TY - JOUR
T1 - Bimetallic Ag–Cu nanosheets assembled flower-like structure for oxygen reduction reaction
AU - Chen, Jianan
AU - Wang, Zhenyu
AU - Mao, Jianjun
AU - Liu, Chang
AU - Chen, Yue
AU - Lu, Zhouguang
AU - Feng, Shien-Ping
PY - 2021/3/5
Y1 - 2021/3/5
N2 - Fabricating low-cost and Pt-free fuel cell catalysts towards highly active and durable oxygen-reduction reaction catalysis remains a great challenge. Herein, we synthesize a bimetallic Ag–Cu nanosheets assembled flower-like structure by our developed cyclic scanning electrodeposition (CSE) method. The formation mechanism of this structure is investigated systematically, where Cu2+ can affect oxidative etching during the formation process. The prepared bimetallic nanostructure is studied for kinetics towards oxygen reduction reaction (ORR) in alkaline media. The electrochemical test results indicate that the ORR catalytic ability of bimetallic Ag–Cu nanostructure is competitive with Pt/C-20%, better than Pt disk, and far superior to the pure Ag nanostructure. The electrons transfer number (n) is close to four, which is further proved by scanning electrochemical microscope (SECM) experiments. Density functional theory (DFT) calculations reveal that the high ORR activity is attributable to the widely distributed Ag–Cu steps, which is formed by decorating Cu atoms on the Ag nanosheets.
AB - Fabricating low-cost and Pt-free fuel cell catalysts towards highly active and durable oxygen-reduction reaction catalysis remains a great challenge. Herein, we synthesize a bimetallic Ag–Cu nanosheets assembled flower-like structure by our developed cyclic scanning electrodeposition (CSE) method. The formation mechanism of this structure is investigated systematically, where Cu2+ can affect oxidative etching during the formation process. The prepared bimetallic nanostructure is studied for kinetics towards oxygen reduction reaction (ORR) in alkaline media. The electrochemical test results indicate that the ORR catalytic ability of bimetallic Ag–Cu nanostructure is competitive with Pt/C-20%, better than Pt disk, and far superior to the pure Ag nanostructure. The electrons transfer number (n) is close to four, which is further proved by scanning electrochemical microscope (SECM) experiments. Density functional theory (DFT) calculations reveal that the high ORR activity is attributable to the widely distributed Ag–Cu steps, which is formed by decorating Cu atoms on the Ag nanosheets.
KW - Ag–Cu
KW - DFT
KW - Electrocatalyst
KW - Oxygen reduction reaction
KW - SECM
UR - http://www.scopus.com/inward/record.url?scp=85092617373&partnerID=8YFLogxK
UR - https://www.scopus.com/record/pubmetrics.uri?eid=2-s2.0-85092617373&origin=recordpage
U2 - 10.1016/j.jallcom.2020.157379
DO - 10.1016/j.jallcom.2020.157379
M3 - RGC 21 - Publication in refereed journal
SN - 0925-8388
VL - 856
JO - Journal of Alloys and Compounds
JF - Journal of Alloys and Compounds
M1 - 157379
ER -