光催化
氮气
氮化碳
固氮
氮化物
光化学
材料科学
固碳
量子产额
化学
碳纤维
化学工程
纳米技术
催化作用
有机化学
物理
二氧化碳
光学
复合材料
工程类
复合数
荧光
图层(电子)
作者
Gang Dong,Peng Qiu,Qingze Chen,Cong Huang,Feiyang Chen,Xueqin Liu,Zhen Li,Yang Wang,Yanli Zhao
标识
DOI:10.1016/j.cej.2021.133573
摘要
Photocatalytic nitrogen fixation is one of the most promising sustainable energy conversion technologies and might serve as a cheaper and more energy-efficient alternative to the capital- and energy-intensive Haber-Bosch process. However, the solution to solve the nitrogen fixation kinetic problem induced by high reduction potential of intermediates remains a grand challenge. In this work, the kinetic problem of nitrogen fixation is addressed under ambient conditions using K+-intercalated crystalline carbon nitride (KCCN) with an electron storage property. Combined with vigorous N2 chemisorption and activation properties of nitrogen vacancies (NVs), a photocatalytic nitrogen fixation system is constructed, where the NVs on KCCN chemisorb and activate N2 molecule, and subsequently reduce it to NH3 by multielectron reactions facilitated by the stored electrons of KCCN. The unique structure of KCCN-NVs demonstrates a high NH3 production rate of 3.51 mmol h−1 g−1 under visible light irradiation and an apparent quantum yield of 2.05% at λ = 430 nm. This work offers an intriguing solution toward the development of nitrogen-fixing photocatalysts.
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