Coupled Heterojunction Sn2Ta2O7@SnO2: Cooperative Promotion of Effective Electron–Hole Separation and Superior Visible-light Absorption
Source abstract
Abstract
In this work, a novel heterostructure integrated by two wide-band gap semiconductors, SnO2 and Sn2Ta2O7, is successfully prepared via a hydrothermal approach. Hollow Sn2Ta2O7 spheres were first formed, and small SnO2 particles were then well-dispersed onto the outside surface of the spheres, forming a p-n heterostructure. This heterostructure exhibits a higher potential edge that yielded enhanced photoredox ability. Further, the heterostructure is of Z-type with a consistent internal electric field direction, which effectively separates the photogenerated electron-hole pairs. Although both component semiconductors do not absorb visible light, the resulted p-n heterostructure is surprisingly observed to show an outstanding photocatalytic performance under visible light illumination. Such a visible light response is concluded to be the consequence of the impurity band formed by Sn(2+) doped in SnO2 and Sn(4+) in Sn2Ta2O7 via in situ redox. The existence of coupled Sn(2+) and Sn(4+) ions in p-n heterostructure is responsible for the absence of defects and the regenerated catalytic activities. The findings reported here may provide an approach to fabricate the new types of photocatalysts with a synergetic promotion for visible light absorption and sustained photocatalytic activities by coupling different wide-band semiconductors.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · TiO2 Photocatalysis and Solar Cells · Ga2O3 and related materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot City 010021, People’s Republic of China
National Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Chemistry College, Jilin University, Changchun 130023, People’s Republic of China
Funding
National Natural Science Foundation of China · Inner Mongolia University
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