Journal
FARADAY DISCUSSIONS
Volume 213, Issue -, Pages 99-113Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c8fd00098k
Keywords
-
Categories
Funding
- MEXT/JSPS AKENES [16K05732, JP17H05383]
- Research Grant from the Institute for Science and Engineering at Chuo University
- Science Research Promotion Fund from the Promotion and Mutual Aid Corporation for Private Schools of Japan
Ask authors/readers for more resources
A new type of memristor inspired by bio-membranes is presented, based on the proton movement resulting from proton -coupled electron transfer (PCET) processes in dinuclear Ru complexes, whereby a two -terminal device based on said Ru complexes and a proton -conducting polymer was constructed as a proof -of -concept. Two ITO electrodes were modified separately with dinuclear Ru complexes that bear tetraphosphonic acid linkers at both ends and a 2,6,2',6'-tetrakis(benzimidazol-2-yl)-4,4'-bipyridine (RuNH-OH) or 1,3,1',3'-tetrakis(benzimidazol-2-yl)-5,5'-biphenyl (RuCH-OH) bridging ligand, and both ITO electrodes exhibit PCET processes with different redox potentials and pKa values. Poly(4-vinylpyridine) (P4VP; pK(a) = 4-5), a proton-conducting polymer, was sandwiched between the two modified ITO electrodes to construct a two-terminal device of the type ITOI(RuNH-OH)(3)vertical bar P4VP vertical bar(RuCH-OH)(3)vertical bar ITO. Initially, the oxidation state of the metal centers in RuNH-OH and RuCH-OH is Ru(ii) and Ru(ui), respectively. Upon applying a bias voltage between the two ITO electrodes, the high and low current states switch at approximately +/- 1.10 V due to Ru(iiiiii) redox reactions. At the RuNH-OHIP4VP and RuCH-OH vertical bar P4VP interfaces, a proton is released from Ru(u)NH-OH and subsequently captured by RuOu)CH-OH through the hydrogen -bonding interaction with the P4VP polymer, which is driven by the changes in the pK(a) values of the Ru complexes from 4.1-8.8 [Ru(II)NH-OH] to <3.8 [Ru(III)NH-OH] and from <8.4 [Ru(II)CH-OH] to 5.2-9.8 [Ru(III)CH-OH] under these conditions. The redox reactions on the modified Ru films create a large proton gradient between the two electrodes, enhancing the proton conductivity through the P4VP layer (pK(a) = 4-5). When the applied bias potential was inverted, the pK(a) gradient returned to the original state and the current decreased. Such a proton-conductivity enhancement is relevant to the transport of protons by proton gradients in bio-membranes. Therefore, the present protonic coordination -network films containing metal complexes that exhibit PCET should open new avenues for the design of a new type of memristor devices mimicking the function of synapses.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available