Enhanced carbon dioxide adsorption performance and kinetic study of K and Al co-doped Li4SiO4

Herein, we report the effects of doped K and Al on the carbon dioxide （CO2） adsorption performance of the Li4SiO4-based adsorbents. The CO2 adsorption capacity of 0.8 wt% K and 1.5 wt% AI doped Li4SiO4 is ～2.2 times and ～1.3 times higher than that of the pristine Li4SiO4 at 500 and 600℃, respectively. The kinetic study further indicated that the reaction rates of the lithium diffusion process is greatly improved by K and AI doping, and the lithium diffusion rate of 0.8 wt% K and 1.5 wt% AI doped Li4SiO4 is ～2 times higher than that of the pristine Li4SiO4 at 575-650 ℃. K and AI doping increases the adsorption capacity of Li4SiO4-based adsorbents, and widens its effective adsorption temperature range

One-step electrochemical in-situ Li doping and LiF coating enable ultra-stable cathode for sodium ion batteries

Despite of the higher energy density and inexpensive characteristics,commercialization of layered oxide cathodes for sodium ion batteries(SIBs)is limited due to the lack of structural stability at the high voltage.Herein,the one-step electrochemical in-situ Li doping and LiF coating are successfully achieved to obtain an advanced Na0.79Lix[Li_(0.13)Ni_(0.20)Mn_(0.67)]O_(2)@LiF(NaLi-LNM@LiF)cathode with superlattice structure.The results demonstrate that the Li^(+)doped into the alkali metal layer by electrochemical cycling act as"pillars"in the form of Li-Li dimers to stabilize the layered structure.The supplementation of Li to the superlattice structure inhibits the dissolution of transition metal ions and lattice mismatch.Furthermore,the in-situ LiF coating restrains side reactions,reduces surface cracks,and greatly improves the cycling stability.The electrochemical in-situ modification strategy significantly enhances the electrochemical performance of the half-cell.The NaLi-LNM@LiF exhibits high reversible specific capacity(170.6 m A h g^(-1)at 0.05 C),outstanding capacity retention(92.65%after 200 cycles at 0.5 C)and excellent rate performance(80 mA h g^(-1)at 7 C)in a wide voltage range of 1.5-4.5 V.This novel method of in-situ modification by electrochemical process will provide a guidance for the rational design of cathode materials for SIBs.

Enhancing carrier transport in flexible CZTSSe solar cells via doping Li strategy

The passivation of non-radiative states and inhibition of band tailings are desirable for improving the open-circuit voltage(V_(oc))of CZTSSe thin-film solar cells.Recently,alkali metal doping has been investigated to passivate defects in CZTSSe films.Herein,we investigate Li doping effects by applying Li OH into CZTSSe precursor solutions,and verify that carrier transport is enhanced in the CZTSSe solar cells.Systematic characterizations demonstrate that Li doping can effectively passivate non-radiative recombination centers and reduce band tailings of the CZTSSe films,leading to the decrease in total defect density and the increase in separation distance between donor and acceptor.Fewer free carriers are trapped in the band tail states,which speeds up carrier transport and reduces the probability of deep-level defects capturing carriers.The charge recombination lifetime is about twice as long as that of the undoped CZTSSe device,implying the heterojunction interface recombination is also inhibited.Besides,Li doping can increase carrier concentration and enhance build-in voltage,leading to a better carrier collection.By adjusting the Li/(Li+Cu)ratio to 18%,the solar cell efficiency is increased significantly to 9.68%with the fill factor(FF)of 65.94%,which is the highest FF reported so far for the flexible CZTSSe solar cells.The increased efficiency is mainly attributed to the reduction of V_(oc)deficit and the improved CZTSSe/Cd S junction quality.These results open up a simple route to passivate non-radiative states and reduce the band tailings of the CZTSSe films and improve the efficiency of the flexible CZTSSe solar cells.

Study of the structural,ferroelectric,dielectric,and pyroelectric properties of the K0.5Na0.5NbO3 system doped with Li+,La3+,and Ti4+

Pure Ko.sNao sNbO3(KNN)and KNN doped with Lit(6%mole),Lat(1.66%,5%,6%mole),and Ti+t(10%mole)were prepared by mixture of oxides using high-energy milling and conventional solid-state reaction.The effects of the dopant on the physical properties of pure KNN have been evaluated based on the structural,ferroelectric,pyroelectric,and dielectric measurements.The XRD measurements show that KNN pure sample contains a mixture of monoclinic and orthorhombic crystalline phases,with a slightly higher concentration of monoclinic phase.In contrast,all doped samples show a higher concentration of the orthorhombic phase,as well as the presence of a secondary phase(K6Nb10.8O3o),also detected by Raman measurements.The samples with a higher concentration of this secondary phase,also present greater dielectric losses and lower values of remnant polarization.The dielectric measurements allowed us to detect temperatures of structural transitions(orthorhombic-tetragonal,O-T)previous to the ferroelectric paraelectric transition(tetragonal-cubic,T-C),and also in this set of samples,a direct correlation was found between the values of remnant polarization and the corresponding pyroelectric signal response.