Amorphization Activated Multimetallic Pd Alloys for Boosting Oxygen Reduction Catalysis

被引:14
作者
Yu, Zhiyong [1 ]
Chen, Yuwen [2 ,3 ,4 ,5 ,6 ]
Xia, Jing [7 ]
Yao, Qing [1 ]
Hu, Zhiwei [8 ]
Huang, Wei-Hsiang [9 ]
Pao, Chih-Wen [9 ]
Hu, Wenfeng [2 ,3 ,4 ,5 ,6 ]
Meng, Xiang-Min [7 ]
Yang, Li-Ming [2 ,3 ,4 ,5 ,6 ]
Huang, Xiaoqing [1 ,10 ]
机构
[1] Xiamen Univ, Coll Chem & Chem Engn, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Huazhong Univ Sci & Technol, Key Lab Mat Chem Energy Convers & Storage, Minist Educ, Wuhan 430074, Peoples R China
[3] Huazhong Univ Sci & Technol, Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China
[4] Huazhong Univ Sci & Technol, Hubei Key Lab Bioinorgan Chem & Mat Med, Wuhan 430074, Peoples R China
[5] Huazhong Univ Sci & Technol, Hubei Engn Res Ctr Biomat & Med Protect Mat, Wuhan 430074, Peoples R China
[6] Huazhong Univ Sci & Technol, Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
[7] Chinese Acad Sci, Tech Inst Phys & Chem, Key Lab Photochem Convers & Optoelect Mat, Beijing 100190, Peoples R China
[8] Max Planck Inst Chem Phys Solids, D-01187 Dresden, Germany
[9] Natl Synchrotron Radiat Res Ctr, Hsinchu 30076, Taiwan
[10] Innovat Lab Sci & Technol Energy Mat Fujian Prov I, Xiamen 361005, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
Palladium; Multimetallic; Amorphization; Alkaline; Oxygen reduction reaction; ELECTROOXIDATION; NANOCRYSTALS; ETHANOL; ELECTROCATALYSTS; SITES;
D O I
10.1021/acs.nanolett.3c04045
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Amorphous nanomaterials have drawn extensive attention owing to their unique features, while amorphization on noble metal nanomaterials still remains formidably challenging. Herein, we demonstrate a universal strategy to synthesize amorphous Pd-based nanomaterials from unary to quinary metals through the introduction of phosphorus (P). The amorphous Pd-based nanoparticles (NPs) exhibit generally promoted oxygen reduction reaction (ORR) activity and durability compared with their crystalline counterparts. Significantly, the quinary P-PdCuNiInSn NPs, benefiting from the amorphous structure and multimetallic component effect, exhibit mass activities as high as 1.04 A mgPd(-1) and negligible activity decays of 1.8% among the stability tests, which are much better than values for original Pd NPs (0.134 A mgPd(-1) and 28.4%). Experimental and theoretical analyses collectively reveal that the synergy of P-induced amorphization and the expansion of metallic components can considerably lower the free energy changes in the rate-determined step, thereby explaining the positive correlation with the catalytic activity.
引用
收藏
页码:1205 / 1213
页数:9
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