Single-atom Rh/N-doped carbon electrocatalyst for formic acid oxidation

被引:513
作者
Xiong, Yu [1 ,2 ]
Dong, Juncai [3 ]
Huang, Zheng-Qing [4 ]
Xin, Pingyu [1 ]
Chen, Wenxing [1 ]
Wang, Yu [5 ]
Li, Zhi [1 ]
Jin, Zhao [6 ,7 ]
Xing, Wei [6 ,7 ]
Zhuang, Zhongbin [8 ]
Ye, Jinyu [9 ]
Wei, Xing [10 ]
Cao, Rui [11 ]
Gu, Lin [12 ]
Sun, Shigang [9 ]
Zhuang, Lin [10 ]
Chen, Xiaoqing [2 ]
Yang, Hua [2 ]
Chen, Chen [1 ]
Peng, Qing [1 ]
Chang, Chun-Ran [4 ]
Wang, Dingsheng [1 ]
Li, Yadong [1 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing, Peoples R China
[2] Cent South Univ, Coll Chem & Chem Engn, Changsha, Hunan, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Beijing Synchrotron Radiat Facil, Beijing, Peoples R China
[4] Xi An Jiao Tong Univ, Sch Chem Engn & Technol, Shaanxi Key Lab Energy Chem Proc Intensificat, Xian, Peoples R China
[5] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai Synchrotron Radiat Facil, Shanghai, Peoples R China
[6] Chinese Acad Sci, Changchun Inst Appl Chem, Lab Adv Power Sources, Changchun, Jilin, Peoples R China
[7] Jilin Prov Key Lab Low Carbon Chem Power Sources, Changchun, Jilin, Peoples R China
[8] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, State Key Lab Organ Inorgan Composites, Beijing, Peoples R China
[9] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem, State Key Lab Phys Chem Solid Surfaces, Xiamen, Peoples R China
[10] Wuhan Univ, Coll Chem & Mol Sci, Hubei Key Lab Electrochem Power Sources, Wuhan, Peoples R China
[11] SLAC Natl Accelerator Lab, Stanford Synchrotron Radiat Lightsource, Menlo Pk, CA USA
[12] Chinese Acad Sci, Inst Phys, Beijing Natl Lab Condensed Matter Phys, Beijing, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划; 中国博士后科学基金;
关键词
INITIO MOLECULAR-DYNAMICS; OXYGEN REDUCTION; PALLADIUM NANOSHEETS; CATALYSTS; IDENTIFICATION; TRANSITION; GRAPHENE; ELECTROOXIDATION; DECOMPOSITION; CONVERSION;
D O I
10.1038/s41565-020-0665-x
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
To meet the requirements of potential applications, it is of great importance to explore new catalysts for formic acid oxidation that have both ultra-high mass activity and CO resistance. Here, we successfully synthesize atomically dispersed Rh on N-doped carbon (SA-Rh/CN) and discover that SA-Rh/CN exhibits promising electrocatalytic properties for formic acid oxidation. The mass activity shows 28- and 67-fold enhancements compared with state-of-the-art Pd/C and Pt/C, respectively, despite the low activity of Rh/C. Interestingly, SA-Rh/CN exhibits greatly enhanced tolerance to CO poisoning, and Rh atoms in SA-Rh/CN resist sintering after long-term testing, resulting in excellent catalytic stability. Density functional theory calculations suggest that the formate route is more favourable on SA-Rh/CN. According to calculations, the high barrier to produce CO, together with the relatively unfavourable binding with CO, contribute to its CO tolerance. Atomically dispersed Rh on N-doped carbon exhibits 28- and 67-fold enhancements compared with state-of-the-art Pd/C and Pt/C, despite the low activity of Rh/C. The Rh single atoms exhibit high tolerance to CO poisoning compared to Rh nanoparticles.
引用
收藏
页码:390 / +
页数:11
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