Structural and Phase Engineering of a Hierarchical 2D-2D Nickel MOF/Hydroxide-Derived Ni0.85Se/NiTe2 Heterointerface for Robust HER, OER, and Overall Water Splitting

被引:4
|
作者
Pathak, Ishwor [1 ,2 ]
Prabhakaran, Sampath [1 ]
Acharya, Debendra [1 ]
Chhetri, Kisan [1 ]
Muthurasu, Alagan [1 ]
Rosyara, Yagya Raj [1 ]
Kim, Taewoo [1 ]
Ko, Tae Hoon [1 ]
Kim, Do Hwan [3 ]
Kim, Hak Yong [1 ,4 ]
机构
[1] Jeonbuk Natl Univ, Dept Nano Convergence Engn, Jeonju 54896, South Korea
[2] Tribhuvan Univ, Dept Chem, Amrit Campus, Kathmandu 44613, Nepal
[3] Jeonbuk Natl Univ, Dept Energy Storage Convers Engn BK21 FOUR, Div Sci Educ, Jeonju 54896, Jeonbuk, South Korea
[4] Jeonbuk Natl Univ, Dept Organ Mat & Fiber Engn, Jeonju 561756, South Korea
基金
新加坡国家研究基金会;
关键词
metal-organic framework; Ni0.85Se/NiTe2; heterointerface; selenotellurization; water splitting; HYDROGEN EVOLUTION; ELECTROCATALYSTS;
D O I
10.1002/smll.202406732
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of a nonnoble metal-based cost-effective, efficient, and durable bifunctional electrocatalyst is crucial to achieving the goal of carbon neutrality. In this study, a structural and interfacial engineering approach is employed to design a 2D-2D hierarchical nickel MOF/nickel hydroxide-derived nickel selenide/nickel telluride dual-phase material through a single-step selenotellurization process. The rational design of highly ordered nanoarchitectures provides well-defined voids and ample pathways for ion diffusion. Furthermore, hierarchical nickel selenide/nickel telluride works synergistically at heterojunctions, providing a local ion enrichment mechanism for the catalytic process. As a result, Ni0.85Se/NiTe2@Ni-NH@CC needs an overpotential of 69 and 240 mV to deliver a current density of 10 mA cm(-2) for the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER), respectively, with an outstanding stability observed for over 100 h. Moreover, the Ni0.85Se/NiTe2@Ni-NH@CC (+, -) device exhibits excellent overall water-splitting performance with a cell voltage of 1.50 V at 10 mA cm(-2) and can be operated steadily for >100 h at 100 mA cm(-2). Density functional theory (DFT) calculations indicate favorable kinetics for H-adsorption at the selenotelluride heterojunction, thereby promoting the HER. This work highlights a new approach for designing a unique nanoarchitecture of MOF/hydroxide-derived selenotelluride heterojunctions for high-efficiency energy conversion applications.
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页数:14
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