Research articles

103. NiO-MnO₂ and NiO-CuO Anchored on rGO as Ternary Electrode Materials for  Energy Storage Applications 

A. Salim, S. Khan, M. Bhoi, A. Mishra, G. D. Sharma, R. Vishnoi, R. Singhal

   New J. Chem. 2025, DOI: 10.1039/d4nj05462h (IF = 2.5)

102. Efficient All-Small-Molecule Organic Solar Cells Based on Asymmetric Coumarin-Anthracene Donor 

   N. N. Bhuyan, S. Shankar S, M. Bhoi, H Dahiya, R. Singhal, G. D. Sharma, A. Mishra*

   ACS Appl. Energy Mater. 2025, 8, 2335–2345 (IF = 5.5)

101. Influence of Alkyl Chain Length on Solar Cell Performance of Molecular Organic Semiconductors: A Review

   A. Mishra, S. Mahalik, A. Mishra* 

  Chem. Commun. 2025, 61, 3649-3668  (IF = 4.3)  (Invited Article)

100. An Asymmetric Coumarin-Anthracene Conjugate as Efficient Fullerene-Free Acceptor for Organic Solar Cells

   N. N. Bhuyan, S. S. Shankar, S. J. Panda, C. S. Purohit, R. Singhal, G. D. Sharma,* A. Mishra* 

   Angew. Chem. Int. Ed. 2024, 63, e202406272 (IF = 16.82)

99. Advances in Layer-by-Layer Processing for Efficient and Reliable Organic Solar Cells 

A. Mishra,* N. N. Bhuyan, H.-J. Xu, G. D. Sharma*

Mater. Adv., 2023, 4, 6031-6063 (IF = 5.0)

98. Correlation of Functional Coumarin Dye Structure with Molecular Packing and Organic Solar Cells Performance

R. Pradhan, K. Khandelwal, S. S. Shankar, S. J. Panda, C. S. Purohit, B. P. Bag, R. Singhal, W. Liu, X. Zhu, G. D. Sharma,* A. Mishra* 

Solar RRL 2023, 7, 2300487 (IF = 9.17)

97. Diketopyrrolopyrrole-Coumarin Conjugates for Efficient Binary Organic Solar Cells

K. S. More, H. A. Mirgane, Shyam Shankar S, N. N. Bhuyan, A. Mishra* S. V. Bhosale,* G. D. Sharma* 

ACS Appl. Energy Mater. 2023, 6, 8857–8866 (IF = 5.5)

96. Achieving High-Efficiency in Binary Organic Solar Cells by the Structural Fine-Tuning of Coumarin-based Donor 

R. Pradhan, K. Khandelwal, S. J. Panda, C. S. Purohit, B. P. Bag, R. Singhal, W. Liu, X. Zhu, G. D. Sharma,* A. Mishra* 

Solar RRL 2023, 7, 2300032 (IF = 9.17) (Front Cover Page)

95. Harnessing the Structure-Performance Relationships in Designing Non-Fused Ring Acceptors for Organic Solar Cells 

A. Mishra,* G. D. Sharma*

Angew. Chem. Int. Ed. 2023, 62, e202219245 (IF = 16.82)

94. All-Small-Molecule Efficient Ternary Organic Solar Cells Employing Two Fullerene-Free Acceptors and a Coumarin Donor

G. D. Sharma,* R. Pradhan, K. Khandelwal, R. Singhal, W. Liu, X. Zhu, A. Mishra* 

J. Mater. Chem. C 2023, 11, 1919-1926 (IF = 8.07)

93. Optical and structural modifications of copper nanoparticles in a matrix of fullerene C60 under 220 keV Ag ion irradiation 

V. Chaudhary, R. Vishnoi, A. Salim, J. Bhardwaj, D. Gupta, G. R. Umapathy, S. Ojha, U. K. Dwivedi, P. Kumar, M. Reza, A. Mishra, S. Aggarwal, G. D. Sharma, R. Singhal

Appl. Surf. Sci. Adv. 2022,  11, 100305 (IF = 6.2)

92. High-Efficiency Ternary Organic Solar Cells Enabled by Synergizing Dicyanomethylene-Functionalized Coumarin Donors and Fullerene-Free Acceptors 

R. Pradhan, A. Agrawal, B. P. Bag, R. Singhal, G. D. Sharma, A. Mishra,* 

ACS Appl. Energy Mater. 2022,  5, 9020-9030 (IF = 6.4)

91. Conformational selectivity of merocyanine on nanostructured silver films: Surface enhanced resonance Raman scattering (SERRS) and Density Functional Theoretical (DFT) Study

A. Das, R. Chadha, A. Mishra, N. Maiti

Front. Chem., 2022, 10, 902585  (IF = 5.54)

90. Semitransparent Organic Solar Cells: From Molecular Design to Structure-Performance Relationships

K. Khandelwal, S. Biswas, A. Mishra,* G. D. Sharma,* 

J. Mater. Chem. C 2022, 10, 13-43 (Invited Review) (IF = 8.07)

89. Exploring the Inclusion Complex Formation of 3-Acetylcoumarin with β-Cyclodextrin and its Delivery to a Carrier Protein: A Spectroscopic and Computational Study

 N. N. Bhuyan, A. Joardar, B. P. Bag, H. Chakraborty,* A. Mishra,* 

 J. Mol. Liq. 2021, 344, 117752 (IF = 6.63)

88. Fullerene-Free All Small Molecule Ternary Organic Solar Cells with Two Compatible Fullerene-Free Acceptors and a Coumarin Donor Enabling Power Conversion Efficiency of 14.5% 

G. D. Sharma,* A. Agrawal, R. Pradhan, M. L. Keshtov, R. Singhal, W. Liu, X. Zhu, A. Mishra,* 

ACS Appl. Energy Mater. 2021, 4, 11537–11544 (IF = 6.4)

87. Incorporation of a Guaiacol-Based Small Molecule Guest Donor Enables Efficient Non-Fullerene Acceptor-Based Ternary Organic Solar Cells

 R. Barla, B. Lochap, A. Agrawal, A. Mishra, M.L. Keshtov, G. D. Sharma

Solar RRL 2021, 5, 2100402 (IF = 9.17)

86. Exploring membrane viscosity at the headgroup region utilizing a hemicyanine-based fluorescent probe 

 N. N. Bhuyan, G. P. Pattanaik. A. Mishra,* H. Chakraborty*

J. Mol. Liq. 2021, 325, 115152. (IF = 6.63)

85. Energy-Level Modulation of Coumarin-Based Molecular donors for Efficient All Small Molecule Fullerene-Free Organic Solar Cell

R. Pradhan, H. Dahiya, B. P. Bag, M. L. Keshtov, R. Singhal, G. D. Sharma,* A. Mishra*

J. Mater. Chem. A 2021,  9, 1563-1573. (IF = 14.51)

84. Material Perceptions and Advances in Molecular Heteroacenes for Organic Solar Cells  

 A. Mishra*

Energy Environ. Sci. 2020, 13, 4738-4793. (IF = 39.71)

83. Efficient Fullerene-Free Organic Solar Cells Using a Coumarin-Based Wide Bandgap Donor Material 

 R. Pradhan, P. Malhotra, G. Gupta, R. Singhal, G. D. Sharma,* A. Mishra*

ACS Appl. Mater. Interfaces 2020, 12, 41869–41876. (IF = 10.38)

82. Perovskite Solar Cells with S,Si-Heteropentacene Based Hole Conductor Yield High Open Circuit Voltage of 1.55 V

M. I. Dar, N. Arora,* C. Steck, A. Mishra,* M. Alotaibi, P. Bäuerle, S. M. Zakeeruddin, M. Grätzel

Eur. J. Inorg. Chem. 2018, 4573-4578. (IF = 2.55)

81. Low Energy Gap Triphenylamine-Hetero­penta­cene-Dicyanovinyl Triad for Solution-Processed Bulk Heterojunction Solar Cells

A. Mishra,* C. Wetzel, R. Singhal, P. Bäuerle, G. D. Sharma*

J. Phys. Chem. C, 2018, 122, 11262–11269. (IF = 4.18) 

80. Transition-Metal-Based Layered Double Hydroxides Tailored for Energy Conversion and Storage

R. Patel, J. T. Park, M. Patel, J. K. Dash, E. Bhoje Gowde, R. Karpoormath, A. Mishra, J. Kwak, J. H. Kim

J. Mater. Chem. A. 2018, 6, 12-29 (IF = 14.51) 

79. Donor-Acceptor-Type S,N-Heteroacene Based Hole Transporting Materials for Efficient Perovskite Solar Cells 

N. Arora, C. Wetzel, M. I. Dar,* A. Mishra,* P. Yadav, C. Steck, S. M. Zakeeruddin, P. Bäuerle, M. Grätzel

ACS Appl. Mater. Interfaces, 2017, 9, 44423–44428 (IF = 10.38)

78. The Origin of Photoelectrochemical Generation of Dihydrogen by a Dye-Sensitized Photo­ca­thode Without an Intentionally Introduced Catalyst

D. A. Hoogeveen, M. Fournier, S. A. Bonke, A. Nattestad, A. Mishra, P. Bäuerle, L. Spiccia, A. J. Mozer, A. N. Simonov

J. Phys. Chem. C, 2017, 121, 25836–25846 (IF = 4.18)

77. Unprecedented low energy losses in organic solar cells with high external quantum efficiencies by employing non-fullerene electron acceptors 

A. Mishra,* M. L. Keshtov, A. Looser, R. Singhal, M. Stolte, F. Würthner, P. Bäuerle, G. D. Sharma*

J. Mater. Chem. A, 2017, 5, 14887-14897 (IF = 14.51)

76. The Influence of the Central Acceptor Unit on the Optoelectronic Properties and Photovoltaic Performance of A-D-A-D-A-Type Co-oligomers

I. Ata, D. Popovic, M. Lindén, A. Mishra, P. Bäuerle

Org. Chem. Front. 2017, 4, 755-766. (IF = 5.46)

75. Photo-Electrocatalytic Hydrogen Generation at Dye-Sensitised Electrodes Functionalised with a Heterogeneous Metal Catalyst

D. A. Hoogeveen, M. Fournier, S. Bonke, X.-Y. Fan, A. Mozer, A. Mishra, P. Bäuerle, A. N. Simonov, L. Spiccia

Electrochim. Acta, 2016, 219, 773–780 (IF = 7.34) 

74. High Performance A‑D‑A Oligothiophene-based Organic Solar Cells Employing Two-Step Annealing and Solution-Processable Copper Thiocyanate (CuSCN) as an interfacial hole transporting layer

A. Mishra,* T. Rana, A. Looser, M. Stolte, F. Würthner, P. Bäuerle, G. D. Sharma*

 J. Mater. Chem. A, 2016, 4, 17344-17353 (IF = 14.51) 

73. Indium Tin Oxide as a Semiconductor Material in Efficient p-Type Dye-Sensitized Solar Cells

Z. Yu, I. R. Perera, T. Daeneke, S. Makuta, Y. Tachibana, J. J. Jasieniak, A. Mishra, P. Bauerle, L. Spiccia, U. Bach

NPG Asia Mater., 2016, 8, e305; DOI: 10.1038/am.2016.89 (IF = 10.76)

72. The influence of alkyl side chains on molecular packing and solar cell performance of  dithienopyrrole-based oligothiophenes

G. L. Schulz, P. Kar, M. Weidelener, A. Vogt, M. Urdanpilleta, M. Lindén, E. Mena-Osteritz, A. Mishra,* P. Bäuerle*

 J. Mater. Chem. A, 2016, 4, 10514-10523 (IF = 14.51)

71. Development of Strongly Absorbing S,N-Heterohexacene-Based Donor Materials for Efficient Vacuum-Processed Organic Solar Cells

C. Wetzel, A. Mishra, E. Mena-Osteritz, K. Walzer, M. Pfeiffer, P. Bäuerle

J. Mater. Chem. C, 2016, 4, 3715-3725 (Cover page) (IF = 8.07)

70. Modulation of band gap and p- versus n-semiconductor character of ADA dyes by core and acceptor group variation

A. Nowak-Krol, R. Wagener, F. Kraus, A. Mishra, P. Bäuerle, F. Würthner

Org. Chem. Front. 2016, 3, 545-555 (IF = 5.46) 

69. High-Efficiency Perovskite Solar Cells Employing a D‑A-Substituted S,N-Heteropentacene as Hole Transport Material

D. Bi, A. Mishra,* P. Gao, M. Franckevičius, C. Steck, S. M. Zakeeruddin, M. K. Nazeeruddin, P. Bäuerle, M. Grätzel, A. Hagfeldt*

ChemSusChem, 2016, 9, 433-438 (IF = 9.14)

68. A Dopant-free Spirobi[cyclopenta[2,1-b;3,4-b']dithiophene] based Hole-Transport Material for Efficient Perovskite Solar Cells

M. Franckevičius, A. Mishra,* F. Kreuzer, J. Luo, S. M. Zakeeruddin,* M. Grätzel* 

Mater. Horiz. 2015, 2, 613-618 (IF = 15.72)

67. Fused thiophene-pyrrole-containing ring systems up to a Heterodecacene

C. Wetzel, E. Brier, A. Vogt, A. Mishra, E. Mena-Osteritz, P. Bäuerle

Angew. Chem. Int. Ed. 2015, 54, 12334–12338 (IF = 16.82) 

66. A-D-A-type S,N-Heteropentacene-based Hole Transport Materials for Dopant-free Perovskite Solar Cells

C. Steck, M. Franckevičius, S. M. Zakeeruddin,* A. Mishra,* P. Bäuerle, M. Grätzel* 

J. Mater. Chem. A, 2015, 3, 17738-17746 (IF = 14.51)

65. Functional Tuning of A-D-A Oligothiophenes: The Effect of Solvent Vapor Annealing on Blend Morphology and Solar Cell Performance

G. L. Schulz, M. Löbert, I. Ata, M. Urdanpilleta, M. Lindén, A. Mishra,* P. Bäuerle* 

J. Mater. Chem. A, 2015, 3, 13738-13748 (IF = 14.51

64. Acceptor-substituted S,N-heteropentacenes of different conjugation length: Structure-property relationships and solar cell performance

H. Kast, A. Mishra,* G. L. Schulz, M. Urdanpilleta, E. Mena‑Osteritz, P. Bäuerle* 

Adv. Funct. Mater. 2015, 25, 3414–3424 (IF = 19.92)

63. π-Conjugated [2]Catenanes based on Oligothiophenes and Phenanthrolines: Efficient Synthesis and Electronic Properties

G. Götz, X. Zhu, A. Mishra, J.-L. Segura, E. Mena-Osteritz, P. Bäuerle

Chem.–Eur. J. 2015, 21, 7193–7210 (IF = 5.02)

62. Application of the Tris(acetylacetonato)iron(II)/(III) Redox Couple in p-Type Dye-Sensitized Solar Cells

I. R. Perera, T. Daeneke, S. Makuta, Z. Yu, Y. Tachibana, A. Mishra, P. Bäuerle, C. A. Ohlin, U. Bach, L. Spiccia

Angew. Chem. Int. Ed. 2015, 54, 3758–3762 (IF = 16.82) (Cit. = 190)

61. Dominating Energy Losses in NiO p-Type Dye-Sensitized Solar Cells

T. Daeneke, Z. Yu, G. P. Lee, D. Fu, N. W. Duffy, S. Makuta, Y. Tachibana, L. Spiccia, A. Mishra, P. Bäuerle U. Bach

Adv. Energy Mater. 2015, 5, 1401387 (IF = 29.70)

60. A-D-A-type S,N-Heteropentacenes: Next Generation Molecular Donor Materials for Efficient Vacuum-Processed Organic Solar Cells

A. Mishra, D. Popovic, A. Vogt, H. Kast, T. Leitner, K. Walzer, M. Pfeiffer, E. Mena-Osteritz, P. Bäuerle

Adv. Mater. 2014, 26, 7217–7223 (inside cover) (IF = 32.09)

59. Synthesis and Characterization of Organic Dyes with Various Electron-Accepting Substituents for p-Type Dye-Sensitized Solar Cells

M. Weidelener, S. Powar, H. Kast, Z. Yu, P. P. Boix, C. Li, K. Müllen, T. Geiger, S. Kuster, F. Nüesch, U. Bach, A. Mishra,* P. Bäuerle*

Chem.–Asian J. 2014, 7, 3251-3263 (IF = 4.84)

58. A-D-A-Type Oligothiophenes Containing Benzothiadiazole Terminal Units for Small Molecule Organic Solar Cells

S. Steinberger, A. Mishra,* G. Schulz, C. Uhrich, M. Pfeiffer, P. Bäuerle

Org. Photonics Photovolt., 2014, 2, 40-49 (open access)

57. Low Band Gap S,N-Heteroacene-based Oligothiophenes as Hole-Transporting and Light-Absorbing Materials for Efficient Perovskite-based Solar Cells

P. Qin, H. Kast, M. K. Nazeeruddin, S. M. Zakeeruddin, A. Mishra,* P. Bäuerle, M. Grätzel*

Energy Environ. Sci. 2014, 7, 2981-2985 (IF = 39.71) (Cit. = 125)

56. Efficiency Improvement of Solution-Processed Dithienopyrrole-Based A-D-A Oligothiophene Bulk-Heterojunction Solar Cells by Solvent Vapor Annealing

C. D. Wessendorf, G. L. Schulz, A. Mishra, P. Kar, I. Ata, M. Weidelener, M. Urdanpilleta, J. Hanisch, E. Mena-Osteritz, M. Lindén, E. Ahlswede, P. Bäuerle

Adv. Energy Mater. 2014, 4, 1400266 (IF = 29.70) (Cit. = 112)

55. Synthesis and Characterization of Benzo- and Naphtho[2,1-b:3,4-b']dithiophene Containing Oligomers for Photovoltaic Applications

M. Löbert, A. Mishra, C. Uhrich, M. Pfeiffer, P. Bäuerle

J. Mater. Chem. C, 2014, 2, 4879-4892 (IF = 8.07)

54. Acceptor-Donor-Acceptor Oligo­mers Containing Dithieno[3,2-b:2',3'-d]pyrrole and Thieno[2,3-c]pyrrole-4,6-dione Units for Solution-Processed Organic Solar Cells

L. G. Mercier, A. Mishra,* Y. Ishigaki, F. Henne, G. Schulz, P. Bäuerle*

Org. Lett. 2014, 16, 2642–2645 (IF = 6.07)

53. Synthesis and Structural Analysis of Thiophene-pyrrole-based S,N-heteroacenes

C. Wetzel, A. Mishra, E. Mena-Osteritz, A. Liess, M. Stolte, F. Würthner, P. Bäuerle

Org. Lett. 2014, 16, 362-365 (IF = 6.07)

52. Dithienopyrrole-based Oligothiophenes for Solution-Processed Organic Solar Cells

M. Weidelener, C. D. Wessendorf, J. Hanisch, E. Ahlswede, G. Götz, M. Lindén, G. Schulz, E. Mena-Osteritz, A. Mishra, P. Bäuerle

Chem. Commun. 2013, 49, 10865-10867 (IF = 6.06)

51. Synthesis and Ultrafast Time Resolved Spectroscopy of Peripherally Functionalized Zinc Phthalocyanine Bearing Oligothienylene-ethynylene Subunits

O. O. Adegoke, M. Ince, A. Mishra, A. Green, O. Varnavski, M. V. Martínez-Díaz, P. Bäuerle, T. Torres, T. Goodson III

J. Phys. Chem. C, 2013, 117, 20912-20918 (IF = 4.18)

50. Mannose-Functionalized Dendritic Oligothiophenes: Synthesis, Characterizations and Studies on their Interaction with Concanavalin A

S. Schmid, A. Mishra, M. Wunderlin, P. Bäuerle

Org. Biomol. Chem. 2013, 11, 5656-5665 (IF = 3.89)

49. Synthesis, Photophysical and Electrochemical Characteriza­tion of Terpyridine-functionalized Dendritic Oligothiophenes and their Ru(II) Complexes

A. Mishra,* E. Mena-Osteritz, P. Bäuerle* 

Beilstein J. Org. Chem. 2013, 9, 866-876 (IF = 2.54)

48. Highly Efficient p-Type Dye-sensitized Solar Cells based on Tris(1,2-diamino­ethane)cobalt(II)/(III) Electrolytes

S. Powar, T. Daeneke, M. T. Ma, D. Fu, N. W. Duffy, G. Götz, M. Weidelener, A. Mishra, P. Bäuerle, L. Spiccia, U. Bach, 

Angew. Chem. Int. Ed. 2013, 52, 602–605 - Hot article (IF = 16.82) (Cit. = 195)

47. Sustained Solar Hydrogen Generation Using a Dye-Sensitised NiO Photoca­thode/BiVO4 Tandem Photo-Electrochemical Device

L. Tong, A. Iwase, A. Nattestad, U. Bach, M. Weidelener, G. Götz, A. Mishra, P. Bäuerle, R. Amal, G. Wallace, A. Mozer

Energy Environ. Sci. 2012, 5, 9472–9475 (IF = 39.71) (Cit. = 180)

46. Improved Photocurrents for p-Type Dye-Sensitized Solar Cells Using Nano-Structured Nickel(II) Oxide Microballs

S. Powar, Z. Hu, M. Weidelener, A. Nattestad, Q. Wu, A. Mishra, P. Bäuerle, L. Spiccia, Y.-B. Cheng, U. Bach

Energy Environ. Sci. 2012, 5, 8896–8900 (IF = 39.71) (Cit. = 100)

45. Correlation between π-Conjugated Oligomer Structure with Film Morpho­logy and Organic Solar Cell Performance

R. Fitzner, E. Mena-Osteritz, A. Mishra, G. Schulz, E. Reinold, M. Weil, C. Körner, H. Ziehlke, C. Elschner, K. Leo, M. Riede, M. Pfeiffer, C. Uhrich, P. Bäuerle

J. Am. Chem. Soc. 2012, 134, 11064–11067 (IF = 16.38) (Cit. = 279)

44. Synthesis and Structure-Property Correlations of Dicyanovinyl-substituted Oligoselenophenes and their Application in Organic Solar Cells

S. Haid, A. Mishra,* M. Weil, C. Uhrich, M. Pfeiffer, P. Bäuerle*

Adv. Funct. Mater. 2012, 22, 4322–4333 (IF = 19.92)

43. Significant Improvement of Dye-Sensitized Solar Cell Performance by Small Structural Modification in π-Conjugated Donor-Acceptor Dyes

S. Haid, M. Marszatek, A. Mishra,* M. Wielopolski, J. Teuscher, J‑E. Moser, R. Humphry-Baker, S. M. Zakeeruddin,* M. Grätzel,* P. Bäuerle*

Adv. Funct. Mater. 2012, 22, 1291–1302 (IF = 19.92) (Cit. = 385)

42. Click-Functionalized Ru(II) Complexes for Dye-Sensitized Solar Cells

I. Stengel, N. Pootrakulchote, R. R. Dykeman, A. Mishra, S. M. Zakeeruddin, P. J. Dyson, M. Grätzel, P. Bäuerle

Adv. Energy Mater. 2012, 2, 1004–1012 (IF = 29.70)

41. Thiophene-based Donor-Acceptor Co-oligomers by Copper-catalyzed 1,3-Dipolar Cycloaddition 

S. Potratz, A. Mishra, P. Bäuerle

Beilstein J. Org. Chem. 2012, 8, 683–692 (IF = 2.54)

40. Small Molecule Organic Semiconductors on the Move – Promises for Future Solar Energy Technology

A. Mishra,* P. Bäuerle*

Angew. Chem. Int. Ed. 2012, 51, 2020–2067 (Review) (IF = 16.82) (Cit. = 1770)

39. Synthesis and Characterization of Perylene–Bithiophene–Triphenylamine Triads: Studies on the Effect of Alkyl-Substitution in p-Type NiO Based Photocathodes 

M. Weidelener, A. Mishra,* A. Nattestad, S. Powar, A. Mozer, E, Mena-Osteritz, Y.-B. Cheng, U. Bach,* P. Bäuerle*

J. Mater. Chem. 2012, 22, 7366–7379 (IF = 6.1)

38. Synthesis and Characterizations of Red/Near-IR Absorbing A‑D‑A‑D‑A‑type Oligothiophenes Containing Thienothiadiazole and Thienopyrazine Central Units

S. Steinberger, A. Mishra,* E. Reinold, E. Mena-Osteritz, H. Müller, C. Uhrich, M. Pfeiffer, P. Bäuerle* 

 J. Mater. Chem. 2012, 22, 2701–2712 (IF = 6.1) 

37. Dicyanovinylene-substituted Selenophene-Thiophene Co-Oligomers for Small Molecule Organic Solar Cells

S. Haid, A. Mishra,* C. Uhrich, M. Pfeiffer, P. Bäuerle* 

Chem. Mater. 2011, 23, 4435–4444 (IF = 10.51)

36. Synthesis and Characterization of Acceptor-substituted Oligothiophenes for Solar Cell Applications

A. Mishra,* C. Uhrich, E. Rynold, M. Pfeiffer, P. Bäuerle* 

Adv. Energy Mater. 2011, 1, 265–273 (IF = 29.70)

35. “Click-Chemistry” Approach in the Design of 1,2,3-Triazolyl-Pyridine Ligands and their Ru(II)-Complexes for Dye-Sensitized Solar Cells 

I. Stengel, A. Mishra, N. Pootrakulchote, S.-J. Moon, S. M. Zakeeruddin, M. Grätzel, P. Bäuerle

J. Mater. Chem. 2011, 21, 3726–3734 (IF = 6.1) (Cit. = 76)

33. Dicyanovinyl–substituted Oligothiophenes: Structure-Property Relationships and Application in Vacuum-Processed Small Molecule Organic Solar Cells 

R. Fitzner, E. Reinold, A. Mishra, E. Mena-Osteritz, H. Ziehlke, C. Körner, K. Leo, M. Riede, M. Weil, O. Tsaryova, A. Weiß, C. Uhrich, M. Pfeiffer, P. Bäuerle

Adv. Funct. Mater. 2011, 21, 897–910 (IF = 19.92) (Cit. = 239)

32. A-D-A-D-A-Type Oligothiophenes for Vacuum-Deposited Organic Solar Cells

S. Steinberger, A. Mishra,* E. Reinold, C. M. Müller, C. Uhrich, M. Pfeiffer, P. Bäuerle*

Org. Lett. 2011, 13, 90–93 (IF = 6.07) (Cit. = 58)

31. Enhanced Open-Circuit Voltage of p-Type DSC with Highly Crystalline NiO Nanoparticles

X. L. Zhang, F. Huang, A. Nattestad, K. Wang, D. Fu, A. Mishra, P. Bäuerle, U. Bach, Y.-B. Cheng 

Chem. Commun. 2011, 47, 4808–4810 (IF = 6.06) (Cit. = 104)

30. Vacuum-Processed Small Molecule Solar Cells based on Novel Acceptor-Substituted Low-Band Gap Oligothiophenes

S. Steinberger, A. Mishra,* E. Reinold, C. Uhrich, M. Pfeiffer, P. Bäuerle* 

Chem. Commun. 2011, 47, 1982–1984 (IF = 6.06) (Cit. = 91)

29. Carbohydrate-Functionalized Oligothiophenes for Concanavalin A Recognition 

S. Schmid, A. Mishra, P. Bäuerle

Chem. Commun. 2011, 47, 1324–1326 (IF = 6.06)

28. D-π-A Sensitizers for Dye-sensitized Solar Cells: Linear vs. Branched Oligothiophenes

M. K. R. Fischer, S. Wenger, M. Wang, A. Mishra,* S. M. Zakeeruddin,* M. Grätzel,* P. Bäuerle*

Chem. Mater. 2010, 22, 1836–1845 (IF = 10.51) (Cit. = 154)

27. Highly Efficient Sensitizers for Dye-Sensitized Photocathodes and Tandem Solar Cells

A. Nattestad, A. Mozer, M. K. R. Fischer, Y.-B. Cheng, A. Mishra, P. Bäuerle, U. Bach

Nature Mater. 2010, 9, 31–35 (IF = 47.66) (Cit. = 604)

Highlighted in NPG Asia Materials, Dye-sensitized photovoltaics: Tailor made. doi:10.1038/asiamat.2010.18 (2010)

26. Design and Synthesis of a Novel Anchoring Ligand for Highly Efficient Thin Film Dye-Sensitized Solar Cells

A. Mishra,* N. Pootrakulchote, M. K. R. Fischer, C. Klein, M. K. Nazeeruddin, S. M. Zakeerud­din,* P. Bäuerle,* M. Grätzel* 

Chem. Commun. 2009, 7146–7148 (IF = 6.06)

25. A Dendritic Oligothiophene Ruthenium Sensitizer for Stable Dye-Sensitized Solar Cells

F. Sauvage, M. K. R. Fischer, A. Mishra, S. M. Zakeeruddin, M. K. Nazeeruddin, P. Bäuerle, M. Grätzel

ChemSusChem, 2009, 2, 761–768 (IF = 9.14)

24. Metal-free Organic Dyes for Dye-Sensitized Solar Cells: From Structure-Property Relationships to Design Rules

A. Mishra, M. K. R. Fischer, P. Bäuerle

Angew. Chem. Int. Ed. 2009, 48, 2474–2499 (Review) (IF = 16.82) (Cit. = 2780)

23. Functional Oligothiophenes: Molecular Design for Multi-Dimensional Nanoarchitectures and their Applications

 A. Mishra, C.-Q. Ma, P. Bäuerle

Chem. Rev. 2009, 109, 1141–1276 (IF = 72.09) (Cit. = 1260)

22. Shape-persistent Oligothienylene-Ethynylene based Dendrimers: Synthesis, Spectroscopy and Electrochemical Characterizations

A. Mishra, C-Q. Ma, R. A. J. Janssen, P. Bäuerle

Chem. Eur. J. 2009, 15, 13521–13534 (IF = 5.02)

21. Studies on Adsorption of Mono- and Multi-Chromophoric Hemicyanine Dyes on Silver Nanoparticles by Surface-Enhanced Reso­nance Raman and Theoretical Calculations

N. Biswas, S. Thomas, S. Kapoor, A. Mishra, S. Wategaonkar, T. Mukherjee

J. Chem. Phys. 2008, 129, 184702(1–15) (IF = 4.30)

20. Surface-Enhanced Resonance Raman Scattering and Density Functional Calculations of Hemicyanine Adsorbed on Colloidal Silver Surface

N. Biswas, S. Thomas, S. Kapoor, A. Mishra, S. Wategaonkar, S. Venkateswaran, T. Mukherjee

J. Phys. Chem. A, 2006, 110, 1805–1811 (IF = 2.94)

19. Synthesis and Charac­te­rization of Spin-Coatable tert-Amine Molecules for Hole-Transport in Organic Light-Emitting Diodes

A. Mishra,* P. K. Nayak, D. Ray, M. P. Patankar, K. L. Narasimhan, N. Periasamy

Tetrahedron Lett. 2006, 47, 4715–4719 (IF = 2.03)

18. Synthesis and Characterization of Soluble Aluminium Complex Dyes based on 5-Substituted-8-Hydroxyquinoline Derivatives for OLED Applications

A. Mishra,* N. Periasamy, M. P. Patankar, K. L. Narasimhan

Dyes Pigm. 2005, 66, 89–97 (IF = 5.12)

17. Synthesis of 5-Alkoxymethyl- and 5-Aminomethyl-Substituted 8-Hydroxyquinoline Derivatives and Their Luminescent Al(III) Complexes for OLED Applications

A. Mishra,* P. K. Nayak, N. Periasamy 

Tetrahedron Lett. 2004, 45, 6265–6268 (IF = 2.03)

16. New Push-Pull Type Dendritic Stilbazolium Dyes: Synthesis, Photophysical and Electrochemical Investigation

A. Mishra,* N. S. Haram,

Dyes Pigm. 2004, 63, 191–202 (IF = 5.12)

15. Synthesis of Water-Soluble, Ester-Terminated Dendrons and Dendrimers Containing Internal PEG Linkages

G. R. Newkome, K. K. Kotta, A. Mishra, C. N. Moorefield

Macromolecules, 2004, 37, 8262–8268 (IF = 6.06)

14. Synthesis, Spectroscopic and Electro­chemical Investigation of Some New Stilbazolium Dyes

A. Mishra,* G. R. Newkome, C. N. Moorefield, L. A. Godínez 

Dyes Pigm. 2003, 58, 227–237 (IF = 5.12)

13. Improved Synthesis of an Ethereal Tetraamine Core for Dendrimer Construction

G. R. Newkome, A. Mishra, C. N. Moorefield

J. Org. Chem. 2002, 67, 3957–3960 (IF = 4.20)

12. Time resolved Fluorescence Studies of Aminostyryl pyridinium Dyes in Organic Solvents and Surfactant Solutions

A. Mishra, G. B. Behera, M. M. G. Krishna, N. Periasamy

J. Luminescence, 2001, 92, 175–188 (IF = 4.17)

11. Cyanines during the 1990s: A Review

A. Mishra, R. K. Behera, P. K. Behera, B. K. Mishra, G. B. Behera

Chem. Rev. 2000, 100, 1973–2011 (Review) (IF = 72.09) (Cit. = 1476)

10. A New Method of Isomerization of Trans-1-Propyl-4-(4'-N,N-Dimethylamino)Styryl Pyridinium Bromide

R. K. Behera, A. Mishra, G. B. Behera

Ind. J. Chem. B, 2000, 39, 783–786 (IF = 0.59)

9. X-Ray Crystallographic Study of 1-Methyl-4-(4-N,N-dimethylamino) Styryl Pyridinium Iodide

A. Mishra, R. K. Behera, F. R. Fronczek, M. Bidyasagar, G. B. Behera

Ind. J. Chem. B, 1999, 38, 982–985 (IF = 0.59)