Key Laboratory of Material Chemistry for Energy Conversion and Storage, Ministry of Education, Hubei Key Laboratory of Material Chemistry and Service Failure, School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology , Wuhan 430073, China.
Center for Functional Nanomaterials, Brookhaven National Laboratory , Upton, New York 11973, United States.
ACS Appl Mater Interfaces. 2017 Aug 9;9(31):26134-26142. doi: 10.1021/acsami.7b08560. Epub 2017 Jul 31.
Exploring nonprecious metal electrocatalysts to replace the noble metal-based catalysts for full water electrocatalysis is still an ongoing challenge. In this work, porous structured ternary nickel-iron-phosphide (Ni-Fe-P) nanocubes were synthesized through one-step phosphidation of a Ni-Fe-based Prussian blue analogue. The Ni-Fe-P nanocubes exhibit a rough and loose porous structure on their surface under suitable phosphating temperature, which is favorable for the mass transfer and oxygen diffusion during the electrocatalysis process. As a result, Ni-Fe-P obtained at 350 °C with poorer crystallinity offers more unsaturated atoms as active sites to expedite the absorption of reactants. Additionally, the introduction of nickel improved the electronic structure and then reduced the charge-transfer resistance, which would result in a faster electron transport and an enhancement of the intrinsic electrocatalytic activities. Benefiting from the unique porous nanocubes and the chemical composition, the Ni-Fe-P nanocubes exhibit excellent hydrogen evolution reaction and oxygen evolution reaction activities in alkaline medium, with low overpotentials of 182 and 271 mV for delivering a current density of 10 mA cm, respectively. Moreover, the Ni-Fe-P nanocubes show outstanding stability for sustained water splitting in the two-electrode alkaline electrolyzer. This work not only provides a facile approach for designing bifunctional electrocatalysts but also further extends the application of metal-organic frameworks in overall water splitting.
探索非贵金属电催化剂来替代基于贵金属的全水析催化剂仍然是一个持续的挑战。在这项工作中,通过一步磷化 Ni-Fe 基普鲁士蓝类似物合成了具有多孔结构的三元镍-铁-磷化物(Ni-Fe-P)纳米立方块。在合适的磷化温度下,Ni-Fe-P 纳米立方块表面呈现出粗糙疏松的多孔结构,有利于电催化过程中的质量传递和氧气扩散。结果表明,在 350°C 下获得的 Ni-Fe-P 具有较差的结晶度,提供了更多的不饱和原子作为活性位点,从而加速反应物的吸收。此外,镍的引入改善了电子结构,从而降低了电荷转移电阻,这将导致更快的电子传输和增强内在电催化活性。得益于独特的多孔纳米立方块和化学成分,Ni-Fe-P 纳米立方块在碱性介质中表现出优异的析氢反应和析氧反应活性,分别在 10 mA cm 的电流密度下提供 182 和 271 mV 的低过电位。此外,Ni-Fe-P 纳米立方块在碱性两电极电解槽中持续水分解表现出出色的稳定性。这项工作不仅为设计双功能电催化剂提供了一种简便的方法,而且进一步扩展了金属有机骨架在全水分解中的应用。