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JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY · 2025 · IF 14.3

Interfacial lattice matched sub-2 nm RuO2 on rutile TiO2 nanorod for visible light driven CO2 conversion to CH4

Wenjiao Chang,Honghuo Wang,Tingting Wu,Shuting Zhang,Yifan Li,Junying Wang,Yongqiang Yang,Lei Wang

Photocatalytic CO 2 reduction reaction is regarded as a potential strategy to convert greenhouse gases into valuable chemicals. However, achieving photocatalysts with high efficiency and target product selectivity under visible light still faces great challenges. Herein, sub-2 nm RuO 2 @TiO 2 (RTO) nanorods with lattice matching interface are rationally designed and prepared via a hydrothermal reaction step-by-step. Due to the strong interaction of the lattice-matched interface with the Ru-O-Ti bond, new energy levels have emerged at the interface, leading to effective visible light absorbance. Moreover, the photo-generated electrons could be transferred to the RuO 2 efficiently via the lattice-matched interface. As a result, the RTO photocatalyst exhibits superior CO 2 -to-CH 4 conversion performance of 15.6 µmol g −1 with a selectivity of 87.9% under visible light irradiation. Density functional theory (DFT) calculation reveals that the energy barrier of CO* to CO is significantly higher than that of *CHO, resulting in the preferential production of CH 4 . This work provides an effective strategy for designing photocatalyst with promoted visible light absorption and improved product selectivity.

CAS / MDL: 14898-67-0 5593-70-4
研究领域: 材料科学 · 环境科学 · 催化化学
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Journal of Energy Chemistry · 2016 · IF 2.322

p-Type CaFe2O4 semiconductor nanorods controllably synthesized by molten salt method

Xin Liu,Junzhe Jiang,Yushuai Jia,Ailing Jin,Xiangshu Chen,Fei Zhang,Hongxian Han

Pure phase, regular shape and well crystallized nanorods of p-type semiconductor CaFe 2 O 4 have been fabricated for the first time by a facile molten salt assisted method, as confirmed by XRD , TEM, SEM and HRTEM. UV−vis diffuse reflectance spectra and Mott–Schottky plots show that the band structure of the CaFe 2 O 4 nanorods is narrower than that of the CaFe 2 O 4 nanoparticles synthesized by conventional method. The enhancement of the visible-light absorption is due to narrowness of the band gap in CaFe 2 O 4 nanorods. The appropriate ratio between the molten salt and the CaFe 2 O 4 precursors plays an important role in inhibiting the growth of the crystals along the (201) plane to give the desired nanorod morphology. This work not only demonstrates that highly pure p-type CaFe 2 O 4 semiconductor with tunable band structure and morphology could be obtained using the molten salt strategy, but also affirms that the bandgap of a semiconductor may be tunable by monitoring the growth of a particular crystal plane. Furthermore, the facile eutectic molten salt method developed in this work may be further extended to fabricate some other semiconductor nanomaterials with a diversity of morphologies.

CAS / MDL: 13477-34-4 7782-61-8
研究领域: 材料科学 · 半导体物理
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2021 ·Vol. 32 ·期 15 ·20891-20902 · IF 2.478

Facile synthesis of heterojunctions by hydrothermal decoration of CdS on electrospun BiVO4 nanofibers with boosted photocatalytic activity

Peng Long-Gui,Ni Fu-Rong,Liu Jun,Sun Meng,Chang Meng-Jie,Xi Tong,Li Hui-Lu,Du Hui-Ling,Yang Jie,Li Ying

Bismuth vanadate (BiVO 4 ) is a promising photocatalyst material for photocatalytic degradation of organic pollutions. However, the fast recombination of photo-induced charge and insufficient light absorption often lead to poor photocatalytic performance. Herein, novel fibrous BiVO 4 /CdS (BVO/CdS) heterostructures are constructed by uniformly modifying caterpillar shaped electrospun BiVO 4 nanofibers with controllable quantity of CdS nanoparticles through hydrothermal reaction. The absorption of visible light and separation efficiency of photo-generated charge of BiVO 4 are significantly promoted after the decoration of CdS nanoparticles. As a result, the photocatalytic efficiency of the optimized BVO/CdS sample (BVO/CdS-2 stands for the sample synthesized with 0.05 mmol Cd(CH 3 COO) 2 and CH 4 N 2 S) is 90.43%, which is 3.3 times as high as that of pure BiVO 4 after 180 min irradiation under visible light, respectively. Moreover, the .O 2 − and .OH are the predominant active species for the degradation process indicated by scavengers added photocatalytic experiments. Due to the simple, low-cost and controllable synthetic process, the BVO/CdS heterojunctions are suitable for practical usage.

研究领域: 材料科学 · 环境科学
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JOURNAL OF MATERIALS SCIENCE-MATERIALS IN ELECTRONICS · 2020 ·Vol. 31 ·期 19 ·17036-17043 · IF 2.22

A novel CuSbS2–TiO2 nanoparticles synergy structure for photocatalysis

Zhi Guowei,Wang Wei,Zhang Ming,Hao Lingyun,Yang Lu,Liu Jijinhua,Zhao Yijie

In this work, a synergy structure to improve the photocatalytic properties of materials was proposed. CuSbS 2 nanoparticles synthesized by microwave irradiation method were dispersed in TiO 2 sol to form CuSbS 2 –TiO 2 nanoparticles. The properties of composite materials with different TiO 2 sol concentration were investigated by XRD, XPS, etc. The results indicated the as-synthesized CuSbS 2 nanoparticles exhibited chalcostibite structure and the TiO 2 showed anatase phase. The CuSbS 2 –TiO 2 nanoparticles had high absorbance in the visible light and good photocatalysts for the photodegradation reaction of Rhodamine B (RhB). When TiO 2 sol concentration was 0.23 mol/L, the sample possessed a photocatalytic degradation rate of 0.002 min −1 for the degradation of RhB, which was 3 times higher than that by the bare amorphous TiO 2 (0.0007 min −1 ).

研究领域: 材料科学 · 环境科学
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CATALYSIS LETTERS · 2023 · IF 2.8

Construction of p–n Heterojunctions by Co9S8 Modified Rare-Earth Metal Sm-Tungstates for Photocatalytic Hydrogen Evolution

Li Zezhong,Xu Jing,Liu Zhenlu,Liu Xinyu,Xu Shengming,Ma Yue,Li Qian,Shang Yan

The p–n type Sm 2 WO 6 -Co 9 S 8 heterojunction with two-dimensional coupling interface was successfully synthesized by electrostatic self-assembly. The unique rhombic morphology of Sm 2 WO 6 and Co 9 S 8 nanoparticles also effectively improve the light utilization efficiency. The intervention of Co 9 S 8 enhances the visible light absorption capacity of m 2 WO 6 /Co 9 S 8 . The Sm 2 WO 6 /Co 9 S 8 greatly increases the specific surface area and provides a rich reaction site. Recombination of photogenerated carriers in Sm 2 WO 6 /Co 9 S 8 heterojunctions is effectively inhibited. The p–n type Sm 2 WO 6 -Co 9 S 8 heterojunction results show that the optimized Sm 2 WO 6 /Co 9 S 8 heterojunction exhibits significant hydrogen evolution activity, and the optimal Sm 2 WO 6 /Co 9 S 8 -25 composite has 117.5 μmol hydrogen evolution activity, it’s close to four times Co 9 S 8 , close to 143 times Sm 2 WO 6 . The stability of the composite Sm 2 WO 6 /Co 9 S 8 is the better. Under the built-in electric field induced by p–n heterojunction, using of p–n heterojunction interactions and electron transport modes, the Sm 2 WO 6 /Co 9 S 8 can effectively achieve the remarkable effect of its internal carrier separation. This work also provides new opportunities for studying rare earth element tungstate photocatalysts. Graphical Abstract

研究领域: 材料科学 · 能源化学
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CATALYSIS LETTERS · 2025 ·Vol. 155 ·期 5 ·1-13 · IF 2.4

In situ Growth of NiS Nanoparticles on CdS Nanorods for Highly Efficient Photocatalytic Hydrogen Evolution

Lu Xingyu,Sun Jiahao,Yang Pengfei,Yang Xianjun,Hu Qin,Chen Liuyun,Qin Zuzeng,Su Tongming

CdS photocatalysts have attracted extensive attention in the area of photocatalytic hydrogen generation, yet their limited light absorption and charge transfer efficiencies still restrict their photocatalytic performance. In this study, NiS was grown on CdS to synthesize xNiS/CdS composites via a hydrothermal method and was used for photocatalytic hydrogen evolution. The introduction of NiS increased the light absorption intensity and broadened the light absorption range in the visible light region. In addition, a close contact interface formed between NiS and CdS, which accelerated the transfer and separation of photogenerated electrons and holes. Furthermore, NiS acts as the electron aggregation center and active site for photocatalytic hydrogen evolution. Therefore, the photocatalytic performance of the xNiS/CdS composites was greatly enhanced. Among the xNiS/CdS composites, the 0.5NiS/CdS composite exhibited the optimal photocatalytic hydrogen evolution rate of 36.75 mmol·h − 1 ·g − 1 , which was 7.84 times greater than that of CdS. A possible mechanism of photocatalytic H 2 production over xNiS/CdS is also proposed. This work provides new inspiration for the rational design of high-efficiency cocatalyst/CdS composites. Graphical

CAS / MDL: 10022-68-1
研究领域: 材料科学 · 能源化学
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RSC Advances · 2016 ·Vol. 6 ·期 76 ·72659-72669 · IF 3.289

In situ growth of TiO2 on TiN nanoparticles for non-noble-metal plasmonic photocatalysis

Chao Li,Weiyi Yang,Lingmei Liu,Wuzhu Sun,Qi Li

Plasmonic photocatalysis could provide a promising solution to the two fundamental problems of current TiO2-based visible-light photocatalysis on low photocatalytic efficiency and low usage of solar illumination. But till now, most plasmonic photocatalysts have relied on noble metal nanostructures of Au or Ag due to their easy synthesis and efficient absorption of visible light. In this study, a TiN/TiO2 nanocomposite photocatalyst was synthesized by the in situ growth of TiO2 nanoparticles on TiN nanoparticles with a fluorine-free, vapor-phase hydrothermal process. In this composite photocatalyst system, the desirable visible light absorption could be attributed to the LSPR effect of a nanostructured TiN phase. Thus, a plasmonic photocatalyst without noble-metal components was developed, and its good visible light photocatalytic activity was demonstrated by both the photodegradation of organic pollutants of RhB and 4-NP and the disinfection of microorganisms of E. coli. From the energy alignment analysis, hot electrons were expected to be completely injected from TiN to TiO2 once they were excited above the Fermi energy level of TiN because no barrier existed, resulting in better electron injection efficiency than previous reported noble-metal-based plasmonic photocatalysts.

研究领域: 材料科学 · 环境科学
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MATERIALS CHEMISTRY AND PHYSICS · 2016 · IF 2.101

Facile in situ hydrothermal synthesis of g-C3N4/SnS2 composites with excellent visible-light photocatalytic activity

Fang Deng,Lina Zhao,Xule Pei,Xubiao Luo,Shenglian Luo

The g-C 3 N 4 /SnS 2 composites were prepared by in situ hydrothermal method , and the effect of g-C 3 N 4 content on the physical and chemical properties, and photocatalytic performance of g-C 3 N 4 /SnS 2 composites was investigated. The introduction of g-C 3 N 4 enhanced the visible-light absorption of SnS 2 , and reduced the recombination rate of electron-hole pairs. The photocatalytic performance of g-C 3 N 4 /SnS 2 composites was also obviously influenced by g-C 3 N 4 content, and it was found that 15% g-C 3 N 4 /SnS 2 composite exhibited the highest photocatalytic activity and excellent regeneration, which was attributed to the most efficient charge separation, the largest specific surface area and the formation of dominant active species (h + and O 2 − radicals) during the photocatalytic process.

研究领域: 材料科学 · 环境科学
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Materials · 2019 ·Vol. 12 ·期 10 ·1713 · IF 2.972

Carbon Dots-Decorated Bi2WO6 in an Inverse Opal Film as a Photoanode for Photoelectrochemical Solar Energy Conversion under Visible-Light Irradiation

Dongxiang Luo,Qizan Chen,Ying Qiu,Baiquan Liu,Menglong Zhang

This work focuses on the crystal size dependence of photoactive materials and light absorption enhancement of the addition of carbon dots (CDs). mac-FTO (macroporous fluorine-doped tin oxide) films with an inverse opal structure are exploited to supply enhanced load sites and to induce morphology control for the embedded photoactive materials. The Bi2WO6@mac-FTO photoelectrode is prepared directly inside a mac-FTO film using a simple in situ synthesis method, and the application of CDs to the Bi2WO6@mac-FTO is achieved through an impregnation assembly for the manipulation of light absorption. The surface morphology, chemical composition, light absorption characteristics and photocurrent density of the photoelectrode are analyzed in detail by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), UV–vis diffuse reflectance spectra (DRS), Energy dispersive X-ray analysis (EDX) and linear sweep voltammetry (LSV).Keywords:photoelectrode;carbon dots;macroporous electrode

研究领域: 材料科学 · 能源转换技术
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2017 · IF 2.625

Facile hydrothermal synthesis of carbon dots (CDs) doped ZnFe2O4/TiO2 hybrid materials with high photocatalytic activity

Yida Lu,Yiping Feng,Fengliang Wang,Xuegang Zou,Zhi-Feng Chen,Ping Chen,Haijin Liu,Yuehan Su,Qianxin Zhang,Guoguang Liu

In this study, a novel and highly efficient ternary photocatalytic ZnFe 2 O 4 /TiO 2 /CDs nanocomposite was successfully synthesized by a hydrothermal method. The properties and structures of the samples were characterized by X-ray diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Fourier transform infrared spectrometry (FT-IR), and photoluminescence spectrum (PL). The UV–vis diffuse reflectance spectrum was used to demonstrate that carbon quantum dots could increase the absorption of visible light wavelengths. When compared with TiO 2 /3.00   wt%CDs and ZnFe 2 O 4 /TiO 2 nanocomposites, the ternary photocatalysts exhibited the enhanced photocatalytic activity under solar-spectrum irradiation. A low CDs content of 3.00   wt% in the ternary photocatalysts possessed excellent performance in the decomposition of Rhodamine B (RhB). Act as donator and receiver, CDs can efficiently improve the ability of electron transfer and separate the electron-hole pairs. OH and O 2 − were confirmed to be involved in the photocatalytic degradation of RhB base on the Electron spin resonance (ESR) tests, and the photocatalytic mechanism of the ZnFe 2 O 4 /TiO 2 /3.00   wt%CDs was proposed. After four sequential operational cycles, the ZnFe 2 O 4 /TiO 2 /CDs maintained its photocatalytic efficiency, indicating its high photocatalytic stability. Therefore, our results provide a high efficient photocatalytic nanocomposite that synthetized by a facile method, and have implications in the removal of environmental persistent pollutants under ternary photocatalysts mediated solar degradation

研究领域: 材料科学 · 环境科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Highly efficient photocatalytic hydrogen production by platinum modified ferroelectric SrBi4Ti4O15

Longbin Chen,Pengqi Hai,Yaodong Yang,Chao Wu,Yongming Hu,Wei-Feng Rao

Combining metal with ferroelectrics is one of the reliable strategies to enhance the photocatalytic water splitting of ferroelectrics dramatically. However, the metal loading ratio is directly related to the synergistic effect of catalysts. In order to find the appropriate loading of Pt, we fabricated SrBi 4 Ti 4 O 15 (SBTO) nanosheets (NSs) and deposited different amounts of Pt nanoparticles (NPs) to form heterojunction. The optoelectronic characterizations verified that the Pt-modified SBTO NSs have broadened absorption of visible light; produce more long-lived charge carriers. The photocatalytic hydrogen production can reach 11700 μmol g −1 under continuous illumination for 3 h from the sample containing 6 wt% Pt, showing a much higher hydrogen evolution rate than other ferroelectric materials under similar reaction systems. Our work provides a valuable and feasible solution to produce hydrogen from water.

研究领域: 材料科学 · 能源科学 · 光催化
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

Red phosphorus decorated and doped TiO2 nanofibers for efficient photocatalytic hydrogen evolution from pure water

Yukun Zhu,Junzhi Li,Chung-Li Dong,Jun Ren,Yu-Cheng Huang,Daming Zhao,Rongsheng Cai,Daixing Wei,Xianfeng Yang,Chunxiao Lv,Wolfgang Theis,Yuyu Bu,Wei Han,Shaohua Shen,Dongjiang Yang

In this study, we report a facile strategy to prepare a new class of red phosphorus (RP) decorated and doped TiO 2 (A: anatase and B: TiO 2 (B)) nanofibers with boosted photocatalytic hydrogen evolution reaction (HER) performance from pure water. The optimized TiO 2 (B)/RP and TiO 2 (A)/RP heterostructure exhibits significantly enhanced photocatalytic performances, with HER rate reaching 11.4 and 5.3 μmol h −1 , respectively. The optical absorption of TiO 2 is significantly extended to the visible light region after decoration of RP. And more oxygen vacancies (V O ) were introduced by phosphorus doping in the TiO 2 (B)/RP than TiO 2 (A)/RP. The theoretical calculations illustrate the formation of V O can decrease the ratio of effective masses of electron to hole, which gives rise to promoted photoinduced charge separation and transfer. These results suggest that the boosted photocatalytic HER performance should be mainly attributed to the synergetic enhancement in light harvesting and charge separation enabled by RP deposition and P 5+ doping.

研究领域: 材料科学 · 能源化学
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