Hasil Pencarian  ::  Simpan CSV :: Kembali

"Lithium titanate, Li4Ti5O12 (LTO) is a promising candidate as lithium ion battery anode material. In this investigation, LTO was synthesized by a solid state method using TiO2 xerogel prepared by the sol-gel method and lithium carbonate (Li2CO3). Three variations of Li2CO3 content addition in mol% or Li2CO3 molar excess were fabricated, i.e., 0, 50 and 100%, labelled as sample LTO-1, LTO-2 and LTO-3, respectively. The characterizations were made using XRD, FESEM, and BET testing. These were performed to observe the effect of lithium excess addition on structure, morphology, and surface area of the resulting samples. Results showed that the crystallite size and surface area of each sample was 50.80 nm, 17.86 m2/gr for LTO-1; 53.14 nm, 22.53 m2/gr for LTO-2; and 38.09 nm, 16.80 m2/gr for LTO-3. Furthermore, lithium excess caused the formation of impure compound Li2TiO3, while a very small amount of rutile TiO2 was found in LTO-1. A near-pure crystalline Li4Ti5O12 compound was successfully synthesized using the present method with stoichiometric composition with 0% excess, indicating very little Li+ loss during the sintering process."

"Lithium Titanate (Li4Ti5O12) or (LTO) has a potential as an anode material for a high performance lithium ion battery. In this work, LTO was synthesized by a hydrothermal method using Titanium Dioxide (TiO2) xerogel prepared by a sol-gel method and Lithium Hydroxide (LiOH). The sol-gel process was used to synthesize TiO2 xerogel from a titanium tetra-n-butoxide/Ti(OC4H9)4 precursor. An anatase polymorph was obtained by calcining the TiO2 xerogel at a low temperature, i.e.: 300oC and then the hydrothermal reaction was undertaken with 5M LiOH aqueous solution in a hydrothermal process at 135oC for 15 hours to form Li4Ti5O12. The sintering process was conducted at a temperature range varying from 550oC, 650oC, and 750oC, respectively to determine the optimum characteristics of Li4Ti5O12. The characterization was based on Scanning Thermal Analysis (STA), X-ray Powder Diffraction (XRD), Field Emission Scanning Electron Microscopy (FESEM), Fourier Transform Infrared spectroscopy (FTIR), and Brunauer-Emmett-Teller (BET) testing results. The highest intensity of XRD peaks and FTIR spectra of the LTO were found at the highest sintering temperature (750oC). As a trade-off, however, the obtained LTO/Li4Ti5O12 possesses the smallest BET surface area (< 0.001 m2/g) with the highest crystallite size (56.45 nm)."

"ABSTRAKLitium titanat (Li4Ti5O12)/LTO merupakan senyawa yang digunakan sebagai anoda baterai litium ion. Untuk meningkatkan performa baterai litium ion maka dilakukan material komposit pada LTO yaitu LTO nanorod/Sn-grafit. Penelitian ini membahas pengaruh variasi temperatur hidrotermal pada Li4Ti5O12 nanorod dan variasi persen berat timah (Sn) pada Li4Ti5O12 nanorod/Sn -grafit sebagai anoda baterai litium. Variasi temperatur hidrotermal pada sintesis LTO nanorod adalah 2000 C, 2200 C, dan 2400 C. Variasi komposisi persen berat Sn adalah 5%, 7,5%,dan 10%. Sementara persen berat grafit adalah konstan sebesar 10%. Karakterisasi material dilakukan dengan XRD dan SEM. Analisis performa baterai dilakukan dengan pengujian EIS, CV, dan CD. Hasil pengujian XRD menunjukkkan terdapat senyawa LTO nanorod, TiO2 rutile, Li2TiO3, Sn dan grafit. Hasil pengujian SEM menunjukkan tidak ada aglomerasi yang terbentuk dan semakin tinggi temperatur hidrotermal maka bentuk LTO nanorod semakin jelas. Hasil pengujian EIS menunjukkan penambahan persen berat Sn menurunkan nilai konduktivitas. Nilai konduktivitas berbanding terbalik dengan nilai resistivitas (Rct). Nilai konduktivitas tertinggi pada sampel L240Sn5dengan nilai Rct 58,04 Ω . Hasil pengujian CD menunjukkan bahwa material Sn pada komposit meningkatkan nilai kapasitas baterai. Tetapi penambahan persen berat Sn akan menurunkan nilai kapasitas baterai secara drastis seperti terlihat di nilai C-rates sampel. Hasil pengujian CV menunjukkan nilai kapasitas yang paling tinggi adalah 179,38 Mah/g yaitu pada sampel L220Sn7,5. Nilai sampel paling rendah adalah 130,02 Mah/g pada sampel L200Sn7,5. Tegangan kerja yang paling baik adalah 1,5585 V pada sampel L240Sn5. Tegangan kerja pada sampel ini mendekati tegangan kerja nominal LTO yaitu 1,55V. Variasi Sn pada komposit LTO nanorod/Sn-grafit yang paling baik adalah 5 % (L240Sn5-G10).

---

ABSTRACTLithium titanate (Li4Ti5O12) / LTO is a compound used as an anode for lithium ion batteries. To improve the performance of lithium ion batteries, composite materials are carried out on LTO, namely LTO nanorod / Sn-graphite. This study discusses the effect of hydrothermal temperature variations on Li4Ti5O12 nanorods and variations in the weight percent of Sn on Li4Ti5O12 nanorod / Sn-graphite as an lithium battery anode. Hydrothermal temperature variations in the synthesis of LTO nanorods are 2000 C, 2200 C, and 2400 C. The variation of the composition of weight percent Sn is 5%, 7.5%, and 10%. While graphite weight percent is constant at 10%. Material characterization is done by using XRD and SEM. The performance analysis of the battery is done by testing the EIS, CV, and CD. The XRD test results showed that there are compounds of LTO nanorod, rutile TiO2, Li2TiO3, Sn and graphite. SEM test results show that no agglomerates are formed and the higher the hydrothermal temperature, the more clear the shape of the LTO nanorod. The EIS test results show that the addition of weight percent Sn decreases the conductivity value. The conductivity value is inversely proportional to the resistivity value (Rct). The highest conductivity value in the L240Sn5 sample with an Rct value of 58.04 Ω. The CD test results show that the Sn material on the composite increases the value of the battery capacity. But the addition of weight percent Sn will reduce the value of battery capacity drastically as seen in the sample C-rates. The CV test results show the highest capacity value is 179.38 Mah / g, ie in the L220Sn7.5 sample. The lowest sample value is 130.02 Mah / g in the L200Sn7.5 sample. The best working voltage is 1.5585 V in the L240Sn5 sample. The working voltage in this sample approaches the nominal working voltage of LTO which is 1.55V. The best variation of Sn in LTO nanorod / Sn-graphite composites is 5% (L240Sn5-G10)."

"Anoda Li4Ti5O12 (LTO) yang didoping dengan Mg dan Fe dalam bentuk Li4-xMgxTi5-xFexO12 (x = 0, 0.05, 0.1) telah berhasil disintesis menggunakan metode solidstatedengan bantuan sonikasi menggunakan sumber prekursor TiO2 dan Fe2O3, baikkomersial maupun hasil sintesis. Hasil SEM menunjukkan sampel dengan co-doping Mgdan Fe pada LTO komersial memiliki morfologi yang relatif sama dan seragam dan terjadipengurangan ukuran partikel co-doping LTO dengan x = 0.05. Namun, co-doping LTOhasil sintesis tidak ditemukan adanya reduksi pada ukuran partikel yang mengindikasikanbahwa co-doping Mg dan Fe tidak berpengaruh pada ukuran partikel. Hasil EDSmenunjukkan kehadiran unsur Mg, Fe, Ti, dan O yang menunjukkan bahwa unsur yangdiinginkan pada sampel co-doping dan persebarannya relatif merata. Karakterisasi XRDmenunjukkan bahwa fasa Mg(OH)2 dan Fe2O3 tidak ditemukan di dalam struktur codopingLTO yang mengindikasikan bahwa atom Mg dan Fe telah bergabung denganstruktur LTO. Sampel dengan prekursor TiO2 dan Fe2O3 komersial dan TiO2 sintesisdengan Fe2O3 hasil purifikasi pada komposisi x = 0,1 memiliki fasa pengotor terendahdibandingkan LTO komersial dan LTO sintesis murni yaitu 12,7% dan 9,9%. Nilai Rctsemua sampel co-doping menunjukkan nilai Rct lebih kecil dibandingkan nilai Rct LTOmurni (Rct co-doping < Rct LTO murni). Hal ini menunjukkan bahwa co-doping Mg danFe mengurangi hambatan difusi LTO, sehingga meningkatkan transfer muatan dankonduktivitas listrik. Dengan demikian, menunjukkan bahwa pergerakan ion Li+ lebihmudah pada sampel LTO yang didoping. Sampel LTO sintesis dengan menggunakanprekursor Fe2O3 hasil purifikasi (x = 0,1) memiliki nilai Rct paling rendah dibandingkansemua sampel yaitu 85,41 Ω dan memiliki nilai koefisien difusi ion litium dankonduktivitas paling besar yaitu 2,081 x 10-11 cm2.s-1 dan 2,913 S.cm-1. Selain itu,memiliki nilai ΔE yang paling rendah, sehingga memiliki derajat polarisasi terendah danreversibilitas yang paling baik. Pada C-rate tinggi (15C), sampel LTO sintesis denganpenambahan Fe2O3 hasil purifikasi (x=0,1) memiliki kapasitas tertinggi dibandingkansampel co-doping LTO sintesis lainnya yaitu 21,716 mAh/g. Sedangkan pada co-dopingLTO komersial, LTO komersial dengan prekursor Fe2O3 komersial (x=0,1) memilikikapasitas tertinggi yaitu 47,70 mAh/g

---

Li4Ti5O12 (LTO) anode doped with Mg and Fe in the form of Li4-xMgxTi5-xFexO12

(x = 0, 0.05, 0.1) was successfully synthesized using the solid-state method with

sonication using TiO2 and Fe2O3 precursor sources, both comercial and synthetic. SEM

results showed that the co-doped samples of Mg and Fe on commersial LTO had

relatively the same and uniform morphology and particle size reduced of the LTO codoped

particles with x = 0.05. However, co-doping of synthesized LTO was not found in

any reduction in particle size, indicating that Mg and Fe co-doping had no effect on

particle size. The EDS results showed the presence of Mg, Fe, Ti, and O elements which

indicated that the desired element in the co-doping sample and its distribution was

relatively even. XRD characterization showed that Mg(OH)2 and Fe2O3 phases were not

found in the LTO co-doping structure indicating that Mg and Fe atoms had joined the

LTO structure. Samples with commercial TiO2 dan Fe2O3 precursor and synthesized TiO2

with purified Fe2O3 at the composition x = 0.1 had the lowest impurity phase compared

to commersial LTO and synthetic LTO, namely 12.7% and 9.9%. The Rct value of all codoping

samples shows that the Rct value is smaller than the Rct value for pure LTO (codoping

Rct < pure LTO Rct). This suggests that the co-doping Mg and Fe reduces the

diffusion resistance of LTO, thereby increasing charge transfer and electrical

conductivity. Thus, it shows that the movement of Li+ ions is easier in the co-doped LTO

samples. Synthesized LTO samples using the purified Fe2O3 precursor (x = 0.1) has the

lowest Rct value compared to all samples, namely 85.41 Ω and has the greatest value of

lithium ion diffusion coefficient and conductivity values of 2.081 x 10-11 cm2.s-1 and 2.913

S.cm-1. In addition, it has the lowest ΔE value, so it has the lowest degree of polarization

and the best reversibility. At a high C-rate (15C), the synthetic LTO sampel with the

addition of purified Fe2O3 (x = 0.1) has the highest capacity compared to other synthetic

LTO co-doping samples, namely, 21.716 mAh/g. While in commersial LTO co-doping,

sampel commercial Fe2O3 precurcor (x = 0.1) has the highest capacity of 47.70 mAh/g."

"Litium titanat (Li4Ti5O12) merupakan kandidat yang menjanjikan sebagai anoda baterai Lithium-ion. Litium titanat disintesis menggunakan metode solid state dengan mencampurkan TiO2 xerogel yang dibuat dengan metode sol gel dan litium karbonat (Li2CO3) komersil. Dalam penelitian ini digunakan tiga variasi penambahan kadar massa Li2CO3, yaitu 0% (sampel LTO 1), 50% (sampel LTO 2), dan 100% (sampel LTO 3) melebihi stoikiometri. Karakterisasi menggunakan pengujian XRD, FESEM, UV-vis spectroscopy, dan BET telah dilakukan untuk mengetahui pengaruh kadar litium berlebih terhadap struktur, morfologi, dan energi celah pita sampel. Hasil penelitian menunjukkan bahwa ukuran kristalit, ukuran diameter partikel, energi celah pita, dan luas permukaan masing-masing sampel berturut-turut adalah 8,27 nm, 8,44 μm, 3,88 eV untuk sampel LTO 1; 8,22 nm, 8,56 μm, 4,02 eV, 22,529 m2/gr untuk sampel LTO 2; 4,76 nm, 2,07 μm, 4,12 eV, 16,804 m2/gr untuk sampel LTO 3. Selain itu, litium berlebih yang digunakan dalam sintesis Li4Ti5O12 menyebabkan terbentuknya pengotor TiO2 rutile dan Li2TiO3. Senyawa Li4Ti5O12 hanya terbentuk pada sampel LTO 1 dan LTO 2. Untuk mensintesis senyawa Li4Ti5O12 menggunakan metode solid state tanpa menghasilkan pengotor dapat mengacu pada diagram fasa Li2O-TiO2 (28,64% mol Li2O-71,36% mol TiO2).

---

Lithium titanate (Li4Ti5O12) is a promising candidate for lithium ion battery anode. Lithium titanate was synthesized by solid state method using xerogel TiO2 was prepared by sol gel method and commercial lithium carbonate (Li2CO3). This research varies the content of Li2CO3 addition, 0% (sample LTO 1), 50% (sample LTO 2), and 100% (sample LTO 3) Li2CO3 mass excess. Characterization using XRD, FESEM, UV-vis spectroscopy, and BET testing was performed to observe the effect of adding lithium excess in structure, morphology, and band gap energy.

The results show that crystallite size, particle diameter, band gap energy, and surface area of each sample is 8,27 nm, 8,44 μm, 3,88 eV for sample LTO 1; 8,22 nm, 8,56 μm, 4,02 eV, 22,529 m2/gr for sample LTO 2; 4,76 nm, 2,07 μm, 4,12 eV, 16,804 m2/gr for sample LTO 3. Furthermore, the excess of lithium used for Li4Ti5O12 synthesis cause the formation of impurity compound such as rutile TiO2 and Li2TiO3. Li4Ti5O12 compound was successfully syntesized in sample LTO 1 and LTO 2. In order to synthesis pure Li4Ti5O12 without any impurities using solid state method, Li2O-TiO2 phase diagram (28,64% mol Li2O-71,36% mol TiO2) can be used as a reference."

"[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.]"

"Jenis baterai yang banyak dipakai saat ini, yaitu baterai ion litium. LTO merupakan material anoda yang menjanjikan karena memiliki siklus yang stabil, kapabilitas tinggi, dan aman dengan elektrolit konvensional. Alasan lain yang menjadikan LTO sebagai material yang menjanjikan untuk digunakan sebagai baterai ion litium yaitu karena memiliki sifat interkalasi dan deinterkalasi ion litium yang baik dan juga mobilitas ion litium yang luar biasa. Untuk meningkatkan kembali performa dari LTO demi memenuhi kebutuhan media penyimpan energi yang tinggi maka pada penelitian kali ini dilakukan doping pada LTO dengan co-doping Mg dan Mn dengan penambahan cerasperse sebagai zat pendispersi pada saat sintesis material aktif. Dispersan cerasperse (Ammonium Polycarbonate) bisa digunakan untuk mendispersikan partikel dan juga menghindari terjadinya agregasi. Dispersan memiliki peran positif terhadap penyebaran material aktif pada elektroda. Ketika penyebaran material aktif merata maka akan meningkatkan performa dari baterai. Metode untuk pencampuran prekursor sintesis awal dilakukan dengan metode solid-state dan dibantu dengan proses sonikasi. Variasi pada penambahan cerasperse yaitu sebesar 0%, 2,5%, 5%, dan 7,5%. Dari hasil pengujian SEM EDS menunjukkan bahwa penambahan cerasperse sebanyak 7,5% bisa mengurangi terjadinya aglomerasi dan meningkatkan persebaran partikel pada serbuk LTO/MgMn. Pada penambahan cerasperse sebanyak 7,5% juga terjadi peningkatan konduktifitas dari baterai berdasarkan pengujian EIS tetapi kapasitas spesifik yang dihasilkan buruk berdasarkan pengujian CV dan CD.

---

The lithium ion battery is the sort of battery that is most frequently used nowadays. LTO is a guaranteed anode material because it has a stable cycle, high capability, and is safe with conventional electrolytes. Another reason that makes LTO a promising material for use in lithium ion batteries is that it has good lithium ion intercalation and deintercalation properties as well as the outstanding mobility of lithium ions. To improve the performance of LTO in order to meet the need for high energy storage media, in this study, LTO was doped with Mg and Mn co-doping with the addition of cerasperse as a dispersing agent during the synthesis of active materials. Dispersants like Cerasperse (Ammonium Polycarbonate) can be employed to spread particles out while also preventing agglomeration. Dispersants have a positive role in the dispersion of the active matter on the electrodes. When the active material is evenly distributed, it will improve the performance of the battery. The method for mixing the precursors of the initial synthesis was carried out by the solid-state method and assisted by the sonication process. Variations in the addition of cerasperse are 0%, 2.5%, 5%, and 7.5%. From the results of the SEM EDS test, it was shown that the addition of 7.5% cerasperse could reduce the occurrence of agglomeration and increase the distribution of particles in LTO/MgMn powder. According to EIS tests, the battery's conductivity increased at a cerasperse addition of 7.5 %, however the specific capacity produced was poor based on chargedischarge."

"Litium Titanat atau Li4Ti5O12 (LTO) merupakan salah satu material yang menguntungkan sebagai bahan dasar anoda baterai lithium ion. Dalam penelitian ini, LTO disintesis dengan karbon aktif (AC) yang berbahan dasar dari sampah pelastik (PET), dengan komposisi karbon aktif yang berbeda sebesar 3 wt%, 5 wt%, and 7 wt%. Karbon aktif tersebut terbuat dari campuran sampah pelastik dan bentonite (9:1) yang dikarbonisasi melalui tungku pembakaran pada suhu 400°C dalam atmosfer inert nitrogen menjadi karbon amorf hitam. Setelah karbonisasi, karbon tersebut diaktivasi melalui empat proses utama: pencampuran dengan NaOH, sintering dalam atmosfir nitrogen, pencucian, dan pengeringan. LTO/AC yang sudah disintesis lalu diubah menjadi anoda baterai lithium-ion setengah sel. Kemudian anoda tersebut dikarakterisasi melalui Uji Voltametri Siklus, Uji Pengisian Daya Muatan (CD) dan Spektroskopi Impedansi Listrik (EIS). Hasil akhir dari pengujian ini menunjukan bahwa penambahan karbon aktif dapat meningkatkan konduktifitas dari baterai lithium-setengah sel. Sesuai dengan hasil pengujian CV, penambahan karbon sebesar 7% wt% menghasilkan kapasitas spesifik sebesar 143.4 (mAh/g). Hasil pengujian pada penelitian ini menunjukan bahwa penambahan karbon aktif optimal adalah sebesar 7 wt%.

---

Lithium titanate or Li4Ti5O12 (LTO) is a favorable contender as lithium-ion battery anode material. In this research, LTO/AC was synthesized with activated carbon made of plastic waste, the different composition of 3 wt%, 5 wt%, and 7 wt% has been carried out. The activated carbon was made using the mixture of plastic waste and bentonite nano clay (9:1) that will go through the slow pyrolysis carbonization process, which is performed under 400°C in an inert atmosphere of N2 with the help of a furnace into black amorphous carbon. After the carbonization, the carbon is activated through four main stages: mixing with NaOH, sintering under a nitrogen atmosphere, washing, and drying. The synthesized LTO/AC materials are then formed into a half-cell lithium-ion battery anode. The half cell lithium-ion battery anodes are then examined using the Cycle Voltammetry Test, Charge Discharge (CD) Test, and Electrical Impedance Spectroscopy (EIS). The final result of this research shows that activated carbon can increase the conductivity of the half-cell lithium battery. According to the results of the CV test, the addition of 7% wt% carbon resulted in a specific capacity of 143.4 (mAh/g). The test results in this research indicate that the optimal addition of activated carbon is 7 wt%."

"Litium Titanat, Li4Ti5O12 (LTO) adalah kandidat yang menjanjikan sebagai bahan anoda baterai lithium ion. Dalam penelitian ini, LTO-ZnO/C yang disintesis dengan metode hidrotermal untuk membentuk struktur LTO nanowire dan di grinding Bersama dengan ZnO nanopartikel dan grafit. Tiga variasi penambahan konten ZnO nanopartikel dalam % berat, yaitu, 4, 7 dan 10%, diberi label sampel LTO-ZnO 4%/C 5%, LTO-ZnO 7%/C 5% dan LTO-ZnO 10%/C 5%. Karakterisasi dilakukan menggunakan XRD dan SEM. Uji performa baterai menggunakan metode EIS, CV, dan CD. Hasil penelitian menunjukkan dari CV dan CD kita bias mengetahui bahwa LTO-ZnO 4%/C 5% memiliki performa terbaik dengan potensial kerja 1.595V dan kurva discharge vs C rate terbaik sementara dari hasil uji EIS kita bisa melihat bahwa sampel LTO-ZnO 10%/C 5% memiliki resistivitas terendah yaitu 28.44Ω.

---

Lithium Titanate, Li4Ti5O12 (LTO) is a promising candidate to be a lithium-ion battery anode. In this experiment LTO-ZnO/C are synthesized with hydrothermal method to form LTO nanowire and grinded with ZnO nanoparticle and graphite to form the composite. Three variables used are the different content of ZnO nanoparticle which are 4, 7 and 10%, labeled as LTO-ZnO 4%/C 5%, LTO-ZnO 7%/C 5% dan LTO-ZnO 10%/C 5%. Characterization is done by XRD and SEM. Battery performance test is done by EIS, CV, and CD.

The result of this research shows that in CV and CD testing LTO-ZnO 4%/C 5% perform best with working potential of 1.595V and the best discharge vs C rate curve while from EIS testing we can see that LTO-ZnO 10%/C 5% has the lowest resistivity at 28.44Ω."

"Litium Titanat, Li4Ti5O12 (LTO) adalah kandidat yang menjanjikan sebagai bahan anoda baterai lithium ion. Dalam penelitian ini, Li4Ti5O12 akan disintesis dengan menggunakan metode solid-state dengan menggunakan komersial TiO2 dan komersial litium hidroksida (LiOH). Setelah itu, komersial bubuk nikel dipanaskan pada suhu 600oC selama 4 jam untuk mendapatkan NiO sebagai logam oksida transisi. Penambahan NiO ke LTO kepada semua sampel sebesar 3%. Tiga variasi penambahan lama waktu proses sintering sebesar 4 jam, 8 jam, 10 jam, diberi label sampel LTO/NiO 3% (4 jam), LTO/NiO 3% (8 jam) and LTO/NiO 3% (10 jam). Karakterisasi dilakukan menggunakan XRD dan SEM untuk mengamati efek penambahan NiO pada struktur dan morfologi sampel yang dibuat. Hasil karakterisasi sampel menunjukkan bahwa penambahan NiO 3% memiliki konduktivitas lebih baik. Hasil dari tes Electrochemical Impedance Spectroscopy juga menunjukkan LTO/NiO 3% (4 jam) memiliki konduktivitas terbaik dengan nilai resistansi terkecil

---

Lithium titanate, Li4Ti5O12 (LTO) is a promising candidate as lithium ion battery anode material. In this investigation, Li4Ti5O12 was synthesized with solid-state method by using TiO2 with the help of lithium hydroxide (LiOH) and nickel powder as the precursor materials, resulting in LTO. Commercial nickel powder was heated at 600oC for 4 hours to obtain NiO as transition metal oxide. NiO addition to the LTO for all samples is 3% in weight%. Three variations of different sintering holding time for 4 hours, 8 hours and 10 hours labelled as LTO/NiO 3% (4 hours), LTO/NiO 3% (8 hours) and LTO/NiO 3% (10 hours), respectively. The characterizations were made using XRD and SEM testing. These were performed to observe the effect of NiO addition and different holding time on structure and morphology of the resulting samples. The result showed that the addition of NiO will make the samples have better conductivity. According to Electrochemical Impedance Spectroscopy, LTO/NiO 3% (4 hours) also has the best conductivity with the lowest resistivity."