Highly Selective TiN-Supported Highly Dispersed Pt Catalyst: Ultra Active toward Hydrogen Oxidation and Inactive toward Oxygen Reduction

被引:51
作者
Luo, Junming
Tang, Haibo
Tian, Xinlong
Hou, Sanying
Li, Xiuhua
Du, Li
Liao, Shijun [1 ]
机构
[1] South China Univ Technol, Key Lab Fuel Cell Technol Guangdong Prov, Sch Chem & Chem Engn, Guangzhou 510641, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
platinum; hydrogen oxidation reaction; oxygen reduction reaction; structure sensitivity; polymer electrolyte membrane fuel cells; SINGLE-ATOM CATALYST; TITANIUM NITRIDE; FUEL-CELLS; PLATINUM; NANOPARTICLES; PERFORMANCE; SURFACES;
D O I
10.1021/acsami.7b15159
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
The severe dissolution of the cathode catalyst, caused by an undesired oxygen reduction reaction at the anode during startup and shutdown, is a fatal challenge to practical applications of polymer electrolyte membrane fuel cells. To address this important issue, according to the distinct structure sensitivity between the sigma-type bond in H-2 and the pi-type bond in O-2, we design a HD-Pt/TiN material by highly dispersing Pt on the TiN surface to inhibit the unwanted oxygen reduction reaction. The highly dispersed Pt/TiN catalyst exhibits excellent selectivity toward hydrogen oxidation and oxygen reduction reactions. With a Pt loading of 0.88 wt %, our catalyst shows excellent hydrogen oxidation reaction activity, close to that of commercial 20 wt % Pt/C catalyst, and much lower oxygen reduction reaction activity than the commercial 20 wt % Pt/C catalyst. The lack of well-ordered Pt facets is responsible for the excellent selectivity of the HD-Pt/TiN materials toward hydrogen oxidation and oxygen reduction reactions. Our work provides a new and cost-effective solution to design selective catalysts toward hydrogen oxidation and oxygen reduction reactions, making the strategy of using oxygen-tolerant anode catalyst to improve the stability of polymer electrolyte membrane fuel cells during startup and shutdown more affordable and practical.
引用
收藏
页码:3530 / 3537
页数:8
相关论文
共 19 条
[1]  
Atanasoski R., 2009, KICK M NEW DOE FUEL
[2]   Scientific aspects of polymer electrolyte fuel cell durability and degradation [J].
Borup, Rod ;
Meyers, Jeremy ;
Pivovar, Bryan ;
Kim, Yu Seung ;
Mukundan, Rangachary ;
Garland, Nancy ;
Myers, Deborah ;
Wilson, Mahlon ;
Garzon, Fernando ;
Wood, David ;
Zelenay, Piotr ;
More, Karren ;
Stroh, Ken ;
Zawodzinski, Tom ;
Boncella, James ;
McGrath, James E. ;
Inaba, Minoru ;
Miyatake, Kenji ;
Hori, Michio ;
Ota, Kenichiro ;
Ogumi, Zempachi ;
Miyata, Seizo ;
Nishikata, Atsushi ;
Siroma, Zyun ;
Uchimoto, Yoshiharu ;
Yasuda, Kazuaki ;
Kimijima, Ken-ichi ;
Iwashita, Norio .
CHEMICAL REVIEWS, 2007, 107 (10) :3904-3951
[3]   Electrocatalyst approaches and challenges for automotive fuel cells [J].
Debe, Mark K. .
NATURE, 2012, 486 (7401) :43-51
[4]   Tailoring the Selectivity and Stability of Chemically Modified Platinum Nanocatalysts To Design Highly Durable Anodes for PEM Fuel Cells [J].
Genorio, Bostjan ;
Subbaraman, Ram ;
Strmcnik, Dusan ;
Tripkovic, Dusan ;
Stamenkovic, Vojislav R. ;
Markovic, Nenad M. .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (24) :5468-5472
[5]  
Genorio B, 2010, NAT MATER, V9, P998, DOI [10.1038/nmat2883, 10.1038/NMAT2883]
[6]   Remarkable Performance of Ir1/FeOx Single-Atom Catalyst in Water Gas Shift Reaction [J].
Lin, Jian ;
Wang, Aiqin ;
Qiao, Botao ;
Liu, Xiaoyan ;
Yang, Xiaofeng ;
Wang, Xiaodong ;
Liang, Jinxia ;
Li, Jun ;
Liu, Jingyue ;
Zhang, Tao .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (41) :15314-15317
[7]   Temperature-dependent hydrogen electrochemistry on platinum low-index single-crystal surfaces in acid solutions [J].
Markovic, NM ;
Grgur, BN ;
Ross, PN .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (27) :5405-5413
[8]  
Qiao BT, 2011, NAT CHEM, V3, P634, DOI [10.1038/NCHEM.1095, 10.1038/nchem.1095]
[9]  
Shao Minhua., 2013, ELECTROCATALYSIS FUE
[10]   In situ surface characterization of preferentially oriented platinum nanoparticles by using electrochemical structure sensitive adsorption reactions [J].
Solla-Gullón, J ;
Vidal-Iglesias, FJ ;
Rodríguez, P ;
Herrero, E ;
Feliu, JM ;
Clavilier, J ;
Aldaz, A .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (36) :13573-13575