Rh-M (M: Co, Cu, and Fe) nanoclusters as highly efficient and durable catalysts for the methanolysis of ammonia borane

被引:16
作者
Abay, Bayram [1 ]
Rakap, Murat [2 ]
机构
[1] Yuzuncu Yil Univ, Dept Chem, TR-65080 Van, Turkey
[2] Yuzuncu Yil Univ, Maritime Fac, TR-65080 Van, Turkey
关键词
SUPPORTED RHODIUM(0) NANOPARTICLES; LONG-LIVED CATALYST; HYDROGEN GENERATION; HYDROLYTIC DEHYDROGENATION; HYDRAZINE BORANE; SODIUM-BOROHYDRIDE; H-2; GENERATION; COBALT; PHOTOELECTRON; NANOSPHERES;
D O I
10.1039/d0cy01422b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Herein, we report the preparation, characterization, and employment of hydroxyapatite-supported rhodium-based Rh-M (RhCo, RhCu, and RhFe) nanoclusters as cost-effective, highly efficient and reusable catalysts for hydrogen evolution from ammonia borane methanolysis. Rh-M@HA nanoclusters are formed by in situ reduction of hydroxyapatite-supported related metal cations during ammonia borane methanolysis after ion-exchange. The Rh-M@HA nanoclusters are easily obtained as very stable solids and identified by some advanced analytical techniques like ICP-OES, BET, TEM, XPS, and XRD. After experimental studies, they are found as highly isolable, redispersible, and reusable nanocatalysts to evolve hydrogen from ammonia borane methanolysis under mild conditions. From these three catalysts, the Rh51Co49@HA nanoclusters provide the highest turnover frequency (TOF) value of 193.7 min(-1) while the Rh26Cu74@HA and Rh45Fe55@HA nanoclusters have TOF values of 25.1 and 38.7 min(-1), respectively, in ammonia borane methanolysis at 25 +/- 0.1 degrees C. The apparent activation energies (E-a) of the Rh51Co49@HA, Rh26Cu74@HA, and Rh45Fe55@HA nanoclusters for the same reaction are calculated to be 52.7, 59.7, and 54.1 kJ mol(-1), respectively.
引用
收藏
页码:7270 / 7279
页数:10
相关论文
共 50 条
[1]   Self-assembly of copper nanoparticles (cubes, rods and spherical nanostructures): Significant role of morphology on hydrogen and oxygen evolution efficiencies [J].
Ahmed, Jahangeer ;
Trinh, Phong ;
Mugweru, Amos M. ;
Ganguli, Ashok K. .
SOLID STATE SCIENCES, 2011, 13 (05) :855-861
[2]   A study of catalytic hydrolysis of concentrated ammonia borane solutions [J].
Brockman, Alan ;
Zheng, Yuan ;
Gore, Jay .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2010, 35 (14) :7350-7356
[3]   Zeolite confined rhodium(0) nanoclusters as highly active, reusable, and long-lived catalyst in the methanolysis of ammonia-borane [J].
Caliskan, Salim ;
Zahmakiran, Mehmet ;
Ozkar, Saim .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2010, 93 (3-4) :387-394
[4]   Room temperature hydrogen generation from aqueous ammonia-borane using noble metal nano-clusters as highly active catalysts [J].
Chandra, Manish ;
Xu, Qiang .
JOURNAL OF POWER SOURCES, 2007, 168 (01) :135-142
[5]   Highly efficient colloidal cobalt- and rhodium-catalyzed hydrolysis of H3N•BH3 in air [J].
Clark, Timothy J. ;
Whittell, George R. ;
Manners, Ian .
INORGANIC CHEMISTRY, 2007, 46 (18) :7522-7527
[6]   A Bunch-like Copper Oxide Nanowire Array as an Efficient, Durable, and Economical Catalyst for the Methanolysis of Ammonia Borane [J].
Cui, Liang ;
Cao, Xueying ;
Sun, Xuping ;
Yang, Wenrong ;
Liu, Jingquan .
CHEMCATCHEM, 2018, 10 (04) :710-715
[7]   Ruthenium nanoparticles immobilized in montmorillonite used as catalyst for methanolysis of ammonia borane [J].
Dai, Hong-Bin ;
Kang, Xiang-Dong ;
Wang, Ping .
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY, 2010, 35 (19) :10317-10323
[8]   Hydrogen release by thermolysis of ammonia borane NH3BH3 and then hydrolysis of its by-product [BNHx] [J].
Demirci, U. B. ;
Bernard, S. ;
Chiriac, R. ;
Toche, F. ;
Miele, P. .
JOURNAL OF POWER SOURCES, 2011, 196 (01) :279-286
[9]   Hydrogen generation from the methanolysis of ammonia borane catalyzed by in situ generated, polymer stabilized ruthenium(0) nanoclusters [J].
Erdogan, Huriye ;
Metin, Onder ;
Ozkar, Saim .
CATALYSIS TODAY, 2011, 170 (01) :93-98
[10]   In situ-generated PVP-stabilized palladium(0) nanocluster catalyst in hydrogen generation from the methanolysis of ammonia-borane [J].
Erdogan, Huriye ;
Metin, Oender ;
Oezkar, Saim .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2009, 11 (44) :10519-10525