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The interface of GaP(100) and H2O studied by photoemission and reflection anisotropy spectroscopy

机译:Gap(100)和H2O的界面通过光电子发射和光电子学研究   反射各向异性光谱学

摘要

We study the initial interaction of adsorbed H2O with P-rich and Ga-richGaP(100) surfaces. Atomically well defined surfaces are prepared bymetal-organic vapour phase epitaxy and transferred contamination-free toultra-high vacuum, where water is adsorbed at room temperature. Finally, thesurfaces are annealed in vapour phase ambient. During all steps, the impact onthe surface properties is monitored with in-situ reflection anisotropyspectroscopy (RAS). Photoelectron spectroscopy and low-energy electrondiffraction are applied for further in-system studies. After exposure up tosaturation of the RA spectra, the Ga-rich (2 x 4) surface reconstructionexhibits a sub-monolayer coverage in form of a mixture of molecularly anddissociatively adsorbed water. For the p(2 x 2)/c(4 x 2) P-rich surfacereconstruction, a new c(2 x 2) superstructure forms upon adsorption and theuptake of adsorbate is significantly reduced when compared to the Ga-richsurface. Our findings show that microscopic surface reconstructions of GaP(100)greatly impact the mechanism of initial interface formation with water, whichcould benefit the design of e.g. photoelectrochemical water splitting devices.
机译:我们研究了富P和富GaGaP(100)表面吸附水的初始相互作用。通过金属有机气相外延和转移无污染的超高真空来制备原子定义明确的表面,在室温下水被吸附。最后,将表面在气相环境中退火。在所有步骤中,通过原位反射各向异性光谱(RAS)监视对表面性能的影响。光电子能谱和低能电子衍射被用于进一步的系统内研究。暴露到RA光谱达到饱和后,富含Ga(2 x 4)的表面重建分子和解离吸附水的混合物形式表现出亚单层覆盖。对于p(2 x 2)/ c(4 x 2)富P的表面重建,新的c(2 x 2)上层结构在吸附后形成,与富Ga的表面相比,吸附物的吸收显着减少。我们的研究结果表明,GaP(100)的微观表面重建极大地影响了与水初始界面形成的机制,这可能有益于例如光电化学水分解装置。

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