Quantum Dots of 1T Phase Transitional Metal Dichalcogenides Generated via Electrochemical Li Intercalation

被引:132
作者
Chen, Wenshu [1 ]
Gu, Jiajun [1 ]
Liu, Qinglei [1 ]
Luo, Ruichun [2 ]
Yao, Lulu [1 ]
Sun, Boya [1 ]
Zhang, Wang [1 ]
Su, Huilan [1 ]
Chen, Bin [2 ]
Liu, Pan [2 ]
Zhang, Di [1 ]
机构
[1] Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Mat Sci & Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
2D materials; transitional metal dichalcogenides; quantum dots; 1T phase; electrochemical Li intercalation; HYDROGEN EVOLUTION REACTION; MOS2; NANOSHEETS; IN-SITU; CATALYSIS; LITHIATION; MONOLAYER; CHEMISTRY; MECHANISM; CRYSTALS; 1T-MOS2;
D O I
10.1021/acsnano.7b06364
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We prepare group VI transitional metal dichalcogenides (TMDs, or MX2) from the 1T phase with quantum-sized and monolayer features via a quasi-full electrochemical process. The resulting two-dimensional (2D) MX2 (M = W, Mo; X = S, Se) quantum dots (QDs) are ca. 3.0-5.4 rim in size with a high IT phase fraction of ca. 92%-97%. We attribute this to the high Li content intercalated in the 1T-MX2 lattice (mole ratio of Li:M is over 2:1), which is achieved by an increased lithiation driving force and a reduced electrochemical lithiation rate (0.001 A/g). The high Li content not only promotes the 2H -> 1T phase transition but also generates significant inner stress that facilitates lattice breaking for MX2 crystals. Because of their high proportion of metallic IT phase and sufficient active sites induced by the small lateral size, the 2D 1T-MoS2 QDs show excellent hydrogen evolution reactivity (with a typical eta(10) of 92 mV, Tafel slope of 44 mV/dec, and J(0) of 4.16 x 10(-4) A/cm(2)). This electrochemical route toward 2D QDs might help boost the development of 2D materials in energy-related areas.
引用
收藏
页码:308 / 316
页数:9
相关论文
共 45 条
[1]  
Acerce M, 2015, NAT NANOTECHNOL, V10, P313, DOI [10.1038/nnano.2015.40, 10.1038/NNANO.2015.40]
[2]  
Auerbach S. M., 2004, HDB LAYERED MAT, P517
[3]   In Situ Visualization of Lithium Ion Intercalation into MoS2 Single Crystals using Differential Optical Microscopy with Atomic Layer Resolution [J].
Azhagurajan, Mukkannan ;
Kajita, Tetsuya ;
Itoh, Takashi ;
Kim, Youn-Geun ;
Itaya, Kingo .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (10) :3355-3361
[4]   Intercalation chemistry of molybdenum disulfide [J].
Benavente, E ;
Santa Ana, MA ;
Mendizábal, F ;
González, G .
COORDINATION CHEMISTRY REVIEWS, 2002, 224 (1-2) :87-109
[5]   Chemically exfoliated single-layer MoS2: Stability, lattice dynamics, and catalytic adsorption from first principles [J].
Calandra, Matteo .
PHYSICAL REVIEW B, 2013, 88 (24)
[6]  
Chhowalla M, 2013, NAT CHEM, V5, P263, DOI [10.1038/NCHEM.1589, 10.1038/nchem.1589]
[7]   Understanding catalysis in a multiphasic two-dimensional transition metal dichalcogenide [J].
Chou, Stanley S. ;
Sai, Na ;
Lu, Ping ;
Coker, Eric N. ;
Liu, Sheng ;
Artyushkova, Kateryna ;
Luk, Ting S. ;
Kaehr, Bryan ;
Brinker, C. Jeffrey .
NATURE COMMUNICATIONS, 2015, 6
[8]   Chemically Exfoliated MoS2 as Near-Infrared Photothermal Agents [J].
Chou, Stanley S. ;
Kaehr, Bryan ;
Kim, Jaemyung ;
Foley, Brian M. ;
De, Mrinmoy ;
Hopkins, Patrick E. ;
Huang, Jiaxing ;
Brinker, C. Jeffrey ;
Dravid, Vinayak P. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2013, 52 (15) :4160-4164
[9]   Photoluminescence from Chemically Exfoliated MoS2 [J].
Eda, Goki ;
Yamaguchi, Hisato ;
Voiry, Damien ;
Fujita, Takeshi ;
Chen, Mingwei ;
Chhowalla, Manish .
NANO LETTERS, 2011, 11 (12) :5111-5116
[10]   Structural Transitions in Monolayer MoS2 by Lithium Adsorption [J].
Esfahani, D. Nasr ;
Leenaerts, O. ;
Sahin, H. ;
Partoens, B. ;
Peeters, F. M. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2015, 119 (19) :10602-10609