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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...

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Autores principales: Tian, Shihao, Wang, Haoqi, Dong, Zhiwei, Yang, Yang, Yuan, Hao, Huang, Qiong, Song, Tian-shun, Xie, Jingjing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
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.
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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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