Instituto de Catálisis y Petroleoquímica, CSIC, C/Marie Curie 2, 28049, Madrid, Spain.
European Synchrotron Radiation Facility (ESRF), 71 av. Des Martyrs, Grenoble, France.
Angew Chem Int Ed Engl. 2018 Jan 26;57(5):1199-1203. doi: 10.1002/anie.201709552. Epub 2018 Jan 11.
Understanding how a photocatalyst modulates its oxidation state, size, and structure during a photocatalytic reaction under operando conditions is strongly limited by the mismatch between (catalyst) volume sampled by light and, to date, the physicochemical techniques and probes employed to study them. A synchrotron micro-beam X-ray absorption spectroscopy study together with the computational simulation and analysis (at the X-ray cell) of the light-matter interaction occurring in powdered TiO -based monometallic Cu, Ni and bimetallic CuNi catalysts for hydrogen production from renewables was carried out. The combined information unveils an unexpected key catalytic role involving the phase contact between the reduced and oxidized non-noble metal phases in all catalysts and, additionally, reveals the source of the synergistic Cu-Ni interaction in the bimetallic material. The experimental method is applicable to operando studies of a wide variety of photocatalytic materials.
在实际操作条件下,了解光催化剂在光催化反应过程中如何调节其氧化态、尺寸和结构,受到光采样的(催化剂)体积与迄今为止用于研究它们的物理化学技术和探针之间不匹配的强烈限制。对用于从可再生能源生产氢气的基于 TiO 的单金属 Cu、Ni 和双金属 CuNi 催化剂进行了同步微束 X 射线吸收光谱研究,以及光物质相互作用的计算模拟和分析(在 X 射线电池中)。综合信息揭示了一种意想不到的关键催化作用,涉及所有催化剂中还原和氧化非贵金属相之间的相接触,此外还揭示了双金属材料中 Cu-Ni 相互作用的协同作用的来源。该实验方法适用于各种光催化材料的实际操作研究。