Chongyin Yang

Bio: Chongyin Yang is an academic researcher from University of Maryland, College Park. The author has contributed to research in topics: Electrolyte & Electrochemistry. The author has an hindex of 39, co-authored 63 publications receiving 8831 citations. Previous affiliations of Chongyin Yang include Lucideon & Chinese Academy of Sciences.

Nitrogen-doped mesoporous carbon of extraordinary capacitance for electrochemical energy storage

Abstract: Carbon-based supercapacitors can provide high electrical power, but they do not have sufficient energy density to directly compete with batteries. We found that a nitrogen-doped ordered mesoporous few-layer carbon has a capacitance of 855 farads per gram in aqueous electrolytes and can be bipolarly charged or discharged at a fast, carbon-like speed. The improvement mostly stems from robust redox reactions at nitrogen-associated defects that transform inert graphene-like layered carbon into an electrochemically active substance without affecting its electric conductivity. These bipolar aqueous-electrolyte electrochemical cells offer power densities and lifetimes similar to those of carbon-based supercapacitors and can store a specific energy of 41 watt-hours per kilogram (19.5 watt-hours per liter).

Zn/MnO2 Battery Chemistry With H+ and Zn2+ Coinsertion

Abstract: Rechargeable aqueous Zn/MnO2 battery chemistry in a neutral or mildly acidic electrolyte has attracted extensive attention recently because all the components (anode, cathode, and electrolyte) in a Zn/MnO2 battery are safe, abundant, and sustainable. However, the reaction mechanism of the MnO2 cathode remains a topic of discussion. Herein, we design a highly reversible aqueous Zn/MnO2 battery where the binder-free MnO2 cathode was fabricated by in situ electrodeposition of MnO2 on carbon fiber paper in mild acidic ZnSO4+MnSO4 electrolyte. Electrochemical and structural analysis identify that the MnO2 cathode experience a consequent H+ and Zn2+ insertion/extraction process with high reversibility and cycling stability. To our best knowledge, it is the first report on rechargeable aqueous batteries with a consequent ion-insertion reaction mechanism.

Non-flammable electrolyte enables Li-metal batteries with aggressive cathode chemistries

Abstract: Rechargeable Li-metal batteries using high-voltage cathodes can deliver the highest possible energy densities among all electrochemistries. However, the notorious reactivity of metallic lithium as well as the catalytic nature of high-voltage cathode materials largely prevents their practical application. Here, we report a non-flammable fluorinated electrolyte that supports the most aggressive and high-voltage cathodes in a Li-metal battery. Our battery shows high cycling stability, as evidenced by the efficiencies for Li-metal plating/stripping (99.2%) for a 5 V cathode LiCoPO4 (~99.81%) and a Ni-rich LiNi0.8Mn0.1Co0.1O2 cathode (~99.93%). At a loading of 2.0 mAh cm−2, our full cells retain ~93% of their original capacities after 1,000 cycles. Surface analyses and quantum chemistry calculations show that stabilization of these aggressive chemistries at extreme potentials is due to the formation of a several-nanometre-thick fluorinated interphase.

H‐Doped Black Titania with Very High Solar Absorption and Excellent Photocatalysis Enhanced by Localized Surface Plasmon Resonance

Abstract: Black TiO2 attracts enormous attention due to its large solar absorption and induced excellent photocatalytic activity. Herein, a new approach assisted by hydrogen plasma to synthesize unique H-doped black titania with a core/shell structure (TiO2@TiO2-xHx) is presented, superior to the high H-2-pressure process (under 20 bar for five days). The black titania possesses the largest solar absorption (approximate to 83%), far more than any other reported black titania (the record (high-pressure): approximate to 30%). H doping is favorable to eliminate the recombination centers of light-induced electrons and holes. High absorption and low recombination ensure the excellent photocatalytic activity for the black titania in the photo-oxidation of organic molecules in water and the production of hydrogen. The H-doped amorphous shell is proposed to play the same role as Ag or Pt loading on TiO2 nanocrystals, which induces the localized surface plasma resonance and black coloration. Photocatalytic water splitting and cleaning using TiO2-xHx is believed to have a bright future for sustainable energy sources and cleaning environment.

Visible-light photocatalytic, solar thermal and photoelectrochemical properties of aluminium-reduced black titania

Abstract: Utilizing solar energy for hydrogen generation and water cleaning is a great challenge due to insufficient visible-light power conversion. Here we report a mass production approach to synthesize black titania by aluminium reduction. The obtained sample possesses a unique crystalline core–amorphous shell structure (TiO2@TiO2−x). The black titania absorbs ∼65% of the total solar energy by improving visible and infrared absorption, superior to the recently reported ones (∼30%) and pristine TiO2 (∼5%). The unique core–shell structure (TiO2@TiO2−x) and high absorption boost the photocatalytic water cleaning and water splitting. The black titania is also an excellent photoelectrochemical electrode exhibiting a high solar-to-hydrogen efficiency (1.7%). A large photothermic effect may enable black titania “capture” solar energy for solar thermal collectors. The Al-reduced amorphous shell is proved to be an excellent candidate to absorb more solar light and receive more efficient photocatalysis.

Semiconductor-based Photocatalytic Hydrogen Generation

Abstract: 2.3. Evaluation of Photocatalytic Water Splitting 6507 2.3.1. Photocatalytic Activity 6507 2.3.2. Photocatalytic Stability 6507 3. UV-Active Photocatalysts for Water Splitting 6507 3.1. d0 Metal Oxide Photocatalyts 6507 3.1.1. Ti-, Zr-Based Oxides 6507 3.1.2. Nb-, Ta-Based Oxides 6514 3.1.3. W-, Mo-Based Oxides 6517 3.1.4. Other d0 Metal Oxides 6518 3.2. d10 Metal Oxide Photocatalyts 6518 3.3. f0 Metal Oxide Photocatalysts 6518 3.4. Nonoxide Photocatalysts 6518 4. Approaches to Modifying the Electronic Band Structure for Visible-Light Harvesting 6519

Understanding TiO2 photocatalysis: mechanisms and materials.

Abstract: Jenny Schneider,*,† Masaya Matsuoka,‡ Masato Takeuchi,‡ Jinlong Zhang, Yu Horiuchi,‡ Masakazu Anpo,‡ and Detlef W. Bahnemann*,† †Institut fur Technische Chemie, Leibniz Universitaẗ Hannover, Callinstrasse 3, D-30167 Hannover, Germany ‡Faculty of Engineering, Osaka Prefecture University, 1 Gakuen-cho, Sakai Osaka 599-8531, Japan Key Lab for Advanced Materials and Institute of Fine Chemicals, East China University of Science and Technology, Shanghai 200237, China

Design and Mechanisms of Asymmetric Supercapacitors.

Abstract: Ongoing technological advances in diverse fields including portable electronics, transportation, and green energy are often hindered by the insufficient capability of energy-storage devices By taking advantage of two different electrode materials, asymmetric supercapacitors can extend their operating voltage window beyond the thermodynamic decomposition voltage of electrolytes while enabling a solution to the energy storage limitations of symmetric supercapacitors This review provides comprehensive knowledge to this field We first look at the essential energy-storage mechanisms and performance evaluation criteria for asymmetric supercapacitors to understand the wide-ranging research conducted in this area Then we move to the recent progress made for the design and fabrication of electrode materials and the overall structure of asymmetric supercapacitors in different categories We also highlight several key scientific challenges and present our perspectives on enhancing the electrochemical performance of future asymmetric supercapacitors

Brightly Luminescent and Color-Tunable Colloidal CH3NH3PbX3 (X = Br, I, Cl) Quantum Dots: Potential Alternatives for Display Technology.

Abstract: Organometal halide perovskites are inexpensive materials with desirable characteristics of color-tunable and narrow-band emissions for lighting and display technology, but they suffer from low photoluminescence quantum yields at low excitation fluencies. Here we developed a ligand-assisted reprecipitation strategy to fabricate brightly luminescent and color-tunable colloidal CH3NH3PbX3 (X = Br, I, Cl) quantum dots with absolute quantum yield up to 70% at room temperature and low excitation fluencies. To illustrate the photoluminescence enhancements in these quantum dots, we conducted comprehensive composition and surface characterizations and determined the time- and temperature-dependent photoluminescence spectra. Comparisons between small-sized CH3NH3PbBr3 quantum dots (average diameter 3.3 nm) and corresponding micrometer-sized bulk particles (2–8 μm) suggest that the intense increased photoluminescence quantum yield originates from the increase of exciton binding energy due to size reduction as well a...