Zhihui Dai

Ultra‐Uniform SnOx/Carbon Nanohybrids toward Advanced Lithium‐Ion Battery Anodes

Ultra-uniform SnOx/carbon nanohybrids for lithium-ion batteries are successfully prepared by solvent replacement and subsequent electrospinning. The resulting 1D nanostructure with Sn-N bonding between the SnOx and N-containing carbon nanofiber matrix can not only tolerate the substantial volume change and suppress the aggregation of SnOx, but also enhances the transport of both electrons and ions for the embedded SnOx, thus leading to high cycling performance and rate capability.

Pomegranate-like N,P-Doped Mo2C@C Nanospheres as Highly Active Electrocatalysts for Alkaline Hydrogen Evolution.

Well-defined pomegranate-like N,P-doped Mo2C@C nanospheres were prepared by simply using phosphomolybdic acid (PMo12) to initiate the polymerization of polypyrrole (PPy) and as a single source for Mo and P to produce N,P-doped Mo2C nanocrystals. The existence of PMo12 at the molecular scale in the polymer network allows the formation of pomegranate-like Mo2C@C nanospheres with a porous carbon shell as peel and Mo2C nanocrystals well-dispersed in the N-doped carbon matrix as seeds. This nanostructure provides several favorable features for hydrogen evolution application: (1) the conductive carbon shell and matrix effectively prevent the aggregation of Mo2C nanocrystals and facilitate electron transportation; (2) the uniform N,P-doping in the carbon shell/matrix and plenty of Mo2C nanocrystals provide abundant catalytically highly active sites; and (3) nanoporous structure allows the effective exposure of active sites and mass transfer. Moreover, the uniform distribution of P and Mo from the single source of PMo12 and N from PPy in the polymeric PPy-PMo12 precursor guarantees the uniform N- and P-co-doping in both the graphitic carbon matrix and Mo2C nanocrystals, which contributes to the enhancement of electrocatalytic performance. As a result, the pomegranate-like Mo2C@C nanospheres exhibit extraordinary electrocatalytic activity for the hydrogen evolution reaction (HER) in terms of an extremely low overpotential of 47 mV at 10 mA cm(-2) in 1 M KOH, which is one of the best Mo-based HER catalysts. The strategy for preparing such nanostructures may open up opportunities for exploring low-cost high-performance electrocatalysts for various applications.

Wet milled synthesis of an Sb/MWCNT nanocomposite for improved sodium storage

A uniform mixture of nano-sized Sb particles and MWCNTs is achieved by using wet milling to provide fast ionic diffusion and electronic transportation, and the cycling performance and rate capability of the as-obtained nanocomposite are significantly improved when tested as an anode material for sodium-ion batteries.

Self‐Templated Fabrication of MoNi4/MoO3‐x Nanorod Arrays with Dual Active Components for Highly Efficient Hydrogen Evolution

A binder-free efficient MoNi4 /MoO3-x nanorod array electrode with 3D open structure is developed by using Ni foam as both scaffold and Ni source to form NiMoO4 precursor, followed by subsequent annealing in a reduction atmosphere. It is discovered that the self-templated conversion of NiMoO4 into MoNi4 nanocrystals and MoO3-x as dual active components dramatically boosts the hydrogen evolution reaction (HER) performance. Benefiting from high intrinsic activity, high electrochemical surface area, 3D open network, and improved electron transport, the resulting MoNi4 /MoO3-x electrode exhibits a remarkable HER activity with extremely low overpotentials of 17 mV at 10 mA cm-2 and 114 mV at 500 mA cm-2 , as well as a superior durability in alkaline medium. The water-alkali electrolyzer using MoNi4 /MoO3-x as cathode achieves stable overall water splitting with a small cell voltage of 1.6 V at 30 mA cm-2 . These findings may inspire the exploration of cost-effective and efficient electrodes by in situ integrating multiple highly active components on 3D platform with open conductive network for practical hydrogen production.

Preparation of Reactive Oligo(p‐Phenylene Vinylene) Materials for Spatial Profiling of the Chemical Reactivity of Intracellular Compartments

An oligo(p-phenylene vinylene) derivative (OPV-pfp) functionalized with pentafluorophenol active ester is designed and synthesized. The high reactivity of OPV-pfp with biological small molecules or macromolecules containing amino groups under physiological conditions leads to spectral changes of OPV-pfp; thus, spatial reactivity discrimination for different subcellular structures inside cells is realized by triggering and imaging the fluorescence signal change of the OPV-pfp.

Conjugated Polymer-Based Photoelectrochemical Cytosensor with Turn-On Enable Signal for Sensitive Cell Detection

In this work, a new photoelectrochemical (PEC) cytosensor was constructed by using cationic polyfluorene derivative, poly(9,9-bis(6-(N,N,N,-trimethylammonium)hexyl)fluorene-co-alt-1,4-phenylene)bromide (PFP) as the photoelectric-responsive material for sensitive cell detection. Positive-charged PFP with high photoelectric conversion efficiency can generate robust photocurrent under light illumination. In the PEC cytosensor, 3-phosphonopropionic acid was linked to the indium tin oxide electrode, followed by modification with antiepithelial-cell-adhesion-molecule (EpCAM) antibody via amide condensation reaction. Thus, target SKBR-3 cells with overexpressed EpCAM antigen could be captured onto the electrode via the specific antibody-antigen interactions. Upon adding cationic PFP, a favorable electrostatic interaction between cationic PFP and negatively charged cell membrane led to a turn-on detection signal for target SKBR-3 cells. This new cytosensor not only exhibits good sensitivity because of the good photoelectric performance of conjugated polymers, but also offers decent selectivity to target cells by taking advantage of the specific antibody-antigen recognition.