TY - JOUR
T1 - Metal (Hydr)oxides@Polymer Core-Shell Strategy to Metal Single-Atom Materials
AU - Zhang, Maolin
AU - Wang, Yang Gang
AU - Chen, Wenxing
AU - Dong, Juncai
AU - Zheng, Lirong
AU - Luo, Jun
AU - Wan, Jiawei
AU - Tian, Shubo
AU - Cheong, Weng Chon
AU - Wang, Dingsheng
AU - Li, Yadong
N1 - Publisher Copyright:
© 2017 American Chemical Society.
PY - 2017/8/16
Y1 - 2017/8/16
N2 - Preparing metal single-atom materials is currently attracting tremendous attention and remains a significant challenge. Herein, we report a novel core-shell strategy to synthesize single-atom materials. In this strategy, metal hydroxides or oxides are coated with polymers, followed by higherature pyrolysis and acid leaching, metal single atoms are anchored on the inner wall of hollow nitrogen-doped carbon (CN) materials. By changing metal precursors or polymers, we demonstrate the successful synthesis of different metal single atoms dispersed on CN materials (SA-M/CN, M = Fe, Co, Ni, Mn, FeCo, FeNi, etc.). Interestingly, the obtained SA-Fe/CN exhibits much higher catalytic activity for hydroxylation of benzene to phenol than Fe nanoparticles/CN (45% vs 5% benzene conversion). First-principle calculations further reveal that the high reactivity originates from the easier formation of activated oxygen species at the single Fe site. Our methodology provides a convenient route to prepare a variety of metal single-atom materials representing a new class of catalysts.
AB - Preparing metal single-atom materials is currently attracting tremendous attention and remains a significant challenge. Herein, we report a novel core-shell strategy to synthesize single-atom materials. In this strategy, metal hydroxides or oxides are coated with polymers, followed by higherature pyrolysis and acid leaching, metal single atoms are anchored on the inner wall of hollow nitrogen-doped carbon (CN) materials. By changing metal precursors or polymers, we demonstrate the successful synthesis of different metal single atoms dispersed on CN materials (SA-M/CN, M = Fe, Co, Ni, Mn, FeCo, FeNi, etc.). Interestingly, the obtained SA-Fe/CN exhibits much higher catalytic activity for hydroxylation of benzene to phenol than Fe nanoparticles/CN (45% vs 5% benzene conversion). First-principle calculations further reveal that the high reactivity originates from the easier formation of activated oxygen species at the single Fe site. Our methodology provides a convenient route to prepare a variety of metal single-atom materials representing a new class of catalysts.
UR - http://www.scopus.com/inward/record.url?scp=85027396234&partnerID=8YFLogxK
U2 - 10.1021/jacs.7b05372
DO - 10.1021/jacs.7b05372
M3 - Article
C2 - 28759209
AN - SCOPUS:85027396234
SN - 0002-7863
VL - 139
SP - 10976
EP - 10979
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 32
ER -