Fei Xing,Qiang Fu,Shuo Wang,Lin Liu,Tao Liu,Xianfeng Li
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引用次数: 0
摘要
高活性电催化剂是提高钒液流电池功率密度的关键,是长时间大规模储能中最有前途的技术之一。然而,钒离子的加速氧化还原反应通常伴随着析氢。本文报道了Ag/Sn双原子电催化剂(Ag/Sn- das),该催化剂具有较高的电催化活性和析氢过电位。电化学原位表征表明,Ag/Sn-DAs能显著促进[V(H2O)6]3+/[V(H2O)6]2+的脱水,有效抑制析氢反应(HER)。理论计算表明,相邻Sn对Ag的电子结构和d带中心进行了优化,改变了*H的吸附位点,降低了[V(H2O)6]3+/[V(H2O)6]2+的脱水能势。结果表明,采用Ag/Sn-DAs修饰石墨毡(GF)电极组装的VFB单电池在电流密度为200 mA cm-2时的能量效率为81.2%,峰值功率密度为925 mW cm-2,大大高于原始GF(66.7%和700 mW cm-2)。这项工作为vfb的协同催化提供了一个范例。
Ag/Sn Dual-Atoms with Synergistic Electrocatalysis for High-Power Density Vanadium Flow Batteries.
Electrocatalyst with high activity is crucial to improve the power density of a vanadium flow battery (VFB), which is one of the most promising technologies in long duration large-scale energy storage. However, the accelerated redox reaction of vanadium ions normally accompanies hydrogen evolution as well. Herein, the Ag/Sn dual atoms electrocatalysts (Ag/Sn-DAs) are reported, exhibiting both high electrocatalytic activity and hydrogen evolution overpotential. Electrochemical in situ characterization indicates that the Ag/Sn-DAs can significantly promote the dehydration of [V(H2O)6]3+/[V(H2O)6]2+ and effectively inhibit hydrogen evolution reaction (HER). Theoretical calculations reveal that the optimized electronic structure and d-band center of Ag by the adjacent Sn change the *H adsorption sites and reduce the dehydration energy barrier of [V(H2O)6]3+/[V(H2O)6]2+. As a result, a VFB single cell assembled with Ag/Sn-DAs decorated graphite felt (GF) electrode delivers a high energy efficiency (EE) of 81.2% at a current density of 200 mA cm-2 and a peak power density of 925 mW cm-2, which is much higher than pristine GF (66.7% and 700 mW cm-2). This work presents a paradigm for synergistic catalysis in VFBs.
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