Electroanalysis of microbial anodes for bioelectrochemical systems: basics, progress and perspectives

Literature Information

Publication Date 2014-06-20
DOI 10.1039/C4CP01698J
Impact Factor 3.676
Authors

M. Rimboud, D. Pocaznoi, B. Erable, A. Bergel


View Original

Abstract

Over about the last ten years, microbial anodes have been the subject of a huge number of fundamental studies dealing with an increasing variety of possible application domains. Out of several thousands of studies, only a minority have used 3-electrode set-ups to ensure well-controlled electroanalysis conditions. The present article reviews these electroanalytical studies with the admitted objective of promoting this type of investigation. A first recall of basics emphasises the advantages of the 3-electrode set-up compared to microbial fuel cell devices if analytical objectives are pursued. Experimental precautions specifically relating to microbial anodes are then noted and the existing experimental set-ups and procedures are reviewed. The state-of-the-art is described through three aspects: the effect of the polarisation potential on the characteristics of microbial anodes, the electroanalytical techniques, and the electrode. We hope that the final outlook will encourage researchers working with microbial anodes to strengthen their engagement along the multiple exciting paths of electroanalysis.

Related Literature

Correction: Enantiomeric NMR discrimination of carboxylic acids using actinomycin D as a chiral solvating agent

Liwen Bai, Pian Chen, Jiangxia Xiang, Jiarui Sun, Xinxiang Lei

2019-03-28 Correction

DOI: 10.1039/C9OB90055A

Transition-metal free oxidative C–H etherification of acylanilines with alcohols through a radical pathway

Zhengzhou Chu, Chengcai Xia

2019-06-12 Communication

DOI: 10.1039/C9OB01224A

Dehydroamino acids: chemical multi-tools for late-stage diversification

Jonathan W. Bogart, Albert A. Bowers

2019-02-27 Review Article

DOI: 10.1039/C8OB03155J

Visible light-mediated organophotocatalyzed C–H bond functionalization reactions

Mustafa Uygur, Olga García Mancheño

2019-05-10 Review Article

DOI: 10.1039/C9OB00834A

Facile construction of diverse polyheterocyclic scaffolds via gold-catalysed dearomative spirocyclization/1,6-addition cascade

Yi He, Danjun Wu, Zhenghua Li, Koen Robeyns, Luc Van Meervelt

2019-06-10 Paper

DOI: 10.1039/C9OB01299K

Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives

Yulia V. Nelyubina, Alexey Yu. Sukhorukov, Sema L. Ioffe, Andrey A. Tabolin

2019-05-29 Paper

DOI: 10.1039/C9OB01005J

Doxorubicin-reinforced supramolecular hydrogels of RGD-derived peptide conjugates for pH-responsive drug delivery

Leixia Mei, Ziran Zhai, Suyun He, Tingting Zhu

2019-03-25 Paper

DOI: 10.1039/C9OB00046A

N-Heterocyclic carbene-catalyzed diastereoselective synthesis of sulfenylated indanes via sulfa-Michael–Michael (aldol) cascade reactions

Ze-Nan Feng, Jin-Yun Luo, Yang Zhang, Guang-Fen Du, Lin He

2019-04-12 Communication

DOI: 10.1039/C9OB00210C

Copper and palladium-catalyzed sequential reactions: one-pot synthesis of isoindolo[2,1-b]isoquinolin-7(5H)-ones

Hitesh Kumar Saini, Shiv Dhiman, Nitesh Kumar Nandwana, Rangan Krishnan, Anil Kumar

2019-03-26 Paper

DOI: 10.1039/C9OB00440H

Correction: Lacto-N-tetraose synthesis by wild-type and glycosynthase variants of the β-N-hexosaminidase from Bifidobacterium bifidum

Katharina Schmölzer, Melanie Weingarten, Kai Baldenius

2019-06-04 Correction

DOI: 10.1039/C9OB90088H

You might also like

Compound Q&A

What are the main uses of (3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8)?

(3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8) is primari...

79066-03-8(3.beta.)-3-Hydroxy-...
Compound Q&A

What regulatory guidelines apply to 5-(aminomethyl)-2-methoxyphenol (CAS: 89702-89-6)?

5-(Aminomethyl)-2-methoxyphenol (CAS: 89702-89-6) is classified under GHS as a s...

89702-89-65-(aminomethyl)-2-me...
Compound Q&A

What is Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7)?

Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7) is a heterocyclic organic compo...

28981-13-7Thieno[2,3-c]pyridin...
Compound Q&A

Is 1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride (CAS: 1185311-28-7) safe?

1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride is generally ...

1185311-28-71-[(6-Methoxy-3-pyri...
Compound Q&A

What regulatory guidelines apply to [(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2)?

[(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2) is regulated und...

146404-58-2[(2E)-3-Phenyl-2-pro...
Compound Q&A

What regulatory guidelines apply to 6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7)?

6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7) falls under the scope of the Glob...

1620515-86-76-Bromo-7-methoxyqui...
Compound Q&A

What industries use (2R)-1-(1-Benzofuran-2-yl)-N-propyl-2-pentanamine (CAS: 260550-89-8)?

This compound is primarily used in the pharmaceutical industry for the developme...

260550-89-8(2R)-1-(1-Benzofuran...
1228013-15-71-Ethyl-7-[2-methyl-...
Compound Q&A

Are there alternatives to {5-(Acryloylamino)-2-[(dimethylamino)methyl]phenyl}boronic acid (CAS: 1217500-78-1) in synthesis?

Alternative reagents such as 2-[(dimethylamino)methyl]phenylboronic acid or rela...

1217500-78-1{5-(Acryloylamino)-2...
Compound Q&A

What is 3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2)?

3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2) is an organic compound with the...

310881-48-23-(Piperidin-4-yloxy...

Source Journal

Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
Articles per Year: 3036

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.