Shan Cong

Interface engineering toward enhanced efficiency of planar perovskite solar cells

Interface engineering is an efficient method for improving the performance of planar perovskite solar cells (PSCs). In this paper, the performance of PSCs was improved significantly by introducing 4,7-diphenyl-1,10-phenanthroline (Bphen) doped with bis(2-methyldibenzo-[f,h]quinoxaline) (Ir(MDQ)2(acac)) to modify the interface between perovskite (CH3NH3PbI3−xClx)/PCBM (phenyl-C61-butyric acid methyl ester) and an Ag electrode. The power conversion efficiency (PCE) was enhanced up to 15.87%, compared with 10.77% for the reference device without interlayer modification. It was found that the enhanced PCE was attributed to the better interface contact between the perovskite and Ag cathode. A suitable interface roughness is beneficial for reducing the leakage current and the probability of carrier recombination, resulting in an enhanced fill factor and thus improved device efficiency.

A New Member of Electrocatalysts Based on Nickel Metaphosphate Nanocrystals for Efficient Water Oxidation

High-performance electrocatalysts are desired for electrochemical energy conversion, especially in the field of water splitting. Here, a new member of phosphate electrocatalysts, nickel metaphosphate (Ni2 P4 O12 ) nanocrystals, is reported, exhibiting low overpotential of 270 mV to generate the current density of 10 mA cm-2 and a superior catalytic durability of 100 h. It is worth noting that Ni2 P4 O12 electrocatalyst has remarkable oxygen evolution performance operating in basic media. Further experimental and theoretical analyses demonstrate that N dopant boosts the catalytic performance of Ni2 P4 O12 due to optimizing the surface electronic structure for better charge transfer and decreasing the adsorption energy for the oxygenic intermediates.

Organic Small Molecule as the Underlayer Toward High Performance Planar Perovskite Solar Cells

The underlayer plays an important role for organic-inorganic hybrid perovskite formation and charge transport in perovskite solar cells (PSCs). Here, we employ a classical organic small molecule, 5,6,11,12-tetraphenyltetracene (rubrene), as the underlayer of perovskite films to achieve 15.83% of power conversion efficiency with remarkable moisture tolerance exposed to the atmosphere. Experiments demonstrate rubrene hydrophobic underlayer not only drives the crystalline grain growth of high quality perovskite, but also contributes to the moisture tolerance of PSCs. Moreover, the matching energy level of the desirable underlayer is conductive to extracting holes and blocking electrons at anode in PSCs. This introduction of organic small molecule into PSCs provides alternative materials for interface optimization, as well as platform for flexible and wearable solar cells.

Design and synthesis of functional ionic liquids based on pyrrolidinium cations bearing alkyl nitrile moieties

A series of functional ionic liquids based on pyrrolidinium cations bearing alkyl nitrile moieties have been designed, synthesized and characterised with high purity and yield. The influence of the anion structure and methylene chain length of the alkyl nitrile moieties on the thermal properties of functional ionic liquids is comprehensively investigated. Moreover, some of the ionic liquids show obvious plastic crystal phase behavior with rotational disorder and activated vacancies/defects, which can offer a solid bulk matrix for doping 1-propyl-3-methylimidazolium iodine (PMII), LiI and I2 to prepare plastic crystal electrolytes with high melting points and conductivities. Furthermore, the resulting solid-state dye-sensitized solar cell (DSSC) exhibits a power conversion efficiency (PCE) of 5.22% under the simulated air mass 1.5 solar spectrum illumination at 100 mW cm−2, and displays a superior long-term stability compared to conventional liquid-based devices. These results offer us a feasible method to explore new organic plastic crystals and electrolytes for high temperature solid-state DSSCs.

Self-Cleaning Glass of Photocatalytic Anatase TiO2@Carbon Nanotubes Thin Film by Polymer-Assisted Approach

Due to the good photocatalytic activity, the TiO2@CNTs thin film is highly desirable to apply to the self-cleaning glass for green intelligent building. Here, the TiO2@CNTs thin film has been successfully achieved by polymer-assisted approach of an aqueous chemical solution method. The polymer, polyethylenimine, aims to combine the Ti4+ with CNTs for film formation of TiO2@CNTs. The resultant thin film was uniform, highly transparent, and super-hydrophilic. Owing to fast electron transport and effectively hindering electron-hole recombination, the TiO2@CNTs thin film has nearly twofold photocatalytic performance than pure TiO2. The TiO2@CNTs thin films show a good application for self-cleaning glasses.

Emission switching in carbon dots coated CdTe quantum dots driving by pH dependent hetero-interactions

Due to the different emission mechanism between fluorescent carbon dots and semiconductor quantum dots (QDs), it is of interest to explore the potential emission in hetero-structured carbon dots/semiconducting QDs. Herein, we design carbon dots coated CdTe QDs (CDQDs) and investigate their inherent emission. We demonstrate switchable emission for the hetero-interactions of the CDQDs. Optical analyses indicate electron transfer between the carbon dots and the CdTe QDs. A heterojunction electron process is proposed as the driving mechanism based on N atom protonation of the carbon dots. This work advances our understanding of the interaction mechanism of the heterostructured CDQDs and benefits the future development of optoelectronic nanodevices with new functionalities.

Organic–Inorganic Hybrid Interfacial Layer for High-Performance Planar Perovskite Solar Cells

4,7-Diphenyl-1,10-phenanthroline (Bphen) is an efficient electron transport and hole blocking material in organic photoelectric devices. Here, we report cesium carbonate (Cs2CO3) doped Bphen as cathode interfacial layer in CH3NH3PbI3-xClx based planar perovskite solar cells (PSCs). Investigation finds that introducing Cs2CO3 suppresses the crystallization of Bphen and benefits a smooth interface contact between the perovskite and electrode, resulting in the decrease in carrier recombination and the perovskite degradation. In addition, the matching energy level of Bphen film in the PSCs effectively blocks the holes diffusion to cathode. The resultant power conversion efficiency (PCE) achieves as high as 17.03% in comparison with 12.67% of reference device without doping. Besides, experiments also demonstrate the stability of PSCs have large improvement because the suppressed crystallization of Bphen by doping Cs2CO3 as a superior barrier layer blocks the Ag atom and surrounding moisture access to the vulnerable perovskite layer.