催化作用
化学
电子转移
钌
氢
金属
制氢
纳米技术
光化学
材料科学
有机化学
作者
Baoyue Cao,Hu Shi,Qiangqiang Sun,Yan Yu,Liangliang Chang,Xu Shan,Chun‐Sheng Zhou,Hongxia Zhang,Jianghong Zhao,Yanyan Zhu,Pengju Yang
标识
DOI:10.1016/j.renene.2023.03.136
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-π 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.
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