高分辨率透射电子显微镜
材料科学
X射线光电子能谱
可见光谱
金属
漫反射
分解水
共晶体系
纳米颗粒
化学工程
吸附
合金
粒径
催化作用
光催化
光化学
纳米技术
化学
物理化学
透射电子显微镜
光学
冶金
光电子学
生物化学
物理
工程类
作者
Xiying Li,Heng Liu,Shuang Liu,Jing Zhang,Wei Chen,Cunping Huang,Liqun Mao
标识
DOI:10.1016/j.ijhydene.2016.11.059
摘要
Abstract This paper focuses on the bi-metal co-catalyst of CdS in hydrogen generation from water-splitting under visible light. Pt–Pd eutectic alloy NPs was prepared by two-step chemical reduction, and was subsequently loaded on the surface of CdS photo-catalyst by photo-induced electrons when water splitting reaction was occurring under 300 W Xe light ( λ > 420 nm). According to the experimental results, the photo-activity is significantly promoted as bi-metal modified on the surface of CdS. The H 2 evolution rate of Pt–Pd/CdS, 25.28 mmol/h/gCat., is ca. 2.4 times as much as that of Pt/CdS, and 3.8 times as much as that of Pd/CdS. HRTEM/ED/EDS revealed that the so-obtained Pt–Pd hybrid NPs with a particle size of 5–8 nm is of similar twin structure. XPS revealed that the as-prepared Pt–Pd bi-metal NPs mainly composed of metallic Pt 0 and Pd 0 . UV–Vis diffuse reflectance spectrum of CdS nanoparticles interpreted its trait in visible light adsorption, and PL lifetime indicated that the high active of Pt–Pd/CdS lies in its high separation efficiency.
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