Jiseok Kwon

Microstructural control of new intercalation layered titanoniobates with large and reversible d-spacing for easy Na+ ion uptake

H0.43Ti0.93Nb1.07O5 engineered with large d-spacing of ~8.3 Å and two-dimensional ionic channels enables easy Na+ ion uptake. Key issues for Na-ion batteries are the development of promising electrode materials with favorable sites for Na+ ion intercalation/deintercalation and an understanding of the reaction mechanisms due to its high activation energy and poor electrochemical reversibility. We first report a layered H0.43Ti0.93Nb1.07O5 as a new anode material. This anode material is engineered to have dominant (200) and (020) planes with both a sufficiently large d-spacing of ~8.3 Å and two-dimensional ionic channels for easy Na+ ion uptake, which leads to a small volume expansion of ~0.6 Å along the c direction upon Na insertion (discharging) and the lowest energy barrier of 0.19 eV in the [020] plane among titanium oxide–based materials ever reported. The material intercalates and deintercalates reversibly 1.7 Na ions (~200 mAh g−1) without a capacity fading in a potential window of 0.01 to 3.0 V versus Na/Na+. Na insertion/deinsertion takes place through a solid-solution reaction without a phase separation, which prevents coherent strain or stress in the microstructure during cycling and ensures promising sodium storage properties. These findings demonstrate a great potential of H0.43Ti0.93Nb1.07O5 as the anode, and our strategy can be applied to other layered metal oxides for promising sodium storage properties.

Two-dimensional Nafion nanoweb anion-shield for improved electrochemical performances of lithium–sulfur batteries

We first demonstrate a facile and effective strategy to directly deposit a Nafion nanoweb onto a sulfur cathode to address the challenges underlying in Li–S batteries. The Nafion nanoweb not only blocks the diffusion of polysulfides by electrostatic repulsion but also allows fast Li-ion exchange with the sulfur cathode through the selective protection layer. The Nafion nanoweb-sulfur cathode retained an excellent cycle performance over 200 cycles and delivered an improved rate capability, as compared to a sulfur cathode and a Nafion layer-sulfur cathode.

Unusual Na+ Ion Intercalation/Deintercalation in Metal-Rich Cu1.8S for Na-Ion Batteries

A key issue with Na-ion batteries is the development of active materials with stable electrochemical reversibility through the understanding of their sodium storage mechanisms. We report a sodium storage mechanism and properties of a new anode material, digenite Cu1.8S, based on its crystallographic study. It is revealed that copper sulfides (Cu xS) can have metal-rich formulas ( x ≥ 1.6), due to the unique oxidation state of +1 found in group 11 elements. These phases enable the unit cell to consist of all strong Cu-S bonds and no direct S-S bonds, which are vulnerable to external stress/strain that could result in bond cleavage as well as decomposition. Because of its structural rigidness, the Cu1.8S shows an intercalation/deintercalation reaction mechanism even in a low potential window of 0.1-2.2 V versus Na/Na+ without irreversible phase transformation, which most of the metal sulfides experience through a conversion reaction mechanism. It uptakes, on average, 1.4 Na+ ions per unit cell (∼250 mAh g-1) and exhibits ∼100% retention over 1000 cycles at 2C in a tuned voltage range of 0.5-2.2 V through an overall solid solution reaction with negligible phase separation.

Synthesis of transition metal sulfide and reduced graphene oxide hybrids as efficient electrocatalysts for oxygen evolution reactions

The development of electrochemical devices for renewable energy depends to a large extent on fundamental improvements in catalysts for oxygen evolution reactions (OERs). OER activity of transition metal sulfides (TMSs) can be improved by compositing with highly conductive supports possessing a high surface-to-volume ratio, such as reduced graphene oxide (rGO). Herein we report on the relationship between synthetic conditions and the OER catalytic properties of TMSs and rGO (TMS–rGO) hybrids. Starting materials, reaction temperature and reaction time were controlled to synergistically boost the OER catalytic activity of TMS–rGO hybrids. Our results showed that (i) compared with sulfides, hydroxides are favourable as starting materials to produce the desired TMS–rGO hybrid nanostructure and (ii) high reaction temperatures and longer reaction times can increase physico-chemical interaction between TMSs and rGO supports, resulting in highly efficient OER catalytic activity.

Development of a TL Personal Dosimeter Identifiable PA Exposure, a Comparison with Commercial TL Dosimeters

A single-dosimeter worn on the anterior surface of the body of a worker was found to significantly underestimate the effective dose to the worker when the radiation comes from the back. Several researchers suggested that this sort of underestimation can be corrected to a certain extent by using an extra dosimeter on the back. However, use of multiple dosimeters also has disadvantages such as complication in control or incurrence of extra cost. Instead of the common multi-dosimeter approach, in this study, a single dosimeter introducing asymmetric filters which enabled to identify PA exposure was designed, and its dose evaluation algorithm for AP-PA mixed radiation fields was established. A prototype TL personal dosimeter was designed and constructed. The Monte Carlo simulations were utilized in the design process and verified by experiments. The dosimeter and algorithm were applicable to photon radiation having an effective energy beyond 100 keV in AP-PA mixed radiation fields. A simplified performance test based on ANSI N13.ll showed satisfactory results. Considering that the requirements of the International Electrotechnical Commission(IEC) and the American National Standards Institute(ANSI) with regard to the dosimeter on angular dependency is reinforced, the dosimeter and the dose evaluation algorithm developed in this study provides a useful approach in practical personal dosimetry against inhomogeneous high energy radiation fields.