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李箐

教授    博士生导师    硕士生导师

个人信息 更多+
  • 教师英文名称: Qing Li
  • 性别: 男
  • 在职信息: 在职
  • 所在单位: 材料科学与工程学院
  • 学历: 研究生(博士)毕业
  • 学位: 理学博士学位

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论文成果

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Topologically Close-Packed Frank-Kasper C15 Phase Intermetallic Ir Alloy Electrocatalysts Enables High-Performance Proton Exchange Membrane Water Electrolyzer

发布时间:2024-12-29
点击次数:
论文类型:
Research Article
第一作者:
Qin,Zhuhuang
通讯作者:
Li,Qing
合写作者:
Huang, Yunhui,Yan, Pengfei,Cao, Rui,Lu, Gang, Shenzhou,Xie, Linfeng,Mao, Jialun,Lai, Jiaoyang,Liu, Xuan,Sathishkumar, Nadaraj,Wu, Qiyan,Li,Jinhui
发表刊物:
Advanced Materials
所属单位:
华中科技大学
刊物所在地:
美国
文献类型:
Article
卷号:
36
期号:
47
页面范围:
2412541
ISSN号:
1521-4095
关键字:
electrocatalysis; Frank-Kasper C15 phases; hydrogen evolution reaction; intermetallics; proton exchange membrane water electrolyzer
DOI码:
10.1002/adma.202412541
发表时间:
2024-09-30
影响因子:
27.4
摘要:
Chemical synthesis of unconventional topologically close-packed intermetallic nanocrystals (NCs) remains a considerable challenge due to the limitation of large volume asymmetry between the components. Here, a series of unconventional intermetallic Frank-Kasper C15 phase Ir2M (M = rare earth metals La, Ce, Gd, Tb, Tm) NCs is successfully prepared via a molten-salt assisted reduction method as efficient electrocatalysts for hydrogen evolution reaction (HER). Compared to the disordered counterpart (A1-Ir2Ce), C15-Ir2Ce features higher Ir-Ce coordination number that leads to an electron-rich environment for Ir sites. The C15-Ir2Ce catalyst exhibits excellent and pH-universal HER activity and requires only 9, 16, and 27 mV overpotentials to attain 10 mA cm−2 in acidic, alkaline, and neutral electrolytes, respectively, representing one of the best HER electrocatalysts ever reported. In a proton exchange membrane water electrolyzer, the C15-Ir2Ce cathode achieves an industrial-scale current density of 1 A cm−2 with a remarkably low cell voltage of 1.7 V at 80 °C and can operate stably for 1000 h with a sluggish voltage decay rate of 50 µV h−1. Theoretical investigations reveal that the electron-rich Ir sites intensify the polarization of *H2O intermediate on C15-Ir2Ce, thus lowering the energy barrier of the water dissociation and facilitating the HER kinetics.