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"[Telah dilakukan peningkatan konduktivitas listrik LiFePO4 dengan metode penambahan material logam nano Cu dan CNTs. Metode ini menjadi pilihan yang menarik karena mudah dan murah dalam proses pembuatannya. Proses sintesis dilakukan dengan mencampur serbuk LiFePO4 (komersil) dengan variasi presentase berat nano tembaga (komersil) 0, 1, 3, 5, 7 wt. % dan 5 wt. % nano karbon (komersil)kemudian di proses vacuum mixing dan film applicator. Pengujian XRD, SEM dan EDX dilakukan pada serbuk yang diterima untuk mengkonfirmasi fasa, ukuran butir serta ada tidaknya impurities. Hasil XRD dan EDX pada serbuk nano Cu menunjukkan bahwa telah terjadi oksidasi dan terbentuk menjadi CuO dan Cu2O, serta ditemukanadanya impurities elemen S sebesar 8.5 wt. %. Komposisi fasa yang dihasilkan dari proses penambahan didapat dari menganalisis pola difraksi XRD menunjukkan bahwa fasa yang terbentuk adalahLiFePO4 namun ditemukan adanya impurities berupa Cu4O3 pada variasi penambahan 80 wt. % LiFePO4, 5 wt. % Cu, 5 wt. % C, dan 10 wt. % PVDF. Konduktivitas listrik diuji material katoda LiFePO4 dengan EIS, dan hasil uji menunjukkan bahwa konduktivitas listrik LiFePO4 meningkat seiiring dengan penambahan nano Cu namun tidak terlalu signifikan (dalam satu orde), hal ini dikarenakan efek oksidasi pada Cu.Pada variasi penambahan nano C dan nano Cu terjadi peningkatan sebesar 3 orde dengan nilai konduktivitas sebesar 8.4 x 10-5 S/cm pada variasi penambahan 80 wt. % LiFePO4, 5 wt. % Cu, 5 wt. % C. Penambahan nano karbon pada LiFePO4 lebih efektif dalam peningkatan konduktivitas dibandingkan dengan penambahan nano Cudikarenakan efek oksidasi pada Cu yang tidak dapat dihindari. Morfologi material katoda dan distribusi nano Cu dan nano karbon dianalisis menggunakan SEM/EDX, menunjukkan material yang dicampur pada variasi penambahan nano Cu cukup homogen, struktur butir spherical, sedangkan pada variasi penambahan nano Cu dannano karbon struktur butir polyhedral dengan ukuran butir berada pada rentang 100- 500 nm. Struktur butir ini mempengaruhi hasil cole plot dimana pada variasi penambahan Cu terbentuk semicircle sedangkan pada penambahan nano C tidak;Improved of Electrical conductivity of LiFePO4 with the method of adding Cu Nano metal material and CNTs has been done. This method is an attractive option because it is easy and inexpensive in the manufacturing process. Synthesis process isdone by mixing the powder LiFePO4 (commercial) with a variation of the percentage by weight of Nano copper (commercial) 0, 1, 3, 5, 7 wt. % and 5 wt. % CNTs (commercial) and then process in vacuum mixing and film applicator. Testing XRD, SEM and EDX performed on the powder to confirm the phase, grain size and the presence or absence of impurities. Results of XRD and EDX on Nano Cu powder showed that there had been oxidation and formed into CuO and Cu2O, and discovered the existence of impurities elements S of 8.5 wt. %.Phase composition as the result from adding process obtained with analyzing the XRD diffraction pattern showed that the phase formed is LiFePO4 yet found any impurities in the form of Cu4O3 on variations LiFePO4 addition of 80 wt. %, 5 wt. % Cu, 5 wt. % C, and 10 wt. % PVDF. The electrical conductivity of LiFePO4 cathode material was tested by EIS, and the results showed that the electrical conductivity of LiFePO4 increased with the addition of Nano-Cu but not too significant (still on the same order), this is because the effects of oxidation on Cu. On the addition of Nano C and Nano Cu variation there is an increase of 3 order with conductivity value 8.4 x 10-5 S / cm at variations LiFePO4 addition of 80 wt.%, 5 wt.% Cu, 5 wt.% C. The addition of CNTs is more effective in LiFePO4 conductivity increase, compared to the additionof Nano-Cu due to the effects of oxidation on Cu are unavoidable. Cathode material morphology and distribution of CNTs and Nano Cu analyzed using SEM / EDX, showed mixed material on the variation of the addition of Nano Cu quite homogenous, spherical grain structure, while the variation of the addition of Nano Cu and CNTs structures polyhedral grains with a grain size in the range 100-500 nm. This affects the grain structure results in a variation of Cole plot where the addition of Cu is formed semicircle, while the addition of Nano C is not.;Improved of Electrical conductivity of LiFePO4 with the method of adding CuNano metal material and CNTs has been done. This method is an attractive optionbecause it is easy and inexpensive in the manufacturing process. Synthesis process isdone by mixing the powder LiFePO4 (commercial) with a variation of the percentageby weight of Nano copper (commercial) 0, 1, 3, 5, 7 wt. % and 5 wt. % CNTs(commercial) and then process in vacuum mixing and film applicator. Testing XRD,SEM and EDX performed on the powder to confirm the phase, grain size and thepresence or absence of impurities. Results of XRD and EDX on Nano Cu powdershowed that there had been oxidation and formed into CuO and Cu2O, and discoveredthe existence of impurities elements S of 8.5 wt. %.Phase composition as the result from adding process obtained with analyzingthe XRD diffraction pattern showed that the phase formed is LiFePO4 yet found anyimpurities in the form of Cu4O3 on variations LiFePO4 addition of 80 wt. %, 5 wt. %Cu, 5 wt. % C, and 10 wt. % PVDF. The electrical conductivity of LiFePO4 cathodematerial was tested by EIS, and the results showed that the electrical conductivity ofLiFePO4 increased with the addition of Nano-Cu but not too significant (still on thesame order), this is because the effects of oxidation on Cu. On the addition of Nano Cand Nano Cu variation there is an increase of 3 order with conductivity value 8.4 x 10-5 S / cm at variations LiFePO4 addition of 80 wt.%, 5 wt.% Cu, 5 wt.% C. The additionof CNTs is more effective in LiFePO4 conductivity increase, compared to the additionof Nano-Cu due to the effects of oxidation on Cu are unavoidable. Cathode materialmorphology and distribution of CNTs and Nano Cu analyzed using SEM / EDX,showed mixed material on the variation of the addition of Nano Cu quite homogenous,spherical grain structure, while the variation of the addition of Nano Cu and CNTsstructures polyhedral grains with a grain size in the range 100-500 nm. This affects thegrain structure results in a variation of Cole plot where the addition of Cu is formedsemicircle, while the addition of Nano C is not., Improved of Electrical conductivity of LiFePO4 with the method of adding CuNano metal material and CNTs has been done. This method is an attractive optionbecause it is easy and inexpensive in the manufacturing process. Synthesis process isdone by mixing the powder LiFePO4 (commercial) with a variation of the percentageby weight of Nano copper (commercial) 0, 1, 3, 5, 7 wt. % and 5 wt. % CNTs(commercial) and then process in vacuum mixing and film applicator. Testing XRD,SEM and EDX performed on the powder to confirm the phase, grain size and thepresence or absence of impurities. Results of XRD and EDX on Nano Cu powdershowed that there had been oxidation and formed into CuO and Cu2O, and discoveredthe existence of impurities elements S of 8.5 wt. %.Phase composition as the result from adding process obtained with analyzingthe XRD diffraction pattern showed that the phase formed is LiFePO4 yet found anyimpurities in the form of Cu4O3 on variations LiFePO4 addition of 80 wt. %, 5 wt. %Cu, 5 wt. % C, and 10 wt. % PVDF. The electrical conductivity of LiFePO4 cathodematerial was tested by EIS, and the results showed that the electrical conductivity ofLiFePO4 increased with the addition of Nano-Cu but not too significant (still on thesame order), this is because the effects of oxidation on Cu. On the addition of Nano Cand Nano Cu variation there is an increase of 3 order with conductivity value 8.4 x 10-5 S / cm at variations LiFePO4 addition of 80 wt.%, 5 wt.% Cu, 5 wt.% C. The additionof CNTs is more effective in LiFePO4 conductivity increase, compared to the additionof Nano-Cu due to the effects of oxidation on Cu are unavoidable. Cathode materialmorphology and distribution of CNTs and Nano Cu analyzed using SEM / EDX,showed mixed material on the variation of the addition of Nano Cu quite homogenous,spherical grain structure, while the variation of the addition of Nano Cu and CNTsstructures polyhedral grains with a grain size in the range 100-500 nm. This affects thegrain structure results in a variation of Cole plot where the addition of Cu is formedsemicircle, while the addition of Nano C is not.]"

"Litium titanat Li4Ti5O12 merupakan salah satu material yang sedang dikembangkan sebagai anoda pada baterai litium ion. Kelebihan litium titanat diantaranya memiliki sifat zero-strain yaitu tidak terjadi perubahan volume atau perubahan volume yang sangat rendah (<1%) saat charge dan discharge, tidak menimbulkan SEI, dan dapat digunakan untuk high rate. Namun litium titanat memiliki kelemahan berupakonduktivitas listrik dan kapasitas yang rendah. Oleh karena itu perlu dikombinas ika n dengan bahan lain yang memiliki kapasitas tinggi seperti silikon dan bahan yang memilik i konduktivitas listrik tinggi seperti karbon. Dalam penelitian ini komposit Li4Ti5O12-C/Si Nano dibuat untuk mendapat anoda dengan kapasitas dan konduktivitas listrik yang tinggi. Karbon ditambahkan dengan variasi 1, 3, dan 5 wt% pada saat proses sol-gel, sedangkan Si nano ditambahkan sebesar 10 wt% dari total material aktif pada pembuatan slurry. Karbon yang ditambahkan merupakan karbon aktif yang sebelumnya telah dilakukan proses aktivasidengan menggunakan NaOH.Karbon aktif hasil aktivasi dilakukan karakterisasi BET dan SEM-EDS. Sementara, komposit Li4Ti5O12-C/Si Nano di karakterisasi dengan XRD danSEM-EDS, sertadilakukan pengujian EIS, CV, dan CDuntuk mengetahui performa elektrokimia baterai. Karbon aktif memiliki luas permukaan spesifik sebesar 490,007 m2/g serta ditemukan pori pada struktur mikro karbon aktif. Berdasarkan hasil uji EIS diperoleh bahwa konduktivitas listrik tertinggi terdapat padaLi4Ti5O12-1%C/Si Nano. Kapasitas spesifik tertinggiberdasarkan hasil uji CVterdapat pada Li4Ti5O12-3%C/Si Nanoyaitu sebesar 168 mAh/g.Kapasitas charge-discharge tertinggi pada current rate 0,2 C sampai 20 C berdasarkan hasil uji CD terdapat pada Li4Ti5O12-5%C/Si Nano.

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Lithium titanate is one of the materials being developed as anode in Li-ion battery. Lithium titanate has zero-strain properties that does notvolume change or very low volume change (<1%) at charge and discharge, does not cause SEI, and can be used for high rate. However, lithium titanate has a weakness such aslowelectrical conductivit y and low capacity. Therefore,it needs to be combined with high-capacity materials such as silicon and materials that have high electrical conductivity such as carbon.

In this study,the composite Li4Ti5O12-C/Si Nano was made toobtain an anode with high capacity and electricalconductivity. Carbon is added with a variation of 1, 3, and 5 wt% during the sol-gel process, while Si nano is added by 10wt% of the total activematerialingred ie nt in the slurry making. The carbon added is activated carbon which has previously been activated by using NaOH. Activated carbon as activation result ischaracterized by BET and SEM-EDS. Composite Li4Ti5O12-C/Si nano is characterized by XRD and SEM-EDS. Then, to determine the battery performance, EIS, CV, and CD testwere conducted. Activated carbon has a specific surface area of 490.007 m2/g and found pores in the micro structureof activated carbon.

Based on EIS test results obtained that the highest electrical conductivity is found in Li4Ti5O12-1%C/SiNano. The highest specific capacity based on CV test resultsis found inLi4Ti5O12-3%C/Si Nanowhich is168 mAh/gand the highest charge-discharge capacity at current rate 0,2 C to 20 C based on CD test results is found in Li4Ti5O12-5%C/SiNano."

"Lithium Ferro Phosphate (LiFePO4) adalah kandidat yang menjanjikan sebagai bahan sumber energi elektrik yang ramah lingkungan. Penambahan Ni komposit dalam baterai berbasis Li-ion dapat meningkatan performa dari baterai LiFePO4. Dalam penelitian ini, LiFePO4 akan disintesis dengan menggunakan Fe2O3, H3PO4, dan LiOH melalui cara solid-state dan dilakukan perlakuan panas yaitu sintering. Setelah itu, prekursor dikompositkan dengan tiga variasi penambahan konten Nikel dalam % berat, yaitu 5, 7 dan 10% melalui metode solid-state dengan ball mill diberi label LFP/5-Ni, LFP/7.5-Ni dan LFP/10-Ni. Karakterisasi dilakukan menggunakan XRD dan SEM untuk mengamati efek penambahan Nikel pada struktur dan morfologi sampel yang dihasilkan.

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Lithium Ferro Phosphate (LiFePO4) is a promising candidate as an environmental friendly electric energy sources. The addition of Nickel composite in Lithium-ion battery based can enhance the performance of LiFePO4 batteries. In this experiment, LiFePO4 was synthesized using Fe2O3, H3PO4, and LiOH by solid-state method and heat treated with sintering process. After that, the precursor were composited with the various Nickel composition, in % wt, 5, 7.5 and 10% with solid-state method by using ball mill and labeled as LFP/5-Ni, LFP/7.5-Ni and LFP/10-Ni respectively. The characterizations were made using XRD and SEM testing. These were performed to observe the effect of Nickel addition on structure and morphology of the resulting samples."

"Litium-Ferrous-Fosfat, LiFePO4 (LFP) adalah kandidat yang menjanjikan sebagai bahan katoda baterai lithium ion. Dalam penelitian ini, LFP akan disintesis dengan menggunakan Fe2O3 melalui cara solid-state dengan bantuan H3PO4 and LiOH•H2O. Setelah itu, nikel akan ditambahkan ke LFP secara komposit. Penambahan konten glukosa sebagai sumber karbon akan dilakukan dengan tiga variasi, 6%, 8% dan 10%. Karakterisasi dilakukan menggunakan XRD dan SEM untuk mengamati efek variasi konten karbon pada struktur dan morfologi sampel yang dihasilkan.

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Lithium-iron-phosphate, LiFePO4 (LFP) is one of promising candidate in development of battery cathode. In this experiment, the LFP will be synthesize using Fe2O3, H3PO4 and LiOH•H2O as precursors through solid-state process. Nickel will be added to the LFP/C to improve the properties of LFP/C. The addition of varies glucose content as a carbon source will be done, 6%, 8% and 10%. Material characterization of the samples will be done by using Scanning Electron Microscope (SEM) and X-Ray Diffraction (XRD) to observe the effect of glucose content on the material structure and morphology."

"Litium Ferro Phosphate, LiFePO4 (LFP) adalah kandidat yang menjanjikan sebagai bahan katoda baterai lithium ion. Dalam penelitian ini, LFNP/C disintesis dengan metode solid-state dari precursor LFP, Nikel menjadi variasi penambahan konten LFP dalam bentuk doping, yaitu, 6, 7,5 dan 9%, diberi label sampel LFNP/C-Ni6%, LFNP/C-Ni7.5% dan LFNP/C-Ni9%. Karakterisasi dilakukan menggunakan XRD, SEM, EDX, dan MAPPING. Ini dilakukan untuk mengamati efek penambahan Nikel pada struktur, morfologi, dan komposisi sampel. Hasil penelitian menunjukkan bahwa persentase optimum doping Nikel adalah 7.5% karena telah menunjukan hasil yang memuaskan di performa CV,CD, dan EIS dengan ukuran kristal 76.93 nm. Dalam pengujian cyclic voltametry, konduktivitas dan kapasitas sampel meningkat dan disebabkan oleh penambahan Nikel pada LFP.

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Lithium Ferro Phosphate, LiFePO4 (LFP) is a promising candidate as a cathode material for lithium ion batteries. In this study, LFNP / C was synthesized by the solid-state method of the LFP precursors, Nickel became a variation of LFP content addition in the form of doping, namely, 6, 7.5 and 9%, labeled LFNP / C-Ni6% sample, LFNP / C-Ni7.5% and LFNP / C-Ni9%. Characterization was done using XRD, SEM, EDX, and MAPPING. This was done to observe the effect of adding Nickel to the structure, morphology, and composition of the sample. The results showed that the optimum percentage of Nickel doping was 7.5% because it had shown satisfactory results in the performance of CV, CD, and EIS with a crystal size of 76.93 nm. In cyclic voltametry testing, the conductivity and capacity of the sample increases and is caused by the addition of Nickel to LFP."

"Senyawa Li4Ti5O12 merupakan senyawa yang memiliki potensial sebagai material anoda namun memiliki beberapa kekurangan. Kekurangan dari LTO adalah memiliki konduktivias yang rendah dan kapasitas teoritis yang lebih rendah dari grafit yang dipakai sebagai material anoda pada baterai lithium ion. Pada penelitian ini mixing element yang diberikan pada LTO adakah karbon aktif dan SnO2 untuk menutupi kekurangan dari LTO. Jumlah karbon aktif yang diberikan adalah sebanyak 1, 3 dan 5. Persen SnO2 yang ditambahkan adalah 10. Senyawa SnO2 ditambahkan pada komposit LTO/C menggunakan metode deposisi in-situ. Dengan metode deposisi in-situ senyawa SnO2 yang diperoleh memiliki ukuran partikel yang kecil dan tersebar secara merata. Li4Ti5O12 disintesis menggunakan metode sol-gel, hidrothermal dan mekanokimia dengan menggunakan LiOH sebagai sumber ion lithium. Karakterisasi yang digunakan adalah XRD dan SEM-EDX. Untuk pengujian performa baterai dilakukan pengujian EIS, CV dan CD untuk mengetahui efek dari penambahan karbon aktif dan SnO2 pada performa elektrokimia. Hasil pengujian XRD menunjukkan partikel SnO2 telah terbentuk dan tanpa pengotor. Hasil pengujian SEM menunjukkan partikel SnO2 yang terbentuk memiliki ukuran partikel yang kecil dan tersebar merata begitu pula dengan partikel karbon aktif tersebar secara merata. hasil pengujian CV menunjukkan bahwa penambahan karbon aktif meningkatkan kapasitas spesifik LTO. Hasil pengujian CD menunjukkan dengan penambahan karbon aktif, capacity loss pada c-rate tinggi dapat dikurangi.

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Li4Ti5O12 is one of the compound which has potential as anode material on lithium ion battery but with certain limitation. The limitation of Li4Ti5O12 are it hasa low conductivity and low theoritical capacity compared to graphite which is anode material of state of the art litihum ion battery.

In this research mixing element given to LTO are activated carbon and SnO2 to decrease LTO limitation. Activated carbon as mixing element added in LTO are 1, 3 and 5. SnO2 added to LTO are 10. SnO2 added to LTO composite with in situ deposition method.

Using in situ deposition method, SnO2 particle acquired from deposition has small particle size and distribute evenly. Li4Ti5O12 synthetized with sol gel method, hydrotermal method and mechano chemical method using LiOH as ionic Li source. The sample was characterized with XRD and SEM EDX. For battery performance, EIS, CV and CD testing was conducted to determine the effect of addition activated carbon and SnO2 on electrochemical performance.

Based on XRD result, SnO2 particle is formed with no residue from previous reaction. Based on SEM EDS result, SnO2 particle has small size and distribute evenly same with active carbon. The result from CV testing show with addition of activated carbon increase specific capacity of LTO. The result from CD tewting show with addition of activated carbon, capacity loss on high c rate can be reduced."

"Telah dilakukan sintesis LiFePO4/C sebagai material katoda baterai lithium ion dengan menggunakan metode hidrotermal dari bahan LiOH, NH4H2PO4, FeSO4.7H2O, carbon black dan sukrosa. Proses hidrotermal dilakukan pada suhu reaktor 180⁰C dengan lama waktu penahanan 20 jam. Penambahan karbon dilakukan dengan 2 cara. Pertama menggunakan sukrosa sebagai sumber karbon yang dilarutkan bersama prekusor dan kedua menggunakan carbon black yang ditambahkan setelah proses hidrotermal sebelum proses kalsinasi. Temperatur kalsinasi divariasikan pada 500, 600 dan 750⁰C selama 5 jam. Proses dekomposisi termal dianalisis menggunakan DTA-TGA analyzer, karakterisasi fasa dilakukan dengan XRD, morfologi dengan SEM/EDX, nilai konduktifitas dan kapasitansi material dengan LCR-EIS, dan performa baterai dengan pengujian charge-discharge menggunakan baterai analyzer. Hasil LiFePO4/C yang murni berbentuk flake berhasil disintesis dengan penambahan carbon black 5 wt%, sedangkan untuk penambahan karbon melalui pelarutan sukrosa masih terdapat pengotor Fe3(PO4)2 pada hasil kalsinasi. Temperatur kalsinasi optimal adalah 750⁰C dengan ukuran kristalit 39,7 nm, tebal butiran flake 80 nm dan besar butiran rata-rata 427 nm. Konduktifitas LiFePO4 murni terukur 5 x 10-7 S/cm dan konduktifitas LiFePO4/C adalah 2,23 x 10-4 S/cm yang dihasilkan dari sampel dengan tambahan carbon black 5wt% kalsinasi 750⁰C. Dari pengujian charge/discharge didapatkan siklus terbaik dihasilkan oleh sampel LiFePO4/C yang dikalsinasi 750⁰C yang stabil dengan tegangan 3,3-3,4 V, kapasitas spesifik dihasilkan pada 0,1 C = 11,6 mAh/g ; 0,3C = 10,78 mAh./g dan 0,5 C = 9,45 mAh/g.

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LiFePO4/C has been succesfully synthesized through hydrothermal method from LiOH, NH4H2PO4, and FeSO4.7H2O as starting materials and either carbon black or sucrose as carbon source used as cathode material for lithium ion batteries. In this work, hydrothermal reaction temperature was at 180C for 20 hours.Carbon sources were added in two routes. Firstly, sucrose solution was mixed with precursor solution before hydrothermal reaction. Secondly carbon black was added after hydrothermal reaction before calcination process. Calcination temperatures were performed at 500, 600, and 750C each for 5 hours. Thermal decomposition process was analyzed using DTA-TGA analyzer, phases and morphological were characterized by using XRD and SEM/EDX measurement, conductivity and electrical capacity were characterized by EIS measurement, and batteries performance were tested with charge discharge testing by battery analyzer. Pure LiFePO4/C flake shaped was successfully synthesized with the addition of 5 wt% carbon black, while the addition of carbon through the dissolution of sucrose still contained impurity from Fe3(PO4)2 in calcination product. Optimal calcination temperature was obtained at 750⁰C with crytallite size of 39.7 nm, flake particles diameter of 80 nm with particles average length of 427 nm. Pure LiFePO4 conductivity was measured to be 5 x 10-7 S/cm and conductivity LiFePO4/C was 2.23 x 10-4 S/cm produced from samples with carbon black addition of 5 wt% and calcined at 750⁰C. Charge/discharge cycles test showed that best battery performance was obtained from the sample with carbon black of 5wt% calcined at 750⁰C, with a stable voltage 3.3 to 3.4 V, specific capacity of 0.1 C = 11.6 mAh/g ; 0.3C = 10.78 mAh./g dan 0.5 C = 9.45 mAh/g."

"Litium Ferro Phosphate, LiFePO4 (LFP) adalah kandidat yang menjanjikan sebagai bahan katoda baterai lithium ion. Dalam penelitian ini, LFNP/C disintesis dengan metode solid-state dari precursor LFP, Nikel menjadi variasi penambahan konten LFP dalam bentuk doping, yaitu, 6, 7,5 dan 9%, diberi label sampel LFNP/C-Ni6%, LFNP/C-Ni7.5% dan LFNP/C-Ni9%. Karakterisasi dilakukan menggunakan XRD, SEM, EDX, dan MAPPING. Ini dilakukan untuk mengamati efek penambahan Nikel pada struktur, morfologi, dan komposisi sampel. Hasil penelitian menunjukkan bahwa persentase optimum doping Nikel adalah 7.5% karena telah menunjukan hasil yang memuaskan di performa CV,CD, dan EIS dengan ukuran kristal 76.93 nm. Dalam pengujian cyclic voltametry, konduktivitas dan kapasitas sampel meningkat dan disebabkan oleh penambahan Nikel pada LFP.

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Lithium Ferro Phosphate, LiFePO4 (LFP) is a promising candidate as a cathode material for lithium ion batteries. In this study, LFNP / C was synthesized by the solid-state method of the LFP precursors, Nickel became a variation of LFP content addition in the form of doping, namely, 6, 7.5 and 9%, labeled LFNP / C-Ni6% sample, LFNP / C-Ni7.5% and LFNP / C-Ni9%. Characterization was done using XRD, SEM, EDX, and MAPPING. This was done to observe the effect of adding Nickel to the structure, morphology, and composition of the sample. The results showed that the optimum percentage of Nickel doping was 7.5% because it had shown satisfactory results in the performance of CV, CD, and EIS with a crystal size of 76.93 nm. In cyclic voltametry testing, the conductivity and capacity of the sample increases and is caused by the addition of Nickel to LFP."

"Litium Titanat, Li4Ti5O12 (LTO) adalah kandidat yang menjanjikan sebagai bahan anoda baterai lithium ion. LTO dalam bentuk struktur nanorod akan lebih menjanjikan lagi dengan sifatnya yang lebih baik disbanding struktur biasa. Dalam penelitian ini, LTO nanorod akan disintesis dengan menggunakan bubuk TiO2 melalui cara hidrotermal dengan bantuan litium hidroksida (LiOH). Setelah itu, Grafit dan Nano-Timah akan ditambahkan Bersama LTO Nanorod. Tiga variasi penambahan konten Nano-Timah dalam % berat, yaitu, 5, 10 dan 15%, diberi label sampel LTO/C-5%Nano Sn, LTO/C-10%Nano Sn and LTO/C-15%Nano Sn. Karakterisasi dilakukan menggunakan XRD dan SEM untuk mengamati efek penambahan Nano-Timah pada struktur dan morfologi sampel yang dihasilkan. Hasil menunjukkan bahwa penambahan Nano-Ttimah 10% (LTO/C-10%Nano Sn) memiliki kapasitas spesifik tertinggi dengan 87.07 mAh g-1. Hasil dari tes Electrochemical Impedance Spectroscopy juga menunjukkan LTO/C-10%Nano Sn memiliki konduktivitas terbaik dengan nilai resistansi terkecil.

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Lithium titanate, Li4Ti5O12 (LTO) is a promising candidate as lithium ion battery anode material. LTO in nanorod structure could be even more promising as its properties are better than regular structure. In this investigation, LTO nanorod was prepared by using TiO2 powder then processed by hydrothermal method, with the help of lithium hydroxide (LiOH), resulting in LTO. Graphite and Nano Tin are mixed together with LTO using solid-state method. Three variations of Nano Tin content addition in weight%, i.e., 5, 10 and 15%, labelled as sample LTO/C-5%Nano Sn, LTO/C-10%Nano Sn and LTO/C-15%Nano Sn, respectively. The characterizations were made using XRD and SEM testing. These were performed to observe the effect of Nano Tin addition on structure and morphology of the resulting samples. The result showed that the addition of Nano-Tin of 10% (LTO/C-10%Nano Sn) has the highest specific capacity with 87.07 mAh g-1. According to Electrochemical Impedance Spectroscopy, LTO/C-10%Nano Sn also has the best conductivity with the lowest resistivity. "

"Litium Titanat, Li4Ti5O12 (LTO) adalah kandidat yang menjanjikan sebagai bahan anoda baterai lithium ion. Dalam penelitian ini, LTO/C@ZnO disintesis dengan LTO nanorod dengan metode hidrotermal dari TiO2 xerogel yang dibuat dengan metode sol-gel, litium hidroksida (LiOH), Karbon aktif, dan Zinc Oksida (ZnO) nanorod. Tiga variasi penambahan konten ZnO dalam % berat, yaitu, 4, 7 dan 10%, diberi label sampel LTO/C@ZnO-4, LTO C@ZnO-7 dan LTO/C@ZnO-10. Karakterisasi dilakukan menggunakan XRD, SEM, FE-SEM, dan BET. Ini dilakukan untuk mengamati efek penambahan ZnO pada struktur, morfologi, dan luas permukaan sampel yang dihasilkan. Hasil penelitian menunjukkan bahwa kapasitas optimum dari masing- masing sampel adalah 32,84 mAh/g dalam LTO/C@ZnO-4 dengan ukuran kristal 11,86 nm dan luas permukaan 348,736 m2/g. Dalam pengujian cyclic voltametry, menunjukkan pergeseran dalam tegangan reaksi dan pengurangan kapasitas yang disebabkan oleh penambahan C@ZnO dan kurangnya Li4Ti5O12 yang terbentuk.

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Lithium titanate, Li4Ti5O12 (LTO) is a promising candidate as lithium ion battery anode material. In this investigation, LTO/C@ZnO was synthesized with LTO nanorod by hydrothermal method using TiO2 xerogel that prepared by the sol-gel method, lithium hydroxide (LiOH), Activated carbon, and Zinc Oxide (ZnO) nanorod. Three variations of ZnO content addition in weight% , i.e., 4, 7 and 10%, labelled as sample LTO/C@ZnO-4, LTO/C@ZnO-7 and LTO/C@ZnO-10, respectively. The characterizations were made using XRD, SEM, FE-SEM, and BET testing. These were performed to observe the effect of ZnO addition on astructure, morphology, and surface area of the resulting samples. Result showed that the optimum discharge capacity from each samples was 32.84 mAh/g in LTO/C@ZnO-4 with the crystallite size of 11.86 nm and the surface area of 348.736 m2/g. In cyclic voltammetry testing, it shows a shift in reaction voltage and reduction in capacity that caused by the addition of C@ZnO and the lack of Li4Ti5O12 that are formed.

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