Ruthenium single-atom modulated Ti3C2Tx MXene for efficient alkaline electrocatalytic hydrogen production

被引:26
作者
Zou, Yu [1 ]
Kazemi, Seyedeh Alieh [1 ]
Shi, Ge [1 ]
Liu, Junxian [1 ]
Yang, Yuwei [2 ]
Bedford, Nicholas M. [2 ]
Fan, Kaicai [1 ]
Xu, Yiming [1 ]
Fu, Huaiqin [1 ]
Dong, Mengyang [1 ]
Al-Mamun, Mohammad [1 ]
Zhong, Yu Lin [1 ]
Yin, Huajie [3 ]
Wang, Yun [1 ]
Liu, Porun [1 ]
Zhao, Huijun [1 ]
机构
[1] Griffith Univ, Ctr Catalysis & Clean Energy, Sch Environm & Sci, Southport, Qld 4222, Australia
[2] Univ New South Wales, Sch Chem Engn, Sydney, NSW, Australia
[3] Chinese Acad Sci, Anhui Key Lab Nanomat & Nanotechnol, CAS Ctr Excellence Nanosci, Key Lab Mat Phys,Ctr Environm & Energy Nanomat,In, Hefei 230031, Peoples R China
基金
澳大利亚研究理事会;
关键词
electrocatalysis; hydrogen evolution reaction; in-situ characterization; MXene; single atoms; EVOLUTION REACTION; 2-DIMENSIONAL MXENES; RAMAN-SPECTROSCOPY; CATALYST; DESIGN; OXIDATION;
D O I
10.1002/eom2.12274
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Single-atoms (SAs) supported on various substrates have emerged as a new form of electrocatalysts for hydrogen evolution reaction (HER). The exfoliated MXenes possess rich defects/vacancies and surface oxygen groups, can be favorably utilized to anchor SAs. Here, we take advantage of the exfoliated Ti3C2Tx to anchor Ru-SAs on Ti3C2Tx through a wet-chemistry impregnation process. The obtained Ru-SA@Ti3C2Tx possesses excellent HER activity, especially under high current densities. Remarkably, Ru-SA@Ti3C2Tx can readily attain high current densities of 1 and 1.5 A cm(-2) at low over potentials of 425.7 and 464.6 mV, respectively, demonstrating its potential for practical applications. The A(1g) vibration frequency shift of the Raman spectrum is innovatively used to probe the surface -OH coverage on Ti3C2Tx, providing critical information for mechanistic studies. The experimental and theoretical studies reveal that the superior HER electrocatalytic activity of Ru-SA@Ti3C2Tx results from the Ru-SAs enhanced H2O adsorption and dissociation, and promoted H-2 formation.
引用
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页数:13
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