Interest in hybrid organic-inorganic lead halide compounds with perovskite-like two-dimensional crystal structures is growing due to the unique electronic and optoelectronic properties of these compounds. Herein, we demonstrate the synthesis, thermal and optical properties, and calculations of the electronic band structures for one- and two-layer compounds comprising both cesium and guanidinium cations: Cs[C(NH)]PbI (I), Cs[C(NH)]PbBr (II), and Cs[C(NH)]PbBr (III). Compounds I and II exhibit intense photoluminescence at low temperatures, whereas compound III is emissive at room temperature. All of the obtained substances are stable in air and do not thermally decompose until 300 °C. Since Cs and C(NH) are increasingly utilized in precursor solutions for depositing polycrystalline lead halide perovskite thin films for photovoltaics, exploring possible compounds within this compositional space is of high practical relevance to understanding the photophysics and atomistic chemical nature of such films.
Two-dimensional
hybrid organic–inorganic lead halides perovskite-type
compounds have attracted immense scientific interest due to their
remarkable optoelectronic properties and tailorable crystal structures.
In this work, we present a new layered hybrid lead halide, namely
[CH(NH2)2][C(NH2)3]PbI4, wherein puckered lead-iodide layers are separated by two
small and stable organic cations: formamidinium, CH(NH2)2+, and guanidinium, C(NH2)3+. This perovskite is thermally stable up to 255
°C, exhibits room-temperature photoluminescence in the red region
with a quantum yield of 3.5%, and is photoconductive. This study highlights
a vast structural diversity that exists in the compositional space
typically used in perovskite photovoltaics.
Since the inception of the unprecedented rise of halide
perovskites
for photovoltaic research, ion migration has shadowed this material
class with undesirable hysteresis and degradation effects, limiting
its practical implementations. Unfortunately, the localized doping
and electrochemical reactions triggered by ion migration cause many
more undesirable effects that are often unreported or misinterpreted
because they deviate from classical semiconductor behavior. In this
Perspective, we provide a concise overview of such effects in halide
perovskites, such as operational instability in photovoltaics, polarization-induced
abnormal external quantum efficiency in light-emitting diodes, and
energy channel shift and anomalous sensitivities in hard radiation
detection. Finally, we highlight a unique use case of exploiting ion
migration as a boon to design emerging memory technologies
such as memristors for information storage and computing.
The goal of cryptography is to make it impossible to take a cipher and reproduce the original plain text without the corresponding key. With good cryptography, your messages are encrypted in such a way that brute force attacks against the algorithm or the key are all but impossible. Good cryptography gets its security by using incredibly long keys and using encryption algorithms that are resistant to other form attack. The neural net application represents a way of the next development in good cryptography. This paper deals with using neural network in cryptography, e.g. designing such neural network that would be practically used in the area of cryptography. This paper also includes an experimental demonstration.
Hybrid
organic–inorganic main-group metal halide compounds
are the subject of intense research owing to their unique optoelectronic
characteristics. In this work, we report the synthesis, structure,
and electronic and optical properties of a family of hybrid tin (II)
bromide compounds comprising guanidinium [G, C(NH
2
)
3
+
] and mixed cesium–guanidinium cations:
G
2
SnBr
4
, CsGSnBr
4
, and Cs
2
GSn
2
Br
7
. G
2
SnBr
4
has
a one-dimensional structure that consists of chains of corner-sharing
[SnBr
5
]
2–
square pyramids and G cations
situated in between the chains. Cs
+
exhibits a pronounced
structure-directing effect where a mixture of Cs
+
and G
cations forms mono- and bilayered two-dimensional perovskites: CsGSnBr
4
and Cs
2
GSn
2
Br
7
. Furthermore,
the flat shapes of the guanidinium cations induce anisotropic out-of-plane
tilts of the [SnBr
6
]
4–
octahedra in the
CsGSnBr
4
and Cs
2
GSn
2
Br
7
compounds. In G
2
SnBr
4
, the Sn lone pair is
highly stereoactive and favors non-octahedral, that is, square pyramidal
coordination of Sn(II). G
2
SnBr
4
exhibits bright
broad-band emission from self-trapped excitonic states, owing to its
soft lattice and electronic localization. This emission in G
2
SnBr
4
is characterized by a photoluminescence (PL) quantum
yield of 2% at room temperature (RT; 75 ± 5% at 77 K) and a fast
PL lifetime of 18 ns at room temperature.
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