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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2023 · IF 9.9

Facile construction of robust Ru-Co3O4 Mott-Schottky catalyst enabling efficient dehydrogenation of ammonia borane for hydrogen generation

Jing Jiang,Wei Wei,Zhen Ren,Yang Luo,Xinzhi Wang,Ying Xu,Mingming Chang,Lunhong Ai

Developing efficient catalysts for the dehydrogenation of ammonia borane (AB) is important for the safe storage and controlled release of hydrogen, but it is a challenging task. In this study, we designed a robust Ru-Co 3 O 4 catalyst using the Mott-Schottky effect to induce favorable charge rearrangement. The self-created electron-rich Co 3 O 4 and electron-deficient Ru sites at heterointerfaces are indispensable for the activation of the B-H bond in NH 3 BH 3 and the O H bond in H 2 O, respectively. The synergistic electronic interaction between the electron-rich Co 3 O 4 and electron-deficient Ru sites at the heterointerfaces resulted in an optimal Ru-Co 3 O 4 heterostructure that exhibited outstanding catalytic activity for the hydrolysis of AB in the presence of NaOH. The heterostructure had an extremely high hydrogen generation rate (HGR) of 12238 mL min −1 g cat -1 and an expected high turnover frequency (TOF) of 755 mol H2 mol Ru -1 min −1 at 298 K. The activation energy needed for the hydrolysis was low (36.65 kJ mol −1 ). This study opens up a new avenue for the rational design of high-performance catalysts for AB dehydrogenation based on the Mott-Schottky effect.

研究领域: 催化化学 · 能源材料 · 纳米材料科学 · 表面科学 · 氢能源技术
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APPLIED SURFACE SCIENCE · 2016 · IF 3.15

One-dimensional Fe2O3/TiO2 photoelectrode and investigation of its photoelectric properties in photoelectrochemical cell

Xi-Ming Song,Xin Zhou,Chunxue Yuan,Yu Zhang,Qiang Tong,Ying Li,Luxia Cui,Daliang Liu,Wei Zhang

We reported a novel Fe 2 O 3 /rutile TiO 2 nanorod (NR) arrays with the heterogeneous structure for photoelectrochemical (PEC) cells, which were fabricated on fluorine-doped tin oxide glass (FTO) substrates that serve as model architecture via a hydrothermal method. Fe 2 O 3 was revealed as an inexpensive and eco-friendly semiconductor sensitizer to make TiO 2 respond to visible light . By using this photoanode, the photoelectric conversion and water splitting properties of PEC cells based on the one-dimensional (1D) Fe 2 O 3 /TiO 2 heterostructures were investigated in detail under simulated sunlight. Meanwhile, the optimization of photovoltaic performance was also achieved by regulating the amount of Fe 2 O 3 . The open circuit voltage and short circuit current of the Fe 2 O 3 /TiO 2 solar cell can reach 0.435   V and 1.840   mA/cm 2 , respectively. In addition, theoretical analysis of the photoelectric effect is preliminarily explored on the basis of the flat band potential results.

研究领域: 材料科学 · 物理化学 · 能源科学 · 纳米科技 · 光催化
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OPTICAL MATERIALS · 2024 · IF 3.8

Facile sulfur-assisted synthesis of GaAs nanowires /si heterojunctions for broadband self-powered photodetector

Zhi Yang,Shufang Ma,Yu Shi,Xiaodong Hao,Lin Shang,Bin Han,Bocang Qiu,Bingshe Xu

Nanowires (NWs)-based heterojunction photodetectors (PDs) have been widely applied in the fields of remote sensing, night vision, environmental monitoring, and optical communications with high light absorption coefficient and photoelectric conversion efficiency. Here, S-GaAs NWs/Si heterojunction was developed to form a broadband self-powered PDs by growing GaAs NWs on Si substrate through the sulfur-catalyzed assisted chemical vapor deposition (CVD) technology. Compared with the pure GaAs NWs, the sulfur-assisted catalysts could not only inhibit Ostwald ripening of Au seeds to improve the crystalline quality of NWs but also form a thin Ga–S bond passivation layer to reduce surface defects and enhance the optoelectronic performance of the PDs. The fabricated GaAs NWs/Si heterojunction PDs exhibit excellent performances with the large responsivity of 10.3 mA W −1 and high detectivity of 9.59 × 10 12  cm Hz 1/2  W −1 . Additionally, the designed PDs have the broadband wavelength photoresponse from visible to near infrared and fast response speed (rise/fall time of 3.8/21.8 ms). Importantly, the develop strategy of hybrid heterojunction PDs can be extended to other semiconductor materials for facilitating the practical application of high-performance optoelectronic devices .

研究领域: 半导体材料 · 纳米电子学 · 光电子学 · 凝聚态物理 · 功能材料 · 器件物理
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CHEMICAL ENGINEERING JOURNAL · 2020 · IF 10.652

Interface engineering induced selenide lattice distortion boosting catalytic activity of heterogeneous CoSe2@NiSe2 for lithium-oxygen battery

Ranxi Liang,Chaozhu Shu,Anjun Hu,Minglu Li,Zhiqun Ran,Ruixin Zheng,Jianping Long

The sluggish oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) kinetics greatly limit the development of lithium-oxygen (Li-O 2 ) batteries. Therefore, developing efficient electrocatalysts with high stability to boost oxygen involved reactions is particularly important for promoting the application of Li-O 2 batteries. Here, CoSe 2 @NiSe 2 heterostructure with distinct heterogeneous interfaces was fabricated via deliberate interface engineering. The formation of heterogeneous interface promotes local fine atomic array distortion that can act as an additional active site of ORR/OER. In addition, CoSe 2 @NiSe 2 with a distinct heterogeneous interface is favorable for the formation of built-in electric field during charging/discharging to enable electrodes with fast electrical transfer rates and reaction kinetics. Synergistically, the additional active sites brought by the fine atomic array distortion are highly conducive to the reversible formation and decomposition of the product. Undoubtedly, batteries with CoSe 2 @NiSe 2 exhibit excellent discharge/charge capacity (3530.1 mA h g −1 and 3485.6 mA h g −1 ), low overpotential (1.21 V) and excellent electrochemical stability for over 1200 h.

研究领域: 材料科学 · 电化学 · 能源化学 · 纳米催化 · 电池技术
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Small · 2023 ·Vol. 20 ·期 14 ·2306666 · IF 13.3

Exceptional Hole-Selective Properties of Ta2O5 Films via Sn4+ Doping for High Performance Silicon Heterojunction Solar Cells

Wuqi Liu,Wang Fu,Yaju Wei,Guoqiang Yu,Tao Wang,Lingbo Xu,Xiaoping Wu,Ping Lin,Xuegong Yu,Can Cui,Peng Wang

Carrier-selective passivating contacts using transition metal oxides (TMOs) have attracted great attention for crystalline silicon (c-Si) heterojunction solar cells recently. Among them, tantalum oxide (Ta 2 O 5 ) exhibits outstanding advantages, such as a wide bandgap, good surface passivation, and a small conduction band offset with c-Si, which is typically used as an electron-selective contact layer. Interestingly, it is first demonstrated that solution-processed Ta 2 O 5 films exhibit a high hole selectivity, which blocks electrons and promotes hole transport simultaneously. Through the ozone pre-treatment of Ta 2 O 5 /p-Si interface and optimization of the film thickness (≈9 nm), the interfacial recombination is suppressed and the contact resistivity is reduced from 178.0 to 29.3 mΩ cm 2 . Moreover, the Sn 4+ doping increases both the work function and oxygen vacancies of the film, contributing to the improved hole-selective contact performance. As a result, the photoelectric conversion efficiencies of Ta 2 O 5 /p-Si heterojunction solar cells are significantly improved from 14.84% to 18.47%, with a high thermal stability up to 300 °C. The work has provided a feasible strategy to explore new features of TMOs for carrier-selective contact applications, that is, bipolar carrier transport properties.

研究领域: 材料科学 · 光伏技术 · 半导体器件 · 表面物理 · 纳米材料 · 能源材料
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Journal of Environmental Chemical Engineering · 2021 ·Vol. 9 ·期 4 ·105292 · IF 5.909

0D/1D Z-scheme g-C3N4 quantum dot/WO3 composite for efficient Cr (VI) photoreduction under visible light

Jie Zhou,Wenyi Cai,Jing Ding,Hui Wan,Guofeng Guan

The appropriate construct of Z-scheme heterostructure composite with high photocatalytic activity has created new opportunities for environmental protection. Herein, graphitic carbon nitride quantum dots/tungsten trioxide (CNQDs/WO 3 ) was firstly fabricated using CNQDs decorated onto the surface of WO 3 nanorod grown along the [110] orientation in hydrothermal environment to construct a Z-scheme heterostructure composite. By various characterization methods, the crystal structure, micro morphology, atomic valence state and surface functional groups of the catalyst were systematically revealed. The results indicated that Z-scheme heterojunctions between CNQDs and WO 3 were successfully constructed. Compared with pure WO 3 , CNQDs/WO 3 exhibited prominent photoreduction performance under visible light irradiation. The optimal 5% CNQDs/WO 3 could reduce almost 100% Cr (VI) under acidic condition with the best photocatalytic activity within 90 min. More than this, 5% CNQDs/WO 3 also displayed excellent stability and recyclability even after five cycles of photoreduction experiments. Based on the free radical quenching experiments, the possible photoreduction reaction mechanism had been proposed in detail. The Z-scheme heterostructure provided the possibility of the generation, rapidly transfer and efficient separation of photogenerated electrons, which were major active species in the Cr (VI) photoreduction process.

研究领域: 环境催化 · 材料化学 · 纳米科技 · 光催化 · 环境污染治理 · 半导体异质结
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2019 · IF 14.229

In-situ synthesis of monodispersed CuxO heterostructure on porous carbon monolith for exceptional removal of gaseous Hg0

Liyuan Zhang,Shu Yang,Yuekun Lai,Hui Liu,Yiang Fan,Cao Liu,Haiying Wang,Liyuan Chai

Gaseous Hg 0 is one of the most deadly and hard-to-dispose pollutants. The oxidation of Hg 0 is a promising route, but the rational design and synthesis of highly efficient catalysts still remain grand challenges. Herein, CuO@Cu 2 O (or Cu x O) heterostructured nanoparticles uniformly monodispersing on porous carbon monolith were designed and successfully synthesized using oligo( m -phenylenediamine)-Cu 2+ complex as raw material. The Cu x O-carbon catalyst contains ∼28 wt% of Cu. Based on density functional theory calculation, the CuO@Cu 2 O junction interfaces can accelerate the Hg 0 oxidation by significantly reducing the energy barriers of reaction. Only 1 mg of the catalyst can catalyze the oxidation of more than 90 % of Hg 0 with [HCl] = 0.5 ppm, [O 2 ] = 6 vol%, T = 150 °C. The poisoning effect of either SO 2 or H 2 O on the catalysts is weak. Moreover, a long-term test confirmed that the Hg 0 oxidation rate can maintain more than 90 % even in the co-presence of SO 2 (5000 ppm) and H 2 O (10 vol%).

研究领域: 环境催化 · 材料化学 · 大气污染控制 · 纳米材料 · 表面科学
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Nano Energy · 2019 · IF 15.548

Elevated polysulfide regulation by an ultralight all-CVD-built ReS2@N-Doped graphene heterostructure interlayer for lithium–sulfur batteries

Nan Wei,Jingsheng Cai,Ruochen Wang,Menglei Wang,Wei Lv,Haina Ci,Jingyu Sun,Zhongfan Liu

Lithium–sulfur battery is amongst the most promising next-generation energy storage technology owing to their high theoretical capacity and energy density . Nevertheless, the notorious shuttle effect of lithium polysulfides (LiPSs) seriously impedes its practical applications. Here, we report an all-CVD approach to realize the direct growth of ReS 2 @N-doped graphene (NG) heterostructure , which serves as an ultralight high-performance interlayer for elevated LiPS regulation via easy transfer onto the commercial separator. In contrast to the traditional interlayers constructed via vacuum filtration of nanostructured materials that inevitably increase the thickness and weight of the separator, our all-CVD-enabled ReS 2 @NG film possesses an area of 15 mm × 100 mm, a thickness of ~0.5 μm and a negligible areal weight of 80–90 μg cm −2 . Benefiting from the two-dimensional (2D) vertically-erected nanostructure , adsorptive ReS 2 -conductive NG interface, and favorable electrical conductivity , thus-derived ReS 2 @NG interlayer readily enhances reaction kinetics for LiPS conversion and boosts the reutilization of trapped LiPS whilst guaranteeing smooth transportation of lithium ions . Accordingly, an initial discharge capacity of 854 mAh g −1 with an average capacity decay of 0.064% per cycle after 800 cycles can be harvested at 2.0 C. Even at a high sulfur loading of 6.4 mg cm −2 , an initial areal capacity of 6.1 mAh cm −2 can be gained, which still retains 5.8 mAh cm −2 after 40 cycles at 0.1 C. This work is anticipated to shed light upon the construction of CVD-enabled versatile 2D heterostructures for enriching the interlayer design with multifunctionality and cost-effectiveness.

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米材料 · 界面工程 · 电池技术
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2018 · IF 5.091

Colloidal Cu2ZnSn(S1-x,Sex)4-Au nano-heterostructures for inorganic perovskite photovoltaic applications as photocathode alternative

Shuai Ma,Lifeng Dong,Hongzhou Dong,Jie Wang,Yingjie Chen,Beili Pang,Jianguang Feng,Liyan Yu,Mei Zhao

We concretely report feasible synthesis procedures of colloidal Cu 2 ZnSn(S 1- x ,Se x ) 4 -Au (CZTSSe-Au) nano-heterostructured composites, and creatively employ them as the counter electrodes (CEs) of all-solid-state solar cells with inorganic CsSnI 2.95 F 0.05 perovskite hole conductor. Acquired optical characterization indicates that integration of noble metal nanoparticles with cuprum-chalcogenide could heighten light absorption within visible-band due to localized surface plasmon resonance (LSPR) generated by Au, and the forbidden gap of nanocomposites gets adjustment accordingly. It is demonstrated that this novel photocathode alternative with favorable conductivity can not only match the energy level within the device band structure construction, but also restrain recombination so that accelerate charge transfer and extraction occurring on the photocathode. The photocurrent and photoelectric conversion efficiency (PCE) of cells conjugating CZTS-Au photocathodes turn to be respectively 43% and 25% higher than those using pure CZTS. Moreover, it has been demonstrated that CZTS-Au, coupling very well with inorganic perovskite, owns comparable electrocatalytic performance and even higher output photocurrent with respect to platinum CEs, which portends a potential substitution for conventional costly photocathodes. A comprehensive analysis on impedance spectroscopy data is subsequently carried out for the sake of deep understanding charge accumulation and transfer response at CsSnI 2.95 F 0.05 /CE interface, attempting to orient further optimization of device performance.

研究领域: 材料科学 · 能源科学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2014 · IF 6.007

Single-crystalline AgIn(MoO4)2 nanosheets grafted Ag/AgBr composites with enhanced plasmonic photocatalytic activity for degradation of tetracycline under visible light

Xu Yan,Xiyou Wang,Wei Gu,MiaoMiao Wu,Yan Yan,Bo Hu,Guangbo Che,Donglai Han,Jinghai Yang,Weiqiang Fan,Weidong Shi

Single-crystalline AgIn(MoO 4 ) 2 nanosheets have been successfully fabricated by facile hydrothermal method without any surfactants. Subsequently, Ag/AgBr-grafted AgIn(MoO 4 ) 2 nanosheets were synthesized by the in situ photoreduction of AgBr/AgIn(MoO 4 ) 2 composites prepared by a deposition–precipitation method. Under visible light irradiation. The Ag/AgBr/AgIn(MoO 4 ) 2 composites exhibit a strong absorbance in the visible region because of the surface plasmon resonance absorption of Ag nanocrystals. Compared with bare AgIn(MoO 4 ) 2 nanosheets, Ag/AgBr nanoparticles and Ag/AgIn(MoO 4 ) 2 composites, a dramatic enhancement in the degradation rate of tetracycline (TC) is observed over the Ag/AgBr/AgIn(MoO 4 ) 2 composites. The immense enhancement of the photocatalytic activity is attributed to the extended absorption in the visible-light region, effective charge separation, and synergistic enhancement induced by surface plasmon resonance (SPR) in the heterostructured Ag/AgBr/AgIn(MoO 4 ) 2 . This study provides new insight into the fabrication of highly efficient and stable ternary metal molybdate based plasmonic photocatalysts and facilitates their practical application to solve environmental issues. The mechanism for the photodegradation of TC over Ag/AgBr/AgIn(MoO 4 ) 2 is discussed in detail.

研究领域: 材料科学 · 环境化学 · 光催化 · 纳米材料 · 无机化学 · 物理化学
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SURFACE & COATINGS TECHNOLOGY · 2023 · IF 5.4

Gradient multilayer interface–coupled FeNi@C@SiO2 for enhanced anti–corrosion and preeminent microwave absorption

Yang Guo,Xiaoying Guo,Haipeng Lu,Xian Jian

Developing high–efficient microwave absorbing (MA) materials with anti–corrosion (AC) properties to tackle the harsh hygrothermal marine conditions remains a challenge. Herein, we employed catalytic chemical vapor deposition and the Stöber technique to fabricate gradient multilayer interface–coupled FeNi@C@SiO 2 composites, guided by the hetero–interface engineering. The resulting composites exhibited exceptional MA properties and AC behavior. Specifically, they showcased a remarkable effective absorption bandwidth of 6.27 GHz at 1.40 mm, outperforming that of FeNi (3.80 GHz). This improved bandwidth was attributed to the electron conduction pathway provided by the C layer, which facilitated electron migration and hopping. The C@SiO 2 layer, containing defects and –OH functional groups, induced abundant dipole polarization and optimizes the impedance matching of FeNi. Furthermore, the RCS reduction value of FeNi@C@SiO 2 could reach 16.73 dB·m 2 . Moreover, the corrosion rate of FeNi@C@SiO 2 was 7.48 × 10 −11  m/s, significantly lower than that of FeNi (1.29 × 10 −10  m/s). This reduction was primarily due to the intrinsic inertness and impermeability of the C@SiO 2 layer, effectively isolating the corrosive medium from the substrate. This investigation presents a novel point of reference for the advancement of bifunctional MA materials intended to cope with extreme environments.

研究领域: 材料科学 · 纳米复合材料 · 表面工程 · 电磁功能材料 · 腐蚀防护
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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2022 ·Vol. 47 ·期 33 ·14916-14929 · IF 7.139

A nano-spherical structure Ni3S2/Ni(OH)2 electrocatalyst prepared by one-step fast electrodeposition for efficient and durable water splitting

Hongzhi Wang,Chunxiao Wang,Weiguo Zhang,Suwei Yao

Developing non-noble metal catalysts with excellent electrocatalytic performance and stability is of great significance to hydrogen production by water electrolysis, but there are still problems of low activity, complex preparation and high cost. Herein, we fabricated a novel Ni 3 S 2 /Ni(OH) 2 dual-functional electrocatalyst by a one-step fast electrodeposition on nickel foam (NF). While maintaining the electrocatalytic performance of Ni 3 S 2 , the existence of heterostructure and Ni(OH) 2 co-catalyst function greatly improves the overall water splitting performance of Ni 3 S 2 /Ni(OH) 2 –NF. Hence, It shows a low overpotential of 66 mV at 10 mA cm −2 for HER and 249 mV at 20 mA cm −2 for OER. The dual-functional electrocatalyst needs only 1.58 V at 20 mA cm −2 when assembled two-electrode electrolytic cell. Impressively, the electrocatalyst also shows outstanding catalytic stability for about 800 h when 20 and 50 mA cm −2 constant current was applied, respectively which demonstrates a potential electrocatalyst for overall water splitting.

研究领域: 材料科学 · 电化学 · 能源催化 · 纳米材料 · 可持续能源 · 功能材料 · 界面化学
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