Chu Jiayu, Sun Guoji, Han Xijiang, Chen Xin, Wang Jiajun, Hu Wen, Waluyo Iradwikanari, Hunt Adrian, Du Yunchen, Song Bo, Xu Ping
MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin 150001, China.
State Key Laboratory of Advanced Welding and Joining, Harbin Institute of Technology, Shenzhen Graduate School, Shenzhen 518055, China.
Nanoscale. 2019 Sep 7;11(33):15633-15640. doi: 10.1039/c9nr05086h. Epub 2019 Aug 13.
In order to further enhance the performance of photocatalysts, cocatalysts are used to accelerate the photocatalytic reactions. Herein, ultrafine cobalt oxide (CoO) nanoparticles are synthesized through a novel bottom-up strategy and explored as an efficient non-noble cocatalyst to dramatically promote the photocatalytic hydrogen evolution rate of CdS nanorods. CdS/CoO heterostructures, consisting of highly dispersed 3-5 nm CoO nanoparticles anchored on the CdS nanorods, can provide a high photocatalytic hydrogen evolution rate of 6.45 mmol g h (∼36 times higher than that of bare CdS nanorods) in the visible-light region (>420 nm). Combined X-ray photoelectron spectroscopy and X-ray absorption near edge spectroscopy analyses suggest Co-S bond formation between CoO and CdS, which guarantees efficient migration and separation of photogenerated charge carriers. This work provides a new avenue for adopting CoO as an effective cocatalyst for enhanced photocatalytic hydrogen production in the visible-light region.
为了进一步提高光催化剂的性能,助催化剂被用于加速光催化反应。在此,通过一种新型的自下而上策略合成了超细微氧化钴(CoO)纳米颗粒,并将其作为一种高效的非贵金属助催化剂进行探索,以显著提高硫化镉(CdS)纳米棒的光催化析氢速率。由高度分散在CdS纳米棒上的3 - 5纳米CoO纳米颗粒组成的CdS/CoO异质结构,在可见光区域(>420纳米)可提供6.45 mmol g h的高光催化析氢速率(比裸CdS纳米棒高约36倍)。结合X射线光电子能谱和X射线吸收近边光谱分析表明,CoO和CdS之间形成了Co - S键,这保证了光生电荷载流子的有效迁移和分离。这项工作为采用CoO作为可见光区域增强光催化产氢的有效助催化剂提供了一条新途径。