Yunhao Zheng , Yurui Xue , Yang Gao , Siao Chen , Siyi Chen , Yuliang Li
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引用次数: 0
摘要
电催化水分离是一种绿色、可持续的制氢解决方案,但其整体性能仍然受到缓慢、低效的氧进化反应(OER)的限制。在此,我们报告了钒铱氧化物(VIrOx)在石墨二乙烯(GDY)表面受控生长的情况,从而在 GDY 和 VIrOx 之间生成了定义明确的界面。扫描电子显微镜和高分辨率透射电子显微镜图像显示,VIrOx 量子点在 GDY 纳米片表面成功生长并均匀分布。X 射线光电子能谱显示,在 GDY 和 VIrOx 量子点之间的界面上发生了有效的电荷转移,并形成了混合价金属物种。这些催化剂优势显著增加了活性位点的数量,提高了系统的整体内在活性,从而实现了出色的电催化 OER 性能,在 10 mA cm-2 时过电位低至 121 mV,在 300 mV 时翻转频率高至 0.914 s-1,并且在碱性电解质中具有长期稳定性(100 mA cm-2 时 100 h)。
Selective growth of graphdiyne-based vanadium–iridium oxide interfaces for efficient alkaline oxygen evolution reaction
Electrocatalytic water splitting is a green and sustainable solution for hydrogen production, but its overall performance is still limited by the sluggish and inefficient oxygen evolution reaction (OER). Here, we report the controlled growth of vanadium–iridium oxides (VIrOx) on the surface of graphdiyne (GDY) to generate well-defined interfaces between GDY and VIrOx. The scanning electron microscopy and high-resolution transmission electron microscopy images showed the successful growth and uniform distribution of VIrOx quantum dots on the surface of the GDY nanosheets. The X-ray photoelectron spectra revealed that efficient charge transfer occurred at the interfaces between GDY and VIrOx quantum dots and led to the formation of mixed-valence metal species. These catalyst advantages notably increased the number of active sites and improved the overall intrinsic activity of the system, resulting in excellent electrocatalytic OER performance with a low overpotential of 121 mV at 10 mA cm−2, high turnover frequency of 0.914 s−1 at 300 mV, and long-term stability (100 h at 100 mA cm–2) in alkaline electrolytes.