TiO2 Nanorod Array Conformally Coated with a Monolayer MoS2 Film: An Efficient Electrocatalyst for Hydrogen Evolution Reaction

被引:13
|
作者
Anh Duc Nguyen [1 ]
Thi Hue Pham [2 ]
Tri Khoa Nguyen [3 ]
Ullah, Hamid [2 ]
Tahir, Zeeshan [1 ]
Park, Yun Chang [4 ]
Park, Jongwoo [1 ]
Jang, Joon Ik [5 ]
Shin, Young Han [2 ]
Kim, Yong Soo [1 ]
机构
[1] Univ Ulsan, Dept Phys & Energy, Harvest Storage Res Ctr, Ulsan 44610, South Korea
[2] Univ Ulsan, Dept Phys, Multiscale Mat Modeling Lab, Ulsan 44610, South Korea
[3] Nguyen Tat Thanh Univ, NTT Hitech Inst, Ho Chi Minh City 70000, Vietnam
[4] Natl Nanofab Ctr, Measurement & Anal Div, Daejeon 34141, South Korea
[5] Sogang Univ, Dept Phys, Seoul 04107, South Korea
基金
新加坡国家研究基金会;
关键词
monolayer MoS2; TiO2; nanorods; metal-organic chemical vapor deposition; conformal growth; hydrogen evolution reaction; density functional theory;
D O I
10.1021/acsaem.0c01889
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
Heterostructures, particularly the shell-core (2D@1D) nanostructure with atomically thin layers of transition metal dichalcogenides, exhibit an excellent electrocatalytic hydrogen evolution reaction (HER) activity. Herein, we introduce a facile and precisely controlled synthesis of a shell-core heterostructure that comprises TiO2 nanorods (TNRs) as a core array conformally covered by a continuous monolayer molybdenum disulfide (ML-MoS2) film as a shell. The TNR array was grown by a hydrothermal process, followed by the conformal coating of the ML-MoS2 film via metalorganic chemical vapor deposition. Interestingly, the shell-core hetero- structure (ML-MoS2@TNRs) shows a significant enhancement in the HER activity with an onset overpotential at 140 mV vs reversible hydrogen electrode and a Tafel slope of similar to 80 mV/dec. Based on our experimental results together with first-principle calculations, we attribute the enhanced HER performance of ML-MoS2@TNRs to the synergetic effect of the following characteristics. (i) A large number of active sites owing to TNRs' high surface to volume ratio. (ii) A considerable reduction in the charge transfer resistance caused by the direct growth of ML-MoS2 over the TNR array, naturally rendering low electrical loss contacts compared to the conventional transfer process. Moreover, the direction of the built-in electric field in the MoS2/TiO2 heterostructure also facilitates the flow of electrons from the electrode to the electrocatalyst surface, consequently decreasing the charge transfer resistance. (iii) The high intrinsic HER activity of the active sites owing to the low Gibbs free energy of the catalytic surface (ML-MoS2@TNRs). Moreover, by virtue of the high crystalline quality of ML-MoS2, the ML-MoS2@TNRs sample shows excellent stability and working durability. Clearly, these characteristics suggest that our proposed method has great potential for practical applications in the form of large-scale HER devices.
引用
收藏
页码:10854 / 10862
页数:9
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