柯肯德尔效应
半导体
材料科学
光催化
分解水
纳米技术
模板
纳米晶
扩散
化学工程
光电子学
催化作用
化学
工程类
物理
热力学
生物化学
冶金
作者
Yuemei Li,Jia Liu,Xinyuan Li,Xiaodong Wan,Rongrong Pan,Hongpan Rong,Jiajia Liu,Wenxing Chen,Jiatao Zhang
标识
DOI:10.1021/acsami.9b05325
摘要
Hollow-structured semiconductor nanocrystals (NCs) have aroused tremendous research interest because of their compelling structure-related properties that can facilitate the development of many important applications including solar water splitting. However, the creation of multicomponent semiconductor NCs (such as I-III-VI2 and I2-II-IV-VI4 semiconductors) possessing a hollow architecture still remains a great challenge because of the difficulty in balancing the reactivities of multiple precursors. In this study, we report an effective strategy to prepare hollow CuInS2 nanododecahedrons featuring high uniformity in morphology and composition, based on the Kirkendall effect driven by the cation exchange between Cu+ and In3+ using Cu2-xS nanododecahedrons as templates. The unequal diffusion rates of cations result in an inward flux of vacancies favorably along the (0 16 0) facets of Cu2-xS dodecahedrons, forming a Cu2-xS@CuInS2 core-shell intermediate with striped voids in the core region. Optical absorption studies and photoelectrochemical measurements imply that the increase in the hollowing degree of the NCs benefits enhanced light harvesting and separation of photogenerated charge carriers. As a result, the obtained hollow CuInS2 nanododecahedrons present a high activity in photocatalytic hydrogen evolution, much superior to previously reported CuInS2 photocatalysts with different architectures. We envision that the multifarious morphologies attainable for the Cu2-xS NC templates and the advantages of Cu+ for cation exchange can make this method adaptable to a vast variety of previously intractable structures and compositions.
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