| Literature DB >> 31265235 |
Qinghua Liang1, Lixiang Zhong1, Chengfeng Du1, Yubo Luo1, Jin Zhao1, Yun Zheng2, Jianwei Xu2, Jianmin Ma3,4, Chuntai Liu4, Shuzhou Li1, Qingyu Yan1.
Abstract
Heterostructures with abundant phase boundaries are compelling for surface-mediated electrochemical applications. However, rational design of such bifunctional electrocatalysts for efficient hydrogen and oxygen evolution reactions (HER and OER) is still challenging. Here, due to the well-matched lattice parameters, we easily achieved the epitaxy of two-dimensional ternary nickel thiophosphate (NiPS3) nanosheets with in-grown dinickel phosphide (Ni2P) through an in situ growth strategy. Density functional theory calculations reveal that the NiPS3/Ni2P heterojunction significantly decreases the kinetic barrier for hydrogen adsorption and accelerates electron transfer due to the built-in electric field at the epitaxial interfaces. The significantly improved electrocatalytic performance is shown to be closely related to the epitaxial interfacial area rather than the amount of secondary phase. Notably, the resultant NiPS3/Ni2P heterostructures enable an overall water splitting electrolyzer to achieve 50 mA cm-2 at a lower bias of 1.65 V compared to that for the pristine NiPS3 alone (2.02 V) and even the benchmark Pt/C//IrO2 electrocatalysts (1.69 V).Entities:
Keywords: epitaxial interfaces; heterostructures; hydrogen evolution; nickel thiophosphate; water splitting
Year: 2019 PMID: 31265235 DOI: 10.1021/acsnano.9b02510
Source DB: PubMed Journal: ACS Nano ISSN: 1936-0851 Impact factor: 15.881