Employing Competitive Adsorption and Hollow Nanofiber Strategies toward High-Efficiency Hydrogen Evolution with Ru–Sn/SnO 2 Heterojunction Catalysts

材料科学 吸附 电催化剂 催化作用 纳米纤维 活动站点 化学工程 电化学 纳米技术 碳纳米纤维 合理设计 分解水 电子转移 异质结 传质 纤维 水解 比表面积 碳纳米管 无机化学 活性炭
作者
Huan Liu,Duanduan Yin,Ke Li,Yiran Dong,Dan Li,Feng Li,Ying Yang,Xiangjie Bo,Xiangting Dong
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:17 (51): 69468-69478 被引量:9
标识
DOI:10.1021/acsami.5c18381
摘要

Electrochemical water splitting is regarded as an efficient method for hydrogen production. Ru is theoretically deemed as an effective electrocatalyst for hydrogen evolution reactions (HERs) in alkaline media owing to its fast hydrolysis kinetics. Nevertheless, its strong OH – adsorption affinity can lead to active site blockage, often resulting in a suboptimal performance in practical HER applications. In addition, electrocatalytic reactions predominantly take place at surface-active sites. In the case of conventional solid catalysts, the core active material remains largely inaccessible due to mass transfer limitations, significantly reducing the overall utilization of active sites. To address these challenges, the work introduces a competitive adsorption strategy and a hollow structure strategy for constructing Ru–Sn/SnO 2 hollow carbon nanofiber electrocatalysts (Ru–Sn/SnO 2 HCNFs). The introduction of Sn/SnO 2 helps to modulate the intense interaction between Ru and OH –; OH – adsorption on SnO 2 is more favorable than Ru, thereby successfully mitigating poisoning on Ru. This process also promotes OH – transfer and Ru active site regeneration. Additionally, the specific surface area of Ru–Sn/SnO 2 –HCNFs (606.9 m 2 g –1 ) is higher than that of the solid fiber of Ru–Sn/SnO 2 –CNFs (22.7 m 2 g –1 ), highlighting the beneficial role of hollow fibers in enhancing the exposure of active sites. Consequently, Ru–Sn/SnO 2 –HCNFs exhibit an outstanding HER performance, achieving remarkably low overpotentials of only 6.8 mV in 1 M KOH and 23.3 mV in 0.5 M H 2 SO 4 at 10 mA cm –2, respectively. This research offers a novel approach on rational design for high-efficiency HER electrocatalysts.
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