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首页> 外文期刊>Advanced Materials >Identifying Dense NiSe_2/CoSe_2 Heterointerfaces Coupled with Surface High-Valence Bimetallic Sites for Synergistically Enhanced Oxygen Electrocatalysis
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Identifying Dense NiSe_2/CoSe_2 Heterointerfaces Coupled with Surface High-Valence Bimetallic Sites for Synergistically Enhanced Oxygen Electrocatalysis

机译:识别致密NISE_2 / COSE_2异助料与表面高价双金属位点相结合,用于协同增强的氧电催化

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摘要

Abstract Constructing heterostructures with abundant interfaces is essential for integrating the multiple functionalities in single entities. Herein, the synthesis of NiSe2/CoSe2 heterostructures with different interfacial densities via an innovative strategy of successive ion injection is reported. The resulting hybrid electrocatalyst with dense heterointerfaces exhibits superior electrocatalytic properties in an alkaline electrolyte, superior to other benchmarks and precious metal catalysts. Advanced synchrotron techniques, post structural characterizations, and density functional theory (DFT) simulations reveal that the introduction of atomic‐level interfaces can lower the oxidation overpotential of bimetallic Ni and Co active sites (whereas Ni2+ can be more easily activated than Co2+) and induce the electronic interaction between the core selenides and surface in situ generated oxides/hydroxides, which play a critical role in synergistically reducing energetic barriers and accelerating reaction kinetics for catalyzing the oxygen evolution. Hence, the heterointerface structure facilitates the catalytic performance enhancement via increasing the intrinsic reactivity of metallic atoms and enhancing the synergistic effect between the inner selenides and surface oxidation species. This work not only complements the understanding on the origins of the activity of electrocatalysts based on metal selenides, but also sheds light on further surface and interfacial engineering of advanced hybrid materials.
机译:摘要构造具有丰富接口的异质结构对于整合单个实体中的多个功能至关重要。这里,报道了通过通过连续离子注射的创新策略的具有不同界面密度的NiSE2 / COSE2异质结构的合成。所得具有致密异偶填料的杂种电催化剂在碱性电解质中表现出优异的电催化性质,优于其他基准和贵金属催化剂。先进的同步rotron技术,后结构表征和密度泛函理论(DFT)模拟表明,原子水平界面的引入可以降低双金属Ni和Co活性位点的氧化过度(而Ni2 +比CO2 +更容易激活)并诱导核心硒化物与表面的电子相互作用,原位产生的氧化物/氢氧化物在协同减少能量屏障和加速反应动力学中起重要作用,以催化氧气进化。因此,异煤表面结构通过增加金属原子的内在反应性并增强内硒化物和表面氧化物质之间的协同效应来促进催化性能提高。这项工作不仅补充了基于金属硒化物的电催化剂活动的起源的理解,而且还在先进的混合材料的进一步表面和界面工程上脱光。

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