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ADVANCED FUNCTIONAL MATERIALS · 2020 ·Vol. 31 ·期 8 ·2007591 · IF 16.836

Efficient and Full-Spectrum Photothermal Dehydrogenation of Ammonia Borane for Low-Temperature Release of Hydrogen

Hanlin Huang,Cong Wang,Qi Li,Ruiqi Wang,Yuying Yang,Aidaer Muhetaer,Fuqiang Huang,Bing Han,Dongsheng Xu

Efficient hydrogen release from ammonia borane (AB) with a striking hydrogen content (19.6 wt%) via thermolysis provides a promising pathway for on-board applications utilizing hydrogen energy. However, the sluggish kinetics at low temperatures and high energy consumption of thermal dehydrogenation are major obstacles for hydrogen release from AB. Herein, a novel solar-driven strategy for hydrogen production from AB at low temperature is proposed, in which Ti 2 O 3 is utilized as a full-spectrum light absorber for photothermal-activating solid-state AB reactants to produce hydrogen. Through a reduction transformation method, nanoscale Ti 2 O 3 particles with high chemical stability and narrow band gap are prepared, realizing a rapid production of 2.0 equivalents of hydrogen from AB at ambient temperature, with an excellent recyclable and full-spectrum-responsive photothermal dehydrogenation. Importantly, a record high photothermal activation efficiency of 35% is achieved with nanoscale Ti 2 O 3 particles due to an enhanced local photothermal effect contributed by improved light absorption and decreased thermal conduction. Moreover, assisted with CuCl 2 promoter, a release of 2.0 equivalents of hydrogen under 1.0 solar irradiation at 70 °C is successfully achieved, revealing its potential applications in practical vehicles based on proton exchange membrane fuel cells.

CAS / MDL: 13774-81-7 1317-61-9
研究领域: 材料科学 · 能源化学
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JOURNAL OF SOLID STATE CHEMISTRY · 2022 · IF 3.656

Enhanced UV–Vis–NIR photocatalytic activity of La doped BaBiO2Cl: Role of oxygen vacancies

Jincai Peng,Yuehong Peng,Tianhui Wang,Zhijie Wu,Qi Wang,Yongjin Li,Zhaoyi Yin,Jin Han,Jianbei Qiu,Zhengwen Yang,Zhiguo Song

In order to make the most of solar energy, the development of efficient UV–Vis–NIR activated photocatalysts has attracted more and more attention. In this study, the UV–Vis–NIR broad spectrum activated photocatalysts La-doped BaBiO 2 Cl with abundant oxygen vacancies (OVs) were successfully prepared by solid state reaction . The experimental results and theoretical calculations revealed that La doping induced OVs in BaBiO 2 Cl, formed an intermediate level, extended the light absorption to the NIR region, and promoted carrier separation efficiency. Owing to the synergistic promotion effect, the optimal BaBiO 2 Cl–3%La exhibited obviously enhanced photodegradation rate, which was about 3.26 times higher than that of pure BaBiO 2 Cl under UV–Vis–NIR light irradiation . This work provides a resultful strategy for designing new full-spectrum-activated photocatalysts for environmental protection.

研究领域: 材料科学 · 环境科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Achieving improved full-spectrum responsive 0D/3D CuWO4/BiOBr:Yb3+,Er3+ photocatalyst with synergetic effects of up-conversion, photothermal effect and direct Z-scheme heterojunction

Xintong Yao,Xue Jiang,Dafeng Zhang,Shuya Lu,Mengyao Wang,Sihan Pan,Xipeng Pu,Junchang Liu,Peiqing Cai

The key to obtain effective photocatalysts is to increase the efficiency of light energy conversion, and thus the design and implementation of full-spectrum photocatalysts is a potential approach to solve this problem especially by extending the absorption range to near-infrared (NIR) light. Herein, the improved full-spectrum responsive CuWO 4 /BiOBr:Yb 3+ ,Er 3+ (CW/BYE) direct Z-scheme heterojunction was prepared. The CW/BYE with CW mass ratio of 5% had the best degradation performance, and the removal rate of tetracycline reached 93.9% in 60 min and 69.4% in 12 h under visible (Vis) and NIR light, respectively, which were 5.2 and 3.3 times of BYE. According to the outcome of experimental, the reasonable mechanism of improved photoactivity was put forward on the basis of (i) the up-conversion (UC) effect of Er 3+ ion to convert NIR photon to ultraviolet or visible light, which can be used by CW and BYE, (ii) the photothermal effect of CW to absorb the NIR light, increasing the local temperature of photocatalyst particle to accelerate the photoreaction, and (iii) the formed direct Z-scheme heterojunction between BYE and CW to boost the separation of photogenerated electron-hole pairs. Additionally, the excellent photostability of the photocatalyst was verified by cycle degradation experiments. This work opens up a promising technique for designing and synthesizing full-spectrum photocatalysts by utilizing synergetic effects of UC, photothermal effect and direct Z-scheme heterojunction.

研究领域: 材料科学 · 环境科学
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CERAMICS INTERNATIONAL · 2020 · IF 3.83

Construction of hollow TiO2/CuS nanoboxes for boosting full-spectrum driven photocatalytic hydrogen evolution and environmental remediation

Bo Yu,Fanming Meng,Ting Zhou,Aoyu Fan,Muhammad Wasim Khan,Hao Wu,Xingbin Liu

The plasma semiconductor Cu 2-x S has disclosed enormous potential in the field of broad-spectrum driven photocatalyst design due to its unique LSPR effect in the NIR region. Nevertheless, ineffective carrier separation and severe photocorrosion hinder the further functional applications of this promising material. Here, the TiO 2 @CuS double-shell nanoboxes were successfully constructed via a multistep control strategy involving template participation, and were firstly employed to broad-spectrum photocatalytic hydrogen evolution and pollutant elimination. The hollow core-shell nanocubes with LSPR effect have prominent advantages in broad-spectrum light response, improved photocharge separation and effective photocorrosion inhibition. Besides, the heterogeneous cavity structure also provides a larger specific surface area and ameliorates the light efficiency. Consequently, the optimized TiO 2 @CuS double-shell nanoboxes exhibit superior activity for H 2 production under full-spectrum/NIR light irradiation (2467 and 173 μmol g −1  h −1 , respectively), and maintain high activity in the photodegradation of stubborn pollutants. This work will motivate hollow photocatalysts designed to effectively utilize the spectrum and protect the sulfide core.

研究领域: 材料科学 · 环境科学 · 化学工程
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SEPARATION AND PURIFICATION TECHNOLOGY · 2020 · IF 5.774

Construction of dual ion (Fe3+/Fe2+ and Nb5+/Nb4+) synergy and full spectrum 1D nanorod Fe2O3/NaNbO3 photo-Fenton catalyst for the degradation of antibiotic: Effects of H2O2, S2O82− and toxicity

Chun Tong,Liquan Jing,Minqiang He,Meng Xie,Wei Wei,Yuanguo Xu,Hui Xu,Huaming Li

Designing a green and efficient catalyst to effectively degrade antibiotics is still one of the hot topics of research. Firstly, 1D nanorod Fe 2 O 3 /NaNbO 3 composite was successfully prepared by the two steps strategy through hydrothermal combined calcination method. In addition, the photocatalytic activity of the samples was evaluated by the degradation of tetracycline (TC) under visible light irradiation. The test results show that the 5% Fe 2 O 3 /NaNbO 3 nanorod material exhibits superior degradation rate of TC (89.4% removal efficiency in 90 min), and shows 5.62 times than that of NaNbO 3 nanorods. Under UV–visible light irradiation, 5% Fe 2 O 3 /NaNbO 3 nanorod composite with H 2 O 2 solution can degrade 97.4% of TC in 60 min, which is 12.1 times greater to that of the pure NaNbO 3 nanorods. The outstanding degradation performance may be attributed to the introduction of Fe 2 O 3 nanoparticles, which can activate H 2 O 2 more efficiently and produce more free radicals to degrade pollutants. At the same time, the 5% Fe 2 O 3 /NaNbO 3 nanorod composite can also act as an activate persulfate (PS) and generate SO 4 − to efficiently degrade TC. In addition, the catalyst also showed good performance in degrading TC in the presence of different anions and cations. Plant growth experiment ( mung bean seeds ) results showed that the degradation products have obvious lower toxicity. This study provides new domain about the designing of a photo-Fenton catalyst having dual ion synergy (Fe 3+ /Fe 2+ and Nb 5+ /Nb 4+ ) and full spectrum response.

研究领域: 环境科学 · 催化材料 · 污染控制
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Dual-engine mode based on defective ZnCdS/hierarchical NiCo2S4 for full-spectrum photocatalytic hydrogen evolution

Hanhan Lv,Daniel K. Macharia,Lisha Zhang,Nuo Yu,Yi Zhang,Yumei Zhang,Zhigang Chen,Seeram Ramakrishna

The development of efficient photocatalysts for solar-driven hydrogen production is crucial for addressing energy and environmental challenges. Herein, a full-spectrum responsive “dual-engine” photocatalytic system based on a multifunctional cocatalyst featuring electrons extraction, photothermal heating effect and abundant active sites was successfully designed. In this system, hierarchical NiCo 2 S 4 (NCS)/defective ZnCdS (ZCS-Vs) composite photocatalysts were synthesized through a simple physical mixing method with hierarchical NCS modified ZCS-Vs nanoparticles. Owing to the introduction of black hierarchical NCS, these composite photocatalysts show a wide light absorption range from 300 to 1200 nm due to the introduction of black hierarchical NCS. Under broad-spectrum illumination, the optimized photocatalyst delivered a maximum H 2 production rate of 22.19 mmol·g −1 ·h −1 and an apparent quantum yield of 6.29 % at 420 nm, corresponding to roughly a 42-fold improvement over pure ZCS-Vs. This outstanding H 2 evolution performance originates from three key factors. First, the metallic nature and high work function of NCS enable the formation of a Schottky junction with ZCS-Vs, which efficiently extracts photogenerated electrons from ZCS-Vs for the reduction of H + ions. Second, under photoexcitation, NCS exhibits a strong localized surface plasmon resonance (LSPR) effect, leading to a rapid increase in local temperature on the catalyst surface. This localized heating further elevates the overall reaction solution temperature, thereby reducing the energy barrier for photocatalytic H 2 evolution. Third, 3D hierarchical structure of NCS not only inhibits nanoparticle aggregation and provides abundant active sites, but also enhances light harvesting through internal scattering, thereby maximizing both charge separation and photothermal efficiency. Consequently, this “dual-engine” photocatalytic system provides a feasible pathway for designing photothermal-assisted composite photocatalysts to enhance photocatalytic H 2 evolution efficiency.

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APPLIED SURFACE SCIENCE · 2020 · IF 6.182

Insight into the relationship of the high photocatalytic performance and double photochromic activity of Z-scheme CsxWO3/AgBr heterostructures under UV–Vis-NIR light utilization

Ning Li,Xueyun Gao,Haikuan Fan,Yangqin Gao,Lei Ge

Effective and suitable utilization of solar energy was achieved using a full-spectrum-response photocatalyst AgBr/Cs x WO 3 , applied in the photocatalytic and photochromic field. Benefitting from near-infrared (NIR) absorption ability of Cs x WO 3 , AgBr/Cs x WO 3 exhibits enhanced visible-near-infrared (Vis-NIR) driven photocatalytic activity. Based on X-ray photoelectron spectroscopy (XPS), photoluminescence spectra (PL), and the photoelectrochemical analysis, AgBr and Cs x WO 3 formed a Z-scheme system at the interface to efficiently separate and transfer photo-induced electrons at a fast rate. The quenching experiment and the electron spin resonance (ESR) tests indicated that the photocatalytic reaction is activated by the production of superoxide radicals. Furthermore, the photochromic analysis to different light exhibits the AgBr/Cs x WO 3 heterostructure is stable under visible light with negligible photodeposition of AgBr, and has excellent double photochromic activity with visible-shielding effect of AgBr to Ag 0 and infrared-blocking effect of Cs x WO 3 under ultraviolet light. This research provides new insights into the manufacture of energy-efficient and environmentally friendly materials that provide excellent performance in both thermal insulation and decontamination.

研究领域: 材料科学 · 物理化学 · 纳米催化 · 光化学 · 功能材料 · 环境净化 · 能源材料
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ELECTROCHIMICA ACTA · 2019 · IF 5.383

Full-spectrum responsive photoelectrochemical immunoassay based on β-In2S3@carbon dot nanoflowers

Zhonghua Yu,Lingting Huang,Jialun Chen,Ying Tang,Biyun Xia,Dianping Tang

This work designed a new photoelectrochemical (PEC) immunoassay for the ultrasensitive detection of alpha-fetoprotein (AFP) based on the flower-like β-In 2 S 3 @carbon dots (CDs). The photocurrent of the as-prepared heterogeneous nanostructure was enhanced significantly under ultraviolet (UV), visible (Vis) and near-infrared (NIR) irradiation thanks to the more generation of carriers and less electron-hole pairs recombination with CDs. The three-layer sandwich-like immunocomplex would be formed upon the target AFP existed, the ascorbic acid 2-phosphate (AA2P) was subsequently transformed into ascorbic acid (AA) owing to the catalysis of alkaline phosphatase-conjugated rabbit polyclonal anti-human AFP (ALP-Ab2). Without additional applied voltage, the photocurrent of the β-In 2 S 3 @CDs-modified electrode was positively correlated with the increasing AA level in the detection cell. Under optimal conditions, the developed PEC immunosensing platform exhibited good reproducibility and high sensitivity for the determination of target AFP within a dynamic working range from 0.5 to 50 ng mL −1  at a detection limit of 37.9 pg mL −1 . In addition, the method accuracy relative to human AFP ELISA kit was evaluated by analyzing human serum specimens, and a good match between two methods was obtained. Such the increasing photocurrent through full-spectrum responsive mode gives a new horizon to develop highly sensitive PEC immunoassay in early clinical diagnosis by monitoring disease-related biomarkers.

CAS / MDL: 107-15-3 22519-64-8
研究领域: 分析化学 · 生物医学工程 · 临床诊断
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