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界面金属氧化物调控镍物种周围电子态以实现高效碱性析氢电催化

Interface Metal Oxides Regulating Electronic State around Nickel Species for Efficient Alkaline Hydrogen Electrocatalysis.

作者信息

Ren Jin-Tao, Wang Lei, Chen Lei, Song Xin-Lian, Kong Qing-Hui, Wang Hao-Yu, Yuan Zhong-Yong

机构信息

National Institute for Advanced Materials, School of Materials Science and Engineering, Smart Sensing Interdisciplinary Science Center, Nankai University, Tianjin, 300350, China.

Key Laboratory of Advanced Energy Materials Chemistry (Ministry of Education), Nankai University, Tianjin, 300071, China.

出版信息

Small. 2023 Feb;19(5):e2206196. doi: 10.1002/smll.202206196. Epub 2022 Nov 21.

DOI:10.1002/smll.202206196
PMID:36408769
Abstract

Heterogeneous electrocatalysis typically depends on the surface electronic states of active sites. Modulating the surface charge state of an electrocatalysts can be employed to improve performance. Among all the investigated materials, nickel (Ni)-based catalysts are the only non-noble-metal-based alternatives for both hydrogen oxidation and evolution reactions (HOR and HER) in alkaline electrolyte, while their activities should be further improved because of the unfavorable hydrogen adsorption behavior. Hereto, Ni with exceptional HOR electrocatalytic performance by changing the d-band center by metal oxides interface coupling formed in situ is endowed. The resultant MoO coupled Ni heterostructures exhibit an apparent HOR activity, even approaching to that of commercial 20% Pt/C benchmark, but with better long-term stability in alkaline electrolyte. An exceptional HER performance is also achieved by the Ni-MoO heterostructures. The experiment results are rationalized by the theoretical calculations, which indicate that coupling MoO with Ni results in the downshift of d-band center of Ni, and thus weakens hydrogen adsorption and benefits for hydroxyl adsorption. This concept is further proved by other metal oxides (e.g., CeO , V O , WO , Cr O )-formed Ni-based heterostructures to engineer efficient hydrogen electrocatalysts.

摘要

多相电催化通常取决于活性位点的表面电子态。调节电催化剂的表面电荷状态可用于提高性能。在所有被研究的材料中,镍(Ni)基催化剂是碱性电解质中氢氧化和析氢反应(HOR和HER)仅有的非贵金属基替代物,然而由于其不利的氢吸附行为,它们的活性仍需进一步提高。在此,通过原位形成的金属氧化物界面耦合改变d带中心,赋予了Ni优异的HOR电催化性能。由此产生的MoO耦合Ni异质结构表现出明显的HOR活性,甚至接近商业20% Pt/C基准的活性,但在碱性电解质中具有更好的长期稳定性。Ni-MoO异质结构也实现了优异的HER性能。实验结果通过理论计算得到合理解释,理论计算表明MoO与Ni耦合导致Ni的d带中心下移,从而减弱了氢吸附并有利于羟基吸附。其他金属氧化物(如CeO、V O、WO、Cr O)形成的Ni基异质结构进一步证明了这一概念可用于设计高效的氢电催化剂。

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