Name: iridium oxide-reduced graphene oxide nanohybrid thin film modified screen-printed electrodes as disposable electrochemical paper microfluidic ph sensors
Uploaded: 2016-11-22T12:30:00.000+00:00
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Description: Watch this Scientific Journal Video about Iridium Oxide-reduced Graphene Oxide Nanohybrid Thin Film Modified Screen-printed Electrodes as Disposable Electrochemical Paper Microfluidic pH Sensors at Jo

这项工作是由来自水设备及策略（WEP）NSF工业/大学合作研究中心（I / UCRC）的资助。作者还感谢了亚尔马D.和珍妮特·W·布鲁恩奖学金和路易斯和Elsa汤姆森威斯康辛杰出研究生奖学金在威斯康星大学麦迪逊分校提供给JY

1.μPAD和设备准备<ol><li>刻在底部塑料保持器500微米槽以容纳SPE与由三维（3D）铣床及具有直径为1.6mm铣削位的ABS或兼容塑料片材。与夹持器（ 图1A）在测试过程中保持在适当位置SPE和μPAD牢固。 </li><li>使印模和使用合成树脂片或相容的塑料片材与凹凸花纹，分别真空罩，由3D铣床，以在纸张上焊盘图案疏水PDMS障碍。 <ol><li>制备的PDMS预聚合物和交联剂的混合物中以10:1的比例，或通过制造商的建议，拌入抹刀和应用适当的量到的PDMS印模的凸面。 </li></ol></li><li>放置印章上的滤纸垫预切割成所需要的尺寸，然后在整个纸张印模的相对侧上的真空盖的顶部。应用VACU嗯用于通过手工操作真空泵达30秒。除去从印模和真空罩的纸垫，并在80℃的对流烘箱中烘烤10分钟，以硬化图案化的PDMS（ 图1B）。所得纸垫具有约为0.2 cm 2的感测区和1个厘米×0.4厘米亲水样品芯吸区域。 注:取上施加的PDMS和真空时间的量特别注意事项，以避免在液体样品转移滤纸的内部亲水区的任何可能的PDMS污染。 </li></ol> 2. SPE的修改与2的IrO -RGO纳米杂化薄膜<ol><li>降投3微升所制备的1毫克∙毫升-1 GO SPE上的石墨碳工作电极溶液用微量并让它干燥在培养皿室温。吹扫用N 2的pH 5.0的PBS缓冲液20分钟，浸在SPE中10毫升脱气PBS缓冲液，同时保持Ñ&lt;子&gt; 2流动，并从0.0到-1.5V时重复进行阴极电位循环100次，以减少电化学进入RGO。冲洗用DI水在SPE中一个喷射瓶并在室温下干燥。 注:嗯剥离的GO表，通过静电排斥稳定，从采用改良悍马的方法，其他地方7日报道石墨粉。合成的RGO膜的均匀性是很重要的，因为它充当的IrO 2的薄膜的进一步生长的碳载体。 </li><li>使（IrCl 4）0.15四氯化铱组成100毫升的IrO 2沉积溶液，0.6毫升50％（W / W）过氧化氢（H 2 O 2）和0.5g草酸通过在去离子水中添加它们脱水。逐渐添加无水碳酸钾少量，同时搅拌直到pH达到10.5，通过基于实验室的pH计进行验证。然后，溶液变成淡黄色。老龄化在室温temperatu 48小时解决再次，那么它的颜色是最终关闭的淡蓝色。 </li><li>把RGO-SPE在上述沉积溶液和适用+ 0.6V的恒定电位5分钟。的IrO 2薄膜的厚度可以通过沉积电势和时间被精确地控制。 </li><li>确认通过SEM传感区域的结构。获得SEM照片下面的材料科学中心在威斯康星大学麦迪逊分校的指令，因为我们7以前那样。 </li></ol> 3.价格低廉，便携数字pH计建设<ol><li>通过在任何一个系列的两个单LF356N运算放大器（运算放大器）或者一个INA111高速场效应晶体管（FET） -输入仪表放大器的堵塞建造廉价且小型化的pH计用数字显示（高输入阻抗&gt; 10 12Ω）在面包板，以实现稳定的测量足够高的内部阻抗。 注:所有的部件很容易交流从电子商店够到，并且可以容易地组装。 </li><li>使用税务条例2 -RGO-SPE作为pH探头和运算放大器作为单位增益缓冲器。串联连接两个接地9 V碱性电池消费的pH计的电源插上电线插入基于运算放大器的引脚布局线路板。 </li><li>在阴极和阳极连接到销7和4.又一个数字万用表的正面和负面的探针分别连接到销6和运算放大器5来测量输出电压和显示读数。参考和SPE工作电极连接到引脚2和3水涨船高。详细的连接示于图1D。 </li></ol> 4. pH测量<ol><li>制备100ml的BR缓冲液与0.04M的等摩尔磷酸，乙酸和硼酸和用0.2M氢氧化钠（NaOH）的不同体积（5，25，42，60，78和98），混合到由2-实现不同pH 12，用于校准。 </li><li>禄吃图案在传感区域的顶部μPAD。安装60微升液体样品直接通过微量吸入μPAD的芯吸的亲水区。该μPAD可以在使用或不ABS的盖进行，当它被浸湿。 </li><li>测量的IrO 2 -RGO工作电极和随着时间的推移或者是基于实验室的CHI 660D电化学分析仪或便携式数字pH计，当开路电位（OCP）变得稳定的Ag / AgCl参考电极之间的电压信号（电位变型&lt;5％）。 </li><li>保持浸渍液体样品在纸垫湿感测区域进行测试，如果需要的话，以达到更好的电接触，以及稳定和可重现的读数在长期操作。记录稳态OCP值是在各pH值平均，以确定校准曲线。 </li></ol>

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设备安装 pH传感器的工作原理，通过测量在工作电极和参考电极之间的OCP，因为它按比例改变到的 H +浓度的负对数。测量可以通过一个基于实验室的电位如CHI 660D和与通过万用表阅读面包板构造简单的pH计来实现两者。两个不同的便携式pH计类似地构建在使用两个9伏碱性电池，一个数字万用表，所合成的IrO 2 -RGO-SPE和不同运算放大器，这?...

pH值的测定是在食品，生理，药用和环境研究中无处不在。用于pH检测两种最常用的工具是pH值条和pH计。纸条浸渍有变色的pH指示剂分子，但读数在pH范围，主观和半定量的一些偏差，有时受到限制。另一方面，pH计通常配有玻璃电极可以通过数字用户界面准确到0.01的水平，并显示测量的pH值。基于实验室的pH计不仅需要特别注意维护和校准，也不用对小体积样品很好地工作，往往需要一个干净的容器，如执行测量烧杯中。尽管它的灵敏度，选择性和稳定性的，玻璃电极从酸/碱误差，高阻抗，温度不稳定和机械脆性1受损。因此，这是有利的具有embod的pH测量系统IES pH计和pH条的简易性和成本方面的准确性。 总是有许多发展中地区，其中昂贵的实验室设备或商业实验室是负担不起的未满足的需要对有限资源的条件下，这样的工具。此外，新的易于使用，对现场检测平台的作用越来越被用于点护理检测这样的需求推动。电化学检测是简单，容易小型化和令人满意敏感，在市场上商业化的低成本SPE和各种血糖监测系统作为证明。作为光，灵活和一次性的多孔材料，纸也可具有各种可控的特征，如不同的孔尺寸，官能团，和芯吸速率。 作为纸基材几乎影响分析物扩散和电化学检测2-4，纸流体装置和电分析技术的组合具有recentlŸ受到了广泛的利益。这样的组合的表观优点是样品体积的在其中可以潜在防止在测量过程中的振动和对流的干扰测量中使用的微小量。例如，图案化的微流体垫被施加到芯吸和提供液体样品到SPE的传感区域检测重金属离子和葡萄糖2,5。建立使用纸微流体电化学发光类似的设备来完成检测NADH 4。最近，简单的电化学纸微流体装置可在载玻片上建立与铅笔电极6或使用酶纸张与SPE 3。 使用简便，高效的电化学方法制备的IrO 2和RGO组成的纳米杂化薄膜材料。我们发现，不规则和粗SPE石墨碳表面上，阳极电沉积的IrO 2薄膜不能平滑，稳定，没有RGO的帮助。所得的IrO 2 -RGO SPE被整合到已图案化用于pH传感疏水屏障纸微流体装置。该组装的装置显示，pH值传感出色的分析性能有略微超能斯特行为。结果是可比的常规基于实验室的pH计用玻璃电极。最后，高性价比的小型化pH计是建立在面包板与数字万用表测量开路电位输出信号。便携式pH计的测定良好相关与这些商业实验室pH计的。

<table><tbody><tr><td>Screen-printed electrodes</td><td>Zensor</td><td>TE100</td><td>3-electrode integrated</td></tr><tr><td>Acrylonitrile butadiene styrene (ABS)&amp;nbsp;</td><td></td><td></td><td></td></tr><tr><td>Polydimethylsiloxane (PDMS) prepolymer and cross linker mixture</td><td>Dow-Corning Co.</td><td>Sylgard 184</td><td>10:1 mixture w/w</td></tr><tr><td>Whatman No. 1 filter paper</td><td>GE Healthcare Co.</td><td></td><td></td></tr><tr><td>3D milling system</td><td>Roland DGA Co.</td><td>iModela IM-01</td><td></td></tr><tr><td>PDMS stamp and vacuum cover</td><td>Roland DGA Co.</td><td>Sanmodur</td><td>Synthetic resin tablet</td></tr><tr><td>Hand-operated vacuum pump</td><td>Cole-Parmer Co.</td><td></td><td></td></tr><tr><td>Electrochemical workstation</td><td>CH Instruments</td><td>CHI 660D</td><td></td></tr><tr><td>LF356N operational amplifiers</td><td>Texas Instruments Inc.</td><td></td><td></td></tr><tr><td>INA111 high speed field-effect transistor (FET)-input instrumentation amplifier</td><td>Burr-Brown Inc.</td><td></td><td></td></tr><tr><td>DMM914 digital multimeter&amp;nbsp;</td><td>Tektronix Inc.</td><td>70979101</td><td></td></tr><tr><td>&lt;strong&gt;From Fisher or Sigma:&lt;/strong&gt;</td><td></td><td></td><td></td></tr><tr><td>Iridium tetrachloride (IrCl&lt;sub&gt;4&lt;/sub&gt;)</td><td></td><td></td><td></td></tr><tr><td>50% (w/w) hydrogen peroxide (H&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;2&lt;/sub&gt;)</td><td></td><td></td><td></td></tr><tr><td>Oxalic acid dihydrate</td><td></td><td></td><td></td></tr><tr><td>Potassium carbonate (K&lt;sub&gt;2&lt;/sub&gt;CO&lt;sub&gt;3&lt;/sub&gt;)</td><td></td><td></td><td></td></tr><tr><td>Phosphoric acid</td><td></td><td></td><td></td></tr><tr><td>Acetic acid&amp;nbsp;</td><td></td><td></td><td></td></tr><tr><td>Boric acid</td><td></td><td></td><td></td></tr><tr><td>Sodium hydroxide (NaOH)</td><td></td><td></td><td></td></tr><tr><td>Na&lt;sub&gt;2&lt;/sub&gt;HPO&lt;sub&gt;4&lt;/sub&gt;</td><td></td><td></td><td></td></tr><tr><td>NaH&lt;sub&gt;2&lt;/sub&gt;HPO&lt;sub&gt;4&lt;/sub&gt;</td><td></td><td></td><td></td></tr></tbody></table>

iridium oxide-reduced graphene oxide nanohybrid thin film modified screen-printed electrodes as disposable electrochemical paper microfluidic ph sensors

2的IrO -graphene纳米杂化薄膜的一种简便，可控，价格低廉，绿色电化学合成开发制造一个易于使用的集成微纸电化学pH值资源有限的环境传感器。以优势来自pH计和试纸，pH值检测平台由使用聚二甲基硅氧烷（PDMS）疏水屏障图案纸micropad（μPAD）中，丝网印刷电极（SPE）改性的IrO 2 -graphene薄膜和模塑丙烯腈-丁二烯-苯乙烯（ABS）的塑料保持器。重复阴极电位自行车被用于氧化石墨烯（GO）减少其可以完全具有优良的稳定性和电子属性中删除电化学不稳定含氧组，并生成一个二维无缺陷的均匀的石墨烯薄膜。在纳米颗粒大小均匀，光滑的IrO 2膜阳极电沉积石墨烯薄膜，没有任何观察的裂缝。所得的IrO 2 -RGO电极中的BR（BR），具有良好的线性，迟滞小，低响应时间和再现在不同的缓冲器，以及低敏感性不同干涉缓冲器表明在pH 2-12略微超能斯特响应离子物质和溶解的氧。一个简单的便携式数字pH计是捏造，是用万用表测量其信号，使用高输入阻抗运算放大器和消费电池。与便携式电化学纸微流体pH传感器测得的pH值下分别为与使用商业实验室pH计用玻璃电极测定一致。

电化学的IrO 2 -RGO-SPE pH传感器结合纸微流控的设置显示在图1A。与PDMS疏水屏障的构图纸垫被放置在其上位于ABS塑料支架的IrO 2 -RGO-SPE的敏感区域的顶部。纸垫的感应区进行了仔细的与电极表面对齐。水性亚甲蓝染料溶液用来测试图案化纸垫和所观察到的，将样品灯芯到亲水性区域（ 图1B）与由疏水屏障调节的流体路径。 SEM图像示出...

Watch this Scientific Journal Video about Iridium Oxide-reduced Graphene Oxide Nanohybrid Thin Film Modified Screen-printed Electrodes as Disposable Electrochemical Paper Microfluidic pH Sensors at Jo

Iridium Oxide-reduced Graphene Oxide Nanohybrid Thin Film Modified Screen-printed Electrodes as Disposable Electrochemical Paper Microfluidic pH Sensors

这项研究表明铱-氧化还原的石墨烯氧化物的（的IrO 2 -RGO）生长纳米杂化物通过一个绿色电化学合成不规则和粗丝网印刷碳基板上的薄膜，其作为pH传感器实现具有图案化纸流体平台。

氧化铱还原氧化石墨烯纳米杂化薄膜修饰丝网印刷电极一次性电化学微流控纸pH传感器

A facile, controllable, inexpensive and green electrochemical synthesis of IrO2-graphene nanohybrid thin films is developed to fabricate an easy-to-use ...

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10.5K 次观看.  University of Wisconsin-Madison. 这项研究表明铱-氧化还原的石墨烯氧化物的（的IrO 2 -RGO）生长纳米杂化物通过一个绿色电化学合成不规则和粗丝网印刷碳基板上的薄膜，其作为pH传感器实现具有图案化纸流体平台。 

视频: Iridium Oxide-reduced Graphene Oxide Nanohybrid Thin Film Modified Screen-printed Electrodes as Disposable Electrochemical Paper Microfluidic pH Sensors

Polycrystalline Silicon Thin-film Solar cells with Plasmonic-enhanced Light-trapping

One of major approaches to cheaper solar cells is reducing the amount of semiconductor material used for their fabrication and making cells thinner. To compensate for lower light absorption such physically thin devices have to incorporate light-trapping which increases their optical thickness. Light scattering by textured surfaces is a common technique but it cannot be universally applied to all solar cell technologies. Some cells, for example those made of evaporated silicon, are planar as produced and they require an alternative light-trapping means suitable for planar devices. Metal nanoparticles formed on planar silicon cell surface and capable of light scattering due to surface plasmon resonance is an effective approach.
The paper presents a fabrication procedure of evaporated polycrystalline silicon solar cells with plasmonic light-trapping and demonstrates how the cell quantum efficiency improves due to presence of metal nanoparticles.
To fabricate the cells a film consisting of alternative boron and phosphorous doped silicon layers is deposited on glass substrate by electron beam evaporation. An Initially amorphous film is crystallised and electronic defects are mitigated by annealing and hydrogen passivation. Metal grid contacts are applied to the layers of opposite polarity to extract electricity generated by the cell. Typically, such a ~2 &mu;m thick cell has a short-circuit current density (Jsc) of 14-16 mA/cm2, which can be increased up to 17-18 mA/cm2 (~25% higher) after application of a simple diffuse back reflector made of a white paint.
To implement plasmonic light-trapping a silver nanoparticle array is formed on the metallised cell silicon surface. A precursor silver film is deposited on the cell by thermal evaporation and annealed at 23&deg;C to form silver nanoparticles. Nanoparticle size and coverage, which affect plasmonic light-scattering, can be tuned for enhanced cell performance by varying the precursor film thickness and its annealing conditions. An optimised nanoparticle array alone results in cell Jsc enhancement of about 28%, similar to the effect of the diffuse reflector. The photocurrent can be further increased by coating the nanoparticles by a low refractive index dielectric, like MgF2, and applying the diffused reflector. The complete plasmonic cell structure comprises the polycrystalline silicon film, a silver nanoparticle array, a layer of MgF2, and a diffuse reflector. The Jsc for such cell is 21-23 mA/cm2, up to 45% higher than Jsc of the original cell without light-trapping or ~25% higher than Jsc for the cell with the diffuse reflector only.
Introduction
Light-trapping in silicon solar cells is commonly achieved via light scattering at textured interfaces. Scattered light travels through a cell at oblique angles for a longer distance and when such angles exceed the critical angle at the cell interfaces the light is permanently trapped in the cell by total internal reflection (Animation 1: Light-trapping). Although this scheme works well for most solar cells, there are developing technologies where ultra-thin Si layers are produced planar (e.g. layer-transfer technologies and epitaxial c-Si layers) 1 and or when such layers are not compatible with textures substrates (e.g. evaporated silicon) 2. For such originally planar Si layer alternative light trapping approaches, such as diffuse white paint reflector 3, silicon plasma texturing 4 or high refractive index nanoparticle reflector 5 have been suggested.
Metal nanoparticles can effectively scatter incident light into a higher refractive index material, like silicon, due to the surface plasmon resonance effect 6. They also can be easily formed on the planar silicon cell surface thus offering a light-trapping approach alternative to texturing. For a nanoparticle located at the air-silicon interface the scattered light fraction coupled into silicon exceeds 95% and a large faction of that light is scattered at angles above critical providing nearly ideal light-trapping condition (Animation 2: Plasmons on NP). The resonance can be tuned to the wavelength region, which is most important for a particular cell material and design, by varying the nanoparticle average size, surface coverage and local dielectric environment 6,7. Theoretical design principles of plasmonic nanoparticle solar cells have been suggested 8. In practice, Ag nanoparticle array is an ideal light-trapping partner for poly-Si thin-film solar cells because most of these design principle are naturally met. The simplest way of forming nanoparticles by thermal annealing of a thin precursor Ag film results in a random array with a relatively wide size and shape distribution, which is particularly suitable for light-trapping because such an array has a wide resonance peak, covering the wavelength range of 700-900 nm, important for poly-Si solar cell performance. The nanoparticle array can only be located on the rear poly-Si cell surface thus avoiding destructive interference between incident and scattered light which occurs for front-located nanoparticles 9. Moreover, poly-Si thin-film cells do not requires a passivating layer and the flat base-shaped nanoparticles (that naturally result from thermal annealing of a metal film) can be directly placed on silicon further increases plasmonic scattering efficiency due to surface plasmon-polariton resonance 10.
The cell with the plasmonic nanoparticle array as described above can have a photocurrent about 28% higher than the original cell. However, the array still transmits a significant amount of light which escapes through the rear of the cell and does not contribute into the current. This loss can be mitigated by adding a rear reflector to allow catching transmitted light and re-directing it back to the cell. Providing sufficient distance between the reflector and the nanoparticles (a few hundred nanometers) the reflected light will then experience one more plasmonic scattering event while passing through the nanoparticle array on re-entering the cell and the reflector itself can be made diffuse - both effects further facilitating light scattering and hence light-trapping. Importantly, the Ag nanoparticles have to be encapsulated with an inert and low refractive index dielectric, like MgF2 or SiO2, from the rear reflector to avoid mechanical and chemical damage 7. Low refractive index for this cladding layer is required to maintain a high coupling fraction into silicon and larger scattering angles, which are ensured by the high optical contrast between the media on both sides of the nanoparticle, silicon and dielectric 6. The photocurrent of the plasmonic cell with the diffuse rear reflector can be up to 45% higher than the current of the original cell or up to 25% higher than the current of an equivalent cell with the diffuse reflector only.

Polycrystalline silicon thin-film solar cells on glass are fabricated by deposition of boron and phosphorous doped silicon layers followed by crystallisation, defect passivation and metallisation. Plasmonic light-trapping is introduced by forming Ag nanoparticles on the silicon cell surface capped with a diffused reflector resulting in ~45% photocurrent enhancement.

多晶硅薄膜太阳能电池电浆增强光捕获

One of major approaches to cheaper solar cells is reducing the amount of semiconductor material used for their fabrication and making cells thinner. To ...

科研

工程学

Nanomoulding of Functional Materials, a Versatile Complementary Pattern Replication Method to Nanoimprinting

We describe a nanomoulding technique which allows low-cost nanoscale patterning of functional materials, materials stacks and full devices. Nanomoulding combined with layer transfer enables the replication of arbitrary surface patterns from a master structure onto the functional material. Nanomoulding can be performed on any nanoimprinting setup and can be applied to a wide range of materials and deposition processes. In particular we demonstrate the fabrication of patterned transparent zinc oxide electrodes for light trapping applications in solar cells.

We describe a nanomoulding technique which allows low-cost nanoscale patterning of functional materials, materials stacks and full devices. Nanomoulding can be performed on any nanoimprinting setup and can be applied to a wide range of materials and deposition processes.

Nanomoulding功能材料，灵活的互补模式的复制方法，以奈米

We describe a nanomoulding technique which  allows low-cost nanoscale patterning of functional materials, materials stacks  and full devices. Nanomoulding ...

Development of a 3D Graphene Electrode Dielectrophoretic Device

The design and fabrication of a novel 3D electrode microdevice using 50 &#181;m thick graphene paper and 100 &#181;m double sided tape is described. The protocol details the procedures to construct a versatile, reusable, multiple layer, laminated dielectrophoresis chamber. Specifically, six layers of 50 &#181;m x&#160;0.7 cm x&#160;2 cm graphene paper and five layers of double sided tape were alternately stacked together, then clamped to a glass slide. Then a 700 &#956;m diameter micro-well was drilled through the laminated structure using a computer-controlled micro drilling machine. Insulating properties of the tape layer between adjacent graphene layers were assured by resistance tests. Silver conductive epoxy connected alternate layers of graphene paper and formed stable connections between the graphene paper and external copper wire electrodes. The finished device was then clamped and sealed to a glass slide. The electric field gradient was modeled within the multi-layer device. Dielectrophoretic behaviors of 6 &#956;m polystyrene beads were demonstrated in the 1 mm deep micro-well, with medium conductivities ranging from 0.0001 S/m to 1.3 S/m, and applied signal frequencies from 100 Hz to 10 MHz. Negative dielectrophoretic responses were observed in three dimensions over most of the conductivity-frequency space and cross-over frequency values are consistent with previously reported literature values. The device did not prevent AC electroosmosis and electrothermal flows, which occurred in the low and high frequency regions, respectively. The graphene paper utilized in this device is versatile and could subsequently function as a biosensor after dielectrophoretic characterizations are complete.

A microdevice with high throughput potential is used to demonstrate three-dimensional (3D) dielectrophoresis (DEP) with novel materials. Graphene nanoplatelet paper and double sided tape were alternately stacked; a 700 &#956;m micro-well was drilled transverse to the layers. DEP behavior of polystyrene beads was demonstrated in the micro-well.

三维石墨电极介电泳装置的研制

The design and fabrication of a novel 3D electrode microdevice using 50 &#181;m thick graphene paper and 100 &#181;m double sided tape is described. The ...

Assessment of Boron Doped Diamond Electrode Quality and Application to In Situ Modification of Local pH by Water Electrolysis

Boron doped diamond (BDD) electrodes have shown considerable promise as an electrode material where many of their reported properties such as extended solvent window, low background currents, corrosion resistance, etc., arise from the catalytically inert nature of the surface. However, if during the growth process, non-diamond-carbon (NDC) becomes incorporated into the electrode matrix, the electrochemical properties will change as the surface becomes more catalytically active. As such it is important that the electrochemist is aware of the quality and resulting key electrochemical properties of the BDD electrode prior to use. This paper describes a series of characterization steps, including Raman microscopy, capacitance, solvent window and redox electrochemistry, to ascertain whether the BDD electrode contains negligible NDC i.e. negligible sp2 carbon. One application is highlighted which takes advantage of the catalytically inert and corrosion resistant nature of an NDC-free surface i.e. stable and quantifiable local proton and hydroxide production due to water electrolysis at a BDD electrode. An approach to measuring the local pH change induced by water electrolysis using iridium oxide coated BDD electrodes is also described in detail.

Assessment of Boron Doped Diamond Electrode Quality and Application to In Situ Modification of Local pH by Water Electrolysis

A protocol is described for the characterization of the key electrochemical parameters of a boron doped diamond (BDD) electrode and subsequent application for in situ pH generation experiments.

掺硼金刚石电极质量和应用，以评估<em&gt;原位</em&gt;本地pH值通过水电改造

Boron doped diamond (BDD) electrodes have shown considerable promise as an electrode material where many of their reported properties such as extended ...

化学

Hollow Microneedle-based Sensor for Multiplexed Transdermal Electrochemical Sensing

The development of a minimally invasive multiplexed monitoring system for rapid analysis of biologically-relevant molecules could offer individuals suffering from chronic medical conditions facile assessment of their immediate physiological state. Furthermore, it could serve as a research tool for analysis of complex, multifactorial medical conditions. In order for such a multianalyte sensor to be realized, it must be minimally invasive, sampling of interstitial fluid must occur without pain or harm to the user, and analysis must be rapid as well as selective.
Initially developed for pain-free drug delivery, microneedles have been used to deliver vaccines and pharmacologic agents (e.g., insulin) through the skin.1-2 Since these devices access the interstitial space, microneedles that are integrated with microelectrodes can be used as transdermal electrochemical sensors. Selective detection of glucose, glutamate, lactate, hydrogen peroxide, and ascorbic acid has been demonstrated using integrated microneedle-electrode devices with carbon fibers, modified carbon pastes, and platinum-coated polymer microneedles serving as transducing elements.3-7,8
This microneedle sensor technology has enabled a novel and sophisticated analytical approach for in situ and simultaneous detection of multiple analytes. Multiplexing offers the possibility of monitoring complex microenvironments, which are otherwise difficult to characterize in a rapid and minimally invasive manner. For example, this technology could be utilized for simultaneous monitoring of extracellular levels of, glucose, lactate and pH,9 which are important metabolic indicators of disease states7,10-14 (e.g., cancer proliferation) and exercise-induced acidosis.15

This article details the construction of a multiplexed microneedle-based sensor. The device is being developed for in situ sampling and electrochemical analysis of multiple analytes in a rapid and selective manner. We envision clinical medicine and biomedical research uses for these microneedle-based sensors.

复透皮电化学传感的空心微针为基础的传感器

The development of a minimally invasive multiplexed monitoring system for rapid analysis of biologically-relevant molecules could offer individuals ...

生物工程

Development and Functionalization of Electrolyte-Gated Graphene Field-Effect Transistor for Biomarker Detection

In the current study, graphene and its derivatives have been investigated and used for many applications, including electronics, sensing, energy storage, and photocatalysis. Synthesis and fabrication of high quality, good uniformity, and low defects graphene are critical for high-performance and highly sensitive devices. Among many synthesis methods, chemical vapor deposition (CVD), considered a leading approach to manufacture graphene, can control the number of graphene layers and yield high-quality graphene. CVD graphene needs to be transferred from the metal substrates on which it is grown onto&#160;insulating substrates for practical applications. However, separation and transferring of graphene onto new substrates are challenging for a uniform layer without damaging or affecting graphene&#39;s structures and properties. Additionally, electrolyte-gated graphene field-effect transistor (EGGFET) has been demonstrated for its wide applications in various biomolecular detections because of its high sensitivity and standard device configuration. In this article, poly (methyl methacrylate) (PMMA)-assisted graphene transferring approach, fabrication of graphene field-effect transistor (GFET), and biomarker immunoglobulin G (IgG) detection are demonstrated. Raman spectroscopy and atomic force microscopy were applied to characterize the transferred graphene. The method is shown to be a practical approach for transferring clean and residue-free graphene while preserving the underlying graphene lattice onto an insulating substrate for electronics or biosensing applications.

The present protocol demonstrates the development of electrolyte-gated graphene field-effect transistor (EGGFET) biosensor and its application in biomarker immunoglobulin G (IgG) detection.

用于生物标志物检测的电解质门控石墨烯场效应晶体管的开发与功能化

In the current study, graphene and its derivatives have been investigated and used for many applications, including electronics, sensing, energy storage, ...

Electrochemical Preparation of Poly(3,4-Ethylenedioxythiophene) Layers on Gold Microelectrodes for Uric Acid-Sensing Applications

Two different methods for the synthesis of poly(3,4-ethylenedioxythiophene) (PEDOT) on gold electrodes are described, using electropolymerization of 3,4-ethylenedioxythiophene (EDOT) monomer in an aqueous and an organic solution. Cyclic voltammetry (CV) was used in the synthesis of PEDOT thin layers. Lithium perchlorate (LiClO4) was used as a dopant in both aqueous (aqueous/acetonitrile (ACN)) and organic (propylene carbonate (PC)) solvent systems. After the PEDOT layer was created in the organic system, the electrode surface was acclimatized by successive cycling in an aqueous solution for use as a sensor for aqueous samples. 
The use of an aqueous-based electropolymerization method has the potential benefit of removing the acclimatization step to have a shorter sensor preparation time. Although the aqueous method is more economical and environmentally friendly than the organic solvent method, superior PEDOT formation is obtained in the organic solution. The resulting PEDOT electrode surfaces were characterized by scanning electron microscopy (SEM), which showed the constant growth of PEDOT during electropolymerization from the organic PC solution, with rapid fractal-type growth on gold (Au) microelectrodes.

Electrochemical Preparation of Poly3,4-Ethylenedioxythiophene Layers on Gold Microelectrodes for Uric Acid-Sensing Applications

We describe aqueous and organic solvent systems for the electropolymerization of poly(3,4-ethylenedioxythiophene) to create thin layers on the surface of gold microelectrodes, which are used for sensing low molecular weight analytes.

在金微电极上电化学制备聚（3，4-乙烯二氧噻吩）层在尿酸传感应用中

Two different methods for the synthesis of poly(3,4-ethylenedioxythiophene) (PEDOT) on gold electrodes are described, using electropolymerization of ...

纳米纤维素纸基分析装置的微压花制备  

Microembossing: A Convenient Process for Fabricating Microchannels on Nanocellulose Paper-Based Microfluidics

Nanopaper, derived from nanofibrillated cellulose, has generated considerable interest as a promising material for microfluidic applications. Its appeal lies in a range of excellent&#160;qualities, including an exceptionally smooth surface, outstanding optical transparency, a uniform nanofiber matrix with nanoscale porosity, and customizable chemical properties. Despite the rapid growth of nanopaper-based microfluidics, the current techniques used to create microchannels on nanopaper, such as 3D printing, spray coating, or manual cutting and assembly, which are crucial for practical applications, still possess certain limitations, notably susceptibility to contamination. Furthermore, these methods are restricted to the production of millimeter-sized channels. This study introduces a straightforward process that utilizes convenient plastic micro-molds for simple microembossing operations to fabricate microchannels on nanopaper, achieving a minimum width of 200 &#181;m. The developed microchannel outperforms existing approaches, achieving a fourfold improvement, and can be fabricated within 45 min. Furthermore, fabrication parameters have been optimized, and a convenient quick-reference table is provided for application developers. The proof-of-concept for a laminar mixer, droplet generator, and functional nanopaper-based analytical devices (NanoPADs) designed for Rhodamine B sensing using surface-enhanced Raman spectroscopy was demonstrated. Notably, the NanoPADs exhibited exceptional performance with improved limits of detection. These outstanding results can be attributed to the superior optical properties of nanopaper and the recently developed accurate microembossing method, enabling the integration and fine-tuning of the NanoPADs.

作者聚焦：通过纳米纸上的微通道制造彻底改变微流体 

This protocol describes a straightforward process that utilizes convenient plastic micro-molds for simple microembossing operations to fabricate microchannels on nanofibrillated cellulose paper, achieving a minimum width of 200 &#181;m.

微压花：在纳米纤维素纸基微流控上制造微通道的便捷工艺

Nanopaper, derived from nanofibrillated cellulose, has generated considerable interest as a promising material for microfluidic applications. Its appeal ...

氧化铱还原氧化石墨烯纳米杂化薄膜修饰丝网印刷电极一次性电化学微流控纸pH传感器

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此视频中的章节

多晶硅薄膜太阳能电池电浆增强光捕获

Nanomoulding功能材料，灵活的互补模式的复制方法，以奈米

三维石墨电极介电泳装置的研制

掺硼金刚石电极质量和应用，以评估

复透皮电化学传感的空心微针为基础的传感器

用于生物标志物检测的电解质门控石墨烯场效应晶体管的开发与功能化

在金微电极上电化学制备聚（3，4-乙烯二氧噻吩）层在尿酸传感应用中

微压花：在纳米纤维素纸基微流控上制造微通道的便捷工艺

微压花：在纳米纤维素纸基微流控上制造微通道的便捷工艺

微压花：在纳米纤维素纸基微流控上制造微通道的便捷工艺