{"title":"Boosting large scale capacitive harvesting of osmotic power by dynamic matching of ion exchange kinetics†","authors":"Nicolas Chapuis and Lydéric Bocquet","doi":"10.1039/D4SE01366B","DOIUrl":null,"url":null,"abstract":"<p >Osmotic energy is an untapped source of renewable and non-intermittent energy. However the performances of existing recovery technologies – <em>e.g.</em> pressure retarded osmosis (PRO) and reverse electro-dialysis (RED) – remain too low for sustainable industrial development, while the promising nanopore-based systems remain challenging to scale up. In this study, we explore an alternative osmotic energy harvesting methodology, based on a capacitive recovery process, furthermore at the membrane (large) scale, in contrast to nanopore-based investigations. The approach, here coined capacitive reversed electrodialysis, consists of using porous capacitive electrodes made of (low-cost) activated carbon and periodically alternating the flow through the electrodes with high-salt and low-salt water solutions on each side of a (commercial) cation exchange membrane. Periodic switches prevent full capacitive charging of the electrodes and the harvested power is found to be a non-monotonous function of the switching frequency. Theoretical modelling of the process demonstrates that this optimum results from the internal dynamic properties of the membrane, which has to match the switching frequency for maximal power harvesting. We then demonstrate that the power density accordingly reaches 5.3 W m<small><sup>−2</sup></small> under a 100-fold salinity gradient over a cm<small><sup>2</sup></small> membrane, surpassing both all large-scale studies in the literature and the commonly accepted (economic) break-even point of 5 W m<small><sup>−2</sup></small>. This study demonstrates the feasibility of large-scale, high-power density osmotic energy recovery and suggests a systematic avenue for an informed screening of materials, thus providing a viable pathway for sustainable energy solutions.</p>","PeriodicalId":104,"journal":{"name":"Sustainable Energy & Fuels","volume":" 8","pages":" 2087-2097"},"PeriodicalIF":5.0000,"publicationDate":"2025-02-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sustainable Energy & Fuels","FirstCategoryId":"88","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/se/d4se01366b","RegionNum":3,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Osmotic energy is an untapped source of renewable and non-intermittent energy. However the performances of existing recovery technologies – e.g. pressure retarded osmosis (PRO) and reverse electro-dialysis (RED) – remain too low for sustainable industrial development, while the promising nanopore-based systems remain challenging to scale up. In this study, we explore an alternative osmotic energy harvesting methodology, based on a capacitive recovery process, furthermore at the membrane (large) scale, in contrast to nanopore-based investigations. The approach, here coined capacitive reversed electrodialysis, consists of using porous capacitive electrodes made of (low-cost) activated carbon and periodically alternating the flow through the electrodes with high-salt and low-salt water solutions on each side of a (commercial) cation exchange membrane. Periodic switches prevent full capacitive charging of the electrodes and the harvested power is found to be a non-monotonous function of the switching frequency. Theoretical modelling of the process demonstrates that this optimum results from the internal dynamic properties of the membrane, which has to match the switching frequency for maximal power harvesting. We then demonstrate that the power density accordingly reaches 5.3 W m−2 under a 100-fold salinity gradient over a cm2 membrane, surpassing both all large-scale studies in the literature and the commonly accepted (economic) break-even point of 5 W m−2. This study demonstrates the feasibility of large-scale, high-power density osmotic energy recovery and suggests a systematic avenue for an informed screening of materials, thus providing a viable pathway for sustainable energy solutions.
渗透能是一种尚未开发的可再生和非间歇性能源。然而,现有的回收技术——如压力延迟渗透(PRO)和反电渗析(RED)——的性能仍然太低,无法实现可持续的工业发展,而前景广阔的纳米孔系统在扩大规模方面仍然具有挑战性。在这项研究中,我们探索了一种替代的渗透能量收集方法,基于电容回收过程,并且在膜(大)尺度上,与基于纳米孔的研究相反。这种方法,在这里被称为电容反电渗析,包括使用由(低成本)活性炭制成的多孔电容电极,并在(商业)阳离子交换膜的两侧周期性地交替使用高盐和低盐溶液通过电极。周期性开关防止电极的完全电容充电,并且发现收获的功率是开关频率的非单调函数。该过程的理论建模表明,这种最佳结果来自膜的内部动态特性,它必须匹配开关频率以获得最大的功率。我们随后证明,在一平方厘米的膜上,在100倍盐度梯度下,功率密度达到5.3 W m−2,超过了文献中所有的大规模研究和普遍接受的(经济的)盈亏平衡点5w m−2。这项研究证明了大规模、高功率密度渗透能量回收的可行性,并为材料的知情筛选提供了系统的途径,从而为可持续能源解决方案提供了可行的途径。
期刊介绍:
Sustainable Energy & Fuels will publish research that contributes to the development of sustainable energy technologies with a particular emphasis on new and next-generation technologies.