1. P-Type Cobalt Phosphide Composites (CoP–Co2P) Decorated on Titanium Oxide for Enhanced Noble-Metal-Free Photocatalytic H2 Evolution Activity
- Author
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Rong Liang, Xuehua Chen, Zhizhen Ye, Yanwen Wang, Chao Qin, and Liping Zhu
- Subjects
Photoluminescence ,Materials science ,chemistry.chemical_element ,Heterojunction ,02 engineering and technology ,Surfaces and Interfaces ,engineering.material ,010402 general chemistry ,021001 nanoscience & nanotechnology ,Condensed Matter Physics ,01 natural sciences ,0104 chemical sciences ,Nanomaterials ,Titanium oxide ,Chemical engineering ,chemistry ,Electrochemistry ,engineering ,Photocatalysis ,General Materials Science ,Noble metal ,0210 nano-technology ,Cobalt ,Spectroscopy ,Photocatalytic water splitting - Abstract
Nowadays, transition-metal phosphides have been reported to function well in photocatalytic water splitting and possess great potential to substitute traditional noble-metal cocatalysts in the future. Herein, p-type cobalt phosphide (CoP-Co2P) nanomaterials were synthesized by phosphating the solvothermally prepared Co(OH)2 nanoflowers at a low temperature (300 °C). Then, we combined the phosphides with commercial TiO2 through facile mechanical mixing to fabricate a useful noble-metal-free photocatalyst. The phosphating time that had an influence on the composition of phosphides was tuned, and 3 h was an ideal condition after comparison. The cobalt phosphide-modified TiO2 at the optimal weight percentage (nominal 0.5%) exhibited the highest photocatalytic hydrogen rate of approximately 824.5 μmol g-1 h-1 under simulated sunlight irradiation, which was nearly equal to 160 times that of bare TiO2 and 1.7 times that of single CoP-modified TiO2. The CoPx/TiO2 heterojunction interfaces were studied using photoluminescence (PL), time-resolved PL, and photoelectrochemical methods, which revealed that the effective charge separation and transfer accelerated by the built-in electric field of p-n junction contributed significantly to the photocatalytic performance.
- Published
- 2021