SearcharxivSearch

arXiv subjects

Enting Xu

Publications and source records attributed to Enting Xu.

2 recordsLinked to original sources

Colossal Dielectric Response and Electric Polarization in Lithium Nitrate

Lithium nitrate LiNO$_3$ is identified to possess a dielectric constant $\epsilon$' larger than 6x10$^6$ at 1 kHz in powder samples above the critical temperature $T$$_W$ = 306 K. For single crystalline samples, $\epsilon$' can be sustained to remain above 10$^5$ and the dissipation factor below 10 in the temperature region of 280-340 K after a simple 'activation' process. Moreover, pyroelectric current measurements show LiNO$_3$ to be ferroelectric with an electric polarization of $P$ = 1,200 $\mu$C/cm$^2$. Both $\epsilon$' and $P$ are amongst one of the highest in all known materials. We propose a model suggesting the mechanism underlying the colossal magnitudes of $\epsilon$' and $P$ to stem from a gearing-ungearing process of the planar NO$_3$$^-$ at the macroscopic level. Our results potentially push the boundaries of ceramic capacitors.

cond-mat.mtrl-sci

Magnetism based on nitrate-nitrate interactions: The cases of LiNO$_3$, K$_{0.5}$Rb$_{0.5}$NO$_3$, Ca(NO$_3$)$_2$ and C(NH$_2$)$_3$NO$_3$

Long-range magnetic ordering of the orbital motion of oxygen atoms within NO$_3$$^-$ cations is identified from experimental measurements of the magnetic susceptibility $\chi$($T$) in LiNO$_3$, Ca(NO$_3$)$_2$, K$_{0.5}$Rb$_{0.5}$NO$_3$ and C(NH$_2$)$_3$NO$_3$ at their respective order-disorder, solid-solid phase transitions $T$$_N$. The observed sharp changes in $\chi$($T$) and accompanying hysteretic behavior indicate the phase transitions to be first order. A model employing the law of conservation of angular momentum is used to explain why the librations between neighboring NO$_3$$^-$ become geared below $T$$_N$. Since the periodic motions involve concerted motion of net charges, the associated magnetic moments of the NO$_3$$^-$ ions indirectly establish an antiferromagnetic structure below $T$$_N$. Our findings identify a previously unidentified type of molecular interaction which may be exploited to further increase the enthalpy of the widely-popular hydrated salts employed as energy storage devices.

cond-mat.mtrl-sci