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Dive into the research topics where Mark W. Wilson is active.

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Featured researches published by Mark W. Wilson.


Journal of the American Chemical Society | 2011

Ultrafast Dynamics of Exciton Fission in Polycrystalline Pentacene

Mark W. Wilson; Akshay Rao; Jenny Clark; R. Sai Santosh Kumar; Daniele Brida; Giulio Cerullo; Richard H. Friend

We use ultrafast transient absorption spectroscopy with sub-20 fs time resolution and broad spectral coverage to directly probe the process of exciton fission in polycrystalline thin films of pentacene. We observe that the overwhelming majority of initially photogenerated singlet excitons evolve into triplet excitons on an ∼80 fs time scale independent of the excitation wavelength. This implies that exciton fission occurs at a rate comparable to phonon-mediated exciton localization processes and may proceed directly from the initial, delocalized, state. The singlet population is identified due to the brief presence of stimulated emission, which is emitted at wavelengths which vary with the photon energy of the excitation pulse, a violation of Kashas Rule that confirms that the lowest-lying singlet state is extremely short-lived. This direct demonstration that triplet generation is both rapid and efficient establishes multiple exciton generation by exciton fission as an attractive route to increased efficiency in organic solar cells.


Journal of the American Chemical Society | 2010

Exciton Fission and Charge Generation via Triplet Excitons in Pentacene/C60 Bilayers

Akshay Rao; Mark W. Wilson; Justin M. Hodgkiss; Sebastian Albert-Seifried; H. Bässler; Richard H. Friend

Organic photovoltaic devices are currently studied due to their potential suitability for flexible and large-area applications, though efficiencies are presently low. Here we study pentacene/C(60) bilayers using transient optical absorption spectroscopy; such structures exhibit anomalously high quantum efficiencies. We show that charge generation primarily occurs 2-10 ns after photoexcitation. This supports a model where charge is generated following the slow diffusion of triplet excitons to the heterojunction. These triplets are shown to be present from early times (<200 fs) and result from the fission of a spin-singlet exciton to form two spin-triplet excitons. These results elucidate exciton and charge generation dynamics in the pentacene/C(60) system and demonstrate that the tuning of the energetic levels of organic molecules to take advantages of singlet fission could lead to greatly enhanced photocurrent in future OPVs.


Nature Chemistry | 2014

A transferable model for singlet-fission kinetics

Shane R. Yost; Jiye Lee; Mark W. Wilson; Tony Wu; David Paul McMahon; Rebecca R. Parkhurst; Nicholas J. Thompson; Daniel N. Congreve; Akshay Rao; Kerr Johnson; Moungi G. Bawendi; Timothy M. Swager; Richard H. Friend; Marc A. Baldo; Troy Van Voorhis

Exciton fission is a process that occurs in certain organic materials whereby one singlet exciton splits into two independent triplets. In photovoltaic devices these two triplet excitons can each generate an electron, producing quantum yields per photon of >100% and potentially enabling single-junction power efficiencies above 40%. Here, we measure fission dynamics using ultrafast photoinduced absorption and present a first-principles expression that successfully reproduces the fission rate in materials with vastly different structures. Fission is non-adiabatic and Marcus-like in weakly interacting systems, becoming adiabatic and coupling-independent at larger interaction strengths. In neat films, we demonstrate fission yields near unity even when monomers are separated by >5 Å. For efficient solar cells, however, we show that fission must outcompete charge generation from the singlet exciton. This work lays the foundation for tailoring molecular properties like solubility and energy level alignment while maintaining the high fission yield required for photovoltaic applications.


American Journal of Surgery | 1997

Selective arterial embolization for the control of lower gastrointestinal bleeding

Roy L. Gordon; Kathrin L. Ahl; Robert K. Kerlan; Mark W. Wilson; Jeanne M. LaBerge; Jeet S. Sandhu; Ernest J. Ring; Mark L. Welton

BACKGROUND Transcatheter embolization is accepted as a safe method for treating acute bleeding from the upper gastrointestinal (GI) tract. Hesitancy persists using this technique below the ligament of Treitz, based on the belief that the risk of intestinal infarction is unacceptably high, despite mounting clinical evidence to the contrary. METHODS A series of 17 consecutive patients with angiographically demonstrated small intestinal or colonic bleeding was retrospectively reviewed. The success and complication rate of subselective embolization was assessed. RESULTS Bleeding was stopped in 13 of 14 patients (93%) in whom embolization was possible, and in 13 of 17 patients (76%) where there was an intention to treat. Sufficiently selective catheterization to permit embolization could not be achieved in 3 patients. No clinically apparent bowel infarctions were caused. CONCLUSION Subselective embolization is a safe treatment option for lower GI bleeding, suitable for many patients and effective in most. Careful technique and a readiness to abandon embolization when a suitable catheter position cannot be achieved are important.


Journal of Vascular Surgery | 2000

Endovascular aneurysm repair in high-risk patients☆☆☆★★★

Timothy A.M. Chuter; Linda M. Reilly; Rishad M. Faruqi; Robert B. Kerlan; Rajiv Sawhney; Catherine J. Canto; Jean M. LaBerge; Mark W. Wilson; Roy L. Gordon; Susan D. Wall; Joseph H. Rapp; Louis M. Messina

PURPOSE The purpose of this study was to evaluate the role of endovascular aneurysm repair in high-risk patients. METHODS The elective endovascular repair of infrarenal aortic aneurysm was performed in 116 high-risk patients with either custom-made or commercial stent grafts. The routine follow-up examination included contrast-enhanced computed tomography (CT) before discharge, at 3, 6, and 12 months, and annually thereafter. Patients with endoleak on the initial CT underwent re-evaluation at 2 weeks. Those patients with positive CT results at 2 weeks underwent endovascular treatment. RESULTS Endovascular repair was considered feasible in 67% of the patients. The mean age was 75 years, and the mean aneurysm diameter was 6.3 cm. The American Society of Anesthesiologists grade was II in 3.4%, III in 65.5%, IV in 30.1%, and V in 0.9%. There were no conversions to open repair. Custom-made aortomonoiliac stent grafts were implanted in 77.6% of the cases, custom-made aortoaotic stent grafts in 11.2%, and commercial bifurcated stent grafts in 11.2%. The 30-day rates of mortality, major morbidity, and minor morbidity were 3.4%, 20.7%, and 12%, respectively, in the first 58 patients and 0%, 3.4%, and 3.4%, respectively, in the last 58. The late complications included five cases of stent graft kinking, two cases of femorofemoral graft occlusion, and three cases of proximal stent migration, one of which led to aneurysm rupture. At 2 weeks after repair, endoleak was present in 10.3% of the cases. All the type I (direct perigraft) endoleaks underwent successful endovascular treatment, whereas only one type II (collateral) endoleak responded to treatment. The technical success rate at 2 weeks was 86.2%, and the clinical success rate was 96.6%. The continuing success rate was 87.9%. Seventeen patients died late, unrelated deaths. CONCLUSION Endovascular aneurysm repair is safe and effective in patients at high risk, for whom it may be the preferred method of treatment.


Nano Letters | 2012

Singlet Exciton Fission-Sensitized Infrared Quantum Dot Solar Cells

Bruno Ehrler; Mark W. Wilson; Akshay Rao; Richard H. Friend; Neil C. Greenham

We demonstrate an organic/inorganic hybrid photovoltaic device architecture that uses singlet exciton fission to permit the collection of two electrons per absorbed high-energy photon while simultaneously harvesting low-energy photons. In this solar cell, infrared photons are absorbed using lead sulfide (PbS) nanocrystals. Visible photons are absorbed in pentacene to create singlet excitons, which undergo rapid exciton fission to produce pairs of triplets. Crucially, we identify that these triplet excitons can be ionized at an organic/inorganic heterointerface. We report internal quantum efficiencies exceeding 50% and power conversion efficiencies approaching 1%. These findings suggest an alternative route to circumvent the Shockley-Queisser limit on the power conversion efficiency of single-junction solar cells.


Nature Communications | 2012

In situ measurement of exciton energy in hybrid singlet-fission solar cells

Bruno Ehrler; Brian J. Walker; Marcus L. Böhm; Mark W. Wilson; Yana Vaynzof; Richard H. Friend; Neil C. Greenham

Singlet exciton fission-sensitized solar cells have the potential to exceed the Shockley-Queisser limit by generating additional photocurrent from high-energy photons. Pentacene is an organic semiconductor that undergoes efficient singlet fission--the conversion of singlet excitons into pairs of triplets. However, the pentacene triplet is non-emissive, and uncertainty regarding its energy has hindered device design. Here we present an in situ measurement of the pentacene triplet energy by fabricating a series of bilayer solar cells with infrared-absorbing nanocrystals of varying bandgaps. We show that the pentacene triplet energy is at least 0.85 eV and at most 1.00 eV in operating devices. Our devices generate photocurrent from triplets, and achieve external quantum efficiencies up to 80%, and power conversion efficiencies of 4.7%. This establishes the general use of nanocrystal size series to measure the energy of non-emissive excited states, and suggests that fission-sensitized solar cells are a favourable candidate for third-generation photovoltaics.


Accounts of Chemical Research | 2013

Singlet Exciton Fission in Polycrystalline Pentacene: From Photophysics toward Devices

Mark W. Wilson; Akshay Rao; Bruno Ehrler; Richard H. Friend

Singlet exciton fission is the process in conjugated organic molecules bywhich a photogenerated singlet exciton couples to a nearby chromophore in the ground state, creating a pair of triplet excitons. Researchers first reported this phenomenon in the 1960s, an event that sparked further studies in the following decade. These investigations used fluorescence spectroscopy to establish that exciton fission occurred in single crystals of several acenes. However, research interest has been recently rekindled by the possibility that singlet fission could be used as a carrier multiplication technique to enhance the efficiency of photovoltaic cells. The most successful architecture to-date involves sensitizing a red-absorbing photoactive layer with a blue-absorbing material that undergoes fission, thereby generating additional photocurrent from higher-energy photons. The quest for improved solar cells has spurred a drive to better understand the fission process, which has received timely aid from modern techniques for time-resolved spectroscopy, quantum chemistry, and small-molecule device fabrication. However, the consensus interpretation of the initial studies using ultrafast transient absorption spectroscopy was that exciton fission was suppressed in polycrystalline thin films of pentacene, a material that would be otherwise expected to be an ideal model system, as well as a viable candidate for fission-sensitized photovoltaic devices. In this Account, we review the results of our recent transient absorption and device-based studies of polycrystalline pentacene. We address the controversy surrounding the assignment of spectroscopic features in transient absorption data, and illustrate how a consistent interpretation is possible. This work underpins our conclusion that singlet fission in pentacene is extraordinarily rapid (∼80 fs) and is thus the dominant decay channel for the photoexcited singlet exciton. Further, we discuss our demonstration that triplet excitons generated via singlet fission in pentacene can be dissociated at an interface with a suitable electron acceptor, such as fullerenes and infrared-absorbing inorganic semiconducting quantum dots. We highlight our recent reports of a pentacene/PbSe hybrid solar cell with a power conversion efficiency of 4.7% and of a pentacene/PbSe/amorphous silicon photovoltaic device. Although substantive challenges remain, both to better our understanding of the mechanism of singlet exciton fission and to optimize device performance, this realization of a solar cell where photocurrent is simultaneously contributed from a blue-absorbing fission-capable material and an infrared-absorbing conventional cell is an important step towards a dual-bandgap, single-junction, fission-enhanced photovoltaic device, which could one day surpass the Shockley-Queisser limit.


Chemistry: A European Journal | 2016

Methylammonium Bismuth Iodide as a Lead-Free, Stable Hybrid Organic-Inorganic Solar Absorber.

Robert L. Z. Hoye; Riley E. Brandt; Anna Osherov; Vladan Stevanović; Samuel D. Stranks; Mark W. Wilson; Hyunho Kim; Austin J. Akey; John D. Perkins; Rachel C. Kurchin; Jeremy R. Poindexter; Evelyn N. Wang; Moungi G. Bawendi; Vladimir Bulovic; Tonio Buonassisi

Methylammonium lead halide (MAPbX3 ) perovskites exhibit exceptional carrier transport properties. But their commercial deployment as solar absorbers is currently limited by their intrinsic instability in the presence of humidity and their lead content. Guided by our theoretical predictions, we explored the potential of methylammonium bismuth iodide (MBI) as a solar absorber through detailed materials characterization. We synthesized phase-pure MBI by solution and vapor processing. In contrast to MAPbX3, MBI is air stable, forming a surface layer that does not increase the recombination rate. We found that MBI luminesces at room temperature, with the vapor-processed films exhibiting superior photoluminescence (PL) decay times that are promising for photovoltaic applications. The thermodynamic, electronic, and structural features of MBI that are amenable to these properties are also present in other hybrid ternary bismuth halide compounds. Through MBI, we demonstrate a lead-free and stable alternative to MAPbX3 that has a similar electronic structure and nanosecond lifetimes.


Nature Chemistry | 2016

Real-time observation of multiexcitonic states in ultrafast singlet fission using coherent 2D electronic spectroscopy

Artem A. Bakulin; Sarah Morgan; Tom B. Kehoe; Mark W. Wilson; Alex W. Chin; Donatas Zigmantas; Dassia Egorova; Akshay Rao

Singlet fission is the spin-allowed conversion of a spin-singlet exciton into a pair of spin-triplet excitons residing on neighbouring molecules. To rationalize this phenomenon, a multiexcitonic spin-zero triplet-pair state has been hypothesized as an intermediate in singlet fission. However, the nature of the intermediate states and the underlying mechanism of ultrafast fission have not been elucidated experimentally. Here, we study a series of pentacene derivatives using ultrafast two-dimensional electronic spectroscopy and unravel the origin of the states involved in fission. Our data reveal the crucial role of vibrational degrees of freedom coupled to electronic excitations that facilitate the mixing of multiexcitonic states with singlet excitons. The resulting manifold of vibronic states drives sub-100 fs fission with unity efficiency. Our results provide a framework for understanding singlet fission and show how the formation of vibronic manifolds with a high density of states facilitates fast and efficient electronic processes in molecular systems.

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Maythem Saeed

University of California

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Robert K. Kerlan

United States Department of Veterans Affairs

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Roy L. Gordon

University of California

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Aaron D. Losey

University of California

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S Hetts

University of California

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Loi Do

University of California

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