催化作用
异质结
分解水
材料科学
离解(化学)
吸附
电流密度
电解
化学工程
纳米技术
电解水
离子
光电子学
离子交换
电极
电流(流体)
膜
调制(音乐)
析氧
作者
Jia Liu,Jiawen Sun,Yi‐Ru Hao,Yaqin Chen,Chunhao Li,Le‐Le Ma,Jing Sun,Zhonglong Zhao,Jiangwei Zhang,Hui Xue,Qin Wang
标识
DOI:10.1002/advs.202521184
摘要
Adjusting the d-band center of catalysts through heterojunction construction represents an effective approach for enhancing the catalytic activity. Nevertheless, the precise modulation pathways of d-band centers still require systematic elucidation. In this work, a Ni3Mo/Ni3N junction is constructed to investigate d-band engineering, and a d-band mismatch mechanism has been proposed for the first time to elucidate the synergistic effect between Ni3Mo and Ni3N for improved HER and OER. Specifically, the dissociation of H2O can be achieved on the Ni3Mo surface while the adjacent Ni3N sites catalyze the subsequent evolution reactions. Remarkably, the Ni3Mo-Ni3N/NF achieves ultra-low overpotentials of 15 mV (HER) and 155 mV (OER) at 10 mA cm-2, and just 228 mV (HER) and 459 mV (OER) at 1 A cm-2. Most strikingly, the HER performance of Ni3Mo-Ni3N/NF is superior to that of the Pt/C catalyst across all current densities, marking it as a standout among the NiMo-based catalysts documented so far. Additionally, the Ni3Mo-Ni3N/NF demonstrates outstanding performance in an anion exchange membrane water electrolyzer (AEMWE), delivering the current density of 4 A cm-2 at a mere 2.12 V while maintaining stable operation for 1000 h at 1 A cm-2, showing great potential for practical applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI