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This book is composed of 6 papers. The first paper reports a novel technique for the selective emitter formation by controlling the surface morphology of Si wafers. Selective emitter (SE) technology has attracted renewed attention in the Si solar cell industry to achieve an improved conversion efficiency of passivated-emitter rear-contact (PERC) cells. In the second paper, the temperature dependence of the parameters was compared through the PERC of the industrial-scale solar cells. As a result of their analysis, PERC cells showed different temperature dependence for the fill factor loss as temperatures rose. The third paper reports the effects of carrier selective front contact layer and defect state of hydrogenated amorphous silicon passivation layer/n-type crystalline silicon interface. The results demonstrated the effects of band offset determined by band bending at the interface of the passivation layer and carrier selective front contact layer. In addition, the nc-SiOx: H CSFC layer not only reduces parasitic absorption loss but also has a tunneling effect and field-effect passivation. The fourth paper reports excimer laser annealing of hydrogenated amorphous silicon film for TOPCon solar cell application. This paper analyzes the crystallization of a-Si:H via excimer laser annealing (ELA) and compared this process with conventional thermal annealing. The fifth paper reports the contact mechanism between Ag–Al and Si and the change in contact resistance (Rc) by varying the firing profile. Rc was measured by varying the belt speed and peak temperature of the fast-firing furnace. The sixth paper reports a silicon tandem heterojunction solar cell based on a ZnO/Cu2O subcell and a c-Si bottom subcell using electro-optical numerical modeling. The buffer layer affinity and mobility together with a low conduction band offset for the heterojunction are discussed, as well as spectral properties of the device model.

History of engineering & technology --- fill factor loss analysis --- double-diode model --- PERC --- temperature dependence --- recombination current density --- parasitic resistance --- carrier selective contact --- rear emitter heterojunction --- passivation --- crystallinity --- thermal annealing --- excimer laser annealing --- amorphous hydrogenated silicon film --- metallization --- contact formation --- Ag/Al paste --- p+ emitter --- N-type bifacial solar cells --- silicon tandem heterojunction solar cell --- N-doped Cu2O absorber layer --- Al:ZnO (AZO) --- numerical electro-optical modeling --- scanning electron microscopy (SEM) --- atomic force microscopy (AFM) --- X-ray diffraction (XRD) --- spectroscopic ellipsometry (SE) --- Fourier-transform infrared (FTIR) spectroscopy --- degradation degree --- failure rate --- selective emitter --- surface morphology --- doping process --- solar cell

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The development of micro- and nanodevices for blood analysis continues to be a growing interdisciplinary subject that demands the careful integration of different research fields. Following the success of the book “Micro/Nano Devices for Blood Analysis”, we invited more authors from the scientific community to participate in and submit their research for a second volume. Researchers from different areas and backgrounds cooperated actively and submitted high-quality research, focusing on the latest advances and challenges in micro- and nanodevices for diagnostics and blood analysis; micro- and nanofluidics; technologies for flow visualization and diagnosis; biochips, organ-on-a-chip and lab-on-a-chip devices; and their applications to research and industry.

Information technology industries --- blood viscosity --- Erythrocyte sedimentation rate (ESR) --- T-shaped microfluidic channel --- air-compressed syringe (ACS) --- micro-particle image velocimetry --- viscoelasticity --- microfluidic device --- coflowing streams --- interface --- linear differential equation --- two approximate factors --- dielectrophoresis --- electrophysiological properties --- crossover frequency --- wake or recirculation formation --- dielectric spectra --- air compliance effect --- RBC aggregation --- blood viscoelasticity --- blood velocity fields --- interface in co-flowing streams --- blood flow --- particle tracking --- red blood cells --- manual methods --- automatic methods --- image analysis --- biomicrofluidics --- microfluidics --- blood plasma filtration --- chip extract --- blood molecules --- patient-derived organoids --- colorectal cancer --- 3D model --- drug screening --- diagnostics --- malaria --- optical filters --- reflectance --- spectrophotometry --- TFCalc --- small caliber blood vessel --- composite molding --- micro-nano structure --- tissue repair --- 3D printing --- blood cells --- fourier transform infrared (FTIR) spectroscopy --- functional group --- lab-on-a-chip --- blood viscosity --- Erythrocyte sedimentation rate (ESR) --- T-shaped microfluidic channel --- air-compressed syringe (ACS) --- micro-particle image velocimetry --- viscoelasticity --- microfluidic device --- coflowing streams --- interface --- linear differential equation --- two approximate factors --- dielectrophoresis --- electrophysiological properties --- crossover frequency --- wake or recirculation formation --- dielectric spectra --- air compliance effect --- RBC aggregation --- blood viscoelasticity --- blood velocity fields --- interface in co-flowing streams --- blood flow --- particle tracking --- red blood cells --- manual methods --- automatic methods --- image analysis --- biomicrofluidics --- microfluidics --- blood plasma filtration --- chip extract --- blood molecules --- patient-derived organoids --- colorectal cancer --- 3D model --- drug screening --- diagnostics --- malaria --- optical filters --- reflectance --- spectrophotometry --- TFCalc --- small caliber blood vessel --- composite molding --- micro-nano structure --- tissue repair --- 3D printing --- blood cells --- fourier transform infrared (FTIR) spectroscopy --- functional group --- lab-on-a-chip

Choose an application

• Reference Manager
• EndNote
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The development of micro- and nanodevices for blood analysis continues to be a growing interdisciplinary subject that demands the careful integration of different research fields. Following the success of the book “Micro/Nano Devices for Blood Analysis”, we invited more authors from the scientific community to participate in and submit their research for a second volume. Researchers from different areas and backgrounds cooperated actively and submitted high-quality research, focusing on the latest advances and challenges in micro- and nanodevices for diagnostics and blood analysis; micro- and nanofluidics; technologies for flow visualization and diagnosis; biochips, organ-on-a-chip and lab-on-a-chip devices; and their applications to research and industry.

blood viscosity --- Erythrocyte sedimentation rate (ESR) --- T-shaped microfluidic channel --- air-compressed syringe (ACS) --- micro-particle image velocimetry --- viscoelasticity --- microfluidic device --- coflowing streams --- interface --- linear differential equation --- two approximate factors --- dielectrophoresis --- electrophysiological properties --- crossover frequency --- wake or recirculation formation --- dielectric spectra --- air compliance effect --- RBC aggregation --- blood viscoelasticity --- blood velocity fields --- interface in co-flowing streams --- blood flow --- particle tracking --- red blood cells --- manual methods --- automatic methods --- image analysis --- biomicrofluidics --- microfluidics --- blood plasma filtration --- chip extract --- blood molecules --- patient-derived organoids --- colorectal cancer --- 3D model --- drug screening --- diagnostics --- malaria --- optical filters --- reflectance --- spectrophotometry --- TFCalc --- small caliber blood vessel --- composite molding --- micro-nano structure --- tissue repair --- 3D printing --- blood cells --- fourier transform infrared (FTIR) spectroscopy --- functional group --- lab-on-a-chip --- n/a