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2018
DOI: 10.1039/c8cc06688d
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Fuel-independent and membrane-less self-charging biosupercapacitor

Abstract: A fuel-independent self-charging biosupercapacitor consisting of an enzymatic biocathode and a bioelectrode employing supercapacitive features of immobilized myoglobin is described.

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Cited by 17 publications
(9 citation statements)
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References 31 publications
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“…In the absence of PQQ-GDH, the cyt c-GP electrode displayed a higher OCP of 0.063 V and a gradually increasing OCP during the charge/discharge cycling (Supplementary Figure S2). A similar phenomenon was observed in a recent work regarding a self-charging biosupercapacitor employing a myoglobin-modified electrode [37]. thylakoid membranes-charging/gold nanoparticles-storing patterns, was successfully applied in the construction of hybrid bioelectrochemical systems [5,9].…”
Section: Accepted Manuscriptsupporting
confidence: 75%
“…In the absence of PQQ-GDH, the cyt c-GP electrode displayed a higher OCP of 0.063 V and a gradually increasing OCP during the charge/discharge cycling (Supplementary Figure S2). A similar phenomenon was observed in a recent work regarding a self-charging biosupercapacitor employing a myoglobin-modified electrode [37]. thylakoid membranes-charging/gold nanoparticles-storing patterns, was successfully applied in the construction of hybrid bioelectrochemical systems [5,9].…”
Section: Accepted Manuscriptsupporting
confidence: 75%
“…To suppress fast-self-discharge, a proton exchange separator (PES) can be employed 18 , 30 , 31 . The PES acts as an active barrier for the generated protons at the bioanode preventing the migration towards the biocathode, thus minimizing faradaic side reactions and leading to reduced self-discharge 19 , 20 .…”
Section: Resultsmentioning
confidence: 99%
“…In addition, these complex biological reactions release energy which nBSCs can harness to compensate for any self-discharge [10][11][12][13] . Much effort has gone into exploring and understanding the intricate pathways of this bioenhancement and self-discharge behaviour [14][15][16][17][18] , but the side redox reactions leading to selfdischarge are still true challenges. The low working potential (0.3-0.8 V) and large size (>3 cubic millimetres) of state-of-theart BSCs [14][15][16][17][18] do the rest to deny these devices access to various small spaces in the human vascular system.…”
mentioning
confidence: 99%
“…The biofluids serve as the electrolytes for both the SC modules and BFC modules. Double layer capacitive materials, such as CNTs 93 and porous gold, 94,95 and pseudocapacitive polymers, including conductive polymers (polypyrrole and polyaniline), 96,97 redox polymers, 98–103 and MnO 2 , 104 have been explored to endow traditional BFCs with the capability to store energy. The hybrid device could release electricity in a much higher power density than BFCs resulting from the fast charge‐discharge rate of SCs.…”
Section: Human‐body Biofluids Charged Energy Storage Devicesmentioning
confidence: 99%