Tailored multifunctional hydrazine derivatives for efficient printable hole-conductive-free mesoscopic perovskite solar cells via enhancing defect passivation

The low-cost and easy large-scale fabrication advantages of printable mesoscopic perovskite solar cells(p-MPSCs)are overshadowed by their limited photovoltaic conversion efficiency(PCE).Here,we introduce the hydrazide derivative of 4-Hydroxybenzoylhydrazine(4-HBH)to improve the PCE of p-MPSCs by inducing enhanced defect passivation.Both carbonyl and hydrazine groups in hydrazide groups present strong interaction with perovskite.The hydroxyl group,as an electron donor group,increases the electron cloud density of the hydrazide group in 4-HBH under the conjugation of the benzene ring,and thus enhances its interaction with perovskite.Additionally,the hydroxy group itself interacts with perovskite and passivates defects synergistically.The hydrazine agents can also reduce I2and suppress the loss of iodine in perovskite films,which inhibits the formation of iodine-related defects.Consequently,p-MPSCs with 4-HBH achieve a high PCE of 19.21%,and present well improved stability.

Printed hole-conductor-free mesoscopic perovskite solar cells with excellent long-term stability using PEAI as an additive

Phenethylamine（PEA） was successfully introduced into hole-conductor-free, fully printable mesoscopic MAPbI3 perovskite solar cells（MPSCs） with a carbon electrode by mixing phenethylammonium iodide with MAPbI3 perovskite solution. PEA-MAPbI3 films show better pore filling into TiO2 scaffold that forms better contact, and induce longer exciton lifetime and higher quantum efficiency of photoinduced charge separation. As a result, the power conversion efficiency of PEA-MAPbI3 MPSCs is 37% higher than that of MAPbI3 MPSCs. And PEA-MAPbI3 MPSCs show excellent long-term stability that could keep 90% of origin power conversion efficiency for over 80 days in the air.

High-performance, stable and low-cost mesoscopic perovskite （CH3NH3PbI3） solar cells based on poly（3-hexylthiophene）- modified carbon nanotube cathodes

This work explores the use of poly（3- hexylthiophene） （P3HT） modified carbon nanotubes （CNTs@P3HT） for the cathodes of hole transporter free, mesoscopic perovskite （CH3NH3PbI3） solar cells （PSCs）, simultaneously achieving high-performance, high stability and low-cost PSCs. Here the thin P3HT modifier acts as an electron blocker to inhibit electron transfer into CNTs and a hydrophobic polymer binder to tightly cross-link the CNTs together to compact the carbon electrode film and greatly stabilize the solar cell. On the other hand, the presence of CNTs greatly improve the conductivity of P3HT. By optimizing the concentration of the P3HT modifier （2 mg/mL）, we have improved the power conversion efficiencies （PCEs） of CNTs@P3HT based PSCs up to 13.43% with an average efficiency of 12.54%, which is much higher than the pure CNTs based PSCs （best PCE 10.59%） and the sandwich-type P3HT/CNTs based PSCs （best PCE 9.50%）. In addition, the hysteresis of the CNTs@P3HT based PSCs is remarkably reduced due to the intimate interface between the perovskite and CNTs@P3HT electrodes. Degradation of the CNTs@ P3HT based PSCs is also strongly retarded as compared to cells employing the pure CNTs electrode when exposed to the ambient condition of 20%- 40% humidity.

通过5-氨基-4-甲酰基咪唑盐酸盐提高可印刷介观钙钛矿太阳能电池的光伏性能

基于m-TiO_(2)/m-ZrO_(2)/C的无空穴可印刷介观钙钛矿太阳能电池(p-MPSCs)具有成本低廉、操作简便和稳定性优异的特点,被认为是最具商业应用潜力的新型光伏器件之一.然而,与传统PSC相比,p-MPSCs的开路电压(VOC)损失较大,导致能量转换效率(PCE)与传统PSC存在差距.在此,我们提出了一种利用5-氨基-4甲酰胺咪唑盐酸盐(AICA)提升p-MPSCs开路电压的方法.AICA不仅可以调节钙钛矿膜的功函数,其酰胺基团和氨基还能分别钝化钙钛矿中未配位的Pb2+和I−缺陷,稳定钙钛矿的结构,形成高质量钙钛矿薄膜,从而抑制缺陷诱导的非辐射复合.因此,引入AICA后p-MPSCs获得了16.68%的PCE,并且VOC从0.88提升至0.98 V.

Enhanced perovskite electronic properties via A-site cation engineering

Organic-inorganic halide perovskites have emerged as excellent candidates for low-cost photovoltaics and optoelectronics.While the predominant recent trend in designing perovskites for efficient and stable solar cells has been to mix different A-site cations,the role of A-site cations is still limited to tune the lattice and bandgap of perovskites.Herein we compare the optoelectronic properties of acetamidinum(Ace)and guanidinium(Gua)mixed methylammonium lead iodide perovskites and shed a light on the hidden role of A-site cation on the carrier mobility of mixed-cation lead iodide perovskites.The cations do not affect the bandgap of the perovskites since the orbitals from Ace and Gua do not contribute to the band edges of the material.However,the mobility of the Ace mixed perovskite is significantly enhanced to be an order of magnitude higher than that of the pristine perovskite.We apply the Ace mixed perovskite in hole-conductor-free printable mesoscopic perovskite solar cells and obtain a stabilized PCE of over 18%(certified 17.7%),which is the highest certified efficiency so far.