CATALYSIS LETTERS
·
2021
·Vol. 151
·期 9
·2560-2569
·
IF 3.186
Han Jishu,Wang Ying,Liu Ying,Bai Jiayu,Zhao Ruiyang,Wang Lei
In this paper, novel CdSe/NH 2 -MIL-101(Cr) nanocomposites for photocatalytic hydrogen production were synthesized. When the prepared NH 2 -MIL-101(Cr) MOFs were modified with CdSe QDs, the photocatalytic hydrogen production amount was significantly increased and reached to 17,664 μmol g −1 in 7 h. The formation of CdSe/NH 2 -MIL-101(Cr) nanocomposites enhanced the light absorption intensity, broadened the visible light absorption range, promoted the transfer of photogenerated electrons and inhibited the recombination of photogenerated electron–hole pairs, then effectively improved the photocatalytic hydrogen production performance. In addition, the CdSe/NH 2 -MIL-101(Cr) nanocomposites exhibited high cycle stability, which was beneficial to the practical application in photocatalytic hydrogen production. Graphic Abstract
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Nano Research
·
2020
·Vol. 14
·期 8
·2574-2583
·
IF 8.183
Zhao Xiaojuan,Wan Houzhao,Liang Pei,Wang Nengze,Wang Cong,Gan Yi,Chen Xu,Tan Qiuyang,Liu Xiang,Zhang Jun,Wang Yi,Wang Hanbin,Wang Hao
High-rate battery-type cathode materials have attracted wide attention for advanced battery-supercapacitor hybrid (BSH) devices. Herein, a core-shell structure of the hollow mesoporous carbon spheres (HMCS) supported NiSe 2 nanosheets (HMCS/NiSe 2 ) is constructed through two-step reactions. The HMCS/NiSe 2 shows a max specific capacity of 1,153.5 C·g −1 at the current density of 1 A·g −1 , and can remain at 774.5 C·g −1 even at 40 A·g −1 (the retention rate as high as 67.1%) and then the HMCS/NiSe 2 electrode can keep 80.5% specific capacity after 5,000 cycles at a current density of 10 A·g −1 . Moreover, the density functional theory (DFT) calculation confirmed that the introduction HMCS into NiSe 2 made adsorption/desorption of OH − easier, which can achieve higher rate capability. The HMCS/NiSe 2 //6 M KOH//HMCS hybrid device has energy density of 47.15 Wh·kg −1 and power density of 801.8 W·kg −1 . This work provides a feasible electrode material with a high rate and its preparation method for high energy density and power density energy storage devices.
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Journal of Materials Chemistry A
·
2020
·Vol. 9
·期 4
·2292-2300
·
IF 11.301
Yafang Qi,Xiaoyue Zhao,Yao Liu,Dongxing Kou,Wenhui Zhou,Zhengji Zhou,Shengjie Yuan,Yuena Meng,Sixin Wu
In Cu2ZnSn(S,Se)4 photovoltaic devices, the exceptionally high density of 2CuZn + SnZn donor defects may induce bandgap fluctuations and thus limit Voc and PCE enhancement. We have previously reported that the partial substitution of Ag for Cu in Cu2ZnSn(S,Se)4 provides a promising way to effectively suppress CuZn defects and considerably enhance the cell performance for Cu2ZnSn(S,Se)4 photovoltaic devices. However, the bandgap fluctuations and detrimental band tailing fundamentally still limit cell performance. On the basis of a Ag-substituted CZTSSe system, in this paper, we demonstrate that partially substituting Zn with Mn could be a feasible tactic to pronouncedly decrease the bandgap fluctuations and prevent detrimental band tailing. Our in-depth investigation reveals that Mn substitution could increase depletion width, decrease the defect densities of the CuZn acceptor and 2CuZn + SnZn donor, and enable grain boundary (GB) inversion in a (Cu,Ag)2ZnSn(S,Se)4-based cell. As a result, an impressive PCE of 11.81% was achieved when the Mn substitution level was 10%, with a Voc of 478 mV, a Jsc of 37.89 mA cm−2, and an FF of 65.23%. This is so far the highest efficiency among Mn-substituted CZTSSe-based photovoltaic devices. By thoroughly understanding these photoelectric properties of the CZTSSe-based photovoltaic devices, we believe that the breakthrough in device efficiency will come soon through our continuous efforts.
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Journal of Materials Chemistry A
·
2020
·Vol. 9
·期 1
·413-422
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IF 11.301
Xiaohuan Chang,Junjie Fu,Dongxing Kou,Wenhui Zhou,Zhengji Zhou,Shengjie Yuan,Yafang Qi,Zhi Zheng,Sixin Wu
The introduction of alkali metal (AM) post-deposition treatment (PDT) has led to the consecutive breakthrough of world record efficiencies for Cu(In,Ga)Se2 photovoltaics. However, for the derivative Cu2SnZn(S,Se)4 (CZTSSe) solar cells, the corresponding verdict seems partially unjustified due to the difference in defect chemical environment and phase structure, and the most effective incorporation means of AMs is still a mystery. In this work, for the first time, we developed a dual AM synergistic incorporation strategy combining light and heavy AMs by post-depositing CsF after NaF-PDT to improve the efficiency of CZTSSe solar cells. The relevant microscopic-electrical advantages with regard to the different roles of NaF and CsF PDT are discussed in more detail. It was found that the Na atoms are randomly dispersed both in the grain interior (GI) and grain boundaries (GBs), significantly increasing the acceptor concentration and passivating the deep level defects to enhance the Voc. In contrast, the Cs atoms are mainly segregated at the GBs, primarily increasing the potential of the GBs and improving the FF. The prominent electric benefits of Cs at the GBs and Na in the GI finally increase the device efficiency from 10.12% to 12.16%. Our findings solve the difficulty in obtaining the available Voc and FF for future high efficiency research and should serve as a basis for the in-depth understanding of AM-PDT in kesterite photovoltaics.
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Small
·
2020
·Vol. 16
·期 48
·2004457
·
IF 11.459
Cai Liu,Miaoxin Zhang,Xin Zhang,Biao Wan,Xiaona Li,Huiyang Gou,Yexin Wang,Fuxing Yin,Gongkai Wang
Nano heterostructures relying on their versatile construction and the breadth of combined functionality have shown great potential in energy storage fields. Herein, 2D sandwiched MoSe 2 /TiO 2− x /graphene nano heterostructures are designed by integrating structural and functional effects of each component, aiming to address the rate capability and cyclic stability of MoSe 2 for sodium ion capacitors (SICs). These 2D nano heterostructures based on graphene platform can facilitate the interfacial electron transport, giving rise to fast reaction kinetics. Meanwhile, the 2D open structure induces a large extent of surface capacitive contribution, eventually leading to a high rate capability (415.2 mAh g −1 @ 5 A g −1 ). An ultrathin oxygen deficient TiO 2− x layer sandwiched in these nano heterostructures provides a strong chemical-anchoring regarding the products generated during the sodiation/desodiation process, securing the entire cyclic stability. The associated sodiation/desodiation mechanism is revealed by operando and ex situ characterizations, which exhibits a strong solid electrolyte interphase (SEI) dependence. The simulations verify the dependent sodiation products and enhanced heterostructural chemical-anchoring. Assembled SICs based on these nano heterostructures anode exhibit high initial Coulombic efficiency, energy/power densities, and long cycle life, shedding new light on the design of nano heterostructure electrodes for high performance energy storage application.
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高影响因子
JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2020
·
IF 3.807
KaiBo Zhang,XiaoBing Jiang,Min Zeng,Bo Jing
Lithium-ion batteries have progressively taken the place of conventional power sources and been extensively employed in our daily lives. In this study, a simple hydrothermal method was adopted to develop the two-dimensional layered MoSe 2 into three-dimensional porous microspheres and nanosphere structures hydrangea-like via directional polymerization, self-assembly and Ostwald maturation. Subsequently, the dopamine hydrochloride was polymerized and carbonized to modify the curd-shaped MoSe 2 by N-doped carbon coating. The modified MoSe 2 @N-C anode material exhibited a larger specific capacity, better stability and a higher rate at high current density than MoSe 2 anode material. The modified negative electrode material achieved the specific capacity of 553 mAh/g at a current density of 1 A/g and 300.8 mAh/g at 10 A/g. Under high current density, the long-cycle charge-discharge performance test was performed, and the modified material exhibited a significantly large specific capacity and high stability performance. Its electrochemical performance was enhanced due to the N-doped carbon coating layer on the surface that increased the material conductivity and reduced the shuttle effect of polyselenide.
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CHEMISTRY OF MATERIALS
·
2020
·
IF 9.567
Dong Li,Xiaoli Zhang,Muhammad Ramzan,Kai Gu,Yu Chen,Jiatao Zhang,Bingsuo Zou,Haizheng Zhong
Shell thickness control of core/shell quantum dots (QDs) plays an important role in determining their optical properties as well as the corresponding device performance. PbSe-based core/shell QDs are attractive near-infrared (NIR) light emitters for photonic and optoelectronic applications. We herein report the colloidal synthesis of giant shell PbSe-based core/shell QDs through controllable reactions between preformed PbSe QDs and Cd2+ ions in polar solvents. The preformed PbSe QDs experienced cation-exchange reaction in N,N-dimethylformamide (DMF), while they underwent epitaxial growth of CdS shell in dimethyl sulfoxide (DMSO). The cation exchange of preformed PbSe QDs in DMF result in PbSe/CdSe core/shell QDs with similar size (ca. 6.3 nm) but tunable shell thickness from 0.5 to 2.9 nm. In comparison, the epitaxial growth of preformed PbSe QDs in DMSO produce PbSe/CdS core/shell QDs in DMSO with average core size of ∼5.7 nm but tunable shell thickness from 0.5 to 3.1 nm. These resulting PbSe-based core/shell QDs show tunable photoluminescence emission of 1393–1744 nm for PbSe/CdSe core/shell QDs and 1566–1719 nm for PbSe/CdS core/shell QDs. The cation exchange and epitaxial growth reactions of preformed PbSe QDs were further investigated by comparing the interactions between solvents and cation ions through nuclear magnetic resonance (NMR) measurements. The interactions between Cd2+ and DMSO are stronger than that of DMF, while the interactions between Pb2+ and DMSO are weaker than that of DMF. The difference accounts for the reaction transition from cation exchange to epitaxial growth, providing alternative route for fabricating shell controllable PbSe-based core/shell QDs.
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ACS Applied Nano Materials
·
2020
·
IF 0
He Tian,Xiancheng Meng,Juehan Yang,Chao Fan,Shuo Yuan,Xia An,Chun Sun,Yonghui Zhang,Mengjun Wang,Hongxing Zheng,Zhongming Wei,Erping Li
Two-dimensional (2D) nanomaterials have been attracting intensive interest due to their unique physical and optoelectronic properties. Van der Waals nanolayered heterostructures based on different 2D nanomaterials provide a state-of-the-art platform for investigating the physical phenomena and have extended the applications of 2D nanomaterials, leading to an era of next-generation high-performance electronic and optoelectronic technology. Herein, vertical 2D SnS/SnS2 p–n and SnSe2/SnS2 n–n nanolayered heterostructures are constructed by exfoliating individual materials and stacking them artificially. The two types of back-gate field-effect phototransistors show clear rectifying behaviors with the existence of band offset and excellent optoelectronic performances. The SnS/SnS2 p–n nanolayered heterostructure shows an ambipolar behavior with a hole mobility of 6.96 cm2·V–1·s–1 and electron mobility of 0.68 cm2·V–1·s–1, while the SnSe2/SnS2 n–n nanolayered heterostructure shows an intense n-type behavior with electron mobility of 3.78 cm2·V–1·s–1 and a high on/off ratio of over 105. Interestingly, due to the band alignments and built-in potentials in the two types of nanolayered heterostructures, the phototransistors exhibit enhanced responsive performances to illuminations of three-primary-color lasers (λ = 405, 532, and 650 nm) compared to the individual components. The SnS/SnS2 phototransistor shows a high photoresponsivity of 3567 A W–1, a high detectivity of 3.64 × 1013 Jones, and a fast response time of 0.8 ms. The SnSe2/SnS2 phototransistor also exhibits a high photoresponsivity of 1793 A W–1 and a fast response time of 15.4 ms.
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APPLIED CATALYSIS B-ENVIRONMENTAL
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2020
·
IF 16.683
Zong Liu,Chengzhe Zhang,Hui Liu,Ligang Feng
Herein, we highlighted that a catalyst system of NiSe 2 nanoparticle/NiO nanosheet catalyst exhibited efficient synergism for energy and environmental-relevant urea-assisted water electrolysis reactions. The spectral study and microscopic analysis demonstrated the formation of NiSe 2 nanoparticle/NiO nanosheet heterostructure and efficient Ni O bond and Ni Se bond synergism. Owing to various factors such as the strong synergetic coupling effects between NiSe 2 nanoparticle and NiO nanosheet, unique structure features, increased active sites and amount of intrinsic Ni 3+ ions, efficient synergism was found on the NiSe 2 Nanoparticle/NiO nanosheet for urea-assisted water electrolysis by comparing with the NiSe 2 Nanoparticle and NiO nanosheet alone. It required a cell voltage of 1.39 V, about 210 mV less than that of water electrolysis, confirming the less energy consumption during the electrolysis. Notably, it also shows remarkably superior long-term durability. The current work may extend the nanoparticle-nanosheet catalysts system for simultaneous wastewater treatment and clean energy production.
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BIOMATERIALS
·
2020
·
IF 10.317
Jichun Yang,Shuojiong Pan,Shiqian Gao,Yiheng Dai,Huaping Xu
Thioredoxin reductase (TrxR) is an essential mammalian enzyme that possesses a selenocysteine active site. TrxR is overexpressed in many malignant tumors and has a close relationship with apoptosis, drug resistance, recurrence and metastasis of tumors. Recently, TrxR has emerged as a promising target for anticancer therapy. Herein, we developed a TrxR-interfering drug delivery system (DDS) based on RGD-PEG-PUSeSe-PEG-RGD self-assembling micelles for imaging-guided gemcitabine (GEM) chemosensitization and anti-recurrence/metastasis therapy. The diselenide-containing micelles were degraded in response to TrxR stimuli for GEM releasing. In the meantime, the dissociated polymers’ chain segments targeted the active site of TrxR via Se–Se/Se–S dynamic reactions for activity inhibition. This inhibition by the micelles not only provided chemosensitization, but reduced tumor recurrence/metastasis risk via the induction of residual tumor cell apoptosis by triggering ROS production post-chemotherapy. In this work, we took the transformation between Se-containing dynamic covalent bonds developed by our group from in vitro to in vivo , which furthered the knowledge on the biochemistry of selenium and provided aspects to develop new TrxR inhibitors. Overall, the TrxR-interfering DDS combined excellent antitumor effects for primary solid tumors with the inhibition of tumor recurrence/metastasis during post-treatment care, providing new perspectives for efficient cancer therapy.
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Journal of Materials Chemistry B
·
2020
·Vol. 8
·期 30
·6451-6458
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IF 5.344
Daomeng Liu,Daquan Wang,Xunan Jing,Xiaoping Zhao,Duo Xi,Dongfeng Dang,Lingjie Meng
Nanozymes are a new generation of artificial enzymes that address the limitations of natural enzymes, with numerous reports on the development of high performance nanozymes for various applications. Herein, the phase regulation of network-like MoSe2 from the metal 1T phase to semiconductor 2H phase was achieved under different reaction conditions by a facile but efficient microwave-assisted solvothermal method. The coexisting 1T/2H-MoSe2 with edge enriched and defective nanostructures showed great enhancement of the peroxidase-like properties. This high enzymatic activity may arise from optimized active sites of 1T/2H-MoSe2, effectively leading to a rapid charge transfer within the substrate. In addition, chitosan functionalization not only greatly improves the dispersion stability of MoSe2, but also significantly increases its peroxidase-like activity, probably due to its enhanced affinity to hydrogen peroxide (H2O2). Based on these results we have established a highly sensitive colorimetric assay for the detection of H2O2 and glucose in human serum.
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高影响因子
Nanomaterials
·
2020
·Vol. 10
·期 4
·631
·
IF 4.324
Zhen Li,Libo Yu,Hao Wang,Huiwen Yang,Huan Ma
Light harvesting and electron recombination are essential factors that influence photovoltaic performance of quantum dots sensitized solar cells (QDSSCs). ZnO hollow microspheres (HMS) as architectures in QDSSCs are beneficial in improving light scattering, facilitating the enhancement of light harvesting efficiency. However, this advantage is greatly weakened by defects located at the surface of ZnO HMS. Therefore, we prepared a composite hollow microsphere structure consisting of ZnO HMS coated by TiO2layer that is obtained by immersing ZnO HMS architectures in TiCl4aqueous solution. This TiO2-passivated ZnO HMS architecture is designed to yield good light harvesting, reduced charge recombination, and longer electron lifetime. As a result, the power conversion efficiency (PCE) of QDSSC reaches to 3.16% with an optimal thickness of TiO2passivation layer, which is much higher when compared to 1.54% for QDSSC based on bare ZnO HMS.Keywords:TiO2passivation layer;ZnO hollow microspheres;quantum dots sensitized solar cells
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