ACS Sustainable Chemistry & Engineering
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2021
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IF 8.198
Shen-Gen Gong,Yan-Hong Shi,Yang Su,Yan-Fei Li,Lei Ding,Jian Lin,Guo-Duo Yang,Bing Li,Xing-Long Wu,Jing-Ping Zhang,Hai-Ming Xie,Hai-Zhu Sun
Flexible asymmetric supercapacitor (FASC) systems are expected to exhibit not only excellent energy storage properties and safety but also satisfactory flexibility and robust integration. However, tremendous issues such as low capacitance, narrow voltage window, and poor mechanical properties still exist. In this paper, a novel kind of 3D lamellar Mn(OH)2 nanosheets on Cu-plated carbon cloth with a core-shell integrated framework (CPCC@CuO@Mn(OH)2) is fabricated to obtain the flexible material in the FASC. In this unique CPCC@CuO@Mn(OH)2 electrode material, the high theoretical specific capacity of CuO and Mn(OH)2 brings superior energy storage properties. Meanwhile, as the shell part, the deposited Mn(OH)2 layer and coated CuO layer work as both capacity contributors and substrate protectors, simultaneously maintaining the high capacitance and satisfactory flexibility of the electrodes. Therefore, the capacitance successfully achieves around 8140 mF cm–2 under 0.5 mA cm–2. Significantly, the assembled FASC (named as CPCC@CuO@Mn(OH)2//CC@AC) achieves a working voltage of up to 2.4 V. In the case of a high-power density close to 34.31 mW cm–3, its energy density reaches around 6.29 mW h cm–3. Moreover, the capacity holds 88.9% even after 10,000 cycles, showing its great application potential in the field of wearable electronics.
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高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
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2018
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IF 11.698
Shanshan Su,Chengjin Cao,Yaping Zhao,Dionysios D. Dionysiou
Roxarsone (ROX) is extensively used as a feed additive which tends to leave toxic inorganic arsenic (As) in the natural environment. A composite of reduced graphene oxide and carbon nanotubes was impregnated with goethite designated as α-FeOOH@GCA and tested as an integrated catalyst and adsorbent for ROX decontamination. Nearly 100% of the ROX was transformed in α-FeOOH@GCA activating persulfate (PS) under UV 365 irradiation system at relatively low dosage of the α-FeOOH@GCA catalyst (250 mg L −1 ) in 120 min. The As(V) released in the ROX oxidation was simultaneously adsorbed onto the surface of the α-FeOOH@GCA. A possible ROX transformation pathway is proposed. The As(V) adsorbed on catalyst was recovered and used to form an efficient Ag 3 AsO 4 photocatalyst. This work further extends the oxidation-adsorption technology in solving organoarsenical contamination without producing secondary pollution.
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高影响因子
Nature Communications
·
2025
·Vol. 16
·期 1
·1-19
·
IF 15.7
Tang Yizhang,Yu Xujiang,He Liangrui,Tang Meng,Yue Wenji,Chen Ruitong,Zhao Jie,Pan Qi,Li Wanwan
Reactive oxygen species with evoked immunotherapy holds tremendous promise for cancer treatment but has limitations due to its dependence on exogenous excitation and/or endogenous H 2 O 2 and O 2 . Here we report a versatile oxidizing pentavalent bismuth(V) nanoplatform (NaBi V O 3 -PEG) can generate reactive oxygen species in an excitation-free and H 2 O 2 - and O 2 -independent manner. Upon exposure to the tumor microenvironment, NaBi V O 3 -PEG undergoes continuous H + -accelerated hydrolysis with •OH and 1 O 2 generation through electron transfer-mediated Bi V -to-Bi III conversion and lattice oxygen transformation. The simultaneous release of sodium counterions after endocytosis triggers caspase-1-mediated pyroptosis. NaBi V O 3 -PEG intratumorally administered initiates robust therapeutic efficacies against both primary and distant tumors and activates systemic immune responses to combat tumor metastasis. NaBi V O 3 -PEG intravenously administered can efficiently accumulate at the tumor site for further real-time computed tomography monitoring, immunotherapy, or alternative synergistic immune-radiotherapy. Overall, this work offers a nanomedicine based on high-valence bismuth(V) nanoplatform and underscores its great potential for cancer immunotherapy.
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高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2024
·
IF 8.1
Mingxin Zheng,Keng Xuan,Shuai Yan,Yaoping Guo,Yaxiong Huang,Runling Xu,Kaixuan Zhao,Zebing Li,Xun Li,Hao Jiang,Yadan Guo
A defective metal–organic framework UiO-66–18 synthesized via a facile solvothermal synthesis method with trifluoroacetic acid as modulator was demonstrated to be highly efficient for the elimination of uranium from wastewater. The maximum adsorption capacity of UiO-66–18 toward uranium reached 622.75 mg g −1 , which was approximately 1.43 times higher than that of pristine UiO-66–0 prepared without TFA modulation. The superior elimination performance of UiO-66–18 was because the TFA modulation induced the generation of more missing-linker defects that endowed UiO-66–18 with hierarchical structure and more adsorption active sites for U(VI) capture. Further adsorption mechanism studies indicated that the elimination of U(VI) was endothermic monolayer chemisorption dominated by mass transfer-decomplexation-adsorption process. In addition, the effects of common ions on the elimination efficiency as well as the reusability of UiO-66–0 and UiO-66–18 were studied. This work provides a promising strategy and a theoretical basis for the design and preparation of efficient uranium adsorbent from the points of defects engineering and pore structure design.
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高影响因子
REACTIVE & FUNCTIONAL POLYMERS
·
2024
·
IF 4.5
Xue Liu,Jianguo Deng,Guohong Pu,Zhihua Deng,Lanxiang Ji,Xiaofeng Bai,Quanping Zhang,Yuanlin Zhou
Traditional radiation protection wearable products will inevitably produce a certain degree of mechanical damage during use, leading to breakage or even failure of our wearable products. In this work, we introduce a novel stretchable, self-healing wearable composite, constructed from a double network matrix of Hydrogen-terminated phenyl polysiloxane (HTPP) and Polyborosiloxane (PBS). These composites obtain robustness and elasticity by using phenyl in HTPP as a rigid component and covalent network. In addition, HTPP acts as a scaffold to keep the shape of PBS stable and provide elasticity. Meanwhile, the supramolecular network presented in PBS contributes to high viscoelasticity and improves the self-healing ability to promote rapid autonomous healing. Moreover, tantalum( V ) oxide (Ta 2 O 5 ) as a functional filler enhances the radiation shielding and thermal management performance of the double cross-linked elastomer . This unique combination of thermal management, autonomous self-healing, and mechanical strength , as well as radiation protection, may endow this new composite with a wide range of applications.
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INORGANIC CHEMISTRY
·
2025
·
IF 4.7
Shaopei Jia,Yanfeng Gao,Xiaofei Ma,Yunfei Cao,Quan Huang,Qian Zhang,Zhixin Wang,Yanjie Wang,Yuanyuan Li,Dan Li,Renkai Chang,Yunchao Mu
Designing and synthesizing highly efficient and stable electrocatalysts of seawater electrolysis for the hydrogen evolution reaction is important for realizing green hydrogen production. Herein, a heterostructured V-doped Co2P anchored on N–P-doped three-dimensional covalently cross-linked graphene (V–Co2P@NPPC/3DG) electrocatalysts was synthesized with the help of V-doped ZIF-67 as an intermediate and a controlled phosphidation process. The as-prepared V–Co2P@NPPC/3DG-1:5 had low overpotentials of 98.3 and 88.3 mV (at 10 mA cm–2) in alkaline water and artificial seawater, respectively, and the corresponding Tafel slopes were 56.4 and 51.0 mV dec–1. The electrolyzer with a flowing alkaline artificial seawater assembled from V–Co2P@NPPC/3DG-1:5 with a commercial RuO2 catalyst exhibited a cell voltage of 1.54 V at 10 mA cm–2, which is close to that of Pt/C||RuO2 (1.52 V). Notably, the cell voltage of V–Co2P@NPPC/3DG-1:5||RuO2 was lower than that of Pt/C||RuO2 at a high current density (>58 mA cm–2), which exhibited superior stability. V doping effectively enhanced the intrinsic activity of Co2P, and the complexation with NPPC/3DG achieved full exposure of the active sites while enhancing the charge transfer rate during HER. This work will attract attention to the role of metal compound-carbon support interactions in enhancing the intrinsic activity, conductivity, and stability of electrocatalysts.
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SEPARATION AND PURIFICATION TECHNOLOGY
·
2022
·
IF 9.136
Xinqian Li,Bo Li,Shuqi Li,Yaping Dong,Dandan Gao,Zhengrong Niu,Wu Li,Haitao Feng
Removing impurities from hexavalent chromium system without secondary pollution is the key to the successful development of green chromate production technology. Here, hydrated chromium oxide CrO x (OH) 3-2x with lamellar cluster microsphere structure was prepared by in-situ hydrothermal method and used to simultaneously adsorb Si (IV) and V (V) in high concentration Cr (VI) solution. In the in-situ hydrothermal process of pH 7, 160 ℃ for 8 h, the Si (IV) and V (V) removal rates of the actual chromate production Na 2 Cr 2 O 7 -Na 2 SiO 3 -NaVO 3 -H 2 O solution can reach 92.27 % and 94.81 %, respectively, which is higher than the ex-situ removal efficiency of Si (IV) (62.88 %) and V (V) (63.16 %) under the same conditions. Further characterization of STEM-elemental mapping, XPS and FT-IR results indicate that during in-situ adsorption, Si (IV) and V (V) are mainly adsorbed on the surface of CrO x (OH) 3-2X adsorbent by interacting with surface hydroxyl groups. More importantly, the simultaneous formation and adsorption of the adsorbent are more conducive to the full utilization of active adsorption sites on the adsorbent surface. After that, CrO x (OH) 3-2x was converted into nano Cr 2 O 3 with a purity of 97.87 % by simple desorption and calcination processes. In addition, the results of UV–vis DRS and SEM show that the residual Si and V elements in Cr 2 O 3 unexpectedly increase the size of the particles to about 300 nm, which redshifts the absorption band of the blue region by 3.3 nm. This results in more red absorption and makes Cr 2 O 3 more yellowish-green and exhibits excellent pigment properties. Thus, the in-situ synthesis, synergistic adsorption and green conversion of trivalent chromium adsorbent provide a promising and sustainable technology for the purification of high concentration Cr (VI) solution that avoids the discharge of Cr (VI) containing slag.
研究领域:
环境科学
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材料科学
·
化学工程
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ENZYME AND MICROBIAL TECHNOLOGY
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2020
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IF 3.448
Haikun Zhang,Jingyi Xie,Yanyu Sun,Ailing Zheng,Xiaoke Hu
Antimony trisulfide (Sb 2 S 3 ) is industrially important for processes ranging from a semiconductor dopant through batteries to a flame retardant. Approaches for fabricating Sb 2 S 3 nanostructures or thin films are by chemical or physicochemical methods, while there have been no report focused on the biological synthesis of nano Sb 2 S 3 . In the present study, we fabricated nano-broccoli-like Sb 2 S 3 using Sb(V) reducing bacteria. Thirty four marine and terrestrial strains are capable of fabricating Sb 2 S 3 after 1–5 days of incubation in different selective media. The nano-broccoli-like bio-Sb 2 S 3 was light sensitive between 400–550 nm, acting as a photo-catalyst with the bandgap energy of 1.84 eV. Moreover, kinetic and mechanism studies demonstrated that a k value of ∼0.27 h −1 with an R 2 = 0.99. The bio-Sb 2 S 3 supplemented system exhibited approximately 18.4 times higher photocatalytic activity for degrading methyl orange (MO) to SO 4 2- , CO 2 and H 2 O compared with that of control system, which had a k value of ∼0.015 h −1 (R 2 = 0.99) under visible light. Bacterial community shift analyses showed that the addition of S or Fe species to the media significantly changed the bacterial communities driven by antimony stress. From this work it appears Clostridia, Bacilli and Gammaproteobacteria from marine sediment are potentially ideal candidates for fabricating bio-Sb 2 S 3 due to their excellent electron transfer capability. Based on the above results, we propose a potential visible light bacterially catalyzed self-purification of both heavy metal and persistent organic contamination polluted coastal waters.
研究领域:
材料科学
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环境科学
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生物技术
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化学
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高影响因子
IONICS
·
2023
·Vol. 29
·期 3
·1187-1197
·
IF 2.8
Zhong Xiaoqiu,Yao Qingyun,Tang Shuangmei,Kong Zhenzhen,Yang Chao,Zang Limin,Qiu Jianhui
Fibrous all-solid-state flexible supercapacitors have attracted much attention in the functional field of wearable electronic devices due to their excellent deformability. It is very important to select suitable flexible substrate, active substance, and binding means to improve electrode performance. In this paper, carbon fiber with high conductivity and the active site was used as a flexible substrate, and FeOOH with high specific capacity was grown on the surface of carbon fiber yarn by one-step in situ electrodeposition. The influence of different deposition conditions on the morphology of FeOOH and the electrochemical performance of the flexible electrode was studied. The electrode obtained by deposition at a constant voltage of 2.5 V for 150 min has a high specific capacitance of 10.44 F cm −3 . In addition, the device has a high voltage window of 1.6 V and excellent cycle stability of 7000 cycles when formed as an all-solid-state symmetric supercapacitor.
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ACS Applied Materials & Interfaces
·
2022
·
IF 10.383
Xiaoying Fan,Peng Chen,Xu Yin,Ruo-Xuan Qi,Chao Yang,Ya-Jun Cheng,Kunkun Guo,Cuirong Liu,Yonggao Xia
Increasing working voltage is a promising way to increase the energy density of lithium-ion batteries. Cycling and rate performance deteriorated due to excessive electrolyte decomposition and uncontrolled formation of a cathode–electrolyte interface (CEI) layer at a high voltage. A new concept is proposed to construct a high-voltage-stable electrode–electrolyte interface. An elastomeric poly(dimethyl siloxane) (PDMS) binder is incorporated into the electrode to modify the LiNi0.5Co0.2Mn0.3O2 (NCM 523) particle surface via an in situ cross-linking reaction between hydroxy-terminated PDMS and methyl trimethoxy silane promoted by moisture at ambient conditions (MPDMS). Improved electrochemical performance is achieved with the MPDMS binder in terms of reversible capacity (201 vs 185 mAh·g–1 at 0.2C), capacity retention (80 vs 68%, after 300 cycles at 1C), and rate performance (55.6% increase at 5C), as demonstrated by the NCM 523||Li half-cell. The NCM 523||graphite full-cell also shows improved performance at 4.6 V (147 vs 128 mAh·g–1, 82 vs 76%, after 200 cycles at 1C). The mechanism studies indicate that MPDMS exerts multiple effects, including cathode surface passivation, solvation structure tuning, electrolyte uptake enhancement, and mechanical stress relief. This work provides an inspiring route to realize high-voltage application of lithium-ion battery technology.
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高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2021
·
IF 10.588
Wenjuan Wang,Yanfang Huang,Guihong Han,Bingbing Liu,Shengpeng Su,Yizhuang Wang,Yubin Xue
Environmentally hazardous P(V), Mo(VI) and W(VI) generated oxyanions exist widely in the waste liquid of nonferrous hydrometallurgy . In this work, Fe-MOF material was simply prepared via solvothermal synthesis and then used as an adsorbent to remove P(V), Mo(VI) and W(VI) oxyanions from hydrometallurgical waste liquid . Several important parameters, including solution pH, oxyanion concentration, contact time, adsorbent amount, temperature and coexistent heavy metal ions , were systematically investigated. The results demonstrate that adsorption process was almost pH-independent over a broad range of pH 3.0–10.0. The adsorption efficiency was strongly associated with the chemical species of oxyanions. The higher polymerisation degree of oxyanions was more favourable for removal efficiency. Additionally, the maximum removal efficiencies for P(V), Mo(VI) and W(VI) oxyanions under optimum conditions were approximately 100%. Furthermore, the adsorption kinetics and isotherms of oxyanions on the adsorbent separately belonged to the pseudo-second-order and Langmuir isotherm models. XPS analysis revealed that inner-sphere complexation played a dominant role in the adsorption removal process. Fe-MOFs with pH-independent properties, abundant binding sites and high stability are prospective adsorbents for treating waste liquids in the hydrometallurgical industry.
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高影响因子
JOURNAL OF POWER SOURCES
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2020
·
IF 8.247
Jianhui Li,Zaisheng Wang
Trimethyl borate (TMB) has been identified as electrolyte additive to suppress self-discharge for high voltage layered lithium-rich oxide cathode (LRO) for lithium ion batteries in our previous work. To expand pervious findings, its derivatives, triethyl borate (TEB) and tripropyl borate (TPB) with increased alkyl chains, have been considered as electrolyte additives to mitigate self-discharge behavior of LRO cathode for lithium ion batteries and we make a contrast to explain which one is better and why is better. It is found that fully charged (4.8 V, vs. Li/Li + ) LRO cathode suffers severe self-discharged issue upon storage in standard (STD) electrolyte (1 mol L −1 LiPF 6 -EC/EMC/DEC (3:5:2, in weight)). In contrast, this detrimental self-discharge behavior of LRO cathode at high voltage can be effectively depressed by introducing TEB or TPB into the electrolyte system. Combinations of electrochemical methods and multi spectroscopy techniques have been employed to evaluate effects of TEB and TPB on the LRO cathode surface . They reveal that the B–O and B–F bonds species in the film formed by TEB and TPB prevents electrolyte decomposition and protects LRO from structure transformation. These species in the film formed by TEB is much more than TPB, which explains the better effect for TEB.
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