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Pd@PtRuNi 核壳纳米线作为氧还原电催化剂。

Pd@PtRuNi core-shell nanowires as oxygen reduction electrocatalysts.

机构信息

Hebei Key Laboratory of Applied Chemistry, Yanshan University, Qinhuangdao 066004, People's Republic of China.

Coal Chemical R&D Centr of Kailuan Group, Tangshan 063018, People's Republic of China.

出版信息

Nanotechnology. 2023 Jun 16;34(35). doi: 10.1088/1361-6528/acdad8.

Abstract

Fuel cells, as the alternative to fossil energy, have engaged widespread attention by reason of the high conversion efficiency from the chemical energy to the electric energy combined with low pollution emissions. The cathodic ORR catalysts with excellent performance and cost-effectiveness are the dominant point towards the massive development of fuel cells. Here, our group select the Pd NWs as the template and construct the Pd@PtRuNi core-shell bilayer nanostructure to expand platinum atom utilization. Pd@PtRuNi bilayer core-shell NWs unfold elevated mass activity of1.62Amgmetal-1at 0.9 V versus RHE in alkaline media, 2.03- and 6.23-fold of pristine Pd NWs and benchmark commercial Pt/C, respectively. Meanwhile, the cyclic stability tests reveal the excellent durability of Pd@PtRuNi NWs, whose mass activity is only 13.58% degradation after accelerated durability tests. The catalytic activity and durability towards ORR are better than the U.S. 2025 DOE target (0.44Amgpt-1and less than 40% activity attenuation at 0.9 V after 30 000 potential cycles). The elevated catalytic properties can be traceable to the synergism between the ligand effect of Ni and Ru and one-dimensional structure superiority, which optimizes the electronic structure of active sites, promotes the charge transfer and restrains the agglomeration and detachment.

摘要

燃料电池作为化石能源的替代品,由于其具有将化学能高效转化为电能并同时降低污染排放的特点,引起了广泛关注。具有优异性能和成本效益的阴极 ORR 催化剂是推动燃料电池大规模发展的关键。在这里,我们小组选择 Pd NWs 作为模板,构建了 Pd@PtRuNi 核壳双层纳米结构,以扩展铂原子的利用率。在碱性介质中,Pd@PtRuNi 双层核壳 NWs 在 0.9 V 时的质量活性高达 1.62 Amgmetal-1,分别是原始 Pd NWs 和基准商业 Pt/C 的 2.03 倍和 6.23 倍。同时,循环稳定性测试表明 Pd@PtRuNi NWs 具有优异的耐久性,其质量活性在加速耐久性测试后仅下降了 13.58%。其对 ORR 的催化活性和耐久性优于美国 2025 年 DOE 目标(在 30000 个电位循环后,0.9 V 时的质量活性为 0.44 Amgpt-1,活性衰减小于 40%)。这种增强的催化性能可以归因于 Ni 和 Ru 的配体效应与一维结构优势之间的协同作用,这优化了活性位点的电子结构,促进了电荷转移,并抑制了团聚和脱落。

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