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Journal of Materials Chemistry A · 2023 ·Vol. 11 ·期 39 ·21046-21057 · IF 11.9

A unique octadecahedron SrTiO3 perovskite oxide with a nano step-shaped facet structure for enhanced photoredox and hydrogen evolution performance

Chuyu Wang,Yan Li,Xiaojiao Cai,Dongping Duan,Qibo Jia

As a typical perovskite-type crystal, strontium titanate (SrTiO3, STO) has remarkable photocatalytic activity and is broadly used in solar-driven overall water splitting. The research on controlling the synthesis of polyhedral STO with different exposures of crystal facets to obtain different optoelectronic properties has been greatly carried out in recent years. However, there are few reports of research on the construction of a nano step-shaped facet structure by the reconstruction of the STO crystal facet at a certain temperature, and the formation mechanism and composition analysis have not been explained clearly. In particular, the influence of crystal surface recombination on the hydrogen production reaction hasn't been thoroughly studied. This work presents the existence of a novel STO with the nano step-shaped facet structure parallel to (100) and (110) facets based on octadecahedron STO by a solid-state reaction, and the formation has been monitored by thermogravimetric analysis and in situ X-ray diffraction. In addition, more importantly, the step-shaped facet structure is rich in Sr, and lacks O and Ti, which is evidenced by EPR and XPS characterization, and it affects the transfer and separation of photo carriers. The complex STO catalysts were prepared by photodeposition of Rh, Cr, and Co to compare the hydrogen production capacity of overall water splitting. The novel step-shaped facet SrTiO3 has a good deposition effect on the cocatalysts, and the synthesized catalyst can effectively shorten the band gap to 1.92 eV and prolong the photogenerated carriers' lifetime to 3.7356 ns. Consequently, the novel SrTiO3 sample deposited co-catalysts achieve remarkable activity with the highest H2 evolution rate of 172.0 μmol h−1, which is 4.6 times higher than that of the original octadecahedron SrTiO3 prepared by the hydrothermal method. The DFT calculation results prove that the excellent photocatalytic performance is due to the lower work function and effective electron transfer of the SrTiO3 (100) crystal facet and Sr-rich (110) crystal facet, which is verified by the obvious electron transfer between the CrO42− and the two kinds of crystal facets.

研究领域: 材料科学 · 光催化
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Dendrite-free Zn anode enabled by combining carbon nanoparticles hydrophobic layer with crystal face reconstruction toward high-performance Zn-ion battery

Mengxuan Sun,Xiaohe Ren,Lei Hu,Nengze Wang,Ziwei Gan,Chunyang Jia,Zhijie Li

Aqueous zinc ion batteries (ZIBs) have been considered promising energy storage systems due to their excellent electrochemical performance, environmental toxicity, high safety and low cost. However, uncontrolled dendrite growth and side reactions at the zinc anode have seriously hindered the development of ZIBs. Herein, we prepared the carbon nanoparticles layer coated zinc anode with (1   0   3) crystal plane preferential oriented crystal structure (denoted as C@RZn) by a facile one-step vapor deposition method. The preferential crystallographic orientation of (1   0   3) crystal plane promotes zinc deposition at a slight angle, effectively preventing the formation of Zn dendrites on the surface. In addition, the hydrophobic layer of carbon layer used as an inert physical barrier to prevent corrosion reaction and a buffer during volume changes, thus improving the reversibility of the zinc anode. As a result. the C@RZn anode achieves a stable cycle performance of more than 3000 h at 1 mA cm −2 with CE of 99.77 % at 5 mA cm −2 . The full battery with C@RZn anode and Mn-doped V 6 O 13 (MVO) cathode show stability for 5000 cycles at the current density of 5 A g −1 . This work provides a new approach for the design of multifunctional interfaces for Zn anode.

CAS / MDL: 7785-87-7 62-56-6
研究领域: 材料科学 · 电化学 · 能源存储
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