Photocatalytic hydrogen evolution of nanoporous CoFe2O4 and NiFe2O4 for water splitting

被引:62
作者
He, Gege [1 ,2 ,3 ]
Wen, Yang [1 ,2 ,3 ]
Ma, Chen [1 ,2 ,3 ]
Li, Xiangyang [1 ,2 ,3 ]
Gao, Lumei [4 ]
Sun, Zhanbo [1 ,2 ,3 ]
机构
[1] Xi An Jiao Tong Univ, Sch Sci, MOE Key Lab Nonequilibrium Synth & Modulat Conden, Xian 710049, Peoples R China
[2] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, Xian 710049, Peoples R China
[3] Xi An Jiao Tong Univ, Key Lab Shaanxi Adv Funct Mat & Mesoscop Phys, Xian 710049, Peoples R China
[4] Xi An Jiao Tong Univ, Instrument Anal Ctr, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
CoFe2O4; Mesopores; Hydrogen generation; Photocatalysts; BIOHYDROGEN PRODUCTION; INTERFACE; CATALYST; COBALT; FILMS; AU;
D O I
10.1016/j.ijhydene.2020.11.107
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The spinels CoFe2O4 and NiFe2O4 of nanoporous photocatalysts were prepared by dealloying and calcination. The photocatalytic performance for the hydrogen generation rate via water splitting was measured. The results revealed that CoFe2O4 exhibits a sheet-like nanoporous structure and that abundant mesopores are distributed in the nanosheets. NiFe2O4 shows a typical pore-ligament structure. The measurements show that hydrogen generation is exhibited by both oxides because the bandgap of CoFe2O4 and NiFe2O4 is higher than the water oxidization potential. The hydrogen generation rate is approximately 0.088 mmol h d(-1) g(-1) for CoFe2O4 and 0.026 mmol h d(-1) g(-1) for NiFe2O4 when the TEOA (10 vol%) sacrificial agent is adopted. This performance is significantly higher than that of methanol as the scavenger because TEOA increases the pH value of the solution, changes the negative shift in the conduction band energy level and improves the electron transport efficiency. The higher performance of CoFe2O4 is attributed to its larger specific surface area, ample unimpeded penetration diffusion paths and higher electron transfer rate. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5369 / 5377
页数:9
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