纳米团簇
化学
催化作用
塔菲尔方程
电化学
氢化物
三氟乙酸
结晶学
金属
钯
物理化学
电极
有机化学
作者
Rhone P. Brocha Silalahi,Yongsung Jo,Jian‐Hong Liao,Tzu‐Hao Chiu,Eunsaem Park,Woojun Choi,Hao Liang,Samia Kahlal,Jean‐Yves Saillard,Dongil Lee,C. W. Liu
标识
DOI:10.1002/anie.202301272
摘要
The first hydride-containing 2-electron palladium/copper alloys, [PdHCu11 {S2 P(Oi Pr)2 }6 (C≡CPh)4 ] (PdHCu11 ) and [PdHCu12 {S2 P(Oi Pr)2 }5 {S2 PO(Oi Pr)} (C≡CPh)4 ] (PdHCu12 ), are synthesized from the reaction of [PdH2 Cu14 {S2 P(Oi Pr)2 }6 (C≡CPh)6 ] (PdH2 Cu14 ) with trifluoroacetic acid (TFA). X-ray diffraction reveals that the PdHCu11 and PdHCu12 kernels consist of a central PdH unit encapsulated within a vertex-missing Cu11 cuboctahedron and complete Cu12 cuboctahedron, respectively. DFT calculations indicate that both PdHCu11 and PdHCu12 can be considered as axially-distorted 2-electron superatoms. PdHCu11 shows excellent HER activity, unprecedented within metal nanoclusters, with an onset potential of -0.05 V (at 10 mA cm-2 ), a Tafel slope of 40 mV dec-1 , and consistent HER activity during 1000 cycles in 0.5 M H2 SO4 . Our study suggests that the accessible central Pd site is the key to HER activity and may provide guidelines for correlating catalyst structures and HER activity.
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