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Many cellular functions are regulated by cell surface charges, such as intercellular signaling and metabolism. Noninvasive measurement of surface charge distribution of a single cell plays a vital role in understanding cellular functions via cell membranes. We report a method for cell surface charge mapping via photoelectric interactions. A cell is placed on an array of microelectrodes fabricated on a transparent ITO (indium tin oxide) surface. An incident light irradiates the ITO surface from the backside. Because of the influence of the cell surface charge (or zeta potential), the photocurrent and the absorption of the incident light are changed, inducing a magnitude change of the reflected light. Hence, the cell surface charge distribution can be quantified by analyzing the reflected light intensity. This method does not need physical or chemical modification of the cell surface. We validated this method using charged microparticles (MPs) and two types of cells, i.e., human dermal fibroblast cells (HDFs) and human mesenchymal stem cells (hMSC). The measured average zeta potentials were in good agreement with the standard electrophoresis light scattering method. [ABSTRACT FROM AUTHOR]

Chirality is ubiquitous in nature and it is essential in many fields, but natural materials possess weak and narrow-band chiroptical effects. Here, chiral plasmonic metasurface absorbers are designed and demonstrated to achieve large broadband infrared circular dichroism (CD). The broadband chiral absorber is made of multiple double-rectangle resonators with different sizes, showing strong absorption of left-handed or right-handed circularly polarized (LCP or RCP) light above 0.7 and large CD in absorption more than 0.5 covering the wavelength range from 1.35 µm to 1.85 µm. High broadband polarization-dependent local temperature increase is also obtained. The switchable infrared reflective chiral images are further presented by changing the wavelength and polarization of incident light. The broadband chiral metasurface absorbers promise future applications in many areas such as polarization detection, thermophotovoltaics, and chiral imaging. [ABSTRACT FROM AUTHOR]

Due to its promising benefits in energy and environment, distributed energy system (DES) has increasingly attracted extensive attention worldwide. The application of DES has been increased rapidly in recent years with the supportive government policies and financial incentives. Therefore, it is necessary to systematically summarize and analyze the development status of DES in China. This paper not only presents researches, applications and policies, but provides some relevant suggestion and prospects on DES of China. DES especially the hybrid energy system that gas-fired combined cooling, heating and power (CCHP) with renewable energy (solar and wind) will become the mainstream of future energy supply technologies in China. The paper will be helpful for international stakeholders in energy field to have better understanding on the progress of DES in China, which will benefit them in two aspects: one is that the Chinese situation will be a reference for their own countries or regions to develop energy policy and technology regarding DES, another is that they may be helped to find opportunities in Chinese market, while to contribute to Chinese DES development. [ABSTRACT FROM AUTHOR]

Many bio-functions of cells can be regulated by their surface charge characteristics. Mapping surface charge density in a single cell's surface is vital to advance the understanding of cell behaviors. This article demonstrates a method of cell surface charge mapping via electrostatic cell–nanoparticle (NP) interactions. Fluorescent nanoparticles (NPs) were used as the marker to investigate single cells' surface charge distribution. The nanoparticles with opposite charges were electrostatically bonded to the cell surface; a stack of fluorescence distribution on a cell's surface at a series of vertical distances was imaged and analyzed. By establishing a relationship between fluorescent light intensity and number of nanoparticles, cells' surface charge distribution was quantified from the fluorescence distribution. Two types of cells, human umbilical vein endothelial cells (HUVECs) and HeLa cells, were tested. From the measured surface charge density of a group of single cells, the average zeta potentials of the two types of cells were obtained, which are in good agreement with the standard electrophoretic light scattering measurement. This method can be used for rapid surface charge mapping of single particles or cells, and can advance cell-surface-charge characterization applications in many biomedical fields. [ABSTRACT FROM AUTHOR]

Detection of small biomolecules is critical for understanding molecular mechanisms in biological systems and performing in vitro diagnosis in clinics. Current antibody based detection methods face large challenges in detecting small biomolecules at low concentrations. We report a new method for detecting small biomolecules based on molecular recognition and nanoparticle (NP) counting. Aptamer-functionalized NPs are attached to complementary sequence (CS)-conjugated microparticle (MP) carriers. In the presence of target small biomolecules at ultra low concentrations, NPs would be released from the MP carriers. Coupled with a resistive pulse sensor (RPS) using a micropore that counts the released NPs, this method can measure the concentrations of target biomolecules at low concentrations with high sensitivity and high throughput. Adenosine was used as a model to demonstrate the feasibility of this method. It is demonstrated that this method can detect a wide range of adenosine concentrations with a low detection limit of 0.168 nM, which is 10 times lower than that of the ELISA kit. With its simple structure, high sensitivity, and high reproducibility, this detection method holds great potential for the ultrasensitive detection of low abundance small biomolecules. • Nanoparticles are released from a carrier in the presence of target analytes. • The released nanoparticles can be detected in response to a wide range of analyte concentration. • Ultrasensitive detection of biomolecules can be achieved via molecular recognition coupled with nanoparticle counting. [ABSTRACT FROM AUTHOR]