Liu Yaoda, Chen Ya, Tian Yahui, Sakthivel Thangavel, Liu Hang, Guo Shengwu, Zeng Haibo, Dai Zhengfei
State Key Laboratory for Mechanical Behavior of Materials, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.
MIIT Key Laboratory of Advanced Display Materials and Devices, College of Materials Science and Engineering, Nanjing University of Science and Technology, Nanjing, 210094, P. R. China.
Adv Mater. 2022 Sep;34(37):e2203615. doi: 10.1002/adma.202203615. Epub 2022 Aug 12.
Hydrogen spillover (HSo) has emerged to upgrade the hydrogen evolution reaction (HER) activity of Pt-support electrocatalysts, but it is not applicable to the deprotonated oxygen evolution reaction (OER). Non-precious catalysts that can perform well in both HSo and deprotonation (DeP) are extremely desirable for a sustainable hydrogen economy. Herein, an affordable MoS /NiPS vertical heterostructure catalyst is presented to synergize HSo and DeP for efficient water electrolysis. The internal polarization field (IPF) is clarified as the driving force of HSo in HER electrocatalysis. The HSo from the MoS edge to NiPS can activate the NiPS basal plane to boost the HER activity of the MoS /NiPS heterostructure (112 mV vs reversible hydrogen electrode (RHE) at 10 mA cm ), while for OER, the IPF in the heterostructure can facilitate the hydroxyl diffusion and render MoS -to-NiPS /P-to-S dual-pathways for DeP. As a result, the stacking of OER-inactive MoS on the NiPS surface still brings intriguing OER enhancements. With them serving as electrode couples, the overall water splitting is attested stably with a cell voltage of 1.64 V at 10 mA cm . This research puts forward the IPF as the criterion in the rational design of HSo/DeP-unified non-precious catalysts for efficient water electrolysis.
氢溢流(HSo)已被用于提升铂负载型电催化剂的析氢反应(HER)活性,但它不适用于去质子析氧反应(OER)。对于可持续氢经济而言,能够在氢溢流和去质子化(DeP)过程中均表现良好的非贵金属催化剂是极为理想的。在此,我们展示了一种价格低廉的MoS₂/NiPS垂直异质结构催化剂,它能协同氢溢流和去质子化过程以实现高效水电解。内部极化场(IPF)被确认为HER电催化中氢溢流的驱动力。从MoS₂边缘到NiPS的氢溢流可以激活NiPS基面,从而提升MoS₂/NiPS异质结构的HER活性(在10 mA cm⁻²时相对于可逆氢电极(RHE)为112 mV),而对于OER,异质结构中的IPF可以促进羟基扩散,并为去质子化提供从MoS₂到NiPS以及从P到S的双途径。结果,在NiPS表面堆叠无OER活性的MoS₂仍然带来了引人注目的OER增强效果。以它们作为电极对,在10 mA cm⁻²时,整体水分解在1.64 V的电池电压下得到稳定验证。这项研究提出将IPF作为合理设计用于高效水电解的氢溢流/去质子化统一非贵金属催化剂的标准。