Wang Jiayue, Kumar Abinash, Wardini Jenna L, Zhang Zhan, Zhou Hua, Crumlin Ethan J, Sadowski Jerzy T, Woller Kevin B, Bowman William J, LeBeau James M, Yildiz Bilge
Department of Nuclear Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Department of Materials Science and Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Nano Lett. 2022 Jul 13;22(13):5401-5408. doi: 10.1021/acs.nanolett.2c01439. Epub 2022 Jun 30.
Exsolution synthesizes self-assembled metal nanoparticle catalysts via phase precipitation. An overlooked aspect in this method thus far is how exsolution affects the host oxide surface chemistry and structure. Such information is critical as the oxide itself can also contribute to the overall catalytic activity. Combining X-ray and electron probes, we investigated the surface transformation of thin-film SrTiFeO during Fe exsolution. We found that exsolution generates a highly Fe-deficient near-surface layer of about 2 nm thick. Moreover, the originally single-crystalline oxide near-surface region became partially polycrystalline after exsolution. Such drastic transformations at the surface of the oxide are important because the exsolution-induced nonstoichiometry and grain boundaries can alter the oxide ion transport and oxygen exchange kinetics and, hence, the catalytic activity toward water splitting or hydrogen oxidation reactions. These findings highlight the need to consider the exsolved oxide surface, in addition to the metal nanoparticles, in designing the exsolved nanocatalysts.
离析法通过相沉淀合成自组装金属纳米颗粒催化剂。到目前为止,该方法中一个被忽视的方面是离析如何影响主体氧化物的表面化学和结构。由于氧化物本身也会对整体催化活性产生影响,因此此类信息至关重要。结合X射线和电子探针,我们研究了薄膜SrTiFeO在铁离析过程中的表面转变。我们发现离析产生了一个厚度约为2 nm的高度缺铁近表面层。此外,离析后原本单晶的氧化物近表面区域部分变成了多晶。氧化物表面的这种剧烈转变很重要,因为离析诱导的非化学计量和晶界会改变氧化物离子传输和氧交换动力学,从而改变对水分解或氢氧化反应的催化活性。这些发现凸显了在设计离析纳米催化剂时,除了金属纳米颗粒外,还需要考虑离析氧化物表面。