{"title":"Molecular Photoelectrodes with Enhanced Photogenerated Charge Transport for Efficient Solar Hydrogen Evolution.","authors":"Yifan Gao, Feiqing Sun, Yanjie Fang, Yingke Wen, Feiyang Hong, Bing Shan","doi":"10.1021/jacs.4c17133","DOIUrl":null,"url":null,"abstract":"<p><p>Photoelectrocatalytic cells for seawater splitting have shown promise toward large-scale deployment; however, challenges remain in operation performances, which outline clear research needs to scale up photoelectrodes with small loss of efficiency. Here, we report an approach for scalable and robust solar H<sub>2</sub> evolution by enhancing photogenerated charge transport in a H<sub>2</sub>-evolving molecular photoelectrode. The photoelectrode is based on p-type conjugated polymers that are homogeneously distributed in a polycarbazole network. With a self-assembled NiS<sub>2</sub> catalyst, the photoelectrode under solar irradiation (100 mW cm<sup>-2</sup>, AM 1.5 G) is capable of evolving H<sub>2</sub> from seawater at an external quantum efficiency (EQE) of 34.4% under an applied bias of -0.06 V vs RHE. When scaling up from 1 cm<sup>2</sup> to 25 cm<sup>2</sup>, the photoelectrode generates photocurrents stabilized at 0.4 A and maintains the high EQE at an efficiency loss of less than 1%. Investigation of the photogenerated charge-transport dynamics reveals that the kinetic basis for scaling up lies in the desirable hole diffusion length that far exceeds the spacing between adjacent conjugated-polymer chains due to interchain π-π interactions.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":" ","pages":"7671-7681"},"PeriodicalIF":14.4000,"publicationDate":"2025-03-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of the American Chemical Society","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/jacs.4c17133","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Photoelectrocatalytic cells for seawater splitting have shown promise toward large-scale deployment; however, challenges remain in operation performances, which outline clear research needs to scale up photoelectrodes with small loss of efficiency. Here, we report an approach for scalable and robust solar H2 evolution by enhancing photogenerated charge transport in a H2-evolving molecular photoelectrode. The photoelectrode is based on p-type conjugated polymers that are homogeneously distributed in a polycarbazole network. With a self-assembled NiS2 catalyst, the photoelectrode under solar irradiation (100 mW cm-2, AM 1.5 G) is capable of evolving H2 from seawater at an external quantum efficiency (EQE) of 34.4% under an applied bias of -0.06 V vs RHE. When scaling up from 1 cm2 to 25 cm2, the photoelectrode generates photocurrents stabilized at 0.4 A and maintains the high EQE at an efficiency loss of less than 1%. Investigation of the photogenerated charge-transport dynamics reveals that the kinetic basis for scaling up lies in the desirable hole diffusion length that far exceeds the spacing between adjacent conjugated-polymer chains due to interchain π-π interactions.
用于海水分解的光电催化电池已经显示出大规模部署的前景;然而,在操作性能方面仍然存在挑战,这明确了研究需要在效率损失较小的情况下扩大光电极的规模。在这里,我们报告了一种可扩展和强大的太阳能H2演化方法,通过增强H2演化分子光电极中的光生电荷输运。光电极是基于均匀分布在聚咔唑网络中的p型共轭聚合物。使用自组装的NiS2催化剂,在太阳辐照(100 mW cm-2, AM 1.5 G)下,在-0.06 V vs RHE的应用偏压下,光电极能够以34.4%的外量子效率(EQE)从海水中析出H2。当从1 cm2放大到25 cm2时,光电极产生的光电流稳定在0.4 A,并以小于1%的效率损失保持高EQE。对光生电荷传输动力学的研究表明,放大的动力学基础在于理想的空穴扩散长度远远超过相邻共轭聚合物链之间的间距,这是由于链间π-π相互作用造成的。
期刊介绍:
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