Keisuke Obata, Xinyi Zhang, Tabea Thiel, Michael Schwarze, Reinhard Schomäcker, Roel van de Krol, Fatwa Firdaus Abdi
{"title":"Solar-Driven Upgrading of Biomass by Coupled Hydrogenation Using in Situ Photoelectrochemically Generated H<sub>2</sub>","authors":"Keisuke Obata, Xinyi Zhang, Tabea Thiel, Michael Schwarze, Reinhard Schomäcker, Roel van de Krol, Fatwa Firdaus Abdi","doi":"10.1149/ma2023-01372128mtgabs","DOIUrl":null,"url":null,"abstract":"Green H 2 has been recognized as an important element in efforts to decarbonize our fossil fuel-dependent society. One approach to produce green H 2 is solar water splitting in a photoelectrochemical (PEC) device. Solar-to-hydrogen (STH) efficiencies of up to 30% have been demonstrated 1 but studies have shown that this approach still results in a relatively high levelized cost of hydrogen (LCOH) of ~10 US$ per kg of H 2 . 2-3 This is ca. one order of magnitude higher than that of hydrogen produced via steam methane reforming (SMR), which forms the bulk of the currently produced H 2 . A possible solution is to incorporate an upgrading process of biomass feedstock that generates valuable chemicals into the solar water splitting device. This is expected to not only decrease the overall LCOH but also introduce an alternative renewable pathway in chemical manufacturing. In this study, we propose the concept of solar-driven hydrogenation of biomass-derived feedstock. Photoelectrochemically generated H 2 in our solar water splitting device is coupled in situ with the homogenously catalyzed hydrogenation of itaconic acid (IA) to methyl succinic acid (MSA). IA has been identified by the US Department of Energy as one of the twelve building blocks that possess the potential to be transformed subsequently into several high-value bio-based chemicals or materials. 4 MSA is a valuable chemical compound with an estimated global market size of up to ~15,000 tonnes, whose derivatives are ubiquitously used as solvents in cosmetics, 5 polymer synthesis, 6 binders in powder coatings, 7 and organic synthesis, especially for pharmaceutical synthesis. 8-9 Our coupled hydrogenation approach—performed in the PV-electrolyzer and PEC configurations using III-V PV cells and BiVO 4 -based photoelectrode, respectively—successfully demonstrate solar-driven H 2 -to-MSA conversion efficiencies as high as 60%. In comparison to the non-coupled approach (i.e., direct hydrogenation), our coupled system offers synergistic benefits in terms of prolonged durability and a higher degree of flexibility toward other important chemical transformation reactions. In addition, life-cycle net energy assessment and technoeconomic analysis results show that adding the coupled hydrogenation process significantly lowers the energy payback time and the LCOH, respectively, to a point that is competitive even with SMR-produced H 2 . Further implications and optimization potentials of the coupled PEC hydrogenation approach will be discussed. References Kim, J. H.; Hansora, D.; Sharma, P.; Jang, J.-W.; Lee, J. S., Toward practical solar hydrogen production – an artificial photosynthetic leaf-to-farm challenge. Chem. Soc. Rev. 2019, 48 (7), 1908-1971. Shaner, M. R.; Atwater, H. A.; Lewis, N. S.; McFarland, E. W., A comparative technoeconomic analysis of renewable hydrogen production using solar energy. Energy Environ. Sci. 2016, 9 (7), 2354-2371. Pinaud, B. A.; Benck, J. D.; Seitz, L. C.; Forman, A. J.; Chen, Z.; Deutsch, T. G.; James, B. D.; Baum, K. N.; Baum, G. N.; Ardo, S.; Wang, H.; Miller, E.; Jaramillo, T. F., Technical and economic feasibility of centralized facilities for solar hydrogen production via photocatalysis and photoelectrochemistry. Energy Environ. Sci. 2013, 6 (7), 1983-2002. Werpy, T.; Petersen, G. Top value added chemicals from biomass: volume I--results of screening for potential candidates from sugars and synthesis gas ; National Renewable Energy Lab., Golden, CO (US): 2004. Richard, H.; Muller, B. Use of a 2-methylsuccinic acid diester derivative as solvent in cosmetic compositions; cosmetic compositions containing the same. WO2012119861A3, 2012. Verduyckt, J.; De Vos, D. Method for the production of methylsuccinic acid and the anhydride thereof from citric acid. WO2018065475A1, 2017. Mijolovic, D.; Szarka, Z. J.; Heimann, J.; Garnier, S. Powder coating useful as a coating agent, and for coating metallic- and non-metallic surfaces, comprises a binder comprising methyl succinic acid. DE102011080722A1, 2012. Okabe, M.; Lies, D.; Kanamasa, S.; Park, E. Y., Biotechnological production of itaconic acid and its biosynthesis in Aspergillus terreus. Appl. Microbiol. Biotechnol. 2009, 84 (4), 597-606. Willke, T.; Vorlop, K.-D., Biotechnological production of itaconic acid. Appl. Microbiol. Biotechnol. 2001, 56 (3), 289-295.","PeriodicalId":11461,"journal":{"name":"ECS Meeting Abstracts","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ECS Meeting Abstracts","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1149/ma2023-01372128mtgabs","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Green H 2 has been recognized as an important element in efforts to decarbonize our fossil fuel-dependent society. One approach to produce green H 2 is solar water splitting in a photoelectrochemical (PEC) device. Solar-to-hydrogen (STH) efficiencies of up to 30% have been demonstrated 1 but studies have shown that this approach still results in a relatively high levelized cost of hydrogen (LCOH) of ~10 US$ per kg of H 2 . 2-3 This is ca. one order of magnitude higher than that of hydrogen produced via steam methane reforming (SMR), which forms the bulk of the currently produced H 2 . A possible solution is to incorporate an upgrading process of biomass feedstock that generates valuable chemicals into the solar water splitting device. This is expected to not only decrease the overall LCOH but also introduce an alternative renewable pathway in chemical manufacturing. In this study, we propose the concept of solar-driven hydrogenation of biomass-derived feedstock. Photoelectrochemically generated H 2 in our solar water splitting device is coupled in situ with the homogenously catalyzed hydrogenation of itaconic acid (IA) to methyl succinic acid (MSA). IA has been identified by the US Department of Energy as one of the twelve building blocks that possess the potential to be transformed subsequently into several high-value bio-based chemicals or materials. 4 MSA is a valuable chemical compound with an estimated global market size of up to ~15,000 tonnes, whose derivatives are ubiquitously used as solvents in cosmetics, 5 polymer synthesis, 6 binders in powder coatings, 7 and organic synthesis, especially for pharmaceutical synthesis. 8-9 Our coupled hydrogenation approach—performed in the PV-electrolyzer and PEC configurations using III-V PV cells and BiVO 4 -based photoelectrode, respectively—successfully demonstrate solar-driven H 2 -to-MSA conversion efficiencies as high as 60%. In comparison to the non-coupled approach (i.e., direct hydrogenation), our coupled system offers synergistic benefits in terms of prolonged durability and a higher degree of flexibility toward other important chemical transformation reactions. In addition, life-cycle net energy assessment and technoeconomic analysis results show that adding the coupled hydrogenation process significantly lowers the energy payback time and the LCOH, respectively, to a point that is competitive even with SMR-produced H 2 . Further implications and optimization potentials of the coupled PEC hydrogenation approach will be discussed. References Kim, J. H.; Hansora, D.; Sharma, P.; Jang, J.-W.; Lee, J. S., Toward practical solar hydrogen production – an artificial photosynthetic leaf-to-farm challenge. Chem. Soc. Rev. 2019, 48 (7), 1908-1971. Shaner, M. R.; Atwater, H. A.; Lewis, N. S.; McFarland, E. W., A comparative technoeconomic analysis of renewable hydrogen production using solar energy. Energy Environ. Sci. 2016, 9 (7), 2354-2371. Pinaud, B. A.; Benck, J. D.; Seitz, L. C.; Forman, A. J.; Chen, Z.; Deutsch, T. G.; James, B. D.; Baum, K. N.; Baum, G. N.; Ardo, S.; Wang, H.; Miller, E.; Jaramillo, T. F., Technical and economic feasibility of centralized facilities for solar hydrogen production via photocatalysis and photoelectrochemistry. Energy Environ. Sci. 2013, 6 (7), 1983-2002. Werpy, T.; Petersen, G. Top value added chemicals from biomass: volume I--results of screening for potential candidates from sugars and synthesis gas ; National Renewable Energy Lab., Golden, CO (US): 2004. Richard, H.; Muller, B. Use of a 2-methylsuccinic acid diester derivative as solvent in cosmetic compositions; cosmetic compositions containing the same. WO2012119861A3, 2012. Verduyckt, J.; De Vos, D. Method for the production of methylsuccinic acid and the anhydride thereof from citric acid. WO2018065475A1, 2017. Mijolovic, D.; Szarka, Z. J.; Heimann, J.; Garnier, S. Powder coating useful as a coating agent, and for coating metallic- and non-metallic surfaces, comprises a binder comprising methyl succinic acid. DE102011080722A1, 2012. Okabe, M.; Lies, D.; Kanamasa, S.; Park, E. Y., Biotechnological production of itaconic acid and its biosynthesis in Aspergillus terreus. Appl. Microbiol. Biotechnol. 2009, 84 (4), 597-606. Willke, T.; Vorlop, K.-D., Biotechnological production of itaconic acid. Appl. Microbiol. Biotechnol. 2001, 56 (3), 289-295.