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通过一步合成MoSe -NiSe核壳纳米线阵列实现从碱性/海水中低成本制氢

Low-Cost Hydrogen Production from Alkaline/Seawater over a Single-Step Synthesis of Mo Se -NiSe Core-Shell Nanowire Arrays.

作者信息

Poudel Milan Babu, Logeshwaran Natarajan, Prabhakaran Sampath, Kim Ae Rhan, Kim Do Hwan, Yoo Dong Jin

机构信息

Department of Energy Storage/Conversion Engineering (BK21 FOUR) of Graduate School, Hydrogen and Fuel Cell Research Center, Jeonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju-si, Jeollabuk-do, 54896, Republic of Korea.

Department of Life Science, Jeonbuk National University, 567 Baekje-daero, Deokjin-gu, Jeonju-si, Jeollabuk-do, 54896, Republic of Korea.

出版信息

Adv Mater. 2024 Feb;36(5):e2305813. doi: 10.1002/adma.202305813. Epub 2023 Dec 5.

Abstract

The rational design and steering of earth-abundant, efficient, and stable electrocatalysts for hydrogen generation is highly desirable but challenging with catalysts free of platinum group metals (PGMs). Mass production of high-purity hydrogen fuel from seawater electrolysis presents a transformative technology for sustainable alternatives. Here, a heterostructure of molybdenum selenide-nickel selenide (Mo Se -NiSe) core-shell nanowire arrays constructed on nickel foam by a single-step in situ hydrothermal process is reported. This tiered structure provides improved intrinsic activity and high electrical conductivity for efficient charge transfer and endows excellent hydrogen evolution reaction (HER) activity in alkaline and natural seawater conditions. The Mo Se -NiSe freestanding electrodes require small overpotentials of 84.4 and 166 mV to reach a current density of 10 mA cm in alkaline and natural seawater electrolytes, respectively. It maintains an impressive balance between electrocatalytic activity and stability. Experimental and theoretical calculations reveal that the Mo Se -NiSe interface provides abundant active sites for the HER process, which modulate the binding energies of adsorbed species and decrease the energetic barrier, providing a new route to design state-of-the-art, PGM-free catalysts for hydrogen production from alkaline and seawater electrolysis.

摘要

合理设计并操控储量丰富、高效且稳定的析氢电催化剂是非常必要的,但对于不含铂族金属(PGM)的催化剂而言具有挑战性。通过海水电解大规模生产高纯度氢燃料是一项具有变革性的可持续替代技术。在此,报道了一种通过一步原位水热法在泡沫镍上构建的硒化钼-硒化镍(MoSe₂-NiSe)核壳纳米线阵列异质结构。这种分层结构提高了本征活性和电导率,有利于高效电荷转移,并在碱性和天然海水条件下赋予优异的析氢反应(HER)活性。MoSe₂-NiSe独立电极在碱性和天然海水电解质中分别需要84.4和166 mV的小过电位才能达到10 mA cm⁻²的电流密度。它在电催化活性和稳定性之间保持了令人印象深刻的平衡。实验和理论计算表明,MoSe₂-NiSe界面为HER过程提供了丰富的活性位点,调节了吸附物种的结合能并降低了能垒,为设计用于碱性和海水电解制氢的先进无PGM催化剂提供了一条新途径。

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