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Institution

Jilin University

EducationChangchun, China
About: Jilin University is a education organization based out in Changchun, China. It is known for research contribution in the topics: Catalysis & Apoptosis. The organization has 101453 authors who have published 88966 publications receiving 1444456 citations. The organization is also known as: Jílín Dàxué.
Topics: Catalysis, Apoptosis, Cancer, Adsorption, Cell growth


Papers
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Journal ArticleDOI
TL;DR: In this paper, a new hydrophobic mesoporous polymer-based solid acid catalysts have been successfully synthesized by copolymerization of divinylbenzene (DVB) with sodium p-styrene sulfonate (H-PDVB-x-SO3H's) under solvothermal conditions.
Abstract: Novel excellent hydrophobic- mesoporous- polymer-based solid acid catalysts have been successfully synthesized by copolymerization of divinylbenzene (DVB) with sodium p-styrene sulfonate (H-PDVB-x-SO3H's) under solvothermal conditions. N2 isotherms and TEM images showed that H-PDVB-x-SO3H's have high BET surface areas, large pore volumes, and abundant mesoporosity; CHNS element analysis and acid–base titration technology showed that H-PDVB-x-SO3H's have adjustable sulfur contents (0.31–2.36 mmol/g) and acidic concentrations (0.26–1.86 mmol/g); TG curves showed that H-PDVB-x-SO3H's exhibited much higher stability of the active site (372 °C) than that of the acidic resin of Amberlyst 15 (312 °C); contact angle and water adsorption tests showed that H-PDVB-x-SO3H's exhibited excellent hydrophobic properties. Catalytic tests in esterification of acetic acid with cyclohexanol, esterification of acetic acid with 1-butanol, and condensation of benzaldehyde with ethylene glycol showed that H-PDVB-x-SO3H's were mo...

212 citations

Journal ArticleDOI
30 Aug 2019-ACS Nano
TL;DR: The advantages of Ti3C2T2 host material could be well retained even at high S loading, suggesting the potential of surface-modified MXene for confining sulfur in Li-S battery cathodes.
Abstract: Multiple negative factors, including the poor electronic conductivity of sulfur, dissolution and shuttling of lithium polysulfides (Li2Sn), and sluggish decomposition of solid Li2S, seriously hinder practical applications of lithium-sulfur (Li-S) batteries. To solve these problems, a general strategy was proposed for enhancing the electrochemical performance of Li-S batteries using surface-functionalized Ti3C2 MXenes. Functionalized Ti3C2T2 (T = N, O, F, S, and Cl) showed metallic conductivity, as bare Ti3C2. Among all Ti3C2T2 investigated, Ti3C2S2, Ti3C2O2, and Ti3C2N2 offered moderate adsorption strength, which effectively suppressed Li2Sn dissolution and shuttling. This Ti3C2T2 exhibited effective electrocatalytic ability for Li2S decomposition. The Li2S decomposition barrier was significantly decreased from 3.390 eV to ∼0.4 eV using Ti3C2S2 and Ti3C2O2, with fast Li+ diffusivity. Based on these results, O- and S-terminated Ti3C2 were suggested as promising host materials for S cathodes. In addition, appropriate functional group vacancies could further promote anchoring and catalytic abilities of Ti3C2T2 to boost the electrochemical performance of Li-S batteries. Moreover, the advantages of a Ti3C2T2 host material could be well retained even at high S loading, suggesting the potential of surface-modified MXene for confining sulfur in Li-S battery cathodes.

211 citations

Journal ArticleDOI
TL;DR: It is demonstrated that the HOMO levels are critical for the performance of PSCs and the opportunities for efficient HTMs based on the functionalized nanographenes utilizing the strong interactions of their functional groups with perovskite are opened.
Abstract: Perovskite solar cells (PSCs) have been demonstrated as one of the most promising candidates for solar energy harvesting. Here, for the first time, a functionalized nanographene (perthiolated trisulfur-annulated hexa-peri-hexabenzocoronene, TSHBC) is employed as the hole transporting material (HTM) in PSCs to achieve efficient charge extraction from perovskite, yielding the best efficiency of 12.8% in pristine form. The efficiency is readily improved up to 14.0% by doping with graphene sheets into TSHBC to enhance the charge transfer. By the HOMO–LUMO level engineering of TSHBC homologues, we demonstrate that the HOMO levels are critical for the performance of PSCs. Moreover, beneficial from the hydrophobic nature of TSHBC, the devices show the improved stability under AM 1.5 illumination in the humidity about 45% without encapsulation. These findings open the opportunities for efficient HTMs based on the functionalized nanographenes utilizing the strong interactions of their functional groups with perovs...

211 citations

Journal ArticleDOI
Lei Wang1, Ming Yang1, Guanghua Li1, Zhan Shi1, Shouhua Feng1 
TL;DR: The 1,2,4-BTC ligand shows a novel and unprecedented coordination mode: nine bonds to eight metals with each carboxylate as a tridentate group and exhibits intense photoluminescence at room temperature and shows distinct NLO properties.
Abstract: Employing an unsymmetrical 1,2,4-benzenetricarboxylate as a bridging ligand, a new 3-D chiral cadmium coordination polymer [Cd2(OH)(1,2,4-BTC)] (1,2,4-BTC = 1,2,4-benzenetricarboxylate) has been prepared under hydrothermal conditions and characterized by single crystal X-ray diffraction. This compound crystallizes in the orthorhombic space group P212121, with cell parameters a = 6.900(2) A, b = 7.404(3) A, c = 19.116(5) A, V = 976.5(5) A3, and Z = 4. Its structure contains 2-D Cd−O−Cd connectivity, which is further linked by the 1,2,4-BTC ligand into a 3-D supramolecular framework. The 1,2,4-BTC ligand shows a novel and unprecedented coordination mode: nine bonds to eight metals with each carboxylate as a tridentate group. The compound exhibits intense photoluminescence at room temperature and shows distinct NLO properties. On the basis of the results of TG/DTA analyses, the structure is thermally stable up to ∼ 380 °C.

211 citations

Journal ArticleDOI
TL;DR: In this article, the authors used molybdenum dioxide as a SERS material, showing high enhancement factors and stability to oxidation even at high temperatures, which is the best among the metal oxides and even reaches or approaches to Au/Ag.
Abstract: Compared with noble metals, semiconductors with surface plasmon resonance effect are another type of SERS substrate materials. The main obstacles so far are that the semiconducting materials are often unstable and easy to be further oxidized or decomposed by laser irradiating or contacting with corrosive substances. Here, we report that metallic MoO2 can be used as a SERS substrate to detect trace amounts of highly risk chemicals including bisphenol A (BPA), dichloropheno (DCP), pentachlorophenol (PCP) and so on. The minimum detectable concentration was 10−7 M and the maximum enhancement factor is up to 3.75 × 106. To the best of our knowledge, it may be the best among the metal oxides and even reaches or approaches to Au/Ag. The MoO2 shows an unexpected high oxidation resistance, which can even withstand 300 °C in air without further oxidation. The MoO2 material also can resist long etching of strong acid and alkali. Semiconducting materials are potential SERS substrates as alternatives to noble metals, but often suffer from poor stabilities and sensitivities. Here, the authors use molybdenum dioxide as a SERS material, showing high enhancement factors and stability to oxidation even at high temperatures.

211 citations


Authors

Showing all 101943 results

NameH-indexPapersCitations
Yang Yang1712644153049
Yury Gogotsi171956144520
Lei Jiang1702244135205
Gang Chen1673372149819
Dongyuan Zhao160872106451
Rui Zhang1512625107917
Xiaodong Wang1351573117552
Avelino Corma134104989095
Jie Liu131153168891
Shuai Liu129109580823
Yang Liu1292506122380
Sheng Dai12298563472
Xin Wang121150364930
Simon A. Wilde11839045547
Shaojun Dong11887357337
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023187
20221,197
20218,629
20208,607
20198,049
20186,868