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Acton, J.R.
New York: Academic Press, 1963
621.384 123 ACT c
Buku Teks  Universitas Indonesia Library
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Muhammad Buchari Setia Putra
"Nanopartikel Ni(OH)2 digunakan secara luas sebagai material katoda pada superkapasitor asimetrik karena memiliki sifat elektrokimia yang baik dan mudah didapat. Nanopartikel Ni(OH)2 diproduksi dengan metode hidrotermal. fasa dari hasil sintesis Ni(OH)2 dikarakterisasi menggunakan XRD, tercipta pola difraksi dari fasa Ni(OH)2 tanpa terlihat impurity dari pola difraksi. Didapat ukuran partikel hasil sintesis-Ni(OH)2 sebesar 16.285 +- 4.215 nm dari karakterisasi TEM. Untuk menambah sifat konduktivitas panas, dicampurkan β-Ni(OH)2 dengan karbon mesopori, dan dideposisi pada permukaan glassy carbon electrode. Karakterisasi menggunakan SEM-EDX dan XPS, menghasilkan spektrum perbandingan atom Ni : O sebesar 1 : 2 yang memperkuat dugaan terbentuknya Ni(OH)2. Karakterisasi pendahuluan menggunakan cyclic voltammetry menjelaskan bahwa penambahan material karbon mesopori tidak mendominasi karakter dari Ni(OH)2. Lalu, didapat hasil kapasitas spesifik dalam fungsi discharging sebesar 280C/g, 120 C/g, 30 C/g, dan 10 C/g untuk arus spesifik sebesar 1 A/g, 2 A/g, 5 A/g,dan 10A/g berturut-turut. Serta didapatkan nilai energi spesifik sebesar 39.72; 36.67; 22.92; 15.28 Wh/kg, dan nilai daya spesifik sebesar 0.55; 1.1;2.75; 5.5 kW/kg untuk arus spesifik 1 ;2; 5; 10 A/g secara berturut-turut. Hasil kapasitas spesifik dari Ni(OH)2 masih bertahan 96.59% pada siklus ke 3000.

Ni(OH)2 nanoparticle is widely used as cathode material in asymmetric supercapacitors due to its good electrochemical properties and affordable prices. Ni(OH)2 nanoparticles are synthesized via hydrothermal method. The phase from the as synthesized Ni(OH)2 was characterized using XRD, creating a diffraction pattern from the phase of Ni(OH)2 without any visible impurity from the diffraction pattern. The obtained particle size of Ni(OH)2 was 16.285+- 4.215 nm were measured by TEM characterization. To increase heat conductivity property, Ni(OH)2 was mixed with mesoporous carbon, and deposited on the surface of the glassy carbon electrode. Characterization using SEM-EDX and XPS, resulting in a comparison of determining the ratio of Ni : O at 1 : 2 which strengthens the suspicion of the formation of Ni(OH)2. Preliminary characterization using cyclic voltammetry explains mesoporous carbon material does not dispel characters from Ni(OH)2. the results of specific capacity are 280 C/g, 120 C/g, 30 C/g, and 10 C/g for specific currents of 1 A/g, 2 A/g, 5 A/g, and 10A/g consecutively. Specific energy values obtained were 39.72;36.67; 22,92;15.28 Wh/kg, and specific power values of 0.55; 1.1;2.75;5.5 kW/kg for specific currents 1;2;5;10 A/g respectively. The results of the specific capacity of Ni (OH) 2 still survive at 96.59% in the 3000 cycle.
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Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2019
S-Pdf
UI - Skripsi Membership  Universitas Indonesia Library
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Trivika Lemona
"[ABSTRAK
Hidrogen merupakan salah satu unsur yang dapat dijadikan sebagai bahan bakar alternatif karena BBH atau bahan bakar hidrogen bersifat ecoenergi dengan proses pembakaran yang hanya menghasilkan air dan energi (listrik dan panas). Salah satu teknologi penghasil hidrogen adalah dengan metode Contact Glow Discharge Elektrolisis atau CGDE. Penelitian ini menggunakan metode CGDE dengan multi katoda dan penambahan etanol dengan tujuan dapat meningkatkan laju produksi hidrogen dan efektivitas proses.pada penelitian ini akan dilihat pengaruh penambahan jumlah katoda, pengaruh konsentrasi etanol dan diameter katoda terhadap laju produksi dan efektivitas hidrogen. Dari karakterisasi arus dan tegangan yang diperoleh pada penelitian ini, dapat disimpulkan bahwa arus akan semakin meningkat seiring dengan bertambahnya jumlah katoda. Penggunaan multi katoda pada proses CGDE juga terbukti meningkatkan produksi hidrogen pada tegangan dan konsumsi energi yang sama. Penambahan zat aditif etanol juga dilakukan pada penelitian ini dan memperoleh hasil bahwa semakin tinggi konsentrasi etanol maka akan semakin tinggi produksi dan efektivitas gas Hidrogen yang dihasilkan. Selain itu, penelitian ini juga membuktikan bahwa semakin besar diameter katoda maka laju produksi akan semakin tinggi, namun konsumsi energi menjadi meningkat dan tidak sebanding dengan peningkatan laju produksi sehingga menghasilkan efektivitas yang semakin kecil. Proses CGDE multi katoda pada penelitian ini menunjukkan peningkatan efektivitas proses sebesar 76 kali lipat dibandingkan dengan elektrolisis Faraday.

ABSTRACT
Hydrogen is one of elements that can be used as an alternative energy. The combustion of Hydrogen only produces water and energy. Therefore, hydrogen is called as ecoenergy. One of technology that can produce hydrogen is Contact Glow Discharge Electrolysis or CGDE. CGDE is one of plasma electrolysis that uses electrolyte solution and inert electrode to produce hydrogen in high voltage. This research uses CGDE method with multi-cathode and ethanol in order to increase hydrogen production and the effectivity of process. In this research, we will explore the effect of increasing cathode number, etanol addition, and increasing of cathode diameter. From characterization of current and volatge, we can conclude that the increasing of cathode number can increase the current that through into cathode. Utilization of multi-cathode in CGDE is proven that can increase the hydrogen production at the same voltage and energy consumption. The addition of ethanol has done in this research and we can conclude that when we increase the concentration of ethanol, the hydrogen production will be increased either at the same voltage. In addition, this research also prove that the bigger diameter of a cathode will increase the production rate, but the energy consumption increases higher than the production rate. Therefore, the increasing of diameter of cathode is not effective to use in CGDE. The CGDE multi-cathode on this research indicated increasing of effectiveness as much as 76 times higher than the Faraday Electrolysis., Hydrogen is one of elements that can be used as an alternative energy. The combustion of Hydrogen only produces water and energy. Therefore, hydrogen is called as ecoenergy. One of technology that can produce hydrogen is Contact Glow Discharge Electrolysis or CGDE. CGDE is one of plasma electrolysis that uses electrolyte solution and inert electrode to produce hydrogen in high voltage. This research uses CGDE method with multi-cathode and ethanol in order to increase hydrogen production and the effectivity of process. In this research, we will explore the effect of increasing cathode number, etanol addition, and increasing of cathode diameter. From characterization of current and volatge, we can conclude that the increasing of cathode number can increase the current that through into cathode. Utilization of multi-cathode in CGDE is proven that can increase the hydrogen production at the same voltage and energy consumption. The addition of ethanol has done in this research and we can conclude that when we increase the concentration of ethanol, the hydrogen production will be increased either at the same voltage. In addition, this research also prove that the bigger diameter of a cathode will increase the production rate, but the energy consumption increases higher than the production rate. Therefore, the increasing of diameter of cathode is not effective to use in CGDE. The CGDE multi-cathode on this research indicated increasing of effectiveness as much as 76 times higher than the Faraday Electrolysis.]"
Depok: Fakultas Teknik Universitas Indonesia, 2015
S58845
UI - Skripsi Membership  Universitas Indonesia Library
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Guntur Tri Setiadanu
"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.

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."
Depok: Fakultas Teknik Universitas Indonesia, 2015
T43933
UI - Tesis Membership  Universitas Indonesia Library
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Adlan Mizan
" ABSTRAK
Telah dilakukan proses sintesis LiFe 1-x VxPO4/C untuk katoda baterai litium ion. Pada bahan ini, sintesis diawali dengan pembuatan LiFePO4 yang dilakukan melalui proses hidrotermal dengan bahan dasar LiOH, NH4H2PO4 dan FeSO4.7H2O. Setelah LiFePO4 disintesis, lalu dilakukan penambahan variasi vanadium serbuk yang bersumber dari H4NO3V dan karbon yang berasal dari hasil pirolisis sukrosa selama 2 jam pada 400 C. Bahan-bahan dicampur menggunakan ball-mill lalu dikarakterisasi menggunakan analisis termal STA untuk menentukan temperatur sintering. Hasilnya memperlihatkan bahwa transisi terjadi pada temperatur sekitar 700 C yang kemudian dijadikan patokan untuk menentukan proses sintering. Sintering dilakukan selama 4 jam lalu hasilnya dikarakterisasi menggunakan difraksi sinar-X XRD . Struktur mikto dan morfologi permukaan selanjutnya dianalisis menggunakan mikroskop elektron SEM . Hasil karakterisasi dengan XRD menunjukkan bahwa fasa LiFe 1-x VxPO4/C telah terbentuk dengan struktur berbasis olivin. Hasil SEM menunjukan adanya persebaran partikel LiFe 1-x VxPO4/C walaupun beberapa terlihat masih beraglomerasi. Proses pembuatan baterai dilakukan dari bahan hasil sintesis dan diuji menggunakan electrochemical impedance spectroscopy EIS dan uji performa melalui cyclic voltametry CV dan charge and discharge CD . Hasil EIS menunjukan bahwa doping dengan vanadium meningkatkan konduktifitas yang cukup berarti. Hal yang sama juga terjadi dengan adanya karbon sintesis dari sukrosa walaupun masih lebih rendah jika dibandingkan dengan karbon komersial. Uji performa menunjukan bahwa penambahan vanadium meningkatkan kapasitas 51.06 mAh/g saat charging dan 49.42 mAh/g saat discharging dengan beda potensial 3.581 V saat charging dan 3.319 V saat discharging. Hasil yang didapatkan ini cukup menjanjikan untuk penggunaan selanjutnya sebagai katoda baterai litium ion.
ABSTRACT Synthesis of LiFe 1 x VxPO4 C used for lithium ion battery cathode has been carried out. In the process, the synthesis was begun by synthesizing of LiFePO4 through a hydrothermal method with the precursors of LiOH, NH4H2PO4 and FeSO4.7H2O. The as synthesized LiFePO4 was then mixed with H4NO3V and carbon pyrolyzed from sucrose for 2 hours at 400 C. The mixture was mixed in a ball mill and then was characterized using a thermal analyzer to determine the transition temperature at which sintering at 700 C for 4 hours was obtained. X ray diffraction XRD was performed to analyzed the crystal structure whereas scanning electron microscope SEM was used to examine the microstructure and surface morphology. XRD results show that the phase LiFe 1 x VxPO4 C has been formed with an olivine based structure. SEM results showed the distribution of LiFe 1 x VxPO4 C particles are mostly distributed. The batteries were prepared from the as synthesized materials and was tested using electrochemical impedance spectroscopy EIS , cyclic voltammetry CV and charge and discharge CD performance test. The EIS results showed that doping with vanadium improved the conductivity. The same was true with the carbon even at a smaller value compared to that of the commercial one. The performance test showed that the addition of vanadium increased the capacity of about 51.06 mAh g with a potential of 3.581 V at charging and 49.42 mAh g with a potential of 3.319 V at discharging. These results are promising in terms of using this material for lithium ion battery cathode development."
Depok: Fakultas Teknik Universitas Indonesia, 2017
S66642
UI - Skripsi Membership  Universitas Indonesia Library
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David Ferdiyanto
"Baterai ion-sodium (SiB) saat ini terus dikembangkan sebagai alternatif pengganti baterai ion-litium (LiB) yang lebih ekonomis dan ramah lingkungan. Pada penelitian ini dilakukan karakterisasi dan evaluasi bahan mangan nikel berdoping magnesium yang disintesis secara hidrotermal untuk katoda baterai ion-sodium sebagai alternatif pengganti baterai ion-litium. Hasil yang didapatkan menunjukkan bahwa suhu autoklaf pada proses hidrotermal sangat mempengaruhi sintesis bahan katoda dimana suhu 250oC merupakan suhu optimum proses sintesis bahan. Hal ini dibuktikan melalui  karakterisiasi senyawa kristal bahan dengan uji x-ray diffraxtion (XRD) dan juga pengamatan scanning electron microscope (SEM). Hasil pengujian electric impedance spectroscopy (EIS) menunjukkan bahwa penambahan unsur magnesium sebagai doping pada katoda memberikan hambatan yang lebih rendah dibandingkan tanpa magnesium, sehingga meningkatkan konduktifitas baterai sebesar 9,02%. Tegangan sel mampu mencapai 2,00 V pada pengisian awal dan berada pada rentang 1,50-4,30 V yang terlihat dari hasil uji Cyclic Voltametry (CV). Kapasitas baterai katoda berdoping magnesium (132,12 mAh/g pada saat pengisian dan 14,53 mAh/g pada saat pengosongan) lebih tinggi dibandingkan katoda tanpa magnesium (45,86 mAh/g pada saat pengisian dan 2,37 mAh/g pada saat pengosongan) pada C-rate yang rendah.

Sodium-ion batteries (SiB) are currently being developed as a more economical and environmentally friendly alternative to lithium-ion batteries (LiB). This study involves the characterization and evaluation of manganese nickel materials doped with magnesium, synthesized hydrothermally for use as cathodes in sodium-ion batteries as an alternative to lithium-ion batteries. The results indicate that the autoclave temperature during the hydrothermal process significantly affects the synthesis of the cathode material, with 250°C being the optimal temperature for material synthesis. This is evidenced by the characterization of the material using x-ray diffraction (XRD) and scanning electron microscope (SEM) observations. Electric impedance spectroscopy (EIS) testing shows that adding magnesium as a dopant to the cathode results in lower resistance compared to the one without magnesium, thereby increasing battery conductivity by 9.02%. The cell voltage can reach 2.00 V during initial charging and ranges from 1.50 to 4.30 V, as shown by the Cyclic Voltammetry (CV) test results. The magnesium-doped cathode battery capacity (132.12 mAh/g during charging and 14.53 mAh/g during discharging) is higher than the undoped cathode (45.86 mAh/g during charging and 2.37 mAh/g during discharging) at a low C-rate."
Depok: Fakultas Teknik Universitas Indonesia, 2024
T-pdf
UI - Tesis Membership  Universitas Indonesia Library
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Audiya Dewi Rachmawati
"Telah dilakukan sintesis katoda LiFePO4/V berlapis karbon dari karbon aktif tempurung kelapa untuk katoda baterai lithium ion. Prekursor yang digunakan adalah LiOH, NH4H2PO4, dan FeSO4.7H2O dibuat melalui proses hidrotermal. Selanjutnya, dilakukan pencampuran karbon dari karbon aktif tempurung kelapa sebanyak 4 dan variasi vanadium serbuk yang bersumber dari H4NO3V. Campuran LiFePO4/V/C dikarakterisasi menggunakan analisis termal STA untuk menentukan temperatur sintering. Hasilnya sintesis terjadi pada temperatur di atas 681,950C dan serbuk berwarna abu-abu gelap sebagai karakteristik dari LiFePO4. Kemudian proses sintering dilakukan pada temperatur 8500C selama 4 jam. Serbuk LiFePO4 sintesis dikarakterisasi menggunakan difraksi sinar-X XRD, mikroskop elektron dan pendeteksi unsur SEM-EDS serta sifat listrik melalui spektroskopi impedansi EIS.
Hasil XRD menunjukkan LiFePO4/V/C telah terbentuk dengan struktur berbasis olivin. Hasil SEM-EDS menggambarkan partikel yang teraglomerasi dan LiFePO4/V telah terlapisi karbon. Hasil EIS menunjukkan konduktivitas sebesar 5,33 x 10-5 S/cm untuk LiFePO4/C tanpa vanadium dan 6 x 10-6 S/cm untuk LiFePO4/C dengan doping vanadium 5.

Activated carbon from coconut shell has been used as an additive to form LiFePO4 V C composite for lithium ion battery cathode. Lithium iron phosphate LFP was synthesized from the precursors of LiOH, NH4H2PO4, and FeSO4.7H2O via hydrothermal method. The LiFePO4 V C composite was formed by adding various vanadium concentration 0, 3, 5, 7 at. and a fix concentration of carbon 4 wt. Thermal analysis STA was used to characterize the formation of LFP and the transition temperature of the composite from which a transition temperature of 681.950C was obtained. X ray diffraction XRD was used to characterize the crystal structure, whereas scanning electron microscope SEM equipped with energy dispersive X ray spectroscopy EDX was used to characterize the morphology and composition of the composite. The conductivity of the composite was examined using electrical impendance spectroscopy EIS.
The XRD results showed that LiFePO4 V C has an olivine structure with Pnmb space group. The SEM EDX results depicted aglomerate particles but most LiFePO4 V has been coated by carbon. EIS test results showed a conductivity of 5.33 x 10 5 S cm for LiFePO4 C with no vanadium and 6.0 x 10 6 S cm for 5 wt. vanadium doped LiFePO4 V C.
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Depok: Fakultas Teknik Universitas Indonesia, 2017
S68917
UI - Skripsi Membership  Universitas Indonesia Library
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Budi Setyahandana
"ABSTRACT
High carbon steel generally has a high hardness but lower ductility. To obtain a hard and ductile material, surface hardening can be done on a low carbon steel. Surface hardening can be achieved by hard chrome plating. The objectives of this research were: (1) Conducting the process of hard chrome plating on low carbon steel, (2) Knowing the increasing of surface hardness of low-carbon steel after the plating process in time variations, (3) Knowing the increasing of surface hardness of the low carbon steel after the coating process in anode-cathode distance variations. The specimens was made of low carbon steel. The size of the specimen were 40 mm in length, 35 mm in width and 6.8 mm in thickness. The variables measured were: (1) Coating time (t), (2) The distance between the cathode and anode in the coating process (l). After the coating process completed, the specimen surface hardness was measured by Vickers Hardness Tester. The results showed that up to 532 HV, low carbon steel hardness increased linearly at increasing time plating. At 120 minutes plating, the hardness also increased linearly at current densities up to 1.05 amperes/dm2. While at the current density of 1.1 amperes/dm2, the hardness increased significantly higher."
Yogyakarta: Media Teknika, 2017
620 MT 12:1 (2017)
Artikel Jurnal  Universitas Indonesia Library
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Bian Shafi Muhammad
"Emisi gas CO2 menjadi salah satu faktor terbesar penyumbang efek gas rumah kaca dan perubahan iklim yang ada di bumi. Dampak negatif yang ditimbulkan dari emisi gas CO2 menjadi salah satu fokus perhatian para peniliti untuk menguranginya dan/atau mengubahnya menjadi suatu produk dengan nilai tambah. Pada penelitian kali ini dilakukan konversi CO2 menjadi asam format (HCOOH) secara fotoelektrokimia. Sistem fotoelektrokimia terdiri dari fotoanoda berupa nanokomposit kobalt posfat, bismuth vanadate TiO2 (CoPi/BiVO4/TiO2) dan Grafena Oksida (GO) tereduksi yang akan dilekatkan pada film TiO2 diatas plat logam Ti menjadi (rGO/TiO2) sebagai katoda gelap. Pasangan elektroda tersebut dikemas dalam reaktor gelas berisi elektrolit NaHCO3, sumber cahaya tampak, dan pada kompartemen katoda gelap dibubbling dengan gas CO2. Bismuth vanadate pada fotoanoda CoPi/BiVO4/TiO2 dilekatkan menggunakan metode s-SILAR (successive ionic layer adsorption and reaction) dan untuk kobalt posfat dideposisi kedalam film BiVO4/TiO2 menggunakan metode elektrodeposisi selama 15 menit dengan potensial +1,1 V (vs. Ag/AgCl). Sedangkan katoda gelap difabrikasi dengan melekatkan grafena oksida tereduksi pada film TiO2 diatas plat titanium. Grafena Oksida akan disintesis menggunakan metode hummer termodifikasi kemudian dilekatkan secara elektrodeposisi dan dielektro-reduksi sehingga menjadi rGO/TiO2. Material elektroda dikarakterisasi menggunakan fourier transform infra-red (FTIR), UV-Vis Diffuse Reflectance Spectrocopy (UV-Vis DRS), X-ray Diffraction (XRD), linear sweep voltammetry (LSV), dan multi pulse amperometry (MPA). Dalam sistem fotoelektrokimia katoda gelap rGO/TiO2 berperan sebagai elektroda yang akan mengonversi CO2 menjadi HCOOH. Sedangkan, fotoanoda CoPi/BiVO4/TiO2 berfungsi sebagai sisi oksidasi menghasilkan proton (prekursor hidrogen) dan elektron aktif. Uji aplikasi konversi CO2 menjadi HCOOH dilakukan dengan durasi selama 2 jam, dimana reaktor diisi dengan elektrolit NaHCO3 tersaturasi CO2. Produk yang terbentuk dianalisa menggunakan high-performance liquid chromatography (HPLC). Hasil penelitian menunjukkan bahwa film TiO2 yang digunakan sebagai elektroda memiliki band gap sebesar 3,0 eV, didominasi dengan fase kristal anatase dengan morfologi nantotube. Komposit fotoanoda CoPi/BiVO4/TiO2 memiliki nilai band gap sebesar 2,35 eV dan 2,6 eV: responsif terhadap cahaya tampak. Sedangkan, katoda gelap rGO/TiO2 memiliki nilai band gap sebesar 3,38 eV. Sistem fotoelektrokimia dirancang mampu mengonversi CO2 menjadi asam format, dengan hasil sebesar 20,87 μmol selama 1 jam dengan faradaic efficiency sebesar 52,32%.

Carbon dioxide has been the most significant factor contributing the increase of greenhouse effect worldwide. Adverse impacts from carbon dioxide gas emmisions are becoming the main focus for researchers to decrease and convert carbon dioxide emissions into fine chemicals that benefits our daily lives. In this study, carbon dioxide gas is converted into formic acid (HCOOH) through photoelectrochemical system (PEC). The photoanode used in this research is cobalt phosphate bismuth vanadate TiO2 (CoPi/BiVO4/TiO2), while the dark cathode is reduced graphene oxide that will be attached to TiO2 film on top of titanium foil (rGO/TiO2). Both electrodes are placed into a reactor containing NaHCO3 (pH 7) electrolyte and visible light source, hence on the dark cathode compartment NaHCO3 electrolyte saturated by CO2 gas. Simplified successive ionic layer adsorption and reaction (s-SILAR) is used to paste bismuth vanadate on TiO2, whereas the cobalt phosphate would be deposited to BiVO4/TiO2 film through electrodeposition method for 15 minutes with a potential of +1,1 V (vs. Ag/AgCl). At the same time, the rGO/TiO2 dark cathode is fabricated by attaching reduce graphene oxide on top of TiO2 film. Graphene oxide is attached to TiO2 film by electrodeposition and electroreduction to fabricate rGO/TiO2 film with cyclic voltammetry from a range between -1,7-0,7 V (vs. Ag/AgCl). Electrodes used in this research are analyzed using Fourier transform infrared (FTIR), UV-Vis Diffuse Reflectance Spectroscopy (UV-Vis DRS), Scanning Electron Microscopy (SEM), X-Ray Diffraction, Linear Sweep Voltammetry (LSV), and Multi Pulse Amperometry (MPA). The charazterizations results from this study showed the band gap value from TiO2 film used is 3,0 eV; dominated by the anatase crystal phase with nanotube morphology. Photoanode composite CoPi/BiVO4/TiO2has a band gap value of 2,35 eV and 2,6 eV; which is active under visible light. On the other side, the rGO/TiO2 dark cathode showed a value of 3,38 eV for its band gap. Photoelectrochemical is one of many systems that is designed to be capable for converting CO2 into HCOOH. In the PEC system, rGO/TiO2 dark cathode is the electrode that converts CO2 into HCOOH. The CoPi/BiVO4/TiO2 oxidizes water and produces protons (hydrogen precursor) and active electrons. The PEC system demonstrated that it converts CO2 into HCOOH. The formic acid obtained is analyzed by high-performance liquid chromatography (HPLC), where total of formic acid obtained from this study is 20,87 μmol and with a faradaic efficiency of 52,32%."
Depok: Fakultas Matematika dan Ilmu Pengetahuan Alam Universitas Indonesia, 2024
S-pdf
UI - Skripsi Membership  Universitas Indonesia Library
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Craig, Edwin C.
New York: Springer-Verlag, 1993
621.381 CRA e
Buku Teks  Universitas Indonesia Library
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