Quanzhong Guo

Bio: Quanzhong Guo is an academic researcher from Carnegie Institution for Science. The author has contributed to research in topics: Materials science & Corrosion. The author has an hindex of 3, co-authored 3 publications receiving 776 citations.

Hydrogen clusters in clathrate hydrate.

Abstract: High-pressure Raman, infrared, x-ray, and neutron studies show that H2 and H2O mixtures crystallize into the sII clathrate structure with an approximate H2/H2O molar ratio of 1:2. The clathrate cages are multiply occupied, with a cluster of two H2 molecules in the small cage and four in the large cage. Substantial softening and splitting of hydrogen vibrons indicate increased intermolecular interactions. The quenched clathrate is stable up to 145 kelvin at ambient pressure. Retention of hydrogen at such high temperatures could help its condensation in planetary nebulae and may play a key role in the evolution of icy bodies.

The phase transitions of CoO under static pressure to 104 GPa

Abstract: The phase transitions and equation of state of cobalt oxide (CoO) have been studied at ambient temperature under non-hydrostatic and hydrostatic high pressures, with the diamond-anvil cell technique. We discovered that under hydrostatic pressure conditions the CoO structure transformed from the low-density rhombohedral to a high-density rhombohedral phase at 90 ± 1 GPa with the molecular volume decreasing by about 2.7%. This phase transition with volume discontinuity may be related to magnetic collapse, which was predicted by theory. The pressure of the phase transition of CoO from face-centred cubic B1 to rhombohedral structure was 43 ± 2 GPa. The decompression spectrum data of CoO under non-hydrostatic pressure showed that these phase transitions are reversible.

X-ray diffraction and laser heating: application of a moissanite anvil cell

Abstract: A moissanite anvil cell (MAC) has been used in research at high-pressure recently. In this paper, we describe its application in x-ray diffraction studies with laser heating. A high temperature of 3700 K has been achieved in a MAC; the lattice constants of graphite were determined by means of in situ x-ray diffraction at room temperature and 3700 K, and the results are in good agreement with reference data.

Corrosion and conductivity properties of Ni–P/Ti4O7 coating on carbon steel as bipolar plates for proton exchange membrane fuel cells

Abstract: Purpose The purpose of this paper is to investigate the interfacial conductivity and corrosion resistance of the Ni–P/Ti4O7 composite coating that is deposited on a carbon steel substrate as bipolar plates for proton exchange membrane fuel cells. Design/methodology/approach The Ni–P/Ti4O7 coating was prepared by electroless plating. Scanning electron microscopy, white light interference, energy dispersive spectrometry and X-ray diffraction were used, respectively, to study the surface morphology, chemical composition and phase composition of coated samples. Electrochemical impedance spectroscopy, potentiodynamic and potentiostatic polarization were used to test the electrochemical performance and corrosion behavior. The interfacial contact resistance (ICR) was measured via the standard method. Findings The surface of the Ni–P/Ti4O7 coating is complete and dense and without obvious defects. The electrochemical test results show that the Ni–P/Ti4O7 coating provides better corrosion resistance than the Ni–P coating and substrate. Compared with the Ni–P coating, the ICR of the Ni–P/Ti4O7 coating is lower by about 82.7%. This is because the coating has more conductive contact points. The more exciting thing is that the ICR of the Ni–P/Ti4O7 coating only increases to 12.38 mΩ·cm2 after 5 h of polarization. Originality/value This paper provides a method for achieving surface modification of metal bipolar plates. Introducing Ti4O7 particles in the Ni–P layer reduces the contact resistance before and after polarization while ensuring good corrosion resistance.

Hydrogen storage in metal–organic frameworks

Abstract: New materials capable of storing hydrogen at high gravimetric and volumetric densities are required if hydrogen is to be widely employed as a clean alternative to hydrocarbon fuels in cars and other mobile applications. With exceptionally high surface areas and chemically-tunable structures, microporous metal–organic frameworks have recently emerged as some of the most promising candidate materials. In this critical review we provide an overview of the current status of hydrogen storage within such compounds. Particular emphasis is given to the relationships between structural features and the enthalpy of hydrogen adsorption, spectroscopic methods for probing framework–H2 interactions, and strategies for improving storage capacity (188 references).

Fundamental principles and applications of natural gas hydrates

Abstract: Natural gas hydrates are solid, non-stoichiometric compounds of small gas molecules and water. They form when the constituents come into contact at low temperature and high pressure. The physical properties of these compounds, most notably that they are non-flowing crystalline solids that are denser than typical fluid hydrocarbons and that the gas molecules they contain are effectively compressed, give rise to numerous applications in the broad areas of energy and climate effects. In particular, they have an important bearing on flow assurance and safety issues in oil and gas pipelines, they offer a largely unexploited means of energy recovery and transportation, and they could play a significant role in past and future climate change.

Chemical and Physical Solutions for Hydrogen Storage

Abstract: Hydrogen is a promising energy carrier in future energy systems. However, storage of hydrogen is a substantial challenge, especially for applications in vehicles with fuel cells that use proton-exchange membranes (PEMs). Different methods for hydrogen storage are discussed, including high-pressure and cryogenic-liquid storage, adsorptive storage on high-surface-area adsorbents, chemical storage in metal hydrides and complex hydrides, and storage in boranes. For the latter chemical solutions, reversible options and hydrolytic release of hydrogen with off-board regeneration are both possible. Reforming of liquid hydrogen-containing compounds is also a possible means of hydrogen generation. The advantages and disadvantages of the different systems are compared.

Tuning clathrate hydrates for hydrogen storage

Abstract: The storage of large quantities of hydrogen at safe pressures is a key factor in establishing a hydrogen-based economy. Previous strategies--where hydrogen has been bound chemically, adsorbed in materials with permanent void space or stored in hybrid materials that combine these elements--have problems arising from either technical considerations or materials cost. A recently reported clathrate hydrate of hydrogen exhibiting two different-sized cages does seem to meet the necessary storage requirements; however, the extreme pressures (approximately 2 kbar) required to produce the material make it impractical. The synthesis pressure can be decreased by filling the larger cavity with tetrahydrofuran (THF) to stabilize the material, but the potential storage capacity of the material is compromised with this approach. Here we report that hydrogen storage capacities in THF-containing binary-clathrate hydrates can be increased to approximately 4 wt% at modest pressures by tuning their composition to allow the hydrogen guests to enter both the larger and the smaller cages, while retaining low-pressure stability. The tuning mechanism is quite general and convenient, using water-soluble hydrate promoters and various small gaseous guests.

Stable Low-Pressure Hydrogen Clusters Stored in a Binary Clathrate Hydrate

Abstract: Thermodynamic, x-ray diffraction, and Raman and nuclear magnetic resonance spectroscopy measurements show that clusters of H2 can be stabilized and stored at low pressures in a sII binary clathrate hydrate. Clusters of H2 molecules occupy small water cages, whereas large water cages are singly occupied by tetrahydrofuran. The presence of this second guest component stabilizes the clathrate at pressures of 5 megapascals at 279.6 kelvin, versus 300 megapascals at 280 kelvin for pure H2 hydrate.