16
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Prolonged hydrogen production by engineered green algae photovoltaic power stations

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Interest in securing energy production channels from renewable sources is higher than ever due to the daily observation of the impacts of climate change. A key renewable energy harvesting strategy achieving carbon neutral cycles is artificial photosynthesis. Solar-to-fuel routes thus far relied on elaborately crafted semiconductors, undermining the cost-efficiency of the system. Furthermore, fuels produced required separation prior to utilization. As an artificial photosynthesis design, here we demonstrate the conversion of swimming green algae into photovoltaic power stations. The engineered algae exhibit bioelectrogenesis, en route to energy storage in hydrogen. Notably, fuel formation requires no additives or external bias other than CO 2 and sunlight. The cellular power stations autoregulate the oxygen level during artificial photosynthesis, granting immediate utility of the photosynthetic hydrogen without separation. The fuel production scales linearly with the reactor volume, which is a necessary trait for contributing to the large-scale renewable energy portfolio.

          Abstract

          Cost, scalability, and durability are critical factors determining the application of artificial photosynthesis systems. Here, the authors address these problems by inserting a carbon nanofiber into the chloroplast of green algae to transfer of electrons for photosynthesis and demonstrate H2 production up to 50 days.

          Related collections

          Most cited references38

          • Record: found
          • Abstract: not found
          • Article: not found

          Electrochemical Photolysis of Water at a Semiconductor Electrode

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Powering the planet: chemical challenges in solar energy utilization.

            Global energy consumption is projected to increase, even in the face of substantial declines in energy intensity, at least 2-fold by midcentury relative to the present because of population and economic growth. This demand could be met, in principle, from fossil energy resources, particularly coal. However, the cumulative nature of CO(2) emissions in the atmosphere demands that holding atmospheric CO(2) levels to even twice their preanthropogenic values by midcentury will require invention, development, and deployment of schemes for carbon-neutral energy production on a scale commensurate with, or larger than, the entire present-day energy supply from all sources combined. Among renewable energy resources, solar energy is by far the largest exploitable resource, providing more energy in 1 hour to the earth than all of the energy consumed by humans in an entire year. In view of the intermittency of insolation, if solar energy is to be a major primary energy source, it must be stored and dispatched on demand to the end user. An especially attractive approach is to store solar-converted energy in the form of chemical bonds, i.e., in a photosynthetic process at a year-round average efficiency significantly higher than current plants or algae, to reduce land-area requirements. Scientific challenges involved with this process include schemes to capture and convert solar energy and then store the energy in the form of chemical bonds, producing oxygen from water and a reduced fuel such as hydrogen, methane, methanol, or other hydrocarbon species.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Wireless solar water splitting using silicon-based semiconductors and earth-abundant catalysts.

              We describe the development of solar water-splitting cells comprising earth-abundant elements that operate in near-neutral pH conditions, both with and without connecting wires. The cells consist of a triple junction, amorphous silicon photovoltaic interfaced to hydrogen- and oxygen-evolving catalysts made from an alloy of earth-abundant metals and a cobalt|borate catalyst, respectively. The devices described here carry out the solar-driven water-splitting reaction at efficiencies of 4.7% for a wired configuration and 2.5% for a wireless configuration when illuminated with 1 sun (100 milliwatts per square centimeter) of air mass 1.5 simulated sunlight. Fuel-forming catalysts interfaced with light-harvesting semiconductors afford a pathway to direct solar-to-fuels conversion that captures many of the basic functional elements of a leaf.
                Bookmark

                Author and article information

                Contributors
                whryu@yonsei.ac.kr
                ahnhs@yonsei.ac.kr
                Journal
                Nat Commun
                Nat Commun
                Nature Communications
                Nature Publishing Group UK (London )
                2041-1723
                25 October 2023
                25 October 2023
                2023
                : 14
                : 6768
                Affiliations
                [1 ]Department of Chemistry, Yonsei University, ( https://ror.org/01wjejq96) 50 Yonsei-ro, Seodaemun-gu, Seoul, Republic of Korea
                [2 ]Department of Mechanical engineering, Yonsei University, ( https://ror.org/01wjejq96) 50 Yonsei-ro, Seodaemun-gu, Seoul, Republic of Korea
                Author information
                http://orcid.org/0000-0002-1480-2245
                http://orcid.org/0000-0002-6014-0916
                Article
                42529
                10.1038/s41467-023-42529-3
                10600337
                37880242
                eff92852-88ba-431c-9b23-5cc3edd7b4e7
                © Springer Nature Limited 2023

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 14 June 2023
                : 13 October 2023
                Funding
                Funded by: FundRef https://doi.org/10.13039/501100003725, National Research Foundation of Korea (NRF);
                Award ID: 2022K1A3A1A3109270511
                Award ID: 2020R1A2C3013158
                Award Recipient :
                Funded by: Commercialization Promotion Agency for R&D Outcomes of Korea, Grant Number: NTIS1711198538
                Categories
                Article
                Custom metadata
                © Springer Nature Limited 2023

                Uncategorized
                artificial photosynthesis,electrochemistry,nanobiotechnology,photosynthesis
                Uncategorized
                artificial photosynthesis, electrochemistry, nanobiotechnology, photosynthesis

                Comments

                Comment on this article