Noble metal clusters substitution in porous Ni substrate renders high mass-specific activities toward oxygen evolution reaction and methanol oxidation reaction

Fenglin Wang; Chengwei Kuang; Zhicheng Zheng; Dan Wu; Hao Wan; Gen Chen; Ning Zhang; Xiaohe Liu; Renzhi Ma

doi:10.1016/j.cclet.2024.109989

Journal article Noble metal clusters substitution in porous Ni substrate renders high mass-specific activities toward oxygen evolution reaction and methanol oxidation reaction

Fenglin Wang ; Chengwei Kuang ; Zhicheng Zheng ; Dan Wu ; Hao Wan ; Gen Chen ; Ning Zhang ; Xiaohe Liu ; Renzhi Ma (National Institute for Materials Science)

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Fenglin Wang, Chengwei Kuang, Zhicheng Zheng, Dan Wu, Hao Wan, Gen Chen, Ning Zhang, Xiaohe Liu, Renzhi Ma. Noble metal clusters substitution in porous Ni substrate renders high mass-specific activities toward oxygen evolution reaction and methanol oxidation reaction. Chinese Chemical Letters. 2024, 36 (6), 109989. https://doi.org/10.1016/j.cclet.2024.109989

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The sluggish reaction kinetics of the oxygen evolution reaction (OER) and methanol oxidation reaction (MOR) remain obstacles to the commercial promotion of water splitting and direct methanol fuel cells. Considering the vital role of noble metals in electrocatalytic activity, this work focuses on the rational synthesis of Ni-noble metal composite nanocatalysts for overcoming the drawbacks of high cost and susceptible oxidized surfaces of noble metals. The inherent catalytic activity is improved by the altered electronic structure and effective active sites of the catalyst induced by the size effect of noble metal clusters. In particular, a series of Ni-noble metal nanocomposites are successfully synthesized by partially introducing noble metal into Ni with porous interfacial defects derived from Ni-Al layered double hydroxide (LDH). The Ni10Pd1 nanocomposite exhibits high OER catalytic activity with an overpotential of 0.279 V at 10 mA/cm2, surpassing Ni10Ag1 and Ni10Au1 counterparts. Furthermore, the average diameter of Pd clusters gradually increases from 5.57 nm to 44.44 nm with the increased proportion of doped Pd, leading to the passivation of catalytic activity due to the exacerbated surface oxidation of Pd in the form of Pd2+. After optimization, Ni10Pd1 delivers significantly enhanced OER and MOR electroactivities and long-term stability compared to that of Ni2Pd1, Ni1Pd1 and Ni1Pd2, which is conducive to the effective utilization of Pd and alleviation of surface oxidation.

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