Electron deficiency modulates hydrogen adsorption strength of Ru single-atomic catalyst for efficient hydrogen evolution

被引:15
作者
Cao, Baoyue [1 ]
Shi, Hu [2 ,4 ]
Sun, Qiangqiang [1 ]
Yu, Yan [1 ]
Chang, Liangliang [1 ]
Xu, Shan [1 ]
Zhou, Chunsheng [1 ]
Zhang, Hongxia [2 ]
Zhao, Jianghong [2 ]
Zhu, Yanyan [3 ,5 ]
Yang, Pengju [2 ,5 ]
机构
[1] Shangluo Univ, Shaanxi Engn Res Ctr Mineral Resources Clean & Eff, Shaanxi Key Lab Comprehens Utilizat Tailings Resou, Shangluo 726000, Peoples R China
[2] Shanxi Univ, Sch Chem & Chem Engn, Taiyuan 030006, Peoples R China
[3] Hebei Med Univ, Sch Pharmaceut Sci, Shijiazhuang 050017, Peoples R China
[4] Shanxi Univ, Inst Mol Sci, Taiyuan 030006, Peoples R China
[5] Shangluo Coll, 10 Beixin St, Shangluo, Shaanxi, Peoples R China
基金
中国国家自然科学基金;
关键词
Ruthenium; Single atom; Hydrogen production; Photocatalysis; TOTAL-ENERGY CALCULATIONS; EOSIN Y; PHOTOCATALYST; COCATALYST; GRAPHENE; SEMICONDUCTORS; REDUCTION; G-C3N4;
D O I
10.1016/j.renene.2023.03.136
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
It was found that the Na modification is beneficial to the synthesis of Ru single-atomic catalyst anchored on GONa, which was prepared by one-step hydrothermal process. Importantly, the strong metal-support interaction facilitates the electron transfer from Ru SA to GONa via d-pi conjugation, thus lowering the electron density of Ru SA. Experimental results and DFT calculations confirmed that the low electron density of Ru SA can significantly weaken the absorption of H* intermediates and simultaneously accelerate the desorption of generated H2 from catalyst surface. As a result, the Ru SA/GONa displayed exceptional HER activity with an extremely low over -potential of 20 mV at 10 mA cm-2, outperforming the benchmark commercial Pt (21 mV over-potential) and Ru nanoparticles (212 mV over-potential) catalysts. When Eosin Y was employed as a light harvester, this Ru SA/ GONa achieves outstanding photocatalytic hydrogen production with a record-high apparent quantum efficiency of 65.2% at 520 nm. Moreover, single-atomic Pt, Pd, Au and Rh were also successfully anchored on the Na-functionalized GO support, suggesting the universality of Na-induced single-atomic synthesis. This work not only provides an effective method for the synthesis of single-atomic metal catalysts but also establishes the connection between the electronic structures of catalyst and performances.
引用
收藏
页码:258 / 268
页数:11
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