Dilebo Woldesenbet Bafe, Tsai Meng-Che, Chang Chia-Yu, Edao Habib Gemechu, Nikodimos Yosef, Moges Endalkachew Asefa, Lakshmanan Keseven, Angerasa Fikiru Temesgen, Guta Chemeda Barasa, Ibrahim Kassa Belay, Awoke Yohannes Ayele, Alamirew Tesfaye, Liao Wei-Sheng, Desta Gidey Bahre, Chen Jeng-Lung, Su Wei-Nien, Hwang Bing Joe
Nano-electrochemistry Laboratory, Department of Chemical Engineering, National Taiwan University of Science and Technology, Taipei City 106, Taiwan.
Department of Greenergy, National University of Tainan, Tainan City 70005, Taiwan.
Nanoscale. 2024 Nov 13;16(44):20701-20713. doi: 10.1039/d4nr02788d.
Designing hybrid transition metal phosphosulfide electrocatalysts is critical for the hydrogen evolution reaction (HER). We propose a novel approach by designing a hierarchical structure of cobalt phosphide (CoP) and nickel phosphide (NiP) nanoparticles topotactically developed on nickel sulfide (NiS) nanorods (CoNiP/NiS) a sulfuration-phosphorization strategy using conductive 3D nickel foam. Hierarchical heterostructured nanorods were achieved without the need for template removal steps or the assistance of surfactants. This not only simplifies the process but also improves the exposure of active sites for catalytic purposes. Furthermore, the theoretical calculation results revealed that the high H* adsorption-free energy for CoP and NiP phases significantly decreases upon coupling with NiS, which indicates that the interfacial electronic interaction synergistically modulates both CoP and NiP (CoNiP) at the coupled interfaces and facilitates the adsorption and desorption of H* intermediates during the HER process. The resulting electrode exhibits excellent performance in the HER catalytic process and shows great performance for further exploration in the urea oxidation reaction (UOR). Our work provides a stepping stone toward rational topotactic transformation of active materials on porous substrates, using electronic structure regulation and heterointerfaces to produce promising electrocatalysts for sustainable, large-scale hydrogen production from water electrolysis.
设计混合过渡金属磷硫化物电催化剂对析氢反应(HER)至关重要。我们提出了一种新颖的方法,通过设计在硫化镍(NiS)纳米棒上拓扑生长的磷化钴(CoP)和磷化镍(NiP)纳米颗粒的分级结构(CoNiP/NiS),即使用导电三维泡沫镍的硫化 - 磷化策略。实现了分级异质结构纳米棒,无需去除模板步骤或表面活性剂的辅助。这不仅简化了工艺,还提高了催化活性位点的暴露程度。此外,理论计算结果表明,CoP和NiP相的高H吸附自由能在与NiS耦合后显著降低,这表明界面电子相互作用在耦合界面协同调节CoP和NiP(CoNiP),并促进HER过程中H中间体的吸附和解吸。所得电极在HER催化过程中表现出优异的性能,并在尿素氧化反应(UOR)中显示出进一步探索的巨大潜力。我们的工作为在多孔基底上合理地进行活性材料的拓扑转变提供了一块垫脚石,利用电子结构调控和异质界面来制备用于可持续大规模水电解制氢的有前景的电催化剂。