Underwater adhesion of mussel foot protein on a graphite surface

2020 ◽  
Vol 511 ◽  
pp. 145589
Author(s):  
Mengdi Zhao ◽  
Liyi Bai ◽  
Joonkyung Jang
Author(s):  
Eugene Kim ◽  
Juya Jeon ◽  
Yaguang Zhu ◽  
Ethan D. Hoppe ◽  
Young-Shin Jun ◽  
...  

Author(s):  
Ramesh Kumar Chitumalla ◽  
Kiduk Kim ◽  
Xingfa Gao ◽  
Joonkyung Jang

By employing periodic-DFT simulations, we unveil that the wet adhesion of mussels onto a hydrophobic graphite surface is significantly strong and is comparable with that on a hydrophilic silica surface.


Soft Matter ◽  
2017 ◽  
Vol 13 (48) ◽  
pp. 9122-9131 ◽  
Author(s):  
Ilia Kaminker ◽  
Wei Wei ◽  
Alex M. Schrader ◽  
Yeshayahu Talmon ◽  
Megan T. Valentine ◽  
...  

Single-component peptide coacervates mimicking mussel foot protein-3S were adapted for rapid pressure-sensitive wet adhesion. The coacervate upon compression exhibited orders of magnitude higher underwater adhesion at 2 N m−1 than thin films of the most adhesive mussel-foot-derived peptides reported to date.


2019 ◽  
Author(s):  
Amal Narayanan ◽  
Joshua Menefee ◽  
Qianhui Liu ◽  
Ali Dhinojwala ◽  
Abraham Joy

Inspired from the one-component self-coacervation of tropoelastin and mussel foot protein-3s, we created the first non-ionic, single component coacervates that can coacervate in a all ranges of pH (acidic to basic) and wide range of ionic strengths with degradability, rapid curing and strong underwater adhesion. In contrast to the complex coacervates, these ‘charge-free’ coacervates are potential candidates as tissue adhesives and sealants, adhesives for sensor attachment to wet skin, and as sprayable adhesives. Their potential use in the clinic arises from their enhanced stability to changes in external conditions, cytocompatibility, biodegradability and modular nature in incorporating various functional groups and crosslinkers.


2019 ◽  
Author(s):  
Amal Narayanan ◽  
Joshua Menefee ◽  
Qianhui Liu ◽  
Ali Dhinojwala ◽  
Abraham Joy

Inspired from the one-component self-coacervation of tropoelastin and mussel foot protein-3s, we created the first non-ionic, single component coacervates that can coacervate in a all ranges of pH (acidic to basic) and wide range of ionic strengths with degradability, rapid curing and strong underwater adhesion. In contrast to the complex coacervates, these ‘charge-free’ coacervates are potential candidates as tissue adhesives and sealants, adhesives for sensor attachment to wet skin, and as sprayable adhesives. Their potential use in the clinic arises from their enhanced stability to changes in external conditions, cytocompatibility, biodegradability and modular nature in incorporating various functional groups and crosslinkers.


2018 ◽  
Vol 54 (89) ◽  
pp. 12642-12645 ◽  
Author(s):  
Pulakesh Aich ◽  
Jaeyeon An ◽  
Byeongseon Yang ◽  
Young Ho Ko ◽  
Junghyun Kim ◽  
...  

A spider with mussel: a supramolecular fiber formed by a spider dragline protein was tuned to have underwater adhesion property by genetic fusion of a mussel foot protein.


2018 ◽  
Vol 10 (49) ◽  
pp. 43003-43012 ◽  
Author(s):  
Eugene Kim ◽  
Bin Dai ◽  
James B. Qiao ◽  
Wenlu Li ◽  
John D. Fortner ◽  
...  

Author(s):  
W. Lo ◽  
J.C.H. Spence ◽  
M. Kuwabara

Work on the integration of STM with REM has demonstrated the usefulness of this combination. The STM has been designed to replace the side entry holder of a commercial Philips 400T TEM. It allows simultaneous REM imaging of the tip/sample region of the STM (see fig. 1). The REM technique offers nigh sensitivity to strain (<10−4) through diffraction contrast and high resolution (<lnm) along the unforeshortened direction. It is an ideal technique to use for studying tip/surface interactions in STM.The elastic strain associated with tunnelling was first imaged on cleaved, highly doped (S doped, 5 × 1018cm-3) InP(110). The tip and surface damage observed provided strong evidence that the strain was caused by tip/surface contact, most likely through an insulating adsorbate layer. This is consistent with the picture that tunnelling in air, liquid or ordinary vacuum (such as in a TEM) occurs through a layer of contamination. The tip, under servo control, must compress the insulating contamination layer in order to get close enough to the sample to tunnel. The contaminant thereby transmits the stress to the sample. Elastic strain while tunnelling from graphite has been detected by others, but never directly imaged before. Recent results using the STM/REM combination has yielded the first direct evidence of strain while tunnelling from graphite. Figure 2 shows a graphite surface elastically strained by the STM tip while tunnelling (It=3nA, Vtip=−20mV). Video images of other graphite surfaces show a reversible strain feature following the tip as it is scanned. The elastic strain field is sometimes seen to extend hundreds of nanometers from the tip. Also commonly observed while tunnelling from graphite is an increase in the RHEED intensity of the scanned region (see fig.3). Debris is seen on the tip and along the left edges of the brightened scan region of figure 4, suggesting that tip abrasion of the surface has occurred. High resolution TEM images of other tips show what appear to be attached graphite flakes. The removal of contamination, possibly along with the top few layers of graphite, seems a likely explanation for the observed increase in RHEED reflectivity. These results are not inconsistent with the “sliding planes” model of tunnelling on graphite“. Here, it was proposed that the force due to the tunnelling probe acts over a large area, causing shear of the graphite planes when the tip is scanned. The tunneling current is then modulated as the planes of graphite slide in and out of registry. The possiblity of true vacuum tunnelling from the cleaned graphite surface has not been ruled out. STM work function measurements are needed to test this.


1985 ◽  
Vol 35 (4) ◽  
pp. 469-472 ◽  
Author(s):  
M. Tomášek ◽  
Š. Pick

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Sang-Min Lee ◽  
Junyoung Kim ◽  
Janghyuk Moon ◽  
Kyu-Nam Jung ◽  
Jong Hwa Kim ◽  
...  

AbstractThe realisation of fast-charging lithium-ion batteries with long cycle lifetimes is hindered by the uncontrollable plating of metallic Li on the graphite anode during high-rate charging. Here we report that surface engineering of graphite with a cooperative biphasic MoOx–MoPx promoter improves the charging rate and suppresses Li plating without compromising energy density. We design and synthesise MoOx–MoPx/graphite via controllable and scalable surface engineering, i.e., the deposition of a MoOx nanolayer on the graphite surface, followed by vapour-induced partial phase transformation of MoOx to MoPx. A variety of analytical studies combined with thermodynamic calculations demonstrate that MoOx effectively mitigates the formation of resistive films on the graphite surface, while MoPx hosts Li+ at relatively high potentials via a fast intercalation reaction and plays a dominant role in lowering the Li+ adsorption energy. The MoOx–MoPx/graphite anode exhibits a fast-charging capability (<10 min charging for 80% of the capacity) and stable cycling performance without any signs of Li plating over 300 cycles when coupled with a LiNi0.6Co0.2Mn0.2O2 cathode. Thus, the developed approach paves the way to the design of advanced anode materials for fast-charging Li-ion batteries.


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