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Rev. Lett. 10 486,11 4\nde Gennes P G 1964Rev. Mod. Phys. 36 225\nMooney J B and Redding S B 1982Annu. Rev. Matter. Sci. 12 81\nReddy G S N, Gupta A K, Ojha V N, Walia D K, Kataria N D, Khare N and Tomar V S 1989Mod. Phys: Lett. B3 1311\nSears M W and Gee M A 1988Thin Solid Films 165 265\nSetaka R, Komatsu W, Shibata T and Nakajima M 1988Jpn. J. Appl. Phys. 27 L2100\nWalia D K, Gupta A K, Reddy G S N, Tomar V S, Kataria N D, Ojha V N and Khare N 1989Solid State Commun. 71 987",{"EN":128},"Superconducting Bi-Sr-Ca-Cu-O (2212) films were prepared by spraying stoichiometric aqueous solutions of nitrates of bismuth, strontium, calcium and copper on heated MgO (100) substrates and subsequent annealing in air. TheR-T curves of the films show metallic behaviour above the superconducting transition temperature.T\n                \n                  c\n                 (R=0) is observed between 80 and 85 K. Annealing temperature has a profound effect onT\n                \n                  c\n                 (R=0) and on the orientation of the film. Annealing in air in near-melting region yields highly oriented films withc-axis perpendicular to the substrate. These films show a sharp superconducting transition with zero resistance at 85 K. Microbridges of the dimensions of 50 µm × 50 µm have been patterned photolithographically followed with chemical etching. The 1 V characteristics of the microbridges show Josephson effects due to the presence of grain boundary weaklinks. The temperature dependence of the critical current for these microbridges suggest formation of superconductor-normal-superconductor type weaklinks.",{"EN":130},"Study of Josephson effects in microbridges of Bi-Sr-Ca-Cu-O films made by spray pyrolysis",{"VOID":132},"10.1007\u002FBF02747490","PUBLICATION","VERIFIED","Auto 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C V S, Han X, Zhu Q Y, Mai L Q and Chen W 2006 Microelectron. Eng. 83 281\nNirmala Devi G, Chitra S, Selvasekarapandian S, Premalatha M, Monisha S and Saranya J 2017 Ionics 23 3377\nVanitha D, Bahadur S A, Nallamuthu N and Athimoolam S 2018 Ionics 24 139\nSivadevi S, Selvasekarapandian S, Karthikeyan S, Sanjeeviraja C, Nithya H, Iwai Y et al 2015 Ionics 21 1017\nVanitha D, Bahadur S A, Nallamuthu N and Manikandan A 2017 J. Inorg. Organomet. Polym. 27 257\nShahenoor Basha S K, Ranjit Kumar B, Veera Bhadra Reddy K and Rao M C 2017 Chem. Sci. Rev. Lett. 6 832\nPremalatha M, Vijaya N, Selvasekarapandian S and Selvalakshmi S 2016 Ionics 22 1299\nRamaswamy M, Malayandi T, Subramanium S, Srinivasalu J and Rangaswamy M 2017 Ionics 23 1771\nKhare P K and Jain S K 2000 Bull. Mater. Sci. 23 17\nPolu A R and Kumar R 2011 Bull. Mater. Sci. 34 1063\nAziz S B 2015 Bull. Mater. Sci. 38 1597\nMurugendrappa M V, Khasim S and Ambika Prasad M V N 2005 Bull. Mater. Sci. 28 565\nSarwar M I, Rafiq S, Yousaf S M and Ahmad Z 1998 Int. J. Polym. Mater. Polym. Biomater. 41 185\nLink S and El-Sayed M A 1999 J. Phys. Chem. B. 103 8410\nNath N and Chilkoti A 2004 Anal. Chem. 76 5370\nKulanthaisami S, Managalaraj D and Sa Narayandass K 1995 Eur. Polym. J. 31 969\nAhmed M A and Abo-Ellil M S 1998 J. Mater. Sci. Mater. Electron. 9 391\nRashmi, Narula G K and Pillai P K C 1987 J. Mater. Sci. 22 2006\nSakthivel S, Chandar Shekar B, Mangalaraj D, Sa Narayadass K, Venkatachalam S and Prabhakaran P V 1997 Eur. Polym. J. 33 1747\nBahri R and Singh H P 1979 Thin Solid Films 62 291\nAshcraft C R and Boyd R H 1976 J. Polym. Sci. Polym. Phys. B 14 2153\nLatha C and Venkatachalam K 2017 Polym. Bull. 74 3123\nJeyabanu K, Siva V, Nallamuthu N, Selvanayagam S, Asath Bahadur S and Manikandan A 2018 J. Nanosci. Nanotechnol. 18 1103\nBaraker B M and Lobo B 2016 Indian J. Pure Appl. Phys. 54 634\nHoffman J D, Williams G and Passaglia E 1966 J. Polym. Sci.: Polym. Symp. 14 173\nAlberola N, Cavaille J Y and Perez J 1990 J. Polym. Sci. B: Polym. Phys. 28 569\nRunt J P and Fitzgerald J J 1997 Dielectric spectroscopy of polymeric materials: fundamentals and applications (Washington (DC): American Chemical Society)\nBlochowicz T and Rössler E A 2004 Phys. Rev. Lett. 92 225701\nSundarakannan B, Kakimoto K and Ohsato H 2003 J. Appl. Phys. 94 5182\nYadav V S, Sahu D K, Singh Y and Dhubkarya D C 2010 AIP Conf. Proc. 1285 267\nDebye P 1929 (1st edn) Polar molecules (New York: Chemical Catalog Company)\nCole K S and Cole R H 1941 J. Chem. Phys. 9 341\nQiao J, Fu J, Lin R, Ma J and Liu J 2010 Polymer 51 4850\nMalathi J, Kumaravadivel M, Brahmanandhan G M, Hema M, Baskaran R and Selvasekarapandian S 2010 J. Non-Cryst. Solids 356 2277\nRavi M, Pavani Y, Kumar K K, Bhavani S, Sharma A K and Narasimha Rao V V R 2011 Mater. Chem. Phys. 130 442\nRaja V, Sharma A K and Narasimha Rao V V R 2004 Mater. Lett. 58 3242\nHema M, Selvasekerapandian S, Sakunthala A, Arunkumar D and Nithya H 2008 Physica B 403 2740\nRajeshwari N, Selvasekarapandian S, Prabhu M, Karthikeyan S and Sanjeeviraja C 2013 Bull. Mater. Sci. 36 333\nJonscher A K 1977 Nature 267 673\nFunke K, Roling B and Lange M 1998 Solid State Ion. 105 195\nHirankumar G, Selvasekarapandian S, Bhuvaneswari M S, Baskaran R and Vijayakumar M 2006 J. Solid State Electrochem. 10 193\nHilker B, Fields K B, Stern A, Space B, Zhang X P and Harmon J P 2010 Polymer 51 4790\nRao R V and Shridhar M H 2002 Mater. Lett. 55 34\nYang S, Benitez R, Fuentes A and Lozano K 2007 Compos. Sci. Technol. 67 1159\nGovindaraj G, Baskaran N, Shahi K and Monoravi P 1995 Solid State Ion. 76 47\nMohan V M, Qiu W, Shen J and Chen W 2010 J. Polym. Res. 17 143\nFan L, Dang Z, Wei G, Nan C W and Li M 2003 Mater. Sci. Eng., B 99 340\nRoy A S, Gupta S, Sindhu S, Parveen A and Ramamurthy P C 2013 Composites B 47 314\nPradhan D K, Choudhary R N P and Samantaray B K 2009 Mater. Chem. Phys. 115 557\nPissis P and Kyritsis A 1997 Solid State Ion. 97 105\nPradhan D K, Choudhary R N P and Samantaray B K 2008 Express Polym. Lett. 2 630\nZhang S, Dou S, Colby R H and Runt J 2005 J. Non-Cryst. Solids 351 2825\nAl-Hawarin J, Ayesh A S and Abdel-Rahem R A 2012 Chin. J. Polym. Sci. 30 143\nBhargav P B, Mohan V M, Sharma A K and Rao V V R N 2009 Curr. Appl. Phys. 9 165\nBaraker B M, Hammannavar P B and Lobo B 2015 AIP Conf. Proc. 1665 070037\nBaraker B M and Lobo B 2017 Can. J. Phys. 95 738\nMarzantowicz M, Dygas J R, Krok F, Florjańczyk Z and Zygadło-Monikowska E 2007 J. Non-Cryst. Solids 353 4467\nBaraker B M and Lobo B 2017 Mapana: J. Sci. 16 45\nBaraker B M and Lobo B 2017 J. Polym. Res. 24 84\nHemalatha K S, Sriprakash G, Ambika Prasad M V N, Damle R and Rukmani K 2015 J. Appl. Phys. 118 154103",{"VI":289,"EN":290},"Các quá trình thư giãn phụ thuộc vào nhiệt độ và tần số trong các phim của một hỗn hợp polymer bao gồm copolymer polyvinyl alcohol (PVA)\u002Fpolyvinyl acetate (PVAc) được trộn với polyvinyl pyrrolidone (PVP) theo tỷ lệ bằng nhau theo trọng lượng, và được doping với muối kim loại vô cơ, cadmium chloride $$(\\hbox {CdCl}_{2})$$, ở mức độ doping 0.0 wt% và 10.2 wt%. Sử dụng quang phổ thư giãn điện môi (DRS), các đáp ứng tần số của các thông số điện môi cho các mẫu này đã được nghiên cứu với sự thay đổi nhiệt độ, từ 303 đến 373 K, tại các tần số cố định khác nhau (từ 12 Hz đến 200 kHz). Nghiên cứu các biểu đồ Cole–Cole cho thấy sự giảm điện trở khối của các mẫu khi nhiệt độ tăng, điều này được cho là do sự gia tăng về tính di động của các chuỗi polymer được kích thích bởi nhiệt. Một sự gia tăng gấp 10 lần trong độ dẫn điện khối được quan sát ở các phim đã được dop với mức độ doping là 10.2 wt%, khi so với độ dẫn điện khối của mẫu không có doping (0.0 wt%). Sự phụ thuộc vào nhiệt độ của các thông số điện môi ở các tần số khác nhau đã được nghiên cứu và năng lượng kích hoạt đã được tính toán. Thời gian thư giãn được tìm thấy có độ lớn khoảng vài mili giây, điều này ám chỉ rằng sự dẫn điện trong các phim hỗn hợp PVA\u002FPVAc–PVP dop với $$(\\hbox {CdCl}_{2})$$ chủ yếu là do sự di chuyển của các ion. Sự thay đổi của độ dẫn AC với tần số phù hợp với định luật công suất phổ quát của Jonscher. Độ dẫn AC của mẫu được tìm thấy là tăng đáng kể khi nhiệt độ của mẫu tăng lên. Các thuộc tính điện môi phụ thuộc vào tần số của các phim hỗn hợp PVA\u002FPVAc–PVP dop với $$(\\hbox {CdCl}_{2})$$, ở các mức độ doping khác nhau, cũng được nghiên cứu ở nhiệt độ phòng.","The temperature- and frequency-dependent relaxation processes in films of a polymeric blend comprising a polyvinyl alcohol (PVA)\u002Fpolyvinyl acetate (PVAc) co-polymer blended with polyvinyl pyrrolidone (PVP) in equal proportion by weight, and doped with an inorganic metallic salt, cadmium chloride \n                  \n                    \n                  \n                  $$(\\hbox {CdCl}_{2})$$\n                  \n                    \n                  \n                , at 0.0 wt% and 10.2 wt% doping levels (DLs), have been studied using dielectric relaxation spectroscopy (DRS). The frequency response of dielectric parameters for these samples has been studied with variation in temperature, from 303 up to 373 K, at different fixed frequencies (from 12 Hz up to 200 kHz). Study of Cole–Cole plots reveals a decrease in bulk resistivity of the samples with increase in temperature, which is attributed to thermally induced increase in the mobility of polymer chains. A 10-fold increase in bulk conductivity is observed for doped films with a DL of 10.2 wt%, when compared with the bulk conductivity of the un-doped (0.0 wt% DL) sample. The temperature dependence of dielectric parameters at different frequencies has been studied and the activation energy has been calculated. The relaxation time is found to be of the order of a few milliseconds, which implies that electrical conduction in \n                  \n                    \n                  \n                  $$\\hbox {CdCl}_{2}$$\n                  \n                    \n                  \n                -doped PVA\u002FPVAc–PVP blend films is predominantly due to the migration of ions. The variation of AC conductivity with frequency is in agreement with Jonscher’s universal power law. AC conductivity of the sample is found to increase significantly with an increase in temperature of the sample. Frequency-dependent dielectric properties of \n                  \n                    \n                  \n                  $$\\hbox {CdCl}_{2}$$\n                  \n                    \n                  \n                -doped PVA\u002FPVAc–PVP blend films, for various DLs, are also studied at room temperature.",{"VI":292,"EN":293},"Thư giãn điện môi trong một hỗn hợp polymer được pha dop cadmium chloride","Dielectric relaxation in a cadmium chloride-doped polymeric blend",{"VOID":295},"10.1007\u002Fs12034-018-1690-3",{"VI":297},"","2025-01-23T11:48:35.355+00:00",[300],"VI","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12034-018-1690-3",[303,318],{"id":304,"sortIndex":21,"researcher":20,"roles":305,"affiliations":306,"properties":315},"561b1d67-278e-425f-b0d3-114743c5f09e",[141],[307],{"id":20,"sortIndex":21,"affiliation":308,"properties":20},{"id":309,"createTime":310,"updateTime":310,"relativeEntities":311,"slug":20,"properties":312,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"24053da4-a38f-4fd5-846e-993a14aef67f","2023-12-31T05:34:32.569+00:00",[],{"title":313},{"VI":314},"Department of Physics, Karnatak University’s Karnatak Science College, Dharwad, India",{"title":316},{"VI":317},"Basavarajeshwari M Baraker",{"id":319,"sortIndex":109,"researcher":20,"roles":320,"affiliations":321,"properties":327},"d6a744d4-e7a2-4168-8606-d31669a20f9a",[141],[322],{"id":20,"sortIndex":21,"affiliation":323,"properties":20},{"id":309,"createTime":310,"updateTime":310,"relativeEntities":324,"slug":20,"properties":325,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":326},{"VI":314},{"title":328},{"VI":329},"Blaise Lobo",{"url":301,"publisher":331,"properties":359},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":332,"slug":10,"properties":333,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":337,"manageAffiliations":338,"indexDatabases":339,"url":103,"thumbnailPath":20,"statistic":354,"gsStatistic":20,"type":113,"analyzePriority":20},[],{"issn":334,"eissn":335,"title":336},{"VOID":13},{"VOID":15},{"EN":17},[],[],[340,347],{"id":65,"indexDatabase":341,"url":80,"indexYears":20,"academicFieldIds":346,"indexDatabaseRanking":20},{"id":67,"createTime":68,"updateTime":69,"relativeEntities":342,"label":343,"description":344,"key":76,"publicationTags":345,"standard":20},[],{"EN":72,"VI":72},{"VI":74,"EN":75},[78,79],[82],{"id":84,"indexDatabase":348,"url":97,"indexYears":98,"academicFieldIds":353,"indexDatabaseRanking":102},{"id":86,"createTime":87,"updateTime":88,"relativeEntities":349,"label":350,"description":351,"key":94,"publicationTags":352,"standard":20},[],{"EN":91,"VI":91},{"EN":91,"VI":93},[96],[100,101],{"impactFactor":21,"impactFactorByYear":355,"i10Index":21,"i10IndexLast5Year":21,"totalPublication":106,"totalPublicationByYear":356,"totalCitation":21,"totalCitationByYear":357,"totalCitationPerPublication":21,"totalCitationPerPublicationByYear":358,"hindexLast5Year":21,"hindex":21},{},{"1982":108,"1983":109,"1984":108,"1985":109,"1986":109,"1987":109,"1988":61,"1989":108,"1993":109,"1994":109,"1995":109,"1996":109,"1997":109,"1999":108,"2000":109,"2001":108,"2002":108,"2004":109,"2007":109,"2008":109,"2010":61,"2011":108,"2012":108,"2013":108,"2014":50,"2015":108,"2017":61,"2019":110,"2020":108,"2022":109},{},{},{"volume":360,"pages":362},{"VOID":361},"42",{"VOID":363},"1-16","2019-01-18",2019,{"id":367,"createTime":368,"updateTime":369,"relativeEntities":370,"slug":371,"properties":372,"entityType":133,"verifyStatus":134,"verifyTime":369,"verifyNote":135,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":381,"fullTextUrl":20,"authors":382,"publicationType":241,"publisherRelationship":469,"citationCount":20,"citationInfo":20,"publishDate":502,"publishYear":365,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":278},"ec7c6276-a399-4ca3-a76a-0ebd959f19e8","2024-01-21T09:19:22.537+00:00","2025-02-03T23:59:17.196+00:00",[],"Synthesis-and-thermophysical-studies-of-polyanilines",{"references":373,"abstract":375,"title":377,"doi":379},{"VOID":374},"Stejskal J and Gilbert R G 2002 Pure Appl. Chem. 74 857\nChiang J C and MacDiarmid A G 1986 Synth. Met. 13 193\nMacDiarmid A G, Yang L S, Huang W S and Humphrey B D 1987 Synth. Met. 18 393\nMcCall R P, Ginder J M, Leng J M, Coplin K A, Ye H J, Epstein A J et al 1991 Synth. Met. 41 1329\nTrivedi D C and Dhawan S K 1993 Synth. Met. 59 267\nMakeiff D A and Huber T 2006 Synth. Met. 156 497\nDutta D, Sarma T K, Chowdhury D and Chattopadhyay A 2005 J. Colloid Interface Sci. 283 153\nDrelinkiewicz A, Waksmundzka-Gora A, Sobczak J W and Stejskal J 2007 Appl. Catal. A: Gen. 333 219\nZhao C, Xing S, Yu Y, Zhang W and Wang C 2007 Microelectron. J. 38 316\nWillner I, Willner B and Katz E 2007 Bioelectrochemistry 70 2\nBlinova N V, Stejskal J, Trchova M, Ciric-Marjanovic G and Sapurina I 2007 J. Phys. Chem. B 111 2440\nSun L J, Liu X X, Lau K K T, Chen L and Gu W M 2008 Electrochim. Acta. 53 3036\nBessiere A, Duhamel C, Badot J C, Lucas V and Certiat M C 2004 Electrochim. Acta 49 2051\nHalvorson C, Cao Y, Moses D and Heeger A J 1993 Synth. Met. 57 3941\nWang H L, MacDiarmid A G, Wang Y Z, Gebier D D and Epstein A J 1996 Synth. Met. 78 33\nKaneto K, Kaneko M, Min Y and MacDiarmid A G 1995 Synth. Met. 71 2211\nSoto-Oviedo M A, Araujo O A, Faez R, Rezende M C and DePaoli M A 2006 Synth. Met. 156 1249\nKalendova A, Vesely D and Stejskal J 2008 Progr. Org. Coat. 62 105\nStejskal J, Kratochvıl P and Jenkins A D 1996 Polymer 37 367\nChristina O B, Xinwei H, Wyatt N and Richard B K 2017 Chem. Soc. Rev. 46 1510\nAli E 2010 Nanostructured conductive polymers (Chichester, UK: John Wiley & Sons Ltd.) p 19\nHari Singh N 2001 Handbook of advanced electronic and photonic materials and devices (London, UK: Academic Press) p 1\nHaines P J 1995 Thermal methods of analysis (London, UK: Springer Science)\nShirsath N B, Gupta G R, Gite V V and Meshram J S 2017 Bull. Mater. Sci. 41 63\nZulkhairi Z, Nurul F A H, Mubaraq H V S, Shafiqul Islam A K M, Uda H and Ahmad M N 2015 J. Nanomater. 2015 218204\nJiahua Z, Suying W, Lei Z, Yuanbing M, Jongeun R, Neel H et al 2011 J. Mater. Chem. 21 3952\nArora M and Gupta S K 2008 ICOPVS\nSaini P, Arora M, Arya S K and Tawale J S 2014 Indian J. Pure Appl. Phys. 52 175\nAgrawalla R K, Paul S, Sahoo P K, Chakraborty A K and Mitra A K 2015 J. Appl. Polym. Sci. 132 41692\nAgrawalla R K, Meriga V, Paul R, Chakraborty A K and Mitra A K 2016 EXPRESS Polym. Lett. 9 780\nVenkanna M, Sreeramulu V, Sivaprakash S, Caroline C and Dhanak V R 2015 J. Appl. Polym. Sci. 132 42766\nBurns J A and Verall R E 1974 Thermochim. Acta. 9 277\nDortmund Data Bank. http:\u002F\u002Fwww.ddbst.com\u002Fen\u002FEED\u002FPCP\u002FHCP_C4577.php\nPreeti A T, Yadav S M and Gupta G R 2014 Polym. Bull. 71 1349\nKumar D and Chandra R 2001 Indian J. Eng. Mater. Sci. 8 209\nJiaxing H and Richard B K 2004 J. Am. Chem. Soc. 126 851",{"EN":376},"Aniline was polymerized under different experimental conditions such as interfacial polymerization, rapid mixing in hydrochloric acid medium and classical bulk polymerization method using p-toluene sulphonic acid. The resulting polyanilines were characterized by infrared, X-ray diffraction, conductance and scanning electron microscopic analysis. The main emphasis of the paper is to study the thermal response of the synthesized polyanilines by thermogravimetric analysis and differential scanning calorimetry (DSC). The DSC data were utilized further to calculate the specific heat capacities of the synthesized polyanilines as a function of temperature.",{"EN":378},"Synthesis and thermophysical studies of polyanilines",{"VOID":380},"10.1007\u002Fs12034-018-1705-0","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12034-018-1705-0",[383,398,415,430,445,457],{"id":384,"sortIndex":193,"researcher":20,"roles":385,"affiliations":386,"properties":395},"c22b55a8-b72d-44fe-bb1a-04fa3c8bff6a",[141],[387],{"id":20,"sortIndex":21,"affiliation":388,"properties":20},{"id":389,"createTime":390,"updateTime":390,"relativeEntities":391,"slug":20,"properties":392,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"9e90713b-55e6-44df-96bb-721de56654aa","2023-12-05T23:52:31.975+00:00",[],{"title":393},{"VI":394},"Institute of Chemical Technology, Matunga, Mumbai, India",{"title":396},{"VI":397},"G R Gupta",{"id":399,"sortIndex":61,"researcher":20,"roles":400,"affiliations":401,"properties":412},"6cf7f3c3-cbef-4a9a-9d84-19dcd8681fe5",[141],[402],{"id":20,"sortIndex":21,"affiliation":403,"properties":20},{"id":404,"createTime":405,"updateTime":406,"relativeEntities":407,"slug":408,"properties":409,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"0ceaf430-7c73-44bc-8ce6-bdfa8aa95576","2024-04-15T04:31:34.753+00:00","2024-10-13T03:33:09.975+00:00",[],"School-of-Chemical-Sciences-North-Maharashtra-University-Jalgaon-India",{"title":410},{"EN":411},"School of Chemical Sciences, North Maharashtra University, Jalgaon, India",{"title":413},{"VI":414},"P D Patil",{"id":416,"sortIndex":108,"researcher":20,"roles":417,"affiliations":418,"properties":427},"6a63cbf8-52cf-4e46-98cd-36fd655b1468",[141],[419],{"id":20,"sortIndex":21,"affiliation":420,"properties":20},{"id":421,"createTime":422,"updateTime":422,"relativeEntities":423,"slug":20,"properties":424,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"47fc3b44-886d-48f4-890d-fc4a83f56725","2024-01-21T09:19:22.566+00:00",[],{"title":425},{"VI":426},"SSTs College of Engineering and Technology, Bambhori, Jalgaon, India",{"title":428},{"VI":429},"U T Patil",{"id":431,"sortIndex":50,"researcher":20,"roles":432,"affiliations":433,"properties":442},"5e72efde-aba9-465e-82e8-7accc372fb56",[141],[434],{"id":20,"sortIndex":21,"affiliation":435,"properties":20},{"id":436,"createTime":437,"updateTime":437,"relativeEntities":438,"slug":20,"properties":439,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"63f0b29d-7765-4ba7-b923-2140c940b660","2024-01-21T09:19:22.585+00:00",[],{"title":440},{"VI":441},"Swarnandhra College of Engineering and Technology, Narsapur, India",{"title":443},{"VI":444},"R S Dubey",{"id":446,"sortIndex":21,"researcher":20,"roles":447,"affiliations":448,"properties":454},"b19876af-8470-484f-858a-4513673ebe7f",[141],[449],{"id":20,"sortIndex":21,"affiliation":450,"properties":20},{"id":421,"createTime":422,"updateTime":422,"relativeEntities":451,"slug":20,"properties":452,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":453},{"VI":426},{"title":455},{"VI":456},"K S Patil",{"id":458,"sortIndex":109,"researcher":20,"roles":459,"affiliations":460,"properties":466},"8152cded-0e87-4bec-a24f-7be13e5d8de9",[141],[461],{"id":20,"sortIndex":21,"affiliation":462,"properties":20},{"id":421,"createTime":422,"updateTime":422,"relativeEntities":463,"slug":20,"properties":464,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},[],{"title":465},{"VI":426},{"title":467},{"VI":468},"P H Zope",{"url":381,"publisher":470,"properties":498},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":471,"slug":10,"properties":472,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":476,"manageAffiliations":477,"indexDatabases":478,"url":103,"thumbnailPath":20,"statistic":493,"gsStatistic":20,"type":113,"analyzePriority":20},[],{"issn":473,"eissn":474,"title":475},{"VOID":13},{"VOID":15},{"EN":17},[],[],[479,486],{"id":65,"indexDatabase":480,"url":80,"indexYears":20,"academicFieldIds":485,"indexDatabaseRanking":20},{"id":67,"createTime":68,"updateTime":69,"relativeEntities":481,"label":482,"description":483,"key":76,"publicationTags":484,"standard":20},[],{"EN":72,"VI":72},{"VI":74,"EN":75},[78,79],[82],{"id":84,"indexDatabase":487,"url":97,"indexYears":98,"academicFieldIds":492,"indexDatabaseRanking":102},{"id":86,"createTime":87,"updateTime":88,"relativeEntities":488,"label":489,"description":490,"key":94,"publicationTags":491,"standard":20},[],{"EN":91,"VI":91},{"EN":91,"VI":93},[96],[100,101],{"impactFactor":21,"impactFactorByYear":494,"i10Index":21,"i10IndexLast5Year":21,"totalPublication":106,"totalPublicationByYear":495,"totalCitation":21,"totalCitationByYear":496,"totalCitationPerPublication":21,"totalCitationPerPublicationByYear":497,"hindexLast5Year":21,"hindex":21},{},{"1982":108,"1983":109,"1984":108,"1985":109,"1986":109,"1987":109,"1988":61,"1989":108,"1993":109,"1994":109,"1995":109,"1996":109,"1997":109,"1999":108,"2000":109,"2001":108,"2002":108,"2004":109,"2007":109,"2008":109,"2010":61,"2011":108,"2012":108,"2013":108,"2014":50,"2015":108,"2017":61,"2019":110,"2020":108,"2022":109},{},{},{"volume":499,"pages":500},{"VOID":361},{"VOID":501},"1-9","2019-01-30",{"id":504,"createTime":505,"updateTime":506,"relativeEntities":507,"slug":508,"properties":509,"entityType":133,"verifyStatus":134,"verifyTime":518,"verifyNote":135,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":519,"fullTextUrl":20,"authors":520,"publicationType":241,"publisherRelationship":565,"citationCount":20,"citationInfo":20,"publishDate":599,"publishYear":600,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":278},"10066d9c-7aed-40a7-8711-f308bc13f31b","2023-12-25T23:28:35.623+00:00","2024-12-11T23:58:39.192+00:00",[],"Effect-of-stabilizer-on-the-morphology-of-Au-TiO2-spheres-a-combined-experimental-and-theoretical-study",{"references":510,"abstract":512,"title":514,"doi":516},{"VOID":511},"Qi J, Lai X Y, Wang J Y, Tang H J, Ren H, Yang Y, Jin Q, Zhang L J, Yu R B, Ma G H, Su Z G, Zhao H J and Wang D 2015 Chem. Soc. Rev. 44 6749\nMa Y, Wang X L, Jia Y S, Chen X B, Han H X and Li C 2014 Chem. Rev. 114 9987\nBannat I, Wessels K, Oekermann T, Rathousky J, Bahnemann D and Wark M 2009 Chem. Mater. 21 1645\nDing D W, Liu K, He S N, Gao C B and Yin Y D 2014 Nano Lett. 14 6731\nZheng Z K, Huang B B, Qin X Y, Zhang X Y, Dai Y and Whangbo M H 2011 J. Mater. Chem. 21 9079\nBian Z F, Tachikawa T, Zhang P, Fujitsuka M and Majima T 2014 J. Am. Chem. Soc. 136 458\nCheng L, Li X F and Dong J F 2015 J. Mater. Chem. C 3 6334\nFrisch M J, Trucks G W, Schlegel H B et al 2009 Gaussian 09, Revision A. 02 (Wallingford, CT: Gaussian Inc.)\nLee C, Yang W and Parr R G 1988 Phys. Rev. B 37 785\nHacarlioglu P, Lee D, Gibbs G V and Oyama S T 2008 , J. Membr. Sci. 313 277\nLin Y, Zhang Q, Zhao C, Li H, Kong C, Shen C and Chen L 2015 Chem. Comm. 51 697\nMurugan L, Lakshmipathi S and Bhatia S K 2014 RSC Adv. 4 39576\nZeng Q P, Li H, Duan H N, Guo Y P, Liu X F, Zhang Y Y and Liu H Z 2015 RSC Adv. 5 13430\nYang H G and Zeng H C 2004 J. Phys. Chem. B 108 3492\nYec C C and Zeng H C 2014 J. Mater. Chem. A 2 4843",{"EN":513},"In this study, two different particle sizes of Au nanoparticles (NPs) were synthesized using two different stabilizers, and then two different morphologies Au@TiO2 hollow spheres were obtained when the corresponding Au NPs solutions were added to the TiF4 ethanol–water solution under hydrothermal condition. The computational simulation is employed to provide the fundamental support to explain why different stabilizers yield different sizes of Au NPs, and the main cause for the experimental observation is contributed by the different interactive forces between Au and stabilizer molecules. The experimental strategy adopted different stabilizer in this work is expected to be generally applicable for the synthesis of many other types of micro-nanostructured materials.",{"EN":515},"Effect of stabilizer on the morphology of Au@TiO2 spheres: a combined experimental and theoretical study",{"VOID":517},"10.1007\u002Fs12034-016-1306-8","2024-12-11T23:58:39.191+00:00","https:\u002F\u002Flink.springer.com\u002Farticle\u002F10.1007\u002Fs12034-016-1306-8",[521,538,553],{"id":522,"sortIndex":108,"researcher":20,"roles":523,"affiliations":524,"properties":535},"f1185c6b-416e-4c3d-98b7-b8be5afdeb48",[141],[525],{"id":20,"sortIndex":21,"affiliation":526,"properties":20},{"id":527,"createTime":528,"updateTime":529,"relativeEntities":530,"slug":531,"properties":532,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"0a112086-4fb1-4f1d-9c2b-3c8483824ef7","2023-12-11T10:12:48.907+00:00","2025-06-11T22:59:22.490+00:00",[],"National-Key-Laboratory-of-Biochemical-Engineering-Institute-of-Process-Engineering-Chinese-Academy-of-Sciences-Beijing-People-s-Republic-of-China",{"title":533},{"VI":534},"National Key Laboratory of Biochemical Engineering, Institute of Process Engineering, Chinese 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(Rome) 47 797\nGoodenough J B 1963Magnetism and the chemical bond (New York: Wiley)\nLevinson L M and Wanklyn B M 1970J. Solid State Chem. 3 131\nMilligan W O, Watt L M and Rachford H H 1949J. Phys. Colloid Chem. 53 227\nRobertson B and Kostiner E 1972J. Solid State Chem. 4 29\nSchwartz C M and Young A P 1962Acta Crystallogr. 15 1305\nSchwartz C M, Laves F and Young A P 1964Acta Crystallogr. 17 1476\nSiebert H 1954Z. Anorg. Allg. Chem. 275 225",{"EN":708},"Iron(III) vanadate (FeVO4) is an n-type semiconductor between 300 and 800 K. Electrical conduction in this phase occurs due to small deviation from oxygen stoichiometric composition. The mechanism of electrical transport is of a thermally activated hopping of charge carriers (electrons) on equivalent iron lattice sites. The FeVO4 obeys Curie-Weiss law between 80 and 300 K. The measured magnetic moment (μ\n                eff) of Fe3+ ion in FeVO4 is 5·270 BM at 298 K, which is lower than theμ\n                spin only value. The predominant exchange interactions are the weak 90° M-O-M superexchange and M-O-O-M super-super-exchange. The negative Weiss constantϑ=− 30 K of the phase indicated the possibility of an antiferromagnetic ordering of the iron(III) vanadate lattice. The IR absorption spectrum of FeVO4 gave bands at 990, 900, 825 and 725 cm−1 due to the presence of distorted VO4 polyhedra of the lattice.",{"EN":710},"Electrical and magnetic studies of iron (III) vanadate",{"VOID":712},"10.1007\u002FBF02749660","Author affiliation is blank","http:\u002F\u002Flink.springer.com\u002F10.1007\u002FBF02749660",[716,723],{"id":717,"sortIndex":21,"researcher":20,"roles":718,"affiliations":719,"properties":720},"4a2abb7e-eef1-494d-bc8b-5a6caee8084b",[141],[],{"title":721},{"VI":722},"N Suresh Rao",{"id":724,"sortIndex":109,"researcher":20,"roles":725,"affiliations":726,"properties":735},"e2e8175b-e8be-448b-8d37-e58dd5e6573f",[141],[727],{"id":20,"sortIndex":21,"affiliation":728,"properties":20},{"id":729,"createTime":730,"updateTime":730,"relativeEntities":731,"slug":20,"properties":732,"entityType":49,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21},"8aa3c323-26cb-40bc-81db-6d05d8e52ba3","2023-12-05T06:12:29.669+00:00",[],{"title":733},{"VI":734},"Materials Science Research Laboratory, Department of Chemistry, St. Philomena College, Puttur, India",{"title":736},{"VI":737},"O G Palanna",{"url":714,"publisher":739,"properties":767},{"id":6,"createTime":7,"updateTime":8,"relativeEntities":740,"slug":10,"properties":741,"entityType":18,"verifyStatus":19,"verifyTime":20,"verifyNote":20,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"subjectFields":745,"manageAffiliations":746,"indexDatabases":747,"url":103,"thumbnailPath":20,"statistic":762,"gsStatistic":20,"type":113,"analyzePriority":20},[],{"issn":742,"eissn":743,"title":744},{"VOID":13},{"VOID":15},{"EN":17},[],[],[748,755],{"id":65,"indexDatabase":749,"url":80,"indexYears":20,"academicFieldIds":754,"indexDatabaseRanking":20},{"id":67,"createTime":68,"updateTime":69,"relativeEntities":750,"label":751,"description":752,"key":76,"publicationTags":753,"standard":20},[],{"EN":72,"VI":72},{"VI":74,"EN":75},[78,79],[82],{"id":84,"indexDatabase":756,"url":97,"indexYears":98,"academicFieldIds":761,"indexDatabaseRanking":102},{"id":86,"createTime":87,"updateTime":88,"relativeEntities":757,"label":758,"description":759,"key":94,"publicationTags":760,"standard":20},[],{"EN":91,"VI":91},{"EN":91,"VI":93},[96],[100,101],{"impactFactor":21,"impactFactorByYear":763,"i10Index":21,"i10IndexLast5Year":21,"totalPublication":106,"totalPublicationByYear":764,"totalCitation":21,"totalCitationByYear":765,"totalCitationPerPublication":21,"totalCitationPerPublicationByYear":766,"hindexLast5Year":21,"hindex":21},{},{"1982":108,"1983":109,"1984":108,"1985":109,"1986":109,"1987":109,"1988":61,"1989":108,"1993":109,"1994":109,"1995":109,"1996":109,"1997":109,"1999":108,"2000":109,"2001":108,"2002":108,"2004":109,"2007":109,"2008":109,"2010":61,"2011":108,"2012":108,"2013":108,"2014":50,"2015":108,"2017":61,"2019":110,"2020":108,"2022":109},{},{},{"volume":768,"pages":770},{"VOID":769},"18",{"VOID":771},"229-236","1995-06-01",1995,{"id":775,"createTime":776,"updateTime":777,"relativeEntities":778,"slug":779,"properties":780,"entityType":133,"verifyStatus":134,"verifyTime":777,"verifyNote":135,"syncStatus":19,"languages":20,"translateLanguages":20,"viewCount":21,"primaryUrl":789,"fullTextUrl":20,"authors":790,"publicationType":241,"publisherRelationship":830,"citationCount":20,"citationInfo":20,"publishDate":864,"publishYear":865,"citationAnalyzeStatus":19,"lastCitationAnalyze":20,"indexDatabases":20,"openAccess":20,"references":20,"isForceReanalyzing":278},"755ce92b-09b0-4b70-9d4d-d096de7aa243","2024-02-09T14:42:46.992+00:00","2025-01-17T23:57:48.995+00:00",[],"Transient-charging-and-discharging-current-study-in-pure-PVF-and-PVF-PVDF-fluoro-polyblends-for-application-in-microelectronics",{"references":781,"abstract":783,"title":785,"doi":787},{"VOID":782},"Fisher P and Rahl P 1977 Prog. 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Measurements indicated that transient charging and discharging currents exhibited thermally activated character but did not show mirror image behaviour at different temperatures and field values. The log \n                  \n                    \n                  \n                  $\\emph{I}$\n                –log \n                  \n                    \n                  \n                  $\\emph{t}$\n                 plots were found to follow the Curie–Von Schweidler law with the value of decay constant ‘\n                  \n                    \n                  \n                  $\\emph{n}$\n                ’ lying in the range of 0·029–2·9456. These observed characteristics also indicated that the transient charging in PVF:PVDF fluoro polyblends occur partly due to orientation of dipoles but predominantly due to trapped space charges and hopping of charge carriers amongst localized states. The modification in transient behaviour on blending PVDF with PVF have been explained on the basis of plasticization effect which increases free volume and molecular mobility and T\n                \n                  g\n                 modification in the trap structure.",{"EN":786},"Transient charging and discharging current study in pure PVF and PVF\u002FPVDF fluoro polyblends for application in 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Lumin. 151 149\nKhashan K S, Sulaiman G M and Abdulameer F A 2016 Arab. J. Sci. Eng. 41 301\nJung H J, Yu Y and Choi M Y 2015 Bull. Korean Chem. Soc. 36 3\nMaul J, Brito A S, de Oliveira A L M, Lima S J G, Maurera M A M A, Keyson D, Souza A G and Santos I M G 2011 J. Therm. Anal. Calorim. 106 519\nJiang T, Wang Y, Meng D, Wu X, Wang J and Chen J 2014 Appl. Surf. Sci. 311 602\nChiang C-Y, Aroh K and Ehrman S H 2012 Int. J. Hydrogen Energy 37 4871\nYao W-T, Yu S-H, Zhou Y, Jiang J, Wu Q-S, Zhang L and Jiang J 2005 J. Phys. Chem. B 109 14011\nKassaee M Z, Buazar F and Motamedi E 2010 J. Nanomater. 2010 7\nKarahaliou P K, Svarnas P, Georga S N, Xanthopoulos N I, Delaportas D, Krontiras C A and Alexandrou I 2012 J. Nanopart. Res. 14 1\nGoli M, Haratizadeh H and Abrishami M E 2014 Ceram. Int. 40 16071\nLal A, Bleuler H and Wüthrich R 2008 Electrochem. Commun. 10 488\nWüthrich R and Mandin P 2009 Electrochim. Acta 54 4031\nAllagui A and Wüthrich R 2011 Electrochim. Acta 58 12\nCulity B D and Stock S R 1978 Principles of X-ray Diffraction (Reading: Addision-Wesley)\nWuthrich R and Ziki J D A 2014 Micromachining Using Electrochemical Discharge Phenomenon: Fundamentals and Application of Spark Assisted Chemical Engraving (William Andrew)\nCao X D, Kim B H and Chu C N 2009 Precis. Eng. 4 459\nWang H, Xu J Z, Zhu J-J and Chen H-Y 2002 J. Cryst. Growth 244 88\nRehman S, Mumtaz A and Hasanain S K 2011 J. Nanopart. Res. 13 2497\nPhoka S, Laokul P, Swatsitang E, Promarak V, Seraphin S and Maensiri S 2009 Mater. Chem. Phys. 1 423\nMohamed R M, Harraz F A and Shawky A 2014 Ceram. Int. 40 2127",{"EN":1069},"In the present study, cupric oxide (CuO) nanoparticles were synthesized by electrochemical discharge process using strong base electrolytes. The experiments were carried out separately using NaOH and KOH electrolytes. The mass output rate and the crystal size were obtained with variation of the rotation speed of magnetic stirrer for both types of electrolytes. The mass output rate of CuO nanoparticles increased with the increase in the speed of rotation, and, after an optimum speed, it started decreasing. However, the size of the particles reduced with the increase of the rotation speed. The crystal plane of the obtained CuO nanoparticles was similar for both the electrolytes whereas the yield of nanoparticles was higher in KOH as compared with NaOH under the same experiment conditions. In this set of experiments, the maximum output rates obtained were 21.66 mg h−1 for NaOH and 24.66 mg h−1 for KOH at 200 rpm for a single discharge arrangement. The average crystal size of CuO particles obtained was in the range of 13–18 nm for KOH electrolyte and 15–20 nm for NaOH electrolyte. Scanning electron microscopy images revealed that flower-like and caddice clew-shaped CuO nanocrystalline particles were synthesized by the electrochemical discharge process. Fourier transform infrared spectrum showed that the CuO nanoparticles have a pure and monolithic phase. UV–vis–NIR spectroscopy was used to monitor oxidation course of Cu → CuO and the band gap energy was measured as 2 and 2.6 eV for CuO nanoparticle synthesized in NaOH and KOH solutions, respectively.",{"EN":1071},"Synthesis and characterization of CuO nanoparticles using strong base electrolyte through electrochemical discharge 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