Surface decoration

  • 文章类型: Journal Article
    研究了通过氧化魔芋葡甘聚糖(OKGM)表面修饰来增强原花青素脂质体(PC-Lip)的稳定性。OKGM包被的PC-Lip(OKGM-PC-Lip)的包封率和载药量显著上升。OKGM-PC-Lip的平均大小和PDI增加,而zeta电位与PC-Lip相比降低。用OKGM涂覆后,PC-唇膜流动性降低。OKGM-PC-Lip的形态表明在脂质体表面形成了OKGM“晕层”。氢键在OKGM和PC-Lip的结合中起着不可或缺的作用,用OKGM涂覆后,PC-Lip的相变温度略有升高。OKGM-PC-Lip在极端pH下的保留率高于PC-Lip。体外释放,在胃期,OKGM-PC-Lip和PC-Lip之间的累积释放没有显着差异,肠道期OKGM-PC-Lip的累积释放速率明显低于PC-Lip。OKGM-PC-Lip的抗氧化活性明显高于PC-Lip。这些结果表明,用OKGM涂覆后,PC-Lip对外部影响的抵抗力得到了有效增强。与其他多糖相比,由于多糖对人体健康的益处,OKGM包被的脂质体在功能性食品中可能更有前途和优势。
    The stability enhancement of proanthocyanidin-loaded liposomes (PC-Lip) via surface decoration with oxidized konjac glucomannan (OKGM) was investigated. The encapsulation efficiency and drug loading capacity of OKGM-coated PC-Lip (OKGM-PC-Lip) rose significantly. The average size and PDI of OKGM-PC-Lip increased, while the zeta potential decreased compared to those of PC-Lip. PC-Lip membrane fluidity reduced after coating with OKGM. The morphology of OKGM-PC-Lip showed that OKGM \"halo layer\" was formed on the liposome surface. Hydrogen bonding played an indispensable role in the combination between OKGM and PC-Lip, and the phase transition temperature of PC-Lip slightly increased after coating with OKGM. The retention rate of OKGM-PC-Lip was higher than that of PC-Lip at extreme pH. In vitro release, no significant difference in cumulative release was detected between OKGM-PC-Lip and PC-Lip at gastric stage, while the cumulative release rate of OKGM-PC-Lip was remarkably lower than that of PC-Lip at intestinal stage. The antioxidant activity of OKGM-PC-Lip was notably higher than that of PC-Lip. These results suggested that the resistance of PC-Lip to external influences was fruitfully enhanced after coating with OKGM. Compared with other polysaccharides, OKGM-coated liposomes may be more promising and advantageous in functional foods due to the polysaccharide\'s benefits to human health.
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  • 文章类型: Journal Article
    贵金属纳米晶体在有效催化以电化学乙醇氧化反应(EOR)为代表的多步反应方面面临挑战,由于中间体结合能之间的线性比例关系,多电子转移过程,阻碍各个元素步骤的独立优化。在这里,我们开发的贵金属纳米晶体具有一系列的局部表面结合亲和力,以克服这一挑战。实验上,这通过对Pd表面施加拉伸应变并用离散的Au原子装饰来证明,在客体分子附近形成具有不同亲和力的多种结合位点,CO探测和密度泛函理论计算证明了这一点。这种表面使反应中间体能够根据每个元素步骤的需要在不同的结合位点之间迁移。从而当与单个位点处的反应相比时,降低了总EOR的能量势垒。在这些量身定制的表面上,我们在EOR中获得了32.7mAcm-2和47.8AmgPd-1的比和质量活性,分别超过商用Pd/C10.9倍和43.8倍,分别,和优于现有技术的Pd基催化剂。这些结果突出了这种方法在改进各种多步骤,多电子转移反应,这对能量转换应用至关重要。
    Noble metal nanocrystals face challenges in effectively catalyzing electrochemical ethanol oxidation reaction (EOR)-represented multistep, multielectron transfer processes due to the linear scaling relationship among binding energies of intermediates, impeding independent optimization of individual elemental steps. Herein, we develop noble metal nanocrystals with a range of local surface binding affinities in close proximity to overcome this challenge. Experimentally, this is demonstrated by applying tensile strain to a Pd surface and decorating it with discrete Au atoms, forming a diversity of binding sites with varying affinities in close proximity for guest molecules, as evidenced by CO probing and density functional theory calculations. Such a surface enables reaction intermediates to migrate between different binding sites as needed for each elemental step, thereby reducing the energy barrier for the overall EOR when compared to reactions at a single site. On these tailored surfaces, we attain specific and mass activities of 32.7 mA cm-2 and 47.8 A mgPd-1 in EOR, surpassing commercial Pd/C by 10.9 and 43.8 times, respectively, and outperforming state-of-the-art Pd-based catalysts. These results highlight the promise of this approach in improving a variety of multistep, multielectron transfer reactions, which are crucial for energy conversion applications.
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  • 文章类型: Journal Article
    具有多功能功能的光电传感器已经成为未来光电系统在各种应用中取得突破的基石。特别是,新兴的光电化学(PEC)型装置最近吸引了广泛的兴趣,在基于液体的生物传感应用,由于其天然的电解质辅助操作特性。在这里,通过在硅上使用氮化镓(GaN)p-n同质结半导体纳米线,精心设计和构造了PEC型光传感器,p-GaN段战略掺杂,然后用钴镍氧化物(CoNiOx)装饰。本质上,p-n同质结结构与容易的p-掺杂工程提高载流子分离效率,促进载流子转移到纳米线表面,而CoNiOx装饰进一步增强PEC反应活性和载体动力学在纳米线/电解质界面。因此,构造的光电传感器实现了247.8mAW-1的高响应度,同时具有出色的操作稳定性。引人注目的是,基于设备的显着稳定性和高响应性,建立了一个葡萄糖传感系统,演示了真实人血清中的葡萄糖水平测定。这项工作提供了一种可行和通用的方法,通过合理设计具有战略性掺杂工程的纳米结构体系结构形式的PEC器件,来追求高性能的生物相关传感应用。
    Photosensors with versatile functionalities have emerged as a cornerstone for breakthroughs in the future optoelectronic systems across a wide range of applications. In particular, emerging photoelectrochemical (PEC)-type devices have recently attracted extensive interest in liquid-based biosensing applications due to their natural electrolyte-assisted operating characteristics. Herein, a PEC-type photosensor was carefully designed and constructed by employing gallium nitride (GaN) p-n homojunction semiconductor nanowires on silicon, with the p-GaN segment strategically doped and then decorated with cobalt-nickel oxide (CoNiOx). Essentially, the p-n homojunction configuration with facile p-doping engineering improves carrier separation efficiency and facilitates carrier transfer to the nanowire surface, while CoNiOx decoration further boosts PEC reaction activity and carrier dynamics at the nanowire/electrolyte interface. Consequently, the constructed photosensor achieves a high responsivity of 247.8 mA W-1 while simultaneously exhibiting excellent operating stability. Strikingly, based on the remarkable stability and high responsivity of the device, a glucose sensing system was established with a demonstration of glucose level determination in real human serum. This work offers a feasible and universal approach in the pursuit of high-performance bio-related sensing applications via a rational design of PEC devices in the form of nanostructured architecture with strategic doping engineering.
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  • 文章类型: Journal Article
    铋(Bi)具有很高的理论容量,优异的导电性能,和显着的层间间距,使其成为超级电容器的理想电极材料。然而,在充电和放电过程中,Bi容易体积膨胀和粉化,导致电容下降。在其表面沉积非金属被认为是调节其形态和电子结构的有效方法。在这里,我们采用化学气相沉积技术在镍泡沫(NF)衬底上制造Se装饰的Bi纳米片。各种表征表明,Se在Bi纳米片上的沉积调节了其表面形态和化学状态,同时维持其原始相结构。电化学测试表明,与原始Bi纳米片相比,Se修饰的Bi纳米片表现出51.1%的容量改善(在5A/g的电流密度下,1313F/g与869F/g相比)。在800W/kg的功率密度下,组装的非对称超级电容器中的活性材料的能量密度可以达到151.2Wh/kg。这些发现表明Se修饰是增强Bi纳米片容量的有前途的策略。
    Bismuth (Bi) exhibits a high theoretical capacity, excellent electrical conductivity properties, and remarkable interlayer spacing, making it an ideal electrode material for supercapacitors. However, during the charge and discharge processes, Bi is prone to volume expansion and pulverization, resulting in a decline in the capacitance. Deposition of a nonmetal on its surface is considered an effective way to modulate its morphology and electronic structure. Herein, we employed the chemical vapor deposition technique to fabricate Se-decorated Bi nanosheets on a nickel foam (NF) substrate. Various characterizations indicated that the deposition of Se on Bi nanosheets regulated their surface morphology and chemical state, while sustaining their pristine phase structure. Electrochemical tests demonstrated that Se-decorated Bi nanosheets exhibited a 51.1% improvement in capacity compared with pristine Bi nanosheets (1313 F/g compared to 869 F/g at a current density of 5 A/g). The energy density of the active material in an assembled asymmetric supercapacitor could reach 151.2 Wh/kg at a power density of 800 W/kg. These findings suggest that Se decoration is a promising strategy to enhance the capacity of the Bi nanosheets.
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  • 文章类型: Journal Article
    析氧反应(OER)由于其在可再生能源系统中的关键作用而受到广泛关注。寻求有效和低成本的OER催化剂仍然是一个具有重要意义和重要性的挑战。在这项工作中,据报道,掺入磷酸盐的硅酸钴氢氧化物(表示为CoSi-P)是OER的潜在电催化剂。研究人员首先使用SiO2球体作为模板,通过简单的水热法合成了硅酸钴氢氧化物Co3(Si2O5)2(OH)2(表示为CoSi)的空心球。然后将磷酸盐(PO43-)引入层状CoSi,导致空心球重建为片状建筑。不出所料,所得CoSi-P电催化剂表现出低的过电位(10mA·cm-2时309mV),大电化学活性表面积(ECSA),和低的塔菲尔坡度。这些参数优于CoSi空心球和磷酸钴(表示为CoPO)。此外,在10mA/cm-2下实现的催化性能与大多数过渡金属硅酸盐/氧化物/氢氧化物相当或甚至更好。研究结果表明,在CoSi的结构中掺入磷酸盐可以增强其OER性能。这项研究不仅提供了一种非贵金属催化剂CoSi-P,而且还表明,将磷酸盐掺入过渡金属硅酸盐(TMS)中提供了一种有前途的策略,高效率,和低成本的OER催化剂。
    Oxygen Evolution Reaction (OER) has gained significant attention due to its crucial role in renewable energy systems. The quest for efficient and low-cost OER catalysts remains a challenge of significant interest and importance. In this work, phosphate-incorporated cobalt silicate hydroxide (denoted as CoSi-P) is reported as a potential electrocatalyst for OER. The researchers first synthesized hollow spheres of cobalt silicate hydroxide Co3(Si2O5)2(OH)2 (denoted as CoSi) using SiO2 spheres as a template through a facile hydrothermal method. Phosphate (PO43-) was then introduced to layered CoSi, leading to the reconstruction of the hollow spheres into sheet-like architectures. As expected, the resulting CoSi-P electrocatalyst demonstrated low overpotential (309 mV at 10 mA·cm-2), large electrochemical active surface area (ECSA), and low Tafel slope. These parameters outperform CoSi hollow spheres and cobaltous phosphate (denoted as CoPO). Moreover, the catalytic performance achieved at 10 mA cm-2 is comparable or even better than that of most transition metal silicates/oxides/hydroxides. The findings indicate that the incorporation of phosphate into the structure of CoSi can enhance its OER performance. This study not only provides a non-noble metal catalyst CoSi-P but also demonstrates that the incorporation of phosphates into transition metal silicates (TMSs) offers a promising strategy for the design of robust, high-efficiency, and low-cost OER catalysts.
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  • 文章类型: Journal Article
    具有双极特性的p-n结设置了基本单元来构建电子器件,而其独特的整流行为限制了扩展功能的载流子可调性程度。在这里,报告了在电解质中运行的与氮化镓(GaN)p-n同质结纳米线阵列一起使用的双极结光电极,展示了由不同波长的光控制的双极光响应。重要的是,在理论建模的指导下,对纳米线上的氧化钌(RuOx)层进行合理装饰,所得的RuOx/p-nGaN光电极表现出明确的增强的双极光响应,对正负光电流增强了775%和3000%,分别,与原始纳米线相比。纳米线表面上RuOx层的负载优化了表面带弯曲,这促进了跨GaN/电解质界面的电荷转移,同时提高了对应于负和正光电流的析氢反应和析氧反应的氧化还原反应效率,分别。最后,本发明公开了一种双通道光通信系统,该双通道光通信系统结合了这种光电极,仅使用一个光电极来解码具有加密特性的双频带信号。所提出的双极器件架构提供了一种可行的途径来操纵载流子动力学,以开发过多的多功能光电器件,用于未来的传感。通信,和成像系统。
    The p-n junction with bipolar characteristics sets the fundamental unit to build electronics while its unique rectification behavior constrains the degree of carrier tunability for expanded functionalities. Herein, a bipolar-junction photoelectrode employed with a gallium nitride (GaN) p-n homojunction nanowire array that operates in electrolyte is reported, demonstrating bipolar photoresponse controlled by different wavelengths of light. Significantly, with rational decoration of a ruthenium oxides (RuOx ) layer on nanowires guided by theoretical modeling, the resulting RuOx /p-n GaN photoelectrode exhibits unambiguously boosted bipolar photoresponse by an enhancement of 775% and 3000% for positive and negative photocurrents, respectively, compared to the pristine nanowires. The loading of the RuOx layer on nanowire surface optimizes surface band bending, which facilitates charge transfer across the GaN/electrolyte interface, meanwhile promoting the efficiency of redox reaction for both hydrogen evolution reaction and oxygen evolution reaction which corresponds to the negative and positive photocurrents, respectively. Finally, a dual-channel optical communication system incorporated with such photoelectrode is constructed with using only one photoelectrode to decode dual-band signals with encrypted property. The proposed bipolar device architecture presents a viable route to manipulate the carrier dynamics for the development of a plethora of multifunctional optoelectronic devices for future sensing, communication, and imaging systems.
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  • 文章类型: Journal Article
    溃疡性结肠炎(UC),影响全世界数百万患者,与肠道微生物群的紊乱有关。基于益生菌的治疗积极调节肠道菌群的群落结构被认为是UC的有效干预措施。然而,口服益生菌的递送受到有限的生物活性的限制,短保留时间,复杂的病理状况,和单一的治疗效果。这里,构建用多功能前药涂层装饰的生物工程益生菌以改善上述缺点。葡聚糖硫酸钠诱导的UC小鼠的结果表明,制备的涂层的内在特征整合了肠道微生物保护,结肠靶向药物释放,药物滞留时间延长,和炎症调节。并行,益生菌鼠李糖乳杆菌GG(LGG)可以调节肠道菌群组成,改善上皮屏障功能,从而协同改善UC。这些结果为UC的治疗效果提供了充分的证据,因此,作为UC治疗的潜在治疗策略显示出巨大的希望。
    Ulcerative colitis (UC), affecting millions of patients worldwide, is associated with disorders of the gut microbiota. Probiotics-based therapy positively regulating the community structure of gut microbiota is regarded as an efficient intervention for UC. However, oral probiotics delivery is restricted by limited bioactivity, short retention time, complex pathological condition, and single therapeutic efficacy. Here, a bioengineered probiotic decorated with a multifunctional prodrug coating is constructed to ameliorate the aforementioned shortcomings. The results of UC mice induced by dextran sulfate sodium demonstrate that the intrinsic features of the fabricated coating integrate gut microbes protection, colon-targeted drug release, prolonged drug retention, and inflammation regulation. In parallel, the probiotics Lactobacillus rhamnosus GG (LGG) could regulate the composition of the gut microbiota and improve epithelial barrier function, thereby synergistically ameliorating UC. These results provide ample shreds of evidence of the therapeutic effect on UC, therefore, demonstrate a great promise as the potential therapeutic strategy for UC treatment.
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  • 文章类型: Journal Article
    如今,蛋白质分离在蛋白质组学研究中引起了极大的关注。因为蛋白质的分离有助于许多疾病的早期诊断。磁性纳米粒子是一种有趣且有用的功能材料,并在过去的几十年中引起了广泛的研究兴趣。由于具有优异的性能,例如易于表面功能化,可调节的生物相容性,高饱和磁化强度等,磁性微球已广泛用于蛋白质/肽的分离。值得注意的是,随着表面装饰策略的快速发展,越来越多的功能性磁性吸附剂已被设计和制造,以满足日益增长的生物分离需求。在这次审查中,我们已经收集了有关磁性吸附剂在蛋白质/肽的选择性分离中的应用的最新信息。此外,我们在依靠磁性纳米颗粒的蛋白质分离领域提出了全面的前景和挑战。
    Nowadays, proteins separation has attracted great attention in proteomics research. Because the proteins separation is helpful for making an early diagnosis of many diseases. Magnetic nanoparticles are an interesting and useful functional material, and have attracted extensive research interest during the past decades. Because of the excellent properties such as easy surface functionalization, tunable biocompatibility, high saturation magnetization etc, magnetic microspheres have been widely used in isolation of proteins/peptides. Notably, with the rapid development of surface decoration strategies, more and more functional magnetic adsorbents have been designed and fabricated to meet the growing demands of biological separation. In this review, we have collected recent information about magnetic adsorbents applications in selective separation of proteins/peptides. Furthermore, we present a comprehensive prospects and challenges in the field of protein separation relying on magnetic nanoparticles.
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  • 文章类型: Journal Article
    碳纳米笼(CNCs)由于其多孔结构和改善的传质性能而在多相催化中引起了极大的兴趣。然而,CNCs的控制合成仍然是一个巨大的挑战。在这里,我们已经证明了通过一石双鸟策略成功构建功能化的N掺杂的CNCs(NCNCs)。选择性使用六羰基钼(Mo(CO)6)不仅可以保护ZIF-8前体的轮廓在热处理过程中免于塌陷,而且还可以牺牲热解后NCNCs的功能化。详细的机理研究表明,Mo(CO)6在ZIF-8表面演变成MoO3,然后促进ZIF-8的快速热解,导致形成小尺寸的MoC纳米颗粒(MoC/NCNCs)。这种一石双鸟策略的多功能性已经得到了几代Cr和W装饰NCNCs的验证。此外,MoC/NCNCs可以作为糠醛加氢的选择性和稳定的催化剂。这项工作为制造和功能化CNCs提供了一种简便而通用的策略,这引起了化学领域的研究兴趣,材料科学,催化作用,和超越。
    Carbon nanocages (CNCs) have attracted tremendous interest in heterogeneous catalysis due to their promising properties of porous structure and improved mass transfer. Nevertheless, the controlled synthesis of CNCs remains a great challenge. Herein, we have shown the successful construction of functionalized N-doped CNCs (NCNCs) via a one-stone-two-birds strategy. The selective use of hexacarbonyl molybdenum (Mo(CO)6) can not only protect the profile of the ZIF-8 precursor from collapse during thermal treatment but also be sacrificed for the functionalization of NCNCs after pyrolysis. Detailed mechanism studies reveal that Mo(CO)6 evolves into MoO3 on the surface of ZIF-8 and then facilitates the rapid pyrolysis of ZIF-8, leading to the formation of NCNCs decorated with small-sized MoC nanoparticles (MoC/NCNCs). The versatility of this one-stone-two-birds strategy has been validated by the generations of Cr- and W-decorated NCNCs. Moreover, MoC/NCNCs can serve as a selective and stable catalyst for furfural hydrogenation. This work provides a facile and universal strategy for fabricating and functionalizing CNCs, which attracts research interest in the fields of chemistry, material science, catalysis, and beyond.
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  • 文章类型: Journal Article
    表面费米能级钉扎效应促进了高速GaSb纳米线(NWs)电子器件与金属无关的欧姆接触的形成,然而,它限制了下一代光电器件。在这项工作中,采用具有宽带隙和低功函数的无铅全无机钙钛矿来装饰GaSbNWs的表面,展示了通过表面工程构建肖特基接触的成功。受益于预期的肖特基势垒,暗电流减少到2pA,Ilight/Idark比提高到103,响应时间减少了15倍以上。此外,肖特基接触平行阵列GaSbNWs光电探测器也通过接触印刷技术制造,显示出更高的光电流和15pA的低暗电流,以及对隐蔽目标的良好红外光探测能力。所有结果都指导通过下一代高性能III-VNWs光电子器件的表面装饰来构建肖特基接触。
    The surface Fermi level pinning effect promotes the formation of metal-independent Ohmic contacts for the high-speed GaSb nanowires (NWs) electronic devices, however, it limits next-generation optoelectronic devices. In this work, lead-free all-inorganic perovskites with broad bandgaps and low work functions are adopted to decorate the surfaces of GaSb NWs, demonstrating the success in the construction of Schottky-contacts by surface engineering. Benefiting from the expected Schottky barrier, the dark current is reduced to 2 pA, the Ilight /Idark ratio is improved to 103 and the response time is reduced by more than 15 times. Furthermore, a Schottky-contacted parallel array GaSb NWs photodetector is also fabricated by the contact printing technology, showing a higher photocurrent and a low dark current of 15 pA, along with the good infrared photodetection ability for a concealed target. All results guide the construction of Schottky-contacts by surface decorations for next-generation high-performance III-V NWs optoelectronics devices.
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