光催化
制氢
辐照
材料科学
磷
光化学
化学工程
氢
化学
催化作用
有机化学
冶金
物理
核物理学
工程类
作者
Rugma T.P.,Sandeep Kumar Lakhera,Trilochan Sahoo,Bernaudshaw Neppolian
标识
DOI:10.1016/j.mseb.2022.115873
摘要
• g-C 3 N 4 /CuI (P-CN/CuI) photocatalysts was synthesized via facile wet-impregnation and pyrolysis routes. • P-CN/CuI exihibited high charge-carrier separation efficiency. • Na 2 H 2 PO 4 treatment and CuI incorporation caused a red shift in the bandgap of g-C 3 N 4. • P-CN/CuI photocatalyst produced ∼22 times higher hydrogen than bare g-C 3 N 4 . Polymeric carbon nitride (g-C 3 N 4 ) is a promising 2D semiconducting photocatalyst for solar energy conversion applications. However, it suffers from poor performance due to sluggish charge carrier separation efficiency. Herein, we report a Na 2 H 2 PO 4 treated g-C 3 N 4 /CuI (P-CN/CuI) photocatalysts with enhanced charge carrier separation at the interface of P-g-C 3 N 4 and CuI. Double calcination of melamine at 650 °C caused a large redshift in the band tailing states and the energy bandgap, and treatment of g-C 3 N 4 with Na 2 H 2 PO 4 led to further improvement in the visible light absorption. The introduction of CuI into the P-CN matrix progressively improved the visible light absorption and charge carrier’s separation, as evident from the UV–vis and PL spectra. Due to the improved charge separation and light absorption properties, the P-CN/CuI photocatalyst produced ∼ 22 times higher hydrogen production than the bare g-C 3 N 4 . This work shows that non-metal doping and formation of a p-n heterojunction together could largely inhibit the charge carrier recombination in polymeric g-C 3 N 4 for solar energy conversion applications.
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