Developing easy and effective surface functionalization approaches has required to facilitate the processability of graphene while seeking novel application areas. Herein, an in situ single-step reductive covalent bromination of graphene has been reported for the first time. Highly brominated graphene flakes (>3% Br) were prepared by only subjecting the bromine-intercalated graphite flakes to a reduction reaction with reactive lithium naphthalide. The bromine-functionalized graphene was characterized by X-ray photoelectron spectroscopy and thermogravimetric analysis. Results revealed that Br2 molecules acted as both an intercalating agent for the graphite and a reactant for the surface functionalization of the graphene. After brominating, the remaining negative charges on the reduced graphene surface were further used for the dual surface functionalization of graphene with a long-chain alkyl group (~1% dodecyl group addition). The functionalized graphenes were also characterized by Fourier transform infrared and Raman spectroscopy.

Perovskite solar cells are promising for realizing high power conversion efficiency (PCE) with low manufacturing costs, but efficient coating methods are needed for commercialization. Here, a gas blowing method was used to fabricate perovskite solar cells and was found to create a smooth perovskite layer and to prevent voids in large-area cells, when organic materials were used as scaffolds for forming the perovskite. A PCE of 13% in a 1 cm2 active area is achieved by tuning the band-gap energy of MAPbX3 via substitution of Br for I ions in X sites. Incorporation of a poly(3,4-ethylenedioxythiophene) hole transport layer with a higher work function increased the open circuit voltage of the solar cells. All layers of the cells were fabricated at low temperatures (<140 °C), which makes it possible to incorporate a polymer substrate for producing flexible solar cells and high-throughput fabrication.

In a scenario where ground water enters a canister for spent nuclear fuel in a deep geological repository, the presence of dissolved ions in the water could possibly influence the fuel dissolution due to effects on radiolysis yields. One species of particular interest in this context is bromide, which has a proven ability to scavenge hydroxyl radicals much faster than molecular hydrogen does. As a result, bromide could inhibit the beneficial effect of dissolved hydrogen, which has been shown in γ-radiolysis experiments. However, already a few hundred years after repository closure, α-decay starts to dominate in the radiation field from the spent fuel. Hence, the effects of α-radiolysis are expected to govern the fuel dissolution over the geological timeframes of the repository. In the present work, α-radiolysis experiments have been performed to determine the effect of bromide ions on the yield of hydrogen peroxide by mass spectrometric measurement of its decomposition product oxygen. The use of high activity 238Pu solutions has made it possible to study this effect during pure α-radiolysis from a homogeneously distributed radiation field. To simulate deep bedrock repository conditions, and to minimize the influence of in-leaking O2 from air, the studies were performed using graphite sealed stainless steel autoclaves with an initial atmosphere of 10 bar H2. The results show that addition of 1 mM Br- to the solution gives no significant effect on the O2 yield for radiation doses up to 2 MGy. This lack of effect is most likely explained by the limited radical escape yields from radiation tracks in pure α-radiolysis.

In this work, a planar heterojunction superstrate n-i-p device based on Zn(O,S) electron transport layer and CsPbI2Br absorber material at 1.93 eV bandgap is presented. The CsPbI2Br films are deposited using a 2-step atmospheric solution deposition process and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-vis spectroscopy and photoluminescence (PL). Best device with an efficiency of 12.34 % and 11.94% in reverse and forward scans respectively and stabilized power output of 12.14 mW/cm2 has been demonstrated via atmospheric solution processing with minimal hysteresis between forward and reverse scans. The devices show voltage dependent current collection as well as light-dark crossover in forward bias. Light soaking tests at 65 °C and 1-sun at Voc, resulted in open-circuit voltage and fill-factor degradation. Electroluminescence (EL) after 100 hours of light soaking shows a reduction in overall EL intensity as well a shift in emission to lower wavelength. The devices exhibit a positive temperature coefficient of about 0.14 %/°C. It is found that Zn(O,S) is a viable alternative electron transport layer to replace TiO2. By replacing methylammonium cation with cesium and addition of Br has improved the stability of the perovskite phase.

TlBr crystals have superior radiation detection properties; however, their properties degrade in the range of hours to weeks when an operating electrical field is applied. To account for this rapid degradation using the widely-accepted vacancy migration mechanism, the vacancy concentration must be orders of magnitude higher than any conventional estimates. The present work has incorporated a new analytical variable charge model in molecular dynamics (MD) simulations to examine the structural changes of materials under electrical fields. Our simulations indicate that dislocations in TlBr move under electrical fields. This discovery can lead to new understanding of TlBr aging mechanisms under external fields.

Electrochemical performances of a prototype Lithium-Bromine battery (LBB) employing a solid electrolyte was investigated. It showed the discharge capacity of c.a. 147 mAh/(g-LiBr) for the first cycle, which decreased with repeating charge/discharge cycles. The capacity fading was mainly due to increase of the interfacial resistance between an aqueous active material solution and a solid electrolyte. From the results of symmetric cells and structural analysis of the surface of the solid electrolyte immersed in Br2 solutions, it was suggested that a Li+-depletion layer was formed on the surface of the solid electrolyte by contact with bromine.

Electron-withdrawing halogen atoms are often bonded to the surface of carbon nanotubes to assist in the conversion from metallic to semiconducting properties. Single-walled carbon nanotubes (SWCNTs) were surface modified using UV photolysis with: (i) a broad band of wave lengths from approximately 250 to 400 nm having a maximum intensity at approximately 300 nm for photolysis of Cl2, (ii) low-pressure Hg lamps emitting 253.7 nm photons for photo-decomposition of HBr, and (iii) low-pressure Hg lamps emitting both 253.7 and 184.9 nm for photo-dissociation of HCl and HBr, respectively, and analyzed by x-ray photoelectron spectroscopy. Chlorine atoms adhered more readily than bromine atoms with the π-conjugation of the SWCNTs. The dominant increase with treatment was observed in the singly bonded chlorine moiety. Chlorine atoms, generated by UV photolysis of Cl2, produced a higher Cl saturation level of approximately 36 at.% than previously observed for multi-walled carbon nanotubes (13 at.%).The degree of chlorination depended on the amount of oxygen on the surface of the SWCNTs. Photo-dissociation of gaseous HCl and HBr showed lower amounts of halogenation on SWCNTs (approximately 5.8 at.% Cl and 2.5 at.% Br, respectively) than photolysis of Cl2.