催化作用
石墨烯
钴
氧化物
氧化还原
材料科学
纳米技术
氮气
氧化钴
碳纤维
氨
碳足迹
化学工程
化学
复合数
温室气体
有机化学
冶金
复合材料
生态学
工程类
生物
作者
Haijiao Lu,Yiming Zhao,Sandra Elizabeth Saji,Xinmao Yin,Ary Anggara Wibowo,Chi Sin Tang,Shibo Xi,Pengfei Cao,Mike Tebyetekerwa,Borui Liu,Marc Heggen,Rafal E. Dunin‐Borkowski,Antonio Tricoli,Andrew T. S. Wee,Hieu T. Nguyen,Qing‐Bo Yan,Zongyou Yin
标识
DOI:10.1016/j.apcatb.2021.121001
摘要
Ammonia is an indispensable chemical to the ecosystem and human beings. Storing solar energy in N-H bonds in NH3 is a promising sustainable alternative to the energy-consuming Haber Bosch process. However, nitrogen photofixation with this strategy still suffers from several unsolved issues, such as high-energy consumption with carbon footprint, short lifetime of photocatalysts, and nitrogen contamination in redox reactions. In this study, a room-temperature strategy is developed to two-dimensionally assemble the diminutive CoO-Co3O4 mixed-oxide composites on reduced graphene oxide. They proffer great surface area and deep-red-light absorbing defect states, which enable them to exhibit over 14 times higher photoactivity than template-free single components. The unveiled photoreaction-induced cation oxidation is reversely triggerable by photo-reactivating Co3O4 back to active CoO, with well-maintained photoactivity after six-cycles. All these room-temperature processes, from catalyst synthesis, nitrogen photofixation, to catalyst reactivation, offer facile way towards upscaling and hold great promise for practical zero-emission N2 photofixation.
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