Liu Yuxin, Chen Cailing, He Yiqiang, Zhang Zhe, Li Mingbian, Li Chunguang, Chen Xiao-Bo, Han Yu, Shi Zhan
State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, College of Chemistry, Jilin University, Changchun, 130012, P. R. China.
King Abdullah University of Science and Technology (KAUST), Advanced Membranes and Porous Materials Center, Physical Sciences and Engineering Division, King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Small. 2022 Aug;18(34):e2201556. doi: 10.1002/smll.202201556. Epub 2022 Jul 27.
Design and development of highly efficient photocatalytic materials are key to employ photocatalytic technology as a sound solution to energy and environment related challenges. This work aims to significantly boost photocatalytic activity through rich indium vacancies (V ) In S with atomic p-n homojunction through a one-pot preparation strategy. Positron annihilation spectroscopy and electron paramagnetic resonance reveal existence of V in the prepared photocatalysts. Mott-Schottky plots and surface photovoltage spectra prove rich V In S can form atomic p-n homojunction. It is validated that p-n homojunction can effectively separate carriers combined with photoelectrochemical tests. V decreases carrier transport activation energy (CTAE) from 0.64 eV of V -poor In S to 0.44 eV of V -rich In S . The special structure endows defective In S with multifunctional photocatalysis properties, i.e., hydrogen production (872.7 µmol g h ), degradation of methyl orange (20 min, 97%), and reduction in heavy metal ions Cr(VI) (30 min, 98%) under simulated sunlight, which outperforms a variety of existing In S composite catalysts. Therefore, such a compositional strategy and mechanistic study are expected to offer new insights for designing highly efficient photocatalysts through defect engineering.
设计和开发高效光催化材料是将光催化技术作为解决能源和环境相关挑战的可靠解决方案的关键。这项工作旨在通过一锅法制备策略,通过富含铟空位(V )的In S 形成原子p-n同质结,从而显著提高光催化活性。正电子湮没光谱和电子顺磁共振揭示了所制备的光催化剂中存在V 。莫特-肖特基曲线和表面光电压谱证明富含V 的In S 可以形成原子p-n同质结。结合光电化学测试验证了p-n同质结可以有效地分离载流子。V 将载流子传输活化能(CTAE)从贫V 的In S 的0.64 eV降低到富V 的In S 的0.44 eV。这种特殊结构赋予缺陷In S 多功能光催化性能,即在模拟阳光下产氢(872.7 µmol g h )、降解甲基橙(20分钟,97%)和还原重金属离子Cr(VI)(30分钟,98%),其性能优于多种现有的In S 复合催化剂。因此,这种组成策略和机理研究有望为通过缺陷工程设计高效光催化剂提供新的见解。