Rechargeable zinc-based batteries (RZBs) with the advantages of high safety, low cost, abundant resources and environmental friendliness, are considered as advanced secondary battery systems that can be applied to large-scale energy storage. As an important cathode material for RZBs, NASICON-type Na3V2( PO4)3 (NVP) possesses three-dimensional and large-scale ion channels that facilitate the rapid diffusion of Zn2+, and has a higher average operating voltage compared with other vanadiumbased compounds, thus exhibiting the possibility of realizing RZBs with high energy density. However, NVP still has some problems, such as poor electronic conductivity and spontaneous dissolution in aqueous solution. The sluggish kinetics of Zn2+ (de)intercalation in NVP and dendritic growth on the Zn anode also contribute to the poor rate performance and short cycle life of the batteries. In this review, optimization strategies for the electrochemical performance of RZBs with NVP as cathode are systematically elaborated, including modification of NVP cathode and optimization of electrolyte. Several mainstream energy storage mechanisms and analysis methods in this battery system are sorted out and summarized. On this basis, the development direction of NVP–RZB system is further prospected.

Around 40 years ago, in the mid-1980s, Swedish government approved the KBS-3 method for the direct disposal of spent nuclear fuels (SNF) in Sweden. Since then, this method has become a reference for many countries including Korea, Republic of. The main ideas of the KBS-3 method are to locate SNF at 500 m below the ground surface using a copper disposal canister and a bentonite buffer. In 2016, our government announced the National Plan (NP 2016) regarding the final management of high-level waste (HLW) in Korea. In 2019, new committee were organized to review the NP 2016, and they submitted the final recommendations to the government in 2021. Finally, the government announced the 2nd National Plan in December, 2021. So far, KAERI has developed the technologies related to the final management of SNF in two directions. One follows ‘direct disposal’ based on the KBS-3 concept, and the other ‘recycling’ based on ‘pyroprocessing-and-SFR’ (PYRO-SFR). Even though Posiva and SKB obtained the construction permits with the KBS-3 method in Finland and Sweden, respectively, there are still several technical obstacles to applying directly to our situations. Some examples are as follows: high burnup, huge amounts of SNF, and high geothermal gradient in Korean peninsula. In this work, we try to illustrate some limits of the KBS-3 method. Within our country, currently, the most probable disposal option is the KBS-3 type geological disposal, but no one knows what the best option will be in 20 or 30 years if those kinds of drawbacks are considered. That is, we compare the effects of the drawbacks using our geological data and characteristics of spent fuels. Last year, we reviewed alternative disposal concepts focusing on the direct disposal of SNF and compared the pros and cons of them in order to enhance the disposal efficiency. We selected four candidate concepts. They were multi-level disposal, deep borehole disposal, sub-seabed disposal and mined deep borehole matrix. As mentioned before, KAERI has developed a pyroprocessing technology based on the SFR to reuse fissile radionuclides in SNF. Even though we can consume some fissile nuclides such as 239Pu and 241Pu using PYRO-SFR cycle, there still remain many long-lived radionuclides such as 129I and 135Cs waiting for the final disposal. The authors review and propose several concepts for the future final management of the long-lived radionuclides.

Spherical Li3V2(PO4)3 (LVP) and carbon-coated LVP with a monoclinic phase for the cathode materials are synthesized by a hydrothermal method using N2H4 as the reducing agent and saccharose as the carbon source. The results show that single phase monoclinic LVP without impurity phases such as LiV(P2O7), Li(VO)(PO4) and Li3(PO4) can be obtained after calcination at 800 oC for 4 h. SEM and TEM images show that the particle sizes are 0.5~2 μm and the thickness of the amorphous carbon layer is approximately 3~4 nm. CV curves for the test cell are recorded in the potential ranges of 3.0~4.3 V and 3.0~4.8 V at a scan rate of 0.01 mV s–1 and at room temperature. At potentials between 3.0 and 4.8 V, the third Li+ ions from the carbon-coated LVP can be completely extracted, at voltages close to 4.51 V. The carbon-coated LVP exhibits an initial specific discharge capacity of 118 mAh g–1 in the voltage region of 3.0 to 4.3 V at a current rate of 0.2 C. The results indicate that the reducing agent and carbon source can affect the crystal structure and electrochemical properties of the cathode materials.