Understanding the Role of Removable Solid Additives: Selective Interaction Contributes to Vertical Component Distributions

Author:

Fan Baobing12ORCID,Zhong Wenkai3,Gao Wei24,Fu Huiting24,Lin Francis R.12,Wong Reese W.‐Y.4,Liu Ming24,Zhu Chenhui5,Wang Cheng5,Yip Hin‐Lap24,Liu Feng3,Jen Alex K.‐Y.1246ORCID

Affiliation:

1. Department of Chemistry City University of Hong Kong Kowloon Hong Kong 999077 P. R. China

2. Institute of Clean Energy City University of Hong Kong Kowloon Hong Kong 999077 P. R. China

3. Frontiers Science Center for Transformative Molecules In‐Situ Center for Physical Science and Center of Hydrogen Science School of Chemistry and Chemical Engineering Shanghai Jiao Tong University 200240 Shanghai P. R. China

4. Department of Material Science and Engineering City University of Hong Kong Kowloon Hong Kong 999077 P. R. China

5. Advanced Light Source Lawrence Berkeley National Laboratory Berkeley CA 94720 USA

6. Department of Materials Science and Engineering University of Washington Seattle WA 98195 USA

Abstract

AbstractSequentially deposited organic solar cells (SD‐OSCs) have attracted great attention owing to their ability in achieving a more favorable, vertically phase‐separated morphology to avoid the accumulation of counter charges at absorber/transporting layer interfaces. However, the processing of SD‐OSCs is still quite challenging in preventing the penetration of small‐molecule acceptors into the polymer donor layer via erosion or swelling. Herein, solid additives (SAs) with varied electrostatic potential distributions and steric hinderance are introduced into SD‐OSCs to investigate the effect of evaporation dynamics and selective interaction on vertical component distribution. Multiple modelings indicate that theππinteraction dominates the interactions between aromatic SAs and active layer components. Among them,p‐dibromobenzene shows a stronger interaction with the donor while 2‐chloronaphthalene (2‐CN) interacts more preferably with acceptor. Combining the depth‐dependent morphological study aided by multiple X‐ray scattering methods, it is concluded that the evaporation of SAs can drive the stronger‐interaction component upward to the surface, while having minor impact on the overall molecular packing. Ultimately, the 2‐CN‐treated devices with reduced acceptor concentration at the bottom surface deliver a high power conversion efficiency of 19.2%, demonstrating the effectiveness of applying selective interactions to improve the vertical morphology of OSCs by using SAs with proper structure.

Funder

National Natural Science Foundation of China

China Postdoctoral Science Foundation

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials,General Materials Science

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