Atomic level tailoring of the electrocatalytic activity of Au-Pt core-shell nanoparticles with controllable Pt layers toward hydrogen evolution reaction

被引:33
作者
Shi, Yi [1 ]
Zhai, Ting-Ting [1 ]
Zhou, Yue [1 ]
Xu, Wei-Xuan [1 ]
Yang, Dong-Rui [1 ]
Wang, Feng-Bin [1 ]
Xia, Xing-Hua [1 ]
机构
[1] Nanjing Univ, Sch Chem & Chem Engn, State Key Lab Analyt Chem Sci, Nanjing 210023, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Au-Pt core-shell nanoparticles; Underpotential deposition; Hydrogen evolution reaction; Controllable Pt layers; Electronic interaction; Electrocatalysis; OXYGEN REDUCTION REACTION; TUNGSTEN CARBIDE; PLATINUM; DEPOSITION; CATALYSTS; OXIDATION; ELECTRON; STRAIN; FILMS;
D O I
10.1016/j.jelechem.2017.12.006
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The hydrogen evolution reaction (HER) is a critical step in water splitting and demands efficient and low-cost catalysts for real applications. Pt catalyzes HER efficiently, however, its scarcity and high cost inspire researchers to explore metallic catalysts with core-shell nanostructures. Precise tailoring of Pt catalysts at atomic monolayer level would shed insights on the relationship between electronic structure and electrocatalytic properties. Herein, we report the preparation of Au-Pt core-shell nanoparticles deposited on graphene sheets with tunable Pt monolayer coverage by controlling Cu underpotential deposition (UPD)-Galvanic replacement cycles. The electrochemical results suggest that Au-Pt with monolayer Pt shows superior electrocatalytic activity toward HER. Increasing the thickness of Pt shell results in the decrease of the electrocatalytic activity, which might be attributed to the decreased electronic interactions of Au core with outmost surface Pt atoms as confirmed by X-ray photoelectron spectroscopic characterization. The present research would offer a design criterion for metallic nanostructures in realizing catalysts with high performance.
引用
收藏
页码:442 / 446
页数:5
相关论文
共 29 条
[1]   Layer-by-Layer Evolution of Structure, Strain, and Activity for the Oxygen Evolution Reaction in Graphene-Templated Pt Mono layers [J].
Abdelhafiz, Ali ;
Vitale, Adam ;
Joiner, Corey ;
Vogel, Eric ;
Alamgir, Faisal M. .
ACS APPLIED MATERIALS & INTERFACES, 2015, 7 (11) :6180-6188
[2]   Platinum monolayer fuel cell electrocatalysts [J].
Adzic, R. R. ;
Zhang, J. ;
Sasaki, K. ;
Vukmirovic, M. B. ;
Shao, M. ;
Wang, J. X. ;
Nilekar, A. U. ;
Mavrikakis, M. ;
Valerio, J. A. ;
Uribe, F. .
TOPICS IN CATALYSIS, 2007, 46 (3-4) :249-262
[3]   Alternative energy technologies [J].
Dresselhaus, MS ;
Thomas, IL .
NATURE, 2001, 414 (6861) :332-337
[4]   Platinum-Monolayer Shell on AuNi0.5Fe Nanoparticle Core Electrocatalyst with High Activity and Stability for the Oxygen Reduction Reaction [J].
Gong, Kuanping ;
Su, Dong ;
Adzic, Radoslav R. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2010, 132 (41) :14364-14366
[5]   Computational high-throughput screening of electrocatalytic materials for hydrogen evolution [J].
Greeley, Jeff ;
Jaramillo, Thomas F. ;
Bonde, Jacob ;
Chorkendorff, I. B. ;
Norskov, Jens K. .
NATURE MATERIALS, 2006, 5 (11) :909-913
[6]  
Hammer B, 2000, ADV CATAL, V45, P71
[7]   Atomic layer deposition synthesis of platinum-tungsten carbide core-shell catalysts for the hydrogen evolution reaction [J].
Hsu, Irene J. ;
Kimmel, Yannick C. ;
Jiang, Xiaogiang ;
Willis, Brian G. ;
Chen, Jingguang G. .
CHEMICAL COMMUNICATIONS, 2012, 48 (07) :1063-1065
[8]   Electrochemical design of ultrathin platinum-coated gold nanoparticle monolayer films as a novel nanostructured electrocatalyst for oxygen reduction [J].
Jin, YD ;
Shen, Y ;
Dong, SJ .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (24) :8142-8147
[9]   Carbon paper supported Pt/Au catalysts prepared via Cu underpotential deposition-redox replacement and investigation of their electrocatalytic activity for methanol oxidation and oxygen reduction reactions [J].
Khosravi, Mohsen ;
Amini, Mohammad K. .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2010, 35 (19) :10527-10538
[10]   Electroless deposition of Pt on Ti - catalytic activity for the hydrogen evolution reaction [J].
Kokkinidis, G ;
Papoutsis, A ;
Stoychev, D ;
Milchev, A .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2000, 486 (01) :48-55