A sulfur-tethering synthesis strategy toward high-loading atomically dispersed noble metal catalysts

被引:211
|
作者
Wang, Lei [1 ]
Chen, Ming-Xi [1 ]
Yan, Qiang-Qiang [1 ]
Xu, Shi-Long [1 ]
Chu, Sheng-Qi [2 ]
Chen, Ping [3 ]
Lin, Yue [1 ]
Liang, Hai-Wei [1 ]
机构
[1] Univ Sci & Technol China, Dept Chem, Hefei Natl Lab Phys Sci Microscale, Hefei 230026, Anhui, Peoples R China
[2] Chinese Acad Sci, Inst High Energy Phys, Beijing 100049, Peoples R China
[3] Anhui Univ, Sch Chem & Chem Engn, Hefei 230601, Anhui, 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
SINGLE-SITE; ATOM; HYDROGENATION; OXIDATION; REDUCTION; METHANE; ACID;
D O I
10.1126/sciadv.aax6322
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Metals often exhibit robust catalytic activity and specific selectivity when downsized into subnanoscale clusters and even atomic dispersion owing to the high atom utilization and unique electronic properties. However, loading of atomically dispersed metal on solid supports with high metal contents for practical catalytic applications remains a synthetic bottleneck. Here, we report the use of mesoporous sulfur-doped carbons as supports to achieve high-loading atomically dispersed noble metal catalysts. The high sulfur content and large surface area endow the supports with high-density anchor sites for fixing metal atoms via the strong chemical metalsulfur interactions. By the sulfur-tethering strategy, we synthesize atomically dispersed Ru, Rh, Pd, Ir, and Pt catalysts with high metal loading up to 10 wt %. The prepared Pt and Ir catalysts show 30- and 20-fold higher activity than the commercial Pt/C and Ir/C catalysts for catalyzing formic acid oxidation and quinoline hydrogenation, respectively.
引用
收藏
页数:8
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