材料科学
催化作用
铂金
金属
Atom(片上系统)
氢
费米能级
纳米颗粒
电子结构
原子轨道
结晶学
纳米技术
化学物理
凝聚态物理
物理
电子
嵌入式系统
有机化学
化学
冶金
量子力学
生物化学
计算机科学
作者
Tamás Ollár,Péter Vancsó,Péter Kun,Antal A. Koós,Gergely Dobrik,Ekaterina V. Sukhanova,Захар И. Попов,Miklós Németh,Krisztina Frey,B. Pécz,Péter Nemes‐Incze,Chanyong Hwang,József S. Pap,Levente Tapasztó
标识
DOI:10.1002/adma.202504113
摘要
Abstract Metallic platinum is the best and most widely investigated catalyst for hydrogen evolution, yet little is known about Pt in its semiconducting form. Here, it is shown that semiconducting Pt structures with a thickness of only two atomic layers (0.4 nm) can be stabilized on 2D MoS 2 crystals. Reducing the thickness of Pt particles below the Fermi wavelength (0.5 nm) opens a sizeable (0.3–0.4 eV) gap in their electronic structure. The resulting electronic structure is qualitatively different from both the metallic bands of larger Pt nanoparticles and the atomic orbitals of Pt single atom catalysts while displaying the highest intrinsic activity among them. Semiconducting Pt bilayers enable H 2 production at ten times higher rates (≈1400 H 2 s −1 @ η = 100 mV) than Pt single atom catalysts, and match the activity of commercial Pt nanoparticles (Pt /C catalysts) at three orders of magnitude lower Pt loadings.
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