Co-reporter:Xing Kong, Hongliang Cao, Chang Li, Xin Chen
Journal of Colloid and Interface Science 2017 Volume 487() pp:60-67
Publication Date(Web):1 February 2017
DOI:10.1016/j.jcis.2016.10.005
HypothesisTemplate-free and surfactant-free strategies are highly desirable, which might be used for high efficient platinum catalyst developments.ExperimentsIn this work, a facile one step photochemical synthesis method was developed to prepare sponge-like porous platinum. The present synthesis was performed via ultraviolet light irradiation on a K2PtCl4 aqueous solution at ambient condition. The final pore sizes were in the range of 1–3 nm. The walls of the pores were formed with platinum nanoparticles of 3–5 nm average diameters. For comparisons, pluronic F127 was introduced into the reaction solutions as a surfactant, and sponge-like and dendritic-like platinum nanostructures were obtained. The catalytic activities of these platinum nanomaterials were studied with both menthol oxidation and 4-nitrophenol reduction.FindingsThe sponge-like platinum synthesized without surfactant exhibited higher catalytic activities than the porous platinum with surfactant and the commercial platinum black.
Co-reporter:Hongliang Cao;Xiang Wang;Haiyang Liu;Junsheng Zheng;Wangfan Zhou
Journal of Materials Chemistry A 2017 vol. 5(Issue 39) pp:20729-20736
Publication Date(Web):2017/10/10
DOI:10.1039/C7TA05784A
A double layer hollow structured Cu7S4/NiS material is synthesized using a self-generated sacrificial template method, as an electrode material for supercapacitors. Cu7S4/NiS composites with three different particle sizes are synthesized and tested, which exhibited high specific capacitances of 1204 F g−1, 1028 F g−1 and 857 F g−1, respectively, at a current density of 1 A g−1. The specific capacitance of the nanocomposites remained at 945.5 F g−1 (85.8%), 719.2 F g−1 (84.32%) and 558.5 F g−1 (80.13%) levels after 1000 cycles, respectively, at a current density of 4 A g−1, showing good cycle stability. Compared with the pure NiS and Cu7S4, the development of the hollow Cu7S4/NiS composites is demonstrated to be effective in enhancing the supercapacitive performance.
Co-reporter:Xin Chen;Chang Li;Xing Kong;Hongliang Cao;Hulian Wang;Xiaoqin Zhou
Chinese Journal of Chemistry 2017 Volume 35(Issue 8) pp:1336-1336
Publication Date(Web):2017/08/01
DOI:10.1002/cjoc.201770085
The back cover picture shows schematic of direct in situ liquid cell TEM observation of electron bean induced growth and self-assembly of nanoclusters in water with the aid of a triblock copolymer. The growth and self-assembly of the Pt nanoclusters with the aid of triblock copolymer F127 are directly observed, and a surfactant guided nanocluster formation mechanism is proposed. Dramatic differences are found on the cluster forming behavior and final morphologies between thick and thin liquid regions. The difference in precursor availability and charging effects are attributed to the different growth behavior in different thickness regions. More details are discussed in the article by Chen et al. on page 1278–1283.
Co-reporter:Xin Chen;Chang Li;Xing Kong;Hongliang Cao;Hulian Wang;Xiaoqin Zhou
Chinese Journal of Chemistry 2017 Volume 35(Issue 8) pp:1278-1283
Publication Date(Web):2017/08/01
DOI:10.1002/cjoc.201700017
Triblock copolymers are playing important roles in nanomaterial synthesis, and the nanomaterial forming mechanisms need to be studied in detail. In situ liquid cell transmission electron microscopy (TEM) is a powerful tool for real time observation of the dynamic growth behavior of nanomaterials in liquid with high resolution, and could be used for the above task. Here we report the observation of the growth and self-assembly of Pt nanoclusters with the aid of an ethylene oxide-propylene oxide-ethylene oxide triblock copolymer (PEO-PPO-PEO) F127 using in situ liquid cell TEM, with the nanocluster growth and formation procedures being tracked. Nano objects were seen to appear, drift and rotate with time, and then form into certain shaped nanoclusters under the electron beam irradiation. Further interestingly, in the thicker liquid layer region, the nanoclusters appeared to be fluffy, with average size keeping increase with time, while in the thinner region, the clusters were thinner, and got densified with time. The difference in precursor availability due to liquid layer thickness and charging effects is attributed to such a phenomenon.
Co-reporter:Xin Chen, Chang Li and Hongling Cao
Nanoscale 2015 vol. 7(Issue 11) pp:4811-4819
Publication Date(Web):29 Jan 2015
DOI:10.1039/C4NR07209J
In situ wet cells for transmission electron microscopy (TEM) and scanning transmission electron microscopy (STEM) allow studying structures and processes in a liquid environment with high temporal and spatial resolutions, and have been attracting increasing research interests in many fields. In this review, we highlight the structural and functional developments of the wet cells for TEM and STEM. One of the key features of the wet cells is the sealing technique used to isolate the liquid sample from the TEM/STEM vacuum environments, thus the existing in situ wet cells are grouped by different sealing methods. In this study, the advantages and shortcomings of each type of in situ wet cells are discussed, the functional developments of different wet cells are presented, and the future trends of the wet cell technology are addressed. It is suggested that in the future the in situ wet cell TEM/STEM technology will have an increasing impact on frontier nanoscale research.
Co-reporter:Xin Chen;Lihui Zhou;Ping Wang;Hongliang Cao;Xiaoli Miao
Nano-Micro Letters 2015 Volume 7( Issue 4) pp:385-391
Publication Date(Web):2015 October
DOI:10.1007/s40820-015-0054-4
We studied silicon, carbon, and SiCx nanostructures fabricated using liquid-phase electron-beam-induced deposition technology in transmission electron microscopy systems. Nanodots obtained from fixed electron beam irradiation followed a universal size versus beam dose trend, with precursor concentrations from pure SiCl4 to 0 % SiCl4 in CH2Cl2, and electron beam intensity ranges of two orders of magnitude, showing good controllability of the deposition. Secondary electrons contributed to the determination of the lateral sizes of the nanostructures, while the primary beam appeared to have an effect in reducing the vertical growth rate. These results can be used to generate donut-shaped nanostructures. Using a scanning electron beam, line structures with both branched and unbranched morphologies were also obtained. The liquid-phase electron-beam-induced deposition technology is shown to be an effective tool for advanced nanostructured material generation.
Co-reporter:Xin Chen;Lihui Zhou;Ping Wang;Hongliang Cao;Xiaoli Miao;Feifei Wei
Chinese Journal of Chemistry 2014 Volume 32( Issue 5) pp:399-404
Publication Date(Web):
DOI:10.1002/cjoc.201400139
Abstract
SiCx nano dots and nano wires with sizes from 60 nm to approximately 2 µm were fabricated using liquid cell transmission electron microscope (TEM) technology. A SiCl4 in CH2Cl2 solution was sealed between two pieces of Si3N4 window grids in an in situ TEM liquid cell. Focused 200 keV electron beams were used to bombard the sealed precursors, which caused decomposition of the precursor materials, and deposition of the nano materials on the Si3N4 window substrates. The size of nano dots increased with beam exposure time, following an approximately exponential relationship with the beam doses. Secondary electrons are attributed as the primary sources for the Si and C reduction. A nano device was formed from a deposited nano wire, with its electrical property characterized.
Co-reporter:Xin Chen;Lihui Zhou;Ping Wang;Chongjun Zhao;Xiaoli Miao
Chinese Journal of Chemistry 2012 Volume 30( Issue 12) pp:2839-2843
Publication Date(Web):
DOI:10.1002/cjoc.201201036
Abstract
Several nano material and reaction systems were in situ monitored with an electrochemical TEM wet cell set up. In a 1 g/L sliver particle aqueous solution, the particles were observed to be ca. 10 nm sized, in both discrete particle and nano cluster forms. The silver particles were attached to the 50 nm-thick Si3N4 windows of the wet cell and could not move freely in the liquid. With a SiCl4 liquid loaded in the wet cell, silicon nano materials were controllably grown on the wet cell windows by means of a liquid phase electron beam induced deposition (EBID) method. The deposited nano dots were nicely round-shaped, and demonstrated a power law growth dependency on beam exposure time in a log-log plot. In a NiCl2 solution/Ni system, both electrochemical deposition and dissolution of the nickel nano films were observed while applying electric biases on to the nickel electrodes in the wet cell. Instead of extensional growth on existing crystals, interestingly, it is more commonly observed that new nickel nano particles grow out in front of the existing film first and then merged into the film. The wet cell set up is demonstrated to be a versatile tool for nano liquid system research.