Exploring the potential of calcined nanolayered manganese oxides for water-oxidation reaction

被引:10
作者
Akbari, Nader [1 ]
Allakhverdiev, Suleyman I. [2 ]
Najafpour, Mohammad Mahdi [1 ,3 ,4 ]
机构
[1] Inst Adv Studies Basic Sci IASBS, Dept Chem, Zanjan 4513766731, Iran
[2] Russian Acad Sci, KA Timiryazev Inst Plant Physiol, Botanicheskaya St 35, Moscow 127276, Russia
[3] Inst Adv Studies Basic Sci IASBS, Ctr Climate Change & Global Warming, Zanjan 4513766731, Iran
[4] Inst Adv Studies Basic Sci IASBS, Res Ctr Basic Sci & Modern Technol RBST, Zanjan 4513766731, Iran
基金
俄罗斯科学基金会;
关键词
Artificial photosynthesis; Calcination temperature; Layered manganese oxide; Oxygen; Water-oxidation reaction; Water splitting; EVOLVING PHOTOSYSTEM-II; DIFFERENT METAL-IONS; SOL-GEL SYNTHESIS; HETEROGENEOUS CATALYSTS; THERMAL-DECOMPOSITION; OXIDIZING CATALYSTS; HYDROGEN-PRODUCTION; CRYSTAL-STRUCTURE; OXYGEN EVOLUTION; EFFICIENT;
D O I
10.1016/j.ijhydene.2023.10.025
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
Large-scale electrochemical and photochemical hydrogen production methods from water splitting are limited by the water-oxidation reaction (WOR). This study investigates the influence of calcination temperatures on the WOR efficiency of layered Mn oxides, which are known for their stability and high catalytic activity. The Mn oxides were synthesized via thermal decomposition of KMnO4 and characterized using various techniques including scanning electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, thermal gravimetric analysis, and Raman spectroscopy. The results indicate that even after calcination at high temperatures (>= 400 degrees C), layered Mn oxides remain effective catalysts for WOR. Notably, the calcined sample at 800 degrees C in cerium (IV) ammonium nitrate at concentrations of 0.30 M shows maximum turnover frequency and turnover number of 6.7 x 10(-6)/s and 8.6 x 10(-3) mol (O-2)/mol (Mn) (for 1300 s), respectively.(c) 2023 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:933 / 942
页数:10
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