光催化
甲醇
镓
镍
光化学
人工光合作用
无机化学
化学
碳纤维
烟酰胺腺嘌呤二核苷酸磷酸
制氢
氧化物
电子转移
材料科学
叶绿素
太阳能燃料
光合作用
氧化镍
氮化碳
异构化
烟酰胺腺嘌呤二核苷酸
炭黑
氢
路易斯酸
电化学
氢燃料
分解水
绿色化学
催化作用
化学工程
石墨烯
作者
Rui Song,Zhiwen Chen,Chenyue Qiu,Yangfan Xu,Andrew Wang,Xiaoliang Yan,Yubin Fu,Paul N. Duchesne,Emerson M. MacNeil,Jigang Zhou,Chaoqian Ai,Jiuli Guo,Chaoran Li,Xingda An,Zhijie Chen,Jiajun Han,Dengwei Jing,Athanasios A. Tountas,Jessica Ye,Guangming Cai
标识
DOI:10.1038/s41467-025-65560-y
摘要
Light-driven methanol synthesis from CO2 provides a sustainable fuel source and approach to carbon neutralization. Mimicking natural photosynthesis could improve gas-solid photocatalytic efficiency, but it remains highly challenging due to the absence of well-organized mass and charge transfer networks in artificial materials. Herein, we report a chlorophyll-mimicking, nano-pigment nickel gallium oxide, which facilitates discrete light/dark reactions and proton-mediated charge transfer for efficient photocatalytic hydrogenation of CO2 to methanol. This nano-pigment features surface frustrated Lewis pairs, enabling heterolytic hydrogen splitting into H- and H+. The H- acts analogously to nicotinamide adenine dinucleotide phosphate in natural photosynthesis, with Ni(II)/Ni(III) and OH(-I) respectively serving as conduits for ion transport of H- and H+ to the Ni site, where they subsequently react with CO2, mimicking natural carbon fixation. This approach establishes a chlorophyll-mimetic structure for photocatalytic stepwise CO2 hydrogenation, achieving 3.0% quantum efficiency, 3.20 mmol·h-1·g-1 methanol activity, and 79.6% selectivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI