息请浏览:Lateral Casimir Force on a Rotating Particle near a Planar Surface(点击可以下载原文)或者

Researchers discover a surprising property of glass surfaces

April 10, 2017                                                                

Researchers discover a surprising property of glass surfaces

       A 3D image of the virus on the glass surface. Credit: University of Pennsylvania    

Researchers at the University of Pennsylvania have developed a new technique to study the surface of different types of glass. Using this technique, they discovered a surprising property of the top layer of glasses, which could pave the way to developing better glass materials.  

The research was led by Yue Zhang, a graduate student in the Department of Chemistry in Penn's School of Arts & Sciences, and Zahra Fakhraai, assistant professor of chemistry. Zhang received an APS Padden Award for the research, which recognizes excellence in polymer physics research.

The distinction between crystals and liquids is that, while crystals are ordered and solid, liquids are disordered and can move around to fill whatever container they are in. But if one were to cool a liquid sufficiently, it would remain disordered while the of its molecules would slow down so much that it would seem solid. This is how amorphous materials such as glasses form.

Honey, for instance, is a liquid, but when it is refrigerated its properties become more like that of a solid.

The Penn researchers were investigating how interfaces or surfaces, the boundaries between two phases of matter, would affect the properties of glasses. According to Fakhraai, when a free is introduced to the material, the motion speeds up again, which propagates into the film.

Even though the honey would seem solid, the molecules in the top 5 or 10 nanometers would remain liquid and moving. If a needle were put on the surface of the honey, it would dip and form a meniscus, allowing the molecules to move around, whereas the same needle would have no effect on a solid.

In a previous paper published in Soft Matter, the researchers shrunk this technique down to nanometer length scales using a virus as a needle and watched the come in and slowly try to form a meniscus around the virus. While the molecules in the center of the material may take millions of years to move, for the molecules at the top it would be more like a few hundred seconds.

Researchers discover a surprising property of glass surfaces

       A sketch showing the process of the glass forming a meniscus around the virus. Credit: University of Pennsylvania    

"The technique that we developed is really exciting because in the field there are not many techniques to directly probe the surface motions," Zhang said. "Our technique is very efficient and mathematically simple, and we can easily extend it to other systems."

One of the most challenging aspects of developing the technique, Fakhraai said, was figuring out that they could use viruses to probe the materials.

"For a few years we tried to synthesize nanorods that looked like needles and were long and uniform enough," she said. "Viruses are perfect because they have these crystalline structures that are exactly the right dimensions that we need. Thinking about the virus as a nanoparticle really helped us move forward."

Using this , the researchers wanted to determine how the motion of the molecules on the free surface is coupled with the motion below. In particular, they wanted to see if the molecules on the surface would be affected if the motion of the molecules beneath them was sped up or slowed down.

In another previous paper published in Physical Review Letters, the researchers used different deposition techniques to better pack the molecules and form stable glasses. This made everything extremely slow to the point that it would take longer than the age of the universe for molecules at the center to move.

In their most recent paper, published in the Proceedings of the National Academy of Sciences, they sped everything up by making thinner films, which would have more of a free surface.

"Based on many different theories, we would have expected that the motions at the center and the free surface would be coupled together," Fakhraai said. "The example I like to make is if you're say at the front of the parade and you're moving faster, things should follow you. But it doesn't happen that way. The immediate top layer doesn't really couple: Those molecules can move around without affecting whatever's happening behind them."

Researchers discover a surprising property of glass surfaces

       Meniscus growth on unstable glass. Credit: University of Pennsylvania    

These results, she said, were surprising. While there were many different ideas of whether this correlation exists, no one had really measured it before. They found that, no matter what type of motion, the molecules at the top and the molecules at the center have no effect on each other.

The researchers hope to be able to probe the second and third layers, which may be important in the densification process of the materials during deposition, which is the basis of making stable glasses and is of technological importance. Since the molecules at the first layer aren't affected by the motion of the molecules beneath them, the motion of the underlying layers become crucial in the process.

"We think that it's really the molecules at the second layer and third layer that are participating in this densification process, and the molecules at the free surface are just like a sea of free objects that can provide that mobility but don't necessarily participate in the process," Fakhraai said.

They also hope to better understand the transition from the fast moving particles at the surface to the extremely slow moving molecules at the center. People standing at the front of a parade are free to move around, Fakhraai explained, but the deeper you go into the parade, motion becomes more constrained.

"The question is how deep the effect is and how that process comes about," Fakhraai said. "How do I change from something that takes 100 seconds to move to something that takes billions of years? I think that's the next big challenge in the field: to understand that gradient."

According to Fakhraai, investigating this process will allow to not only better understand theories but to improve coatings on materials and design better .

"We understand what sets the clock in the middle of the film, but we don't know what sets the clock for those surface ," Fakhraai said. "I think that's something to understand more in the future."                                                                

Explore further:Scientists find the temperature at which glass becomes a liquid

More information:                                        Yue Zhang et al. Invariant Fast Diffusion on the Surfaces of Ultrastable and Aged Molecular Glasses, Physical Review Letters (2017). DOI: 10.1103/PhysRevLett.118.066101

Yue Zhang et al. Using tobacco mosaic virus to probe enhanced surface diffusion of molecular glasses, Soft Matter (2016). DOI: 10.1039/C6SM01566B

Yue Zhang et al. Decoupling of surface diffusion and relaxation dynamics of molecular glasses, Proceedings of the National Academy of Sciences (2017). DOI: 10.1073/pnas.1701400114



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