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碳化钼负载的金属有机框架衍生的镍钴磷硫化物异质结构作为高效析氧反应和析氢反应催化剂

Molybdenum carbide supported metal-organic framework-derived Ni, Co phosphosulphide heterostructures as efficient OER and HER catalysts.

作者信息

Naseeb Muhammad Ahsan, Murtaza Maida, Farooq Komal, Shah Waqas Ali, Waseem Amir

机构信息

Department of Chemistry, Quaid-i-Azam University Islamabad-45320 Pakistan

出版信息

Nanoscale Adv. 2025 Jul 22. doi: 10.1039/d5na00510h.

Abstract

Molybdenum carbide (Mo C) has gained attention for water splitting due to its electronic structure resembling to Pt and have high electrochemical performance. We designed porous nanostructured phosphorus/sulfur co-doped Ni, Co phosphosulphide and molybdenum carbide heterostructures Mo C(MoC-MoC) through confined carburization within a metal-organic framework (MOF) matrix combined with a phosphosulfurization strategy. Starting from a carbon source consisting of NiCo-MOF incorporating molybdenum trioxide, we prepared MOF-derived NiCo-Mo C nanorods carbonization, which exhibited decent electrocatalytic performance for the hydrogen evolution reaction (HER) by electrochemical water splitting. The NiCo-Mo C showed low overpotentials of 153 mV and 157 mV RHE at a current density of 10 mA cm in 0.5 M HSO and 1 M KOH, respectively. Phosphosulfurization of NiCo-Mo C, performed under controlled conditions, resulted in the formation of NiPS-CoPS-Mo C, which demonstrated superior HER performance than the precursor NiCo-Mo C with overpotentials of 75.2 mV and 86.6 mV in 0.5 M HSO and 1 M KOH, respectively and an overpotential of 184.5 mV at 10 mA cm for the oxygen evolution reaction (OER). The durability of the NCMCSP-based electrolyzer for the overall water splitting was evaluated by measuring the voltage over time at a constant current density of 20 mA cm for 12 h.

摘要

碳化钼(Mo₂C)因其电子结构类似于铂且具有高电化学性能而在水分解方面受到关注。我们通过在金属有机框架(MOF)基质内进行受限渗碳并结合磷硫化策略,设计了多孔纳米结构的磷/硫共掺杂镍钴磷硫化物与碳化钼异质结构Mo₂C(MoC-MoC)。从由包含三氧化钼的NiCo-MOF组成的碳源开始,我们通过碳化制备了MOF衍生的NiCo-Mo₂C纳米棒,其通过电化学水分解对析氢反应(HER)表现出良好的电催化性能。在0.5 M H₂SO₄和1 M KOH中,电流密度为10 mA cm⁻²时,NiCo-Mo₂C相对于可逆氢电极(RHE)的过电位分别为153 mV和157 mV。在受控条件下对NiCo-Mo₂C进行磷硫化,形成了NiPS-CoPS-Mo₂C,其在0.5 M H₂SO₄和1 M KOH中的析氢过电位分别为75.2 mV和86.6 mV,表现出比前驱体NiCo-Mo₂C更优异的析氢性能,在10 mA cm⁻²时析氧反应(OER)的过电位为184.5 mV。通过在20 mA cm⁻²的恒定电流密度下测量12小时内的电压随时间变化,评估了基于NCMCSP的电解槽用于全水分解的耐久性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/04af/12281582/789b7535a78f/d5na00510h-f1.jpg

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