Satyadeep Waiba, Manami Banerjee, Lindsey Frederiksen, Aleksander Jaworski, Susanna Monti, Giovanni Barcaro, Kaan Karaca, Xiufang He, Anna Rokicińska, Thanh Huyen Vuong, Gianvito Vilé, Piotr Kuśtrowski, Jabor Rabeah, David Reyes, Peng Ren, Sergey Bagnich, Anna Köhler, Daniel Hohenberger, Josef Breu, Paul J Dyson, Shoubhik Das
{"title":"海水到可持续燃料:用原子分散的光催化剂产生阳光驱动的绿色氢。","authors":"Satyadeep Waiba, Manami Banerjee, Lindsey Frederiksen, Aleksander Jaworski, Susanna Monti, Giovanni Barcaro, Kaan Karaca, Xiufang He, Anna Rokicińska, Thanh Huyen Vuong, Gianvito Vilé, Piotr Kuśtrowski, Jabor Rabeah, David Reyes, Peng Ren, Sergey Bagnich, Anna Köhler, Daniel Hohenberger, Josef Breu, Paul J Dyson, Shoubhik Das","doi":"10.1021/jacs.5c11004","DOIUrl":null,"url":null,"abstract":"<p><p>Green hydrogen is widely regarded as a key to a sustainable future, offering a clean and flexible fuel option for decarbonizing the energy, transport, and industrial sectors. While photocatalytic approaches are known for generating hydrogen directly from water, most existing methods require (over)stoichiometric amounts of sacrificial reagents, which is far from ideal for the production of green hydrogen. To address this challenge, we have developed an atomically dispersed Ni-based photocatalyst that achieves hydrogen evolution rates of up to 270 μmol/g/h (168 mmol/g<sub>Ni</sub>/h). Remarkably, this photocatalyst also exhibits high photoreactivity under direct sunlight, producing up to 17 μmol/g/h (10.6 mmol/g<sub>Ni</sub>/h) of hydrogen. Impressively, the catalyst can even generate green hydrogen directly from seawater, up to 144 μmol/g/h, demonstrating significant potential for real-world applications. The photocatalyst is exceptionally stable, remaining active even after 720 h (140 h of irradiation and 580 h resting time) of operation and retaining high performance over more than 15 cycles. Furthermore, comprehensive spectroscopic and structural analyses─including HRTEM, PXRD, ssNMR, XPS, and XAS─provide detailed structural insights and confirm the atomically dispersed nature of the Ni species. In-depth mechanistic studies have elucidated the critical role of atomic dispersion in enabling robust photocatalytic efficiency.</p>","PeriodicalId":49,"journal":{"name":"Journal of the American Chemical Society","volume":" ","pages":""},"PeriodicalIF":15.6000,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Seawater to Sustainable Fuel: Sunlight-Driven Green Hydrogen Generation with an Atomically Dispersed Photocatalyst.\",\"authors\":\"Satyadeep Waiba, Manami Banerjee, Lindsey Frederiksen, Aleksander Jaworski, Susanna Monti, Giovanni Barcaro, Kaan Karaca, Xiufang He, Anna Rokicińska, Thanh Huyen Vuong, Gianvito Vilé, Piotr Kuśtrowski, Jabor Rabeah, David Reyes, Peng Ren, Sergey Bagnich, Anna Köhler, Daniel Hohenberger, Josef Breu, Paul J Dyson, Shoubhik Das\",\"doi\":\"10.1021/jacs.5c11004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Green hydrogen is widely regarded as a key to a sustainable future, offering a clean and flexible fuel option for decarbonizing the energy, transport, and industrial sectors. While photocatalytic approaches are known for generating hydrogen directly from water, most existing methods require (over)stoichiometric amounts of sacrificial reagents, which is far from ideal for the production of green hydrogen. To address this challenge, we have developed an atomically dispersed Ni-based photocatalyst that achieves hydrogen evolution rates of up to 270 μmol/g/h (168 mmol/g<sub>Ni</sub>/h). Remarkably, this photocatalyst also exhibits high photoreactivity under direct sunlight, producing up to 17 μmol/g/h (10.6 mmol/g<sub>Ni</sub>/h) of hydrogen. Impressively, the catalyst can even generate green hydrogen directly from seawater, up to 144 μmol/g/h, demonstrating significant potential for real-world applications. The photocatalyst is exceptionally stable, remaining active even after 720 h (140 h of irradiation and 580 h resting time) of operation and retaining high performance over more than 15 cycles. 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Seawater to Sustainable Fuel: Sunlight-Driven Green Hydrogen Generation with an Atomically Dispersed Photocatalyst.
Green hydrogen is widely regarded as a key to a sustainable future, offering a clean and flexible fuel option for decarbonizing the energy, transport, and industrial sectors. While photocatalytic approaches are known for generating hydrogen directly from water, most existing methods require (over)stoichiometric amounts of sacrificial reagents, which is far from ideal for the production of green hydrogen. To address this challenge, we have developed an atomically dispersed Ni-based photocatalyst that achieves hydrogen evolution rates of up to 270 μmol/g/h (168 mmol/gNi/h). Remarkably, this photocatalyst also exhibits high photoreactivity under direct sunlight, producing up to 17 μmol/g/h (10.6 mmol/gNi/h) of hydrogen. Impressively, the catalyst can even generate green hydrogen directly from seawater, up to 144 μmol/g/h, demonstrating significant potential for real-world applications. The photocatalyst is exceptionally stable, remaining active even after 720 h (140 h of irradiation and 580 h resting time) of operation and retaining high performance over more than 15 cycles. Furthermore, comprehensive spectroscopic and structural analyses─including HRTEM, PXRD, ssNMR, XPS, and XAS─provide detailed structural insights and confirm the atomically dispersed nature of the Ni species. In-depth mechanistic studies have elucidated the critical role of atomic dispersion in enabling robust photocatalytic efficiency.
期刊介绍:
The flagship journal of the American Chemical Society, known as the Journal of the American Chemical Society (JACS), has been a prestigious publication since its establishment in 1879. It holds a preeminent position in the field of chemistry and related interdisciplinary sciences. JACS is committed to disseminating cutting-edge research papers, covering a wide range of topics, and encompasses approximately 19,000 pages of Articles, Communications, and Perspectives annually. With a weekly publication frequency, JACS plays a vital role in advancing the field of chemistry by providing essential research.