纳米棒
纳米花
异质结
光电流
材料科学
光催化
化学工程
硫化镉
金红石
可见光谱
纳米技术
分解水
光电子学
纳米结构
化学
催化作用
工程类
冶金
生物化学
作者
Selvaraj David,Mahadeo A. Mahadik,Hee Suk Chung,Jung Ho Ryu,Jum Suk Jang
标识
DOI:10.1021/acssuschemeng.7b00558
摘要
With the application of ethylenediamine (EDA) as a solvent, a template, and co-ordination agents, novel photoanode architecture of the cadmium sulfide (CdS) nanoflower (NF)/rutile(R)-TiO2 nanorod (NR) heterojunction is successfully synthesized using a facile two-step hydrothermal process. The optimized CdS (medium concentration; MC) NF/R-TiO2 NR heterojunction exhibited a greatly enhanced visible-light photoelectrochemical (PEC) performance, whereby the highest photocurrent density of 3.23 mA cm–2 at 0.1 V versus Ag/AgCl and a photoconversion efficiency (PCE) of 0.46% were achieved under solar light irradiation. The optimal photocurrent density of the CdS (MC) NF/R-TiO2 NR heterojunction, photoanode is 2.54 times (60.68%) higher than that of the pristine R-TiO2 NR because of an effective light absorption, an appropriate band-edge position, and the charge separation. Furthermore, the open circuit voltage (VOC) was shifted from −0.85 V to −1.34 V due to the grafting of the CdS NF onto the R-TiO2 NR facet; this surface modification reveals the synergistic effect. The optimal CdS (MC) NF/R-TiO2 NR heterojunction showed a PEC hydrogen (H2) generation of 1007.98 μmol after 3 h. The design of the novel heterojunction photoanode that is proposed in the present strategy can shed light on the fabrication of new, cheap photocatalysts for an effective H2 generation.
科研通智能强力驱动
Strongly Powered by AbleSci AI