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Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction
BACKGROUND: Microbial electrosynthesis (MES) is a biocathode-driven process, in which electroautotrophic microorganisms can directly uptake electrons or indirectly via H(2) from the cathode as energy sources and CO(2) as only carbon source to produce chemicals. RESULTS: This study demonstrates that...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442412/ https://www.ncbi.nlm.nih.gov/pubmed/30976321 http://dx.doi.org/10.1186/s13068-019-1413-z |
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author | Tian, Shihao Wang, Haoqi Dong, Zhiwei Yang, Yang Yuan, Hao Huang, Qiong Song, Tian-shun Xie, Jingjing |
author_facet | Tian, Shihao Wang, Haoqi Dong, Zhiwei Yang, Yang Yuan, Hao Huang, Qiong Song, Tian-shun Xie, Jingjing |
author_sort | Tian, Shihao |
collection | PubMed |
description | BACKGROUND: Microbial electrosynthesis (MES) is a biocathode-driven process, in which electroautotrophic microorganisms can directly uptake electrons or indirectly via H(2) from the cathode as energy sources and CO(2) as only carbon source to produce chemicals. RESULTS: This study demonstrates that a hydrogen evolution reaction (HER) catalyst can enhance MES performance. An active HER electrocatalyst molybdenum carbide (Mo(2)C)-modified electrode was constructed for MES. The volumetric acetate production rate of MES with 12 mg cm(−2) Mo(2)C was 0.19 ± 0.02 g L(−1) day(−1), which was 2.1 times higher than that of the control. The final acetate concentration reached 5.72 ± 0.6 g L(−1) within 30 days, and coulombic efficiencies of 64 ± 0.7% were yielded. Furthermore, electrochemical study, scanning electron microscopy, and microbial community analyses suggested that Mo(2)C can accelerate the release of hydrogen, promote the formation of biofilms and regulate the mixed microbial flora. CONCLUSION: Coupling a HER catalyst to a cathode of MES system is a promising strategy for improving MES efficiency. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1413-z) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6442412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-64424122019-04-11 Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction Tian, Shihao Wang, Haoqi Dong, Zhiwei Yang, Yang Yuan, Hao Huang, Qiong Song, Tian-shun Xie, Jingjing Biotechnol Biofuels Research BACKGROUND: Microbial electrosynthesis (MES) is a biocathode-driven process, in which electroautotrophic microorganisms can directly uptake electrons or indirectly via H(2) from the cathode as energy sources and CO(2) as only carbon source to produce chemicals. RESULTS: This study demonstrates that a hydrogen evolution reaction (HER) catalyst can enhance MES performance. An active HER electrocatalyst molybdenum carbide (Mo(2)C)-modified electrode was constructed for MES. The volumetric acetate production rate of MES with 12 mg cm(−2) Mo(2)C was 0.19 ± 0.02 g L(−1) day(−1), which was 2.1 times higher than that of the control. The final acetate concentration reached 5.72 ± 0.6 g L(−1) within 30 days, and coulombic efficiencies of 64 ± 0.7% were yielded. Furthermore, electrochemical study, scanning electron microscopy, and microbial community analyses suggested that Mo(2)C can accelerate the release of hydrogen, promote the formation of biofilms and regulate the mixed microbial flora. CONCLUSION: Coupling a HER catalyst to a cathode of MES system is a promising strategy for improving MES efficiency. [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13068-019-1413-z) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-01 /pmc/articles/PMC6442412/ /pubmed/30976321 http://dx.doi.org/10.1186/s13068-019-1413-z Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tian, Shihao Wang, Haoqi Dong, Zhiwei Yang, Yang Yuan, Hao Huang, Qiong Song, Tian-shun Xie, Jingjing Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction |
title | Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction |
title_full | Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction |
title_fullStr | Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction |
title_full_unstemmed | Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction |
title_short | Mo(2)C-induced hydrogen production enhances microbial electrosynthesis of acetate from CO(2) reduction |
title_sort | mo(2)c-induced hydrogen production enhances microbial electrosynthesis of acetate from co(2) reduction |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442412/ https://www.ncbi.nlm.nih.gov/pubmed/30976321 http://dx.doi.org/10.1186/s13068-019-1413-z |
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