In-situ phosphating to synthesize Ni2P decorated NiO/g-C3N4 p-n junction for enhanced photocatalytic hydrogen production

非阻塞I/O 光催化 过电位 磷化物 制氢 材料科学 催化作用 光化学 分解水 化学工程 金属 化学 电极 冶金 物理化学 电化学 工程类 有机化学 生物化学
作者
Jian‐Wen Shi,Yajun Zou,Linhao Cheng,Dandan Ma,Diankun Sun,Siman Mao,Lvwei Sun,Chi He,Zeyan Wang
出处
期刊:Chemical Engineering Journal [Elsevier]
卷期号:378: 122161-122161 被引量:151
标识
DOI:10.1016/j.cej.2019.122161
摘要

Photocatalysis is a promising method to obtain hydrogen without any pollution. The key to improve the efficiency of photocatalytic reaction is to design an excellent catalyst structure which can effectively promote the separation and transfer of photogenerated electrons and holes. In this work, a novel photocatalyst, Ni2P decorated NiO/g-C3N4 p-n junction (NiO/Ni2P/CN, abbreviating g-C3N4 as CN) is successfully developed by a one-step in-situ phosphating of Ni(OH)2/CN. The optimized NiO/Ni2P/CN exhibits an impressive photocatalytic H2 evolution rate of 5.04 μmol h−1 under visible-light irradiation (λ > 420 nm) without any noble metal as co-catalyst, which is 126 times higher than that of pristine CN. This high photocatalytic performance is mainly based on the intimated contact of the three components (Ni2P, NiO and CN), where the photogenerated holes on the valence band (VB) of CN can be transferred to the VB of NiO due to the internal-built electric field created by p-n junction, while the photoexcited electrons on the conduction band (CB) of CN can be migrated to Ni2P co-catalyst with a low overpotential, thus the separation and transfer of charge carriers are significantly promoted, and finally the photocatalytic activity of NiO/Ni2P/CN for the hydrogen evolution from water splitting is enhanced. This work may enlighten on the design of photocatalysts with high efficiency by constructing p-n junction and metal phosphide co-catalyst with low overpotential.

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