量子点
化学
化学物理
光催化
X射线光电子能谱
电子结构
密度泛函理论
表面状态
纳米技术
量子产额
光电发射光谱学
带隙
联轴节(管道)
氧化物
电子
光化学
电子顺磁共振
光谱学
金属
电荷(物理)
四方晶系
电荷密度
量子
共振(粒子物理)
载流子
凝聚态物理
光电子学
作者
Loukas Belles,Areti Zindrou,Nikolaos Effraim Papamatthaiakis,Szymon Smykała,Giannis Mpourmpakis,Yiannis G. Deligiannakis
摘要
Abstract Ultrasmall quantum dots (QDs) exhibit electronic behavior inaccessible to bulk counterparts, yet the role of structurally disordered interfaces remains unresolved, particularly in wide-band gap oxides. Herein, using the flame spray pyrolysis (FSP) technology, we engineered ZrO2/ZrO2–x QDs comprising tetragonal ZrO2 QDs (2–5 nm) tightly interfaced with a semiamorphous, subnanometric ZrO2–x layer. Rather than forming a conventional heterojunction, electronic coupling between a {surface distorted hydroxylated ZrO2–x}, and the {quantum-confined crystalline core} generates shallow interfacial quantum states (IQS). This single-metal-oxide architecture elucidates the synergistic contributions of quantum confinement and interfacial states to photocatalytic H2 evolution. The ZrO2/ZrO2–x QDs exhibit an unprecedented H2 production rate of 32,943 μmol g–1 h–1 and an apparent quantum yield of 3.49% at 252 nm, outperforming bulk-like ZrO2. Experimental results indicate that IQS activate otherwise photoinactive ZrO2, while density functional theory (DFT) calculations elucidate their origin and electronic character. Photoelectrochemical measurements reveal a negative shift in flat-band potential and enhanced interfacial charge conductivity. X-ray photoelectron spectroscopy identifies a highly reduced, hydroxylated surface environment in the ZrO2 QDs, whereas electron paramagnetic resonance (EPR) reveals that {ZrO2/ZrO2–x QDs} form photoactive Zr3+ centers. Additionally, reversible photoinduced (g < 2) and (g > 2) signals consistent with electron and hole trapping, respectively. These findings establish IQS engineering as a novel interphase concept, beyond the quantum-dot limit, to promote charge separation and H2 evolution even in wide-band gap metal oxides. More broadly, coupling metal-oxide QDs with subnanometric, oxygen-deficient layers of the same metal offer a simple chemical route to activate otherwise inefficient oxide photocatalysts.
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