Smolentsev Grigory, Cecconi Bianca, Guda Alexander, Chavarot-Kerlidou Murielle, van Bokhoven Jeroen A, Nachtegaal Maarten, Artero Vincent
Paul Scherrer Institute, 5232 Villigen PSI (Switzerland).
Laboratory of Chemistry and Biology of Metals, Univ. Grenoble Alpes, CEA, CNRS, Grenoble (France).
Chemistry. 2015 Oct 19;21(43):15158-62. doi: 10.1002/chem.201502900. Epub 2015 Sep 4.
Rational development of efficient photocatalytic systems for hydrogen production requires understanding the catalytic mechanism and detailed information about the structure of intermediates in the catalytic cycle. We demonstrate how time-resolved X-ray absorption spectroscopy in the microsecond time range can be used to identify such intermediates and to determine their local geometric structure. This method was used to obtain the solution structure of the Co(I) intermediate of cobaloxime, which is a non-noble metal catalyst for solar hydrogen production from water. Distances between cobalt and the nearest ligands including two solvent molecules and displacement of the cobalt atom out of plane formed by the planar ligands have been determined. Combining in situ X-ray absorption and UV/Vis data, we demonstrate how slight modification of the catalyst structure can lead to the formation of a catalytically inactive Co(I) state under similar conditions. Possible deactivation mechanisms are discussed.
合理开发高效的光催化制氢系统需要了解催化机理以及催化循环中中间体结构的详细信息。我们展示了如何利用微秒时间范围内的时间分辨X射线吸收光谱来识别此类中间体并确定其局部几何结构。该方法用于获得钴肟的Co(I)中间体的溶液结构,钴肟是一种用于从水中进行太阳能制氢的非贵金属催化剂。已经确定了钴与包括两个溶剂分子在内的最近配体之间的距离以及钴原子相对于平面配体形成的平面的平面外位移。结合原位X射线吸收和紫外/可见光谱数据,我们展示了在相似条件下催化剂结构的轻微改变如何导致形成催化无活性的Co(I)状态。讨论了可能的失活机制。