Initial Engineering and Outdoor Stability Assessment of "Gray/Black" Fullerene-Free Organic Photovoltaics Based on Only Two Complementary Absorbing Materials: A Tetrabenzotriazacorrole and a Subphthalocyanine.

Broad absorption is a desired characteristic of materials employed in the photoactive layers of organic photovoltaic (OPV) devices. Here, we have identified tetrabenzotriazacorroles (Tbcs) as complementary absorbing chromophores and electron donors to the promising nonfullerene acceptors boron subphthalocyanines (BsubPcs). These two materials, which can be utilized as donor-acceptor pairs within fullerene-free OPVs, yield spectral coverage over the entire visible range of 300-750 nm. Oxy phosphorus Tbc derivative (POTbc) was employed as an electron donor and paired initially with multiple BsubPc derivatives having a distribution of highest occupied molecular orbital/lowest unoccupied molecular orbital energy levels in planar heterojunction OPVs. These devices were "gray/black" due to the broad absorption across the visible spectrum. Upon screening, the partially halogenated chloro hexachloro BsubPc (Cl-Cl6BsubPc) showed the greatest promise for coupling with POTbc. The thickness ratio and total thickness of the active layer were then probed in order to identify the optical and electrical limitations on the POTbc/Cl-Cl6BsubPc-based OPV device. A maximum power conversion efficiency (PCE) of 2.13% was achieved at 60 nm total thickness of the active layer and 1 to 3 (POTbc to Cl-Cl6BsubPc) thickness ratio. Outdoor stability of the champion device was evaluated using protocols established by International Summits on OPV Stability and was found to be on par with an α-sexithiophene/Cl-Cl6BsubPc baseline OPV.

Boron Subphthalocyanines and Silicon Phthalocyanines for Use as Active Materials in Organic Photovoltaics.

Organic photovoltaics (OPVs) have experienced continued interest over the last 25 years as a viable technology for the generation of power. Phthalocyanines are among the oldest commercial dyes and have been utilized in some of the earliest examples of OPVs. In recent years, the use of boron subphthalocyanines (BsubPcs) and silicon phthalocyanines (SiPcs) has attracted a flurry of interest with some examples of fullerene-free devices reaching power conversion efficiencies >8 %. Unlike other more common divalent phthalocyanines such as copper or zinc, BsubPcs and SiPcs contain additional axial groups that can easily be functionalized without significantly affecting the optoelectronic properties of the macrocycle. This handle facilitates our ability to tune the solid-state arrangement and other physical characteristics such as solubility ultimately giving us the ability to improve the thin film processing and final device performance. This review covers recent studies on the development of BsubPcs and SiPcs for use as active materials in organic photovoltaics.

Phenoxy-(Chloro) n -Boron Subnaphthalocyanines: Alloyed Mixture, Electron-Accepting Functionality, and Enhanced Solubility for Bulk Heterojunction Organic Photovoltaics.

The first set of phenoxy BsubNc compounds, PhO-Cl n BsubNc and F5-Cl n BsubNc, was synthesized through an axial displacement reaction of Cl-Cl n BsubNc with phenol and pentafluorophenol (respectively). Like their precursor, the products were found to be an alloyed mixture of phenoxylated Cl n BsubNcs with random positioning in the solid state yet consistent frequency of bay position chlorination. The average bay position chlorine occupancy was determined to be 0.99 through single crystal diffraction of PhO-Cl n BsubNc. Although the phenoxylation of Cl-Cl n BsubNc did not influence the chromophore photophysical properties, the electrochemical behavior was found to be more stable. Phenoxylation yielded differences in organic photovoltaic (OPV) device metrics. Specifically, a significant increase in open circuit voltage (V OC) was observed, ultimately exceeding 1.0 V when phenoxylated Cl n BsubNcs were paired with alpha-sexithiophene (α-6T) in planar heterojunction OPVs. Phenoxylation enabled the first example of BsubNcs incorporated into polymer-based bulk heterojunction (BHJ) OPVs through enhanced solubility. Phenoxylated Cl n BsubNcs, when paired with poly-3-hexylthiophene, also showed high V OC in BHJ OPVs with broad spectral absorption up to 760 nm. In the BHJ case, simple phenoxy was shown to be a better axial substituent compared to pentafluorophenoxy. This study represents the first example of using Cl n BsubNcs with nonchlorine axial substituents in OPVs and demonstrates that phenoxylation has a significant impact on device metrics while enhancing solubility to enable incorporation of Cl n BsubNcs into BHJ OPVs.

Development of a novel method for the strengthening and toughening of irradiation-sterilized bone allografts.

Reconstruction of large skeletal defects is a significant and challenging issue. Bone allografts are often used for such reconstructions. However, sterilizing bone allografts by using γ-irradiation, damages collagen and causes the bone to become weak, brittle and less fatigue resistant. In a previous study, we successfully protected the mechanical properties of human cortical bone by conducting a pre-treatment with ribose, a natural and biocompatible agent. This study focuses on examining possible mechanisms by which ribose might protect the bone. We examined the mechanical properties, crosslinking, connectivity and free radical scavenging potentials of the ribose treatment. Human cortical bone beams were treated with varying concentration of ribose (0.06-1.2 M) and γ-irradiation before testing them in 3-point bending. The connectivity and amounts of crosslinking were determined with Hydrothermal-Isometric-Tension testing and High-Performance-Liquid-Chromatography, respectively. The free radical content was measured using Electron Paramagnetic Resonance. Ribose pre-treatment improved the mechanical properties of irradiation sterilized human bone in a pre-treatment concentration-dependent manner. The 1.2 M pre-treatment provided >100% of ultimate strength of normal controls and protected 76% of the work-to-fracture (toughness) lost in the irradiated controls. Similarly, the ribose pre-treatment improved the thermo-mechanical properties of irradiation-sterilized human bone collagen in a concentration-dependent manner. Greater free radical content and pentosidine content were modified in the ribose treated bone. This study shows that the mechanical properties of irradiation-sterilized cortical bone allografts can be protected by incubating the bone in a ribose solution prior to irradiation.

Boron Subphthalocyanines as Triplet Harvesting Materials within Organic Photovoltaics.

Singlet fission, the generation of two excited triplet states from a single absorbed photon, is currently an area of significant interest to photovoltaic researchers. In this Letter, we outline how a polychlorinated boron subphthalocyanine, previously hypothesized to be an effective harvester of singlet fission derived triplets from pentacene, is relatively efficient at facilitating the process. As expected, we found a major increase in photocurrent generation at the expense of device voltage. For a direct point of comparison, we also have paired the same polychlorinated boron subphthalocyanine with α-sexithiophene to probe the alternative technique of complementary absorption engineering. The sum of these efforts have let us present new guidelines for the molecular design of boron subphthalocyanine for organic photovoltaic applications.

Evaluating thiophene electron-donor layers for the rapid assessment of boron subphthalocyanines as electron acceptors in organic photovoltaics: solution or vacuum deposition?

In this study, we consider the choice of a standard electron-donating material to be paired with boron subphthalocyanines (BsubPcs) to rapidly assess the viability of new BsubPc derivatives as electron-accepting materials within organic photovoltaic devices (OPVs). Specifically, we evaluate the effectiveness of solution-cast poly(3-hexylthiophene-2,5-diyl) (P3HT) as an electron donor paired with BsubPc derivatives relative to vacuum-deposited sexithiophene (α-6T). By using fullerene (C60 ), boron subphthalocyanine chloride (Cl-BsubPc), and hexachloro boron subphthalocyanine chloride (Cl-Cl6 BsubPc) as electron acceptors, we find that devices made with α-6T outperform those with P3HT. However, the two thiophene-based materials show the same performance trends. Given the preservation of these trends, we can recommend either option for assessing the potential of new BsubPc derivatives; P3HT as a solution-cast electron-donor layer or α-6T as a vacuum-deposited alternative.

Assessing the potential roles of silicon and germanium phthalocyanines in planar heterojunction organic photovoltaic devices and how pentafluoro phenoxylation can enhance π-π interactions and device performance.

In this study, we have assessed the potential application of dichloro silicon phthalocyanine (Cl2-SiPc) and dichloro germanium phthalocyanine (Cl2-GePc) in modern planar heterojunction organic photovoltaic (PHJ OPV) devices. We have determined that Cl2-SiPc can act as an electron donating material when paired with C60 and that Cl2-SiPc or Cl2-GePc can also act as an electron acceptor material when paired with pentacene. These two materials enabled the harvesting of triplet energy resulting from the singlet fission process in pentacene. However, contributions to the generation of photocurrent were observed for Cl2-SiPc with no evidence of photocurrent contribution from Cl2-GePc. The result of our initial assessment established the potential for the application of SiPc and GePc in PHJ OPV devices. Thereafter, bis(pentafluoro phenoxy) silicon phthalocyanine (F10-SiPc) and bis(pentafluoro phenoxy) germanium phthalocyanine (F10-GePc) were synthesized and characterized. During thermal processing, it was discovered that F10-SiPc and F10-GePc underwent a reaction forming small amounts of difluoro SiPc (F2-SiPc) and difluoro GePc (F2-GePc). This undesirable reaction could be circumvented for F10-SiPc but not for F10-GePc. Using single crystal X-ray diffraction, it was determined that F10-SiPc has significantly enhanced π-π interactions compared with that of Cl2-SiPc, which had little to none. Unoptimized PHJ OPV devices based on F10-SiPc were fabricated and directly compared to those constructed from Cl2-SiPc, and in all cases, PHJ OPV devices based on F10-SiPc had significantly improved device characteristics compared to Cl2-SiPc.