Electrostatic-induced green and precise growth of model catalysts

催化作用 电场 静电学 离子键合 化学物理 纳米技术 材料科学 面(心理学) 偶极子 多面体 Crystal(编程语言) 晶体生长 光催化 化学工程 化学 结晶学 物理化学 计算机科学 离子 有机化学 物理 数学 几何学 程序设计语言 五大性格特征 人格 心理学 工程类 社会心理学 量子力学
作者
Qiancheng Xia,Bin Liu,Chao Wang,Tao Shen,Shuang Li,Yongguang Bu,Yuchen Zhang,Zhenda Lu,Guandao Gao
出处
期刊:Proceedings of the National Academy of Sciences of the United States of America [National Academy of Sciences]
卷期号:120 (9): e2217256120-e2217256120 被引量:15
标识
DOI:10.1073/pnas.2217256120
摘要

Crystallographic control of crystals as catalysts with precise geometrical and chemical features is significantly important to develop sustainable chemistry, yet highly challenging. Encouraged by first principles calculations, precise structure control of ionic crystals could be realized by introducing an interfacial electrostatic field. Herein, we report an efficient in situ dipole-sourced electrostatic field modulation strategy using polarized ferroelectret, for crystal facet engineering toward challenging catalysis reactions, which avoids undesired faradic reactions or insufficient field strength by conventional external electric field. Resultantly, a distinct structure evolution from tetrahedron to polyhedron with different dominated facets of Ag 3 PO 4 model catalyst was obtained by tuning the polarization level, and similar oriented growth was also realized by ZnO system. Theoretical calculations and simulation reveal that the generated electrostatic field can effectively guide the migration and anchoring of Ag + precursors and free Ag 3 PO 4 nuclei, achieving oriented crystal growth by thermodynamic and kinetic balance. The faceted Ag 3 PO 4 catalyst exhibits high performance in photocatalytic water oxidation and nitrogen fixation for valuable chemicals production, validating the effectiveness and potential of this crystal regulation strategy. Such an electrically tunable growth concept by electrostatic field provides new synthetic insights and great opportunity to effectively tailor the crystal structures for facet-dependent catalysis.
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