期刊
CHEMICAL ENGINEERING JOURNAL
卷 441, 期 -, 页码 -出版社
ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.136031
关键词
Electrocatalyst; Crystalline; amorphous heterostructure; Transition metal phosphide; Layer double hydroxide; Alkaline water splitting
资金
- Research Development Fund (Tianjin University) [110-0301030146, 110-0505000103]
- State Key Laboratories of Chemical Engineering (Tianjin University)
- (Tianjin University)
- Coal Chemical Industry Joint R&D Center (Baoshun Technology Co., Ltd.)
- Coal Chemical Industry Joint R&D Center (Tianjin University)
- Chemical Engineering Research Center (Tianjin University)
This study develops a non-noble metal catalyst for efficient alkaline electrochemical water splitting. The catalyst, a series of crystalline CoMP-decorated amorphous CoM LDH nanomaterials, shows increased catalytic active sites, optimal intermediate adsorption/dissociation capability, and synergistic effects between transition metals, leading to enhanced catalytic performance. The optimized cell assembled with this catalyst exhibits excellent durability and ultralow cell voltages for driving high current densities.
Rational design of non-noble metal catalysts for alkaline electrochemical water splitting under large current densities is of great significance for realizing hydrogen economy and remains a daunting challenge. Herein, a series of crystalline CoMP-decorated (M = Mn, Fe, Ni, Cu, Zn) amorphous CoM LDH nanomaterials in-situ grown on nickel foam (denoted as c-CoMP/a-CoM LDH/NF) is developed as highly efficient and stable alkaline water splitting electrocatalysts. Crystalline CoMP encountered amorphous CoM LDH structure brings the increased catalytic active sites without sacrificing charge transfer rates, more optimal intermediate adsorption/dissociation capability, and the synergistic effects between binary transition metals, leading to more favorable reaction kinetics, thus enhancing catalytic performance for oxygen evolution reaction and hydrogen evolution reaction. As a result, the optimized cell assembled by the as-proposed electrocatalysts only requires ultralow cell voltages of 1.655 and 1.722 V to drive current densities of 100 and 500 mA cm-2 in 1.0 M KOH and exhibits excellent durability over 85 h (under 100 mA cm-2), which is originated from the well-retentive hybrid crystalline/ amorphous nanostructure even after undergoing surface reconstruction. The presented work deepens the insights of crystalline/amorphous heterostructure catalysts and provides a new inspiration in the design of bifunctional electrocatalysts for high-rate alkaline water splitting.
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