Pulse electrodeposited cathode catalyst layers for PEM fuel cells

Nanostructured Pt and Pt₃Co cathodes for proton exchange membrane fuel cells (PEMFCs) have been prepared by pulse electrodeposition. For high utilization the catalyst nanoparticles are directly deposited on the microporous layer (MPL) of a commercial available gas diffusion layer (GDL). In order to increase the hydrophilic nature of the substrate surface and thus improve drastically the electrodeposition process and the fuel cell performance, prior to electrodeposition, the carbon substrate is submitted to O₂/Ar plasma activation. Cathodes with different amounts and distributions of Aquivion ionomer within the cathode catalyst layer (CCL) thickness (“homogeneous”, “gradient” and “anti-gradient”), different catalysts (Pt and Pt₃Co) at varied plasma duration and catalyst loading have been prepared. The cathodes are analysed via attenuated total reflection (ATR-IR), goniometer, SEM, 0.5 M H₂SO₄ half-cell and 25 cm² H₂/Air single PEMFC. The highest single fuel cell performance is obtained for 2 min plasma activated Pt₃Co cathode.     

Extraction of cobalt from laterite ores by citric acid in presence of ammonium bifluoride

Citric acid was used to selectively extract cobalt from limonite-type laterite ores in the presence of ammonium bifluoride. The results show that ammonium bifluoride enhances the leaching of cobalt by citric acid, and 84.5% cobalt is extracted from a laterite ore containing 0.13% Co when leached at ambient temperature for 2 h with 30 g/L citric acid and 10 g/L ammonium bifluoride. Pyrolusite is reduced by citric acid during leaching, cobalt intergrown with which is liberated and subsequently chelated by the citric acid. The extraction of cobalt is enhanced in the presence of ammonium bifluoride because the matrix of silicate minerals is destroyed by ammonium bifluoride and the adsorbed cobalt is subsequently liberated.     

溶液燃烧法合成掺钴氧化铝

以硝酸铝、尿素为主要原料,首先配制成氧化-还原溶液,然后经加热燃烧制备得到氧化铝/氧化钴聚合物粉体,并研究了钴盐量的投料大小对聚合体颜色的影响效果。结果表明,随着硝酸钴加入量的由小到大,氧化铝-氧化钴聚合物粉体的颜色深度不断增强。经XRD、Raman、IR的测试分析,表明混合粉体具有金刚石氧化物聚合体的结构特征。     

鲁中选矿厂钴回收的探讨

鲁中冶金矿业集团公司所属的港里矿2003年开始首采.随着开采量的不断增加,港里矿矿石成为选厂入选矿的主要来源,钴的赋存状态发生了变化,使钴的回收成为可能.试验表明,采用强磁抛尾-铜、钴混浮-铜、钴分离的流程效果较好.     

Ni3(PO4)2-coated Li[Ni0.8Co0.15Al0.05]O2 lithium battery electrode with improved cycling performance at 55 °C

To improve the cycling performance of LiNi_0.8Co_0.15Al_0.05O₂ at 55 °C, a thin Ni₃(PO₄) layer was homogeneously coated onto the cathode particle via simple ball milling. The morphology of the Ni₃(PO₄)₂-coated LiNi_0.8Co_0.15Al_0.05O₂ particle was characterized using SEM and TEM analysis, and the coating thickness was found to be approximately 10-20 nm. The Ni₃(PO₄)₂-coated LiNi_0.8Co_0.15Al_0.05O₂ cell showed improved lithium intercalation stability and rate capability especially at high C rates. This improved cycling performance was ascribed to the presence of Ni₃(PO₄)₂ on the LiNi_0.8Co_0.15Al_0.05O₂ particle, which protected the cathode from chemical attack by HF and thus suppressed an increase in charge transfer resistance. Transmission electron microscopy of extensively cycled particles confirmed that the particle surface of the Ni₃(PO₄)₂-coated LiNi_0.8Co_0.15Al_0.05O₂ remained almost undamaged, whereas pristine particles were severely serrated. The stabilization of the host structure by Ni₃(PO₄)₂ coating was also verified using X-ray diffraction.     

Significant impact of the current collection material and method on the performance of Ba0.5Sr0.5Co0.8Fe0.2O3−δ electrodes in solid oxide fuel cells

The effects of the current collection material and method on the performance of SOFCs with Ba_0.5Sr_0.5Co_0.8Fe_0.2O_3−δ (BSCF) cathodes are investigated. Ag paste and LaCoO₃ (LC) oxide are studied as current collection materials, and five different current collecting techniques are attempted. Cell performances are evaluated using a current-voltage test and electrochemical impedance spectra (EIS) based on two types of anode-supported fuel cells, i.e., NiO + SDC|SDC|BSCF and NiO + YSZ|YSZ|SDC|BSCF. The cell with diluted Ag paste as the current collector exhibits the highest peak power density, nearly 16 times that of a similar cell without current collector. The electrochemical characteristics of the BSCF cathode with different current collectors are further determined by EIS at 600 °C using symmetrical cells. The cell with diluted Ag paste as the current collector displays the lowest ohmic resistance (1.4 Ω cm²) and polarization resistance (0.1 Ω cm²). Meanwhile, the surface conductivities of various current collectors are measured by a four-probe DC conductivity technique. The surface conductivity of diluted Ag paste is 2-3 orders of magnitude higher than that of LC or BSCF. The outstanding surface conductivity of silver may reduce the contact resistance at the current collector/electrode interface and, thus, contributes to better electrode performance.     

Comparison of the surface changes on cathode during long term storage testing of high energy density cylindrical lithium-ion cells

Nickel-based oxide cathode material taking out from lithium-ion cell after storage for 2 years at 45 °C is analyzed by electron energy-loss spectroscopy in a scanning transmission electron microscope (STEM-EELS) and the result of STEM-EELS is compared with cobalt-based oxide cathode material which is treated as same manor as nickel-based oxide cathode material. The Ni-L_2,3 energy-loss near-edge structure (ELNES) spectra of nickel-based oxide cathode material show peak positions similar to original material before storage. This result indicates that nickel-based oxide material has no significant change in the surface structure. On the other hand, a remarkable shift to low energy is observed in the Co-L_2,3 ELNES spectra of the cobalt-based oxide cathode material after storage. The cycle test at 60 °C under the conditions of aggressive driving cycle (US06) mode for the nickel-based oxide cathode/graphite cell is also carried out. It is clear that cycle performance of the nickel-based oxide cathode/graphite cell is dependent on the depth of discharge (DOD).     

Pd-doped Co nanofibers immobilized on a chemically stable metallic bipolar plate as novel strategy for direct formic acid fuel cells

High contact resistance and corrosion are the main dilemma facing wide application of the metallic bipolar plates. In this study, deposition of thin film from Pd-decorated Co nanofibers on a silicon substrate is introduced as a novel strategy to produce functionalized metallic bipolar plate. The novel active metallic bipolar plate can be prepared by using simple, low cost, high yield and effective technique; electrospinning. The bimetallic nanofibrous film chemically bonds with the silicon substrate due to formation of silicon carbide which leads to merge the deeper nanofibers with the silicon surface. Accordingly, high current density (100 mA cm⁻¹) was obtained when the introduced covered silicon wafer was utilized as anode catalyst for formic acid electrooxidation. Because the bimetallic nanofibers are sheathed in a thin graphite shell, the introduced active bipolar plate reveals very good stability. Overall, the introduced study is opening a new avenue to prepare new class of functionalized metallic bipolar plates.