光催化
星团(航天器)
固氮
质子化
光化学
化学
固氮酶
X射线光电子能谱
分子
催化作用
光电效应
单独一对
脱水
氨
氮气
材料科学
化学工程
有机化学
离子
工程类
生物化学
光电子学
程序设计语言
计算机科学
作者
Binbin Guo,Xiyue Cheng,Yu Tang,Wei Guo,Shuiquan Deng,Ling Wu,Xianzhi Fu
标识
DOI:10.1002/anie.202117244
摘要
This work reports the dehydrated Zr-based MOF UiO-66(SH)2 as a visible-light-driven photocatalyst to mimic the biological N2 fixation process. The 15 N2 and other control experiments demonstrated that the new photocatalyst is highly efficient in converting N2 to ammonia. In-situ TGA, XPS, and EXAFS as well as first-principles simulations were used to demonstrate the role of the thermal treatment and the changes of the local structures around Zr due to the dehydration. It was shown that the dehydration opened a gate for the entry of N2 molecules into the [Zr6 O6 ] cluster where the strong N≡N bond was broken stepwise by μ-N-Zr type interactions driven by the photoelectrons aided by the protonation. This mechanism was discussed in comparison with the Lowe-Thorneley mechanism proposed for the MoFe nitrogenase, and with emphasis on the [Zr6 O6 ] cluster effect and the leading role of photoelectrons over the protonation. The results shed new light on understanding the catalytic mechanism of biological N2 fixation and open a new way to fix N2 under mild conditions.
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