Substantially enhanced rate capability of lithium storage in Na2Ti6O13 with self-doping and carbon-coating.

Na2Ti6O13 (NTO) has recently been reported for lithium ion storage and showed very promising results. In this work, we report substantially enhanced rate capability in NTO nanowires by Ti(iii) self-doping and carbon-coating. Ti(iii) doping and carbon coating were found to work in synergy to increase the electrochemical performances of the material. For 300 cycles at 1C (1C = 200 mA g-1) the charge capacity of the electrode is 206 mA h g-1, much higher than that (89 mA h g-1) of the pristine NTO electrode. For 500 cycles at 5C the electrode can still deliver a charge capacity of 180.5 mA h g-1 with a high coulombic efficiency of 99%. At 20C the capacity of the electrode is 2.6 times that of the pristine NTO. These results clearly demonstrate that the Ti(iii) self-doping and uniform carbon coating significantly enhanced the kinetic processes in the NTO nanowire crystal, making it possible for fast charge and discharge in Li-ion batteries.

Core/Double-Shell Type Gradient Ni-Rich LiNi0.76Co0.10Mn0.14O2 with High Capacity and Long Cycle Life for Lithium-Ion Batteries.

A concentration-gradient Ni-rich LiNi0.76Co0.1Mn0.14O2 layered oxide cathode has been developed by firing a core/double-shell [Ni0.9Co0.1]0.4[Ni0.7Co0.1Mn0.2]0.5[Ni0.5Co0.1Mn0.4]0.1(OH)2 hydroxide precursor with LiOH·H2O, where the Ni-rich interior (core) delivers high capacity and the Mn-rich exterior (shells) provides a protection layer to improve the cyclability and thermal stability for the Ni-rich oxide cathodes. The content of nickel and manganese, respectively, decreases and increases gradually from the center to the surface of each gradient sample particle, offering a high capacity with enhanced surface/structural stability and cyclability. The obtained concentration-gradient oxide cathode exhibits high-energy density with long cycle life in both half and full cells. With high-loading electrode half cells, the concentration-gradient sample delivers 3.3 mA h cm(-2) with 99% retention after 100 cycles. The material morphology, phase, and gradient structure are also maintained after cycling. The pouch-type full cells fabricated with a graphite anode delivers high capacity with 89% capacity retention after 500 cycles at C/3 rate.

Template-free TiO2 hollow submicrospheres embedded with SnO2 nanobeans as a versatile scattering layer for dye-sensitized solar cells.

Nanobean SnO2-embedded TiO2 hollow submicrospheres are presented as a scattering layer for the first time in dye-sensitized solar cells. This designed mesoporous submicrostructure simultaneously promotes dye adsorption, light harvesting, and electron transport, leading to 28% improvement in the conversion efficiency compared to film-based SnO2.

Self-supported single crystalline H2Ti8O17 nanoarrays as integrated three-dimensional anodes for lithium-ion microbatteries.

Well-ordered, one-dimensional H2Ti2O5, H2Ti8O17, TiO2-B, and anatase TiO2/TiO2-B nanowire arrays were innovatively designed and directly grown on current collectors as high performance three dimensional (3D) anodes for binder and carbon free lithium ion batteries (LIBs). The prepared thin nanowires exhibited a single crystalline phase with highly uniform morphologies, diameters ranging from 70-80 nm, and lengths of around 15 µm. Specifically, reversible Li insertion and extraction reactions around 1.6-1.8 V with initial intercalation capacities of 326 and 271 mA h g(-1) at a cycling rate of 0.1 C (where 1 C = 335 mA g(-1)) were observed for H2Ti8O17 and TiO2-B nanowire arrays, respectively. Among the four compounds investigated, the H2Ti8O17 nanowire electrode demonstrated optimal cycling stability, delivering a high specific discharge capacity of 157.8 mA h g(-1) with a coulombic efficiency of 100%, even after the 500th cycle at a current rate of 1 C. Furthermore, the H2Ti8O17 nanowire electrode displayed superior rate performance with rechargeable discharge capacities of 127.2, 111.4, 87.2, and 73.5 mA h g(-1) at 5 C, 10 C, 20 C, and 30 C, respectively. These results present the potential opportunity for the development of high-performance LIBs based on nanostructured Ti-based anode materials in terms of high stability and high rate capability.

Multifunctional TiO2-C/MnO2 core-double-shell nanowire arrays as high-performance 3D electrodes for lithium ion batteries.

The unique TiO2-C/MnO2 core-double-shell nanowires are synthesized for the first time using as anode materials for lithium ion batteries (LIBs). They combine both advantages from TiO2 such as excellent cycle stability and MnO2 with high capacity (1230 mA h g(-1)). The additional C interlayer intends to improve the electrical conductivity. The self-supported nanowire arrays grown directly on current-collecting substrates greatly simplify the fabrication processing of electrodes without applying binder and conductive additives. Each nanowire is anchored to the current collector, leading to fast charge transfer. The unique one-dimensional core-double-shell nanowires exhibit enhanced electrochemical performance with a higher discharge/charge capacity, superior rate capability, and longer cycling lifetime.

Highly catalytic carbon nanotube/Pt nanohybrid-based transparent counter electrode for efficient dye-sensitized solar cells.

Low-cost transparent counter electrodes (CEs) for efficient dye-sensitized solar cells (DSSCs) are prepared by using nanohybrids of carbon nanotube (CNT)-supported platinum nanoparticles as highly active catalysts. The nanohybrids, synthesized by an ionic-liquid-assisted sonochemical method, are directly deposited on either rigid glass or flexible plastic substrates by a facile electrospray method for operation as CEs. Their electrochemical performances are examined by cyclic voltammetry, current density-voltage characteristics, and electrochemical impedance spectroscopy (EIS) measurements. The CNT/Pt hybrid films exhibit high electrocatalytic activity for I(-)/I(3)(-) with a weak dependence on film thickness. A transparent CNT/Pt hybrid CE film about 100 nm thick with a transparency of about 70% (at 550 nm) can result in a high power conversion efficiency (η) of over 8.5%, which is comparable to that of pyrolysis platinum-based DSSCs, but lower cost. Furthermore, DSSC based on flexible CNT/Pt hybrid CE using indium-doped tin oxide-coated polyethylene terephthalate as the substrate also exhibits η=8.43% with J(sc)=16.85 mA cm(-2), V(oc)=780 mV, and FF=0.64, and this shows great potential in developing highly efficient flexible DSSCs.

Dynamic study of highly efficient CdS/CdSe quantum dot-sensitized solar cells fabricated by electrodeposition.

An in situ electrodeposition method is described to fabricate the CdS or/and CdSe quantum dot (QD) sensitized hierarchical TiO(2) sphere (HTS) electrodes for solar cell application. Intensity modulated photocurrent spectroscopy (IMPS), intensity modulated photovoltage spectroscopy (IMVS) and electrochemical impedance spectroscopy (EIS) measurements are performed to investigate the electron transport and recombination of quantum dot-sensitized solar cells (QDSSCs) based on HTS/CdS, HTS/CdSe, and HTS/CdS/CdSe photoelectrodes. This dynamic study reveals that the CdSe/CdS cosensitized solar cell performs ultrafast electron transport and high electron collection efficiency (98%). As a consequence, a power conversion efficiency as high as 4.81% (J(SC) = 18.23 mA cm(-2), V(OC) = 489 mV, FF = 0.54) for HTS/CdS/CdSe photoelectrode based QDSSC is observed under one sun AM 1.5 G illumination (100 mW cm(-2)).

Organic dye bearing asymmetric double donor-π-acceptor chains for dye-sensitized solar cells.

A novel efficient metal free sensitizer containing asymmetric double donor-π-acceptor chains (DC) was synthesized for dye-sensitized solar cells (DSSCs). Comparing to 3.80%, 4.40% and 4.64% for the DSSCs based on the dyes with single chain (SC1, SC2) and cosensitizers (SC1 + SC2), the overall conversion efficiency reaches 6.06% for DC-sensitized solar cells as a result of its longer electron lifetime and higher incident monochromatic photon-to-current conversion efficiency.

Hydrothermal fabrication of quasi-one-dimensional single-crystalline anatase TiO2 nanostructures on FTO glass and their applications in dye-sensitized solar cells.

One-dimensional and quasi-one-dimensional semiconductor nanostructures are desirable for dye-sensitized solar cells (DSSCs), since they can provide direct pathways for the rapid collection of photogenerated electrons, which could improve the photovoltaic performance of the device. Quasi-1D single-crystalline anatase TiO(2) nanostructures have been successfully prepared on transparent, conductive fluorine-doped tin oxide (FTO) glass with a growth direction of [101] through a facile hydrothermal approach. The influences of the initial titanium n-butoxide (TBT) concentration, hydrothermal reaction temperature, and time on the length of quasi-1D anatase TiO(2) nanostructures and on the photovoltaic performance of DSSCs have been investigated in detail. A power conversion efficiency of 5.81% has been obtained based on the prepared TiO(2) nanostructure photoelectrode 6.7 µm thick and commercial N719 dye, with a short-circuit current density of 13.3 mA cm(-2) , an open-circuit voltage of 810 mV, and a fill factor of 0.54.