材料科学
联氨(抗抑郁剂)
催化作用
电化学
解吸
制氢
分解水
化学工程
电极
电子转移
氢
吸附
纳米技术
光化学
物理化学
化学
有机化学
光催化
工程类
色谱法
作者
Yuezhu Wang,Yuezhu Wang,Qiuling Jiang,Siyu Ren,Jiaqi Xu,Ying Wang,Ying Wang,Mengxiao Zhong,Xiaofeng Lu
标识
DOI:10.1002/adma.202504922
摘要
Abstract Manipulating the reconstruction of a heterostructured material is highly desirable to achieve high‐performance electrocatalytic performance. Here, an in situ reconstruction of RuPdO x hollow nanofibers (HNFs) is presented to generate RuO 2 /Pd from both the electrochemical and chemical reconstruction processes. The reconstructed catalyst is highly efficient for both hydrazine oxidation reaction (HzOR) and hydrogen evolution reaction (HER) at industrial‐grade current densities, significantly outperforming the benchmark Pt/C catalyst. Furthermore, it maintains a record‐breaking durability of 500 h for HzOR at 1 A cm −2 . Remarkably, with the catalyst as electrodes, a two‐electrode overall hydrazine splitting (OHzS) cell is constructed, which requires only 0.263 kWh of electricity to produce 1 m 3 H 2 at 100 mA cm −2 , significantly lower than that in overall water splitting (OWS) system (4.286 kWh m −3 H 2 ), exhibiting an exceptional energy‐saving H 2 production property. Density functional theory (DFT) calculations reveal an efficient electron transfer from Pd to RuO 2 at their interface from the reconstruction of RuPdO x HNFs, which regulates the local electronic environment of atoms, modulates the adsorption and desorption for intermediates, and reduces the energy barriers for enhancing the electrocatalytic process. This study offers a robust reconstruction strategy for the design of electrocatalysts that exhibit superior efficiency in energy conversion devices.
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