过电位
材料科学
兴奋剂
光催化分解水
贵金属
催化作用
分解水
石墨氮化碳
光化学
吸收(声学)
氢
光催化
无机化学
化学工程
金属
光电子学
冶金
物理化学
电化学
电极
化学
有机化学
复合材料
生物化学
工程类
作者
Xunfu Zhou,Pai Wang,Meng Li,Min-Fu Wu,Bei Jin,Jin Luo,Meifeng Chen,Xiaoqin Zhou,Yanning Zhang,Xiaosong Zhou
标识
DOI:10.1016/j.jmst.2023.02.041
摘要
Carbon nitride (g-C3N4) is a promising metal-free and visible-light-responsive photocatalyst. However, its photocatalytic efficiency still suffers from high recombination rates of photoinduced charge carriers, slow kinetics of surface redox reactions, and relatively poor light absorption. Herein, a non-noble metal photocatalyst of MoS2 nanodots anchored on P-doped g-C3N4 via in situ photodeposition was constructed. With the synergetic effect of the P-doping and MoS2 co-catalyst, the as-prepared P-doped g-C3N4/MoS2 catalyst has achieved efficient photocatalytic overall water splitting with a hydrogen evolution rate of 121.7 μmol h−1 g−1. Experimental results and Density functional theory (DFT) simulations indicate that the enhanced photo-absorption capacity originates from the reduced band gaps by P doping. Meanwhile, the MoS2 reduces the overpotential of the water oxidation process and improves hydrogen adsorption capability in the hydrogen evolution reaction. This work can pave a new avenue to design and develop noble-metal-free water-splitting photocatalysts for future large-scale applications.
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