Widmer Remo N, Lampronti Giulio I, Casati Nicola, Farsang Stefan, Bennett Thomas D, Redfern Simon A T
Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge, CB2 3EQ, UK.
Paul Scherrer Institute, Photon Science Division, WLGA/229 Forschungsstrasse 111, 5232 Villigen, Switzerland.
Phys Chem Chem Phys. 2019 Jun 21;21(23):12389-12395. doi: 10.1039/c9cp01463b. Epub 2019 May 29.
We report the amorphization of three metal-organic frameworks, ZIF-4, ZIF-62, and ZIF-zni, by synchrotron X-ray radiation. Complete amorphization of these structures occurs on timescales ranging from minutes to hours. This process is non-isokinetic in all three cases, given a varying transformation rate as the transformation proceeds. The underlying mechanism bears the signature of inhomogeneous nucleation, reflected by an increasing local Avrami exponent over time. Furthermore, the amorphization rate accelerates with increasing temperature, even far below the usual thermal stability limit of each crystalline phase. These results not only have important implications for interpretation of X-ray synchrotron studies on the stability of metal-organic frameworks, they also shed light on the rarely-discussed and generally unpredictable experimental problem of beam damage in organic and inorganic compounds in general.
我们报道了通过同步加速器X射线辐射使三种金属有机框架材料ZIF-4、ZIF-62和ZIF-zni发生非晶化的过程。这些结构的完全非晶化发生在从几分钟到几小时的时间尺度上。在这三种情况下,该过程都不是等动力学的,随着转变的进行,转变速率会发生变化。潜在机制具有非均匀成核的特征,表现为局部阿弗拉米指数随时间增加。此外,即使远低于每个晶相通常的热稳定性极限,非晶化速率也会随着温度升高而加快。这些结果不仅对解释金属有机框架材料稳定性的X射线同步加速器研究具有重要意义,还为一般有机和无机化合物中很少被讨论且通常不可预测的束流损伤实验问题提供了线索。