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Selective light absorber-assisted single nickel atom catalysts for ambient sunlight-driven CO(2) methanation

Ambient sunlight-driven CO(2) methanation cannot be realized due to the temperature being less than 80 °C upon irradiation with dispersed solar energy. In this work, a selective light absorber was used to construct a photothermal system to generate a high temperature (up to 288 °C) under weak solar...

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Detalles Bibliográficos
Autores principales: Li, Yaguang, Hao, Jianchao, Song, Hui, Zhang, Fengyu, Bai, Xianhua, Meng, Xianguang, Zhang, Hongyuan, Wang, Shufang, Hu, Yong, Ye, Jinhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6541650/
https://www.ncbi.nlm.nih.gov/pubmed/31142744
http://dx.doi.org/10.1038/s41467-019-10304-y
Descripción
Sumario:Ambient sunlight-driven CO(2) methanation cannot be realized due to the temperature being less than 80 °C upon irradiation with dispersed solar energy. In this work, a selective light absorber was used to construct a photothermal system to generate a high temperature (up to 288 °C) under weak solar irradiation (1 kW m(−2)), and this temperature is three times higher than that in traditional photothermal catalysis systems. Moreover, ultrathin amorphous Y(2)O(3) nanosheets with confined single nickel atoms (SA Ni/Y(2)O(3)) were synthesized, and they exhibited superior CO(2) methanation activity. As a result, 80% CO(2) conversion efficiency and a CH(4) production rate of 7.5 L m(−2) h(−1) were achieved through SA Ni/Y(2)O(3) under solar irradiation (from 0.52 to 0.7 kW m(−2)) when assisted by a selective light absorber, demonstrating that this system can serve as a platform for directly harnessing dispersed solar energy to convert CO(2) to valuable chemicals.