scholarly journals Electrical conductivity of Self-assembling Peptide-semiconducting dye Conjugate nanofibre networks

Author(s):  
Zainab Makinde ◽  
Aakanksha Rani ◽  
Taniela Lolohea ◽  
Laura Domigan ◽  
Duncan McGillivray ◽  
...  

Conjugates comprising a semiconducting dye (Thiophene-diketopyrrolopyrrole, TDPP-dye) attached to a self-assembling peptide (HEFISTAH) assemble into long nanofibers. Well-ordered Langmuir-Blodgett films of these materials can be prepared. Networks of these nanofibres can be deposited to bridge electrodes. Although similar systems have been proposed as organic semiconductors, in this case, no electronic conductivity was observed. Instead, the fibres behaved as ionic (probably proton) conductors as a consequence of adsorbed water. A strong dependence of electrical conductivity on relative humidity and fibre network density was demonstrated. The system of nanofibers bridging gold electrodes behaved as an electrolytic cell, with oxygen reduction as a limiting electrode reaction.

2018 ◽  
Vol 106 (1) ◽  
pp. 107 ◽  
Author(s):  
Jean- Louis Crolet

All that was said so far about passivity and passivation was indeed based on electrochemical prejudgments, and all based on unverified postulates. However, due the authors’ fame and for lack of anything better, the great many contradictions were carefully ignored. However, when resuming from raw experimental facts and the present general knowledge, it now appears that passivation always begins by the precipitation of a metallic hydroxide gel. Therefore, all the protectiveness mechanisms already known for porous corrosion layers apply, so that this outstanding protectiveness is indeed governed by the chemistry of transport processes throughout the entrapped water. For Al type passivation, the base metal ions only have deep and complete electronic shells, which precludes any electronic conductivity. Then protectiveness can only arise from gel thickening and densification. For Fe type passivation, an incomplete shell of superficial 3d electrons allows an early metallic or semimetallic conductivity in the gel skeleton, at the onset of the very first perfectly ordered inorganic polymers (- MII-O-MIII-O-)n. Then all depends on the acquisition, maintenance or loss of a sufficient electrical conductivity in this Faraday cage. But for both types of passive layers, all the known features can be explained by the chemistry of transport processes, with neither exception nor contradiction.


2020 ◽  
Vol 12 (50) ◽  
pp. 56222-56230
Author(s):  
Marten Koopmans ◽  
Miina A. T. Leiviskä ◽  
Jian Liu ◽  
Jingjin Dong ◽  
Li Qiu ◽  
...  

2016 ◽  
Vol 697 ◽  
pp. 327-330 ◽  
Author(s):  
Ke Shan ◽  
Xing Min Guo ◽  
Feng Rui Zhai ◽  
Zhong Zhou Yi

Y0.06Sr0.94Ti0.6Fe0.4O3-δ-YSZ composites were prepared by mixing Y, Fe co-doped SrTiO3 (Y0.06Sr0.94Ti0.6Fe0.4O3-δ known as YSTF) and 8 mol% Y2O3 stabilized ZrO2 (YSZ) in different weight fractions. The phase stability, phase compatibility, microstructure and mixed ionic-electronic conductivity of composites were investigated. Phase analysis by XRD showed no clearly detectable secondary phases. The electrical conductivity measurement on the YSTF-YSZ composites showed a drastic decrease in total electrical and ionic conductivities when more than 10 wt% of YSZ was used in the composites. The total electrical conductivity was 0.102 S/cm for Y0.06Sr0.94Ti0.6Fe0.4O3-δ and 0.043 S/cm for YSTF-20YSZ at 700 oC, respectively. The value at 700 oC is approximately 2.4 times higher than that of YSTF-20YSZ. The ionic conductivity of Y0.06Sr0.94Ti0.8Fe0.2O3-δ varies from 0.015S/cm at 700 oC to 0.02 S/cm at 800 oC, respectively. The value at 800°C is approximately 12.5 times higher than YSTF-20YSZ. The ion transference numbers of YSTF-YSZ composites vary from 0.14 to 0.28 at 800 °C.


2019 ◽  
Vol 7 (42) ◽  
pp. 24059-24091 ◽  
Author(s):  
Hai-Ning Wang ◽  
Xing Meng ◽  
Long-Zhang Dong ◽  
Yifa Chen ◽  
Shun-Li Li ◽  
...  

This review summarizes recent developments of coordination polymers and their derivatives for ionic and electrical conductivity with the discussion about synthetic strategies and possible mechanisms to identify the key structural factors.


2011 ◽  
Vol 192 (1) ◽  
pp. 76-82 ◽  
Author(s):  
Keiji Yashiro ◽  
Satoshi Akoshima ◽  
Takao Kudo ◽  
Masatsugu Oishi ◽  
Hiroshige Matsumoto ◽  
...  

1974 ◽  
Vol 29 (5) ◽  
pp. 782-785
Author(s):  
A. Sdiiraldi ◽  
A. Magistris ◽  
E. Pezzati

Abstract The transport properties of TlI and of the system AgI -TlI were investigated by measuring the electrical conductivity, σ , and the electronic and ionic transport numbers. A particularly high electronic conductivity was detected in β-TlI, while the a phase showed a predominant anionic contribution, as in TlCl and TlBr. The intermediate compounds, AgTl2I3 and AgTlI2, are silver ion conductors, but they exhibit low σ values. A comparison with other poliiodides, with a high silver ion conductivity, is suggested on the basis of the crystal bond ionicity.


2007 ◽  
Vol 336-338 ◽  
pp. 424-427
Author(s):  
Xiang Yong Zhou ◽  
Zeng Fan ◽  
Zi Long Tang ◽  
Zhong Tai Zhang

The Y2O3-ZrO2 binary system ceramic is considered to be most developed in application to the ZrO2-based materials. A cubic fluorite structure is generally achieved, as the metal ion of the additive (Y) takes place of the Zr4+ and oxygen ion vacancies are produced in the lattice to maintain the charge balance. This leads to almost totally ionic conductivity. The introduction of changeable valued CeO2 can further improve the total electronic conductivity through the defect equilibrium reaction between tetravalent Ce4+ and trivalent Ce3+ at high temperature and reducing atmosphere. In this study, solid phase synthesis method was employed for the preparation of (YO1.5)x-(CeO2)0.08-(ZrO2)0.9-x and (YO1.5)0.05-(CeO2)y- (ZrO2)0.95-y ceramics, while four probe DC conductivity measurement method was also applied under the temperature between 300 to 800°C. The results prove that the concentration of Y3+ is the main contribution of the electrical conductivity at low temperature.


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