scholarly journals Cation Substitution in Earth-Abundant Kesterite Photovoltaic Materials

2018 ◽  
Vol 5 (4) ◽  
pp. 1700744 ◽  
Author(s):  
Jianjun Li ◽  
Dongxiao Wang ◽  
Xiuling Li ◽  
Yu Zeng ◽  
Yi Zhang
2018 ◽  
Vol 5 (4) ◽  
pp. 1870021 ◽  
Author(s):  
Jianjun Li ◽  
Dongxiao Wang ◽  
Xiuling Li ◽  
Yu Zeng ◽  
Yi Zhang

2017 ◽  
Vol 7 (11) ◽  
pp. 1602366 ◽  
Author(s):  
Donghyeop Shin ◽  
Bayrammurad Saparov ◽  
David B. Mitzi

2016 ◽  
Vol 18 (7) ◽  
pp. 5121-5128 ◽  
Author(s):  
J. G. Slingsby ◽  
N. A. Rorrer ◽  
L. Krishna ◽  
E. S. Toberer ◽  
C. A. Koh ◽  
...  

Earth abundant semiconducting type II Si clathrates have attracted attention as photovoltaic materials due to their wide band gaps.


2021 ◽  
pp. 2010325
Author(s):  
Yachao Du ◽  
Shanshan Wang ◽  
Qingwen Tian ◽  
Yuechao Zhao ◽  
Xiaohuan Chang ◽  
...  

Author(s):  
Fancong Zeng ◽  
Yingrui Sui ◽  
Meiling Ma ◽  
Na Zhao ◽  
Tianyue Wang ◽  
...  

2020 ◽  
Vol 8 (47) ◽  
pp. 24920-24942
Author(s):  
Qingwen Tian ◽  
Shengzhong (Frank) Liu

Recent theoretical and experimental studies for cation substitution in kesterite-based materials were summarized, with a particular focus on inhibiting defects for mitigating Voc,def.


2020 ◽  
Author(s):  
Lucas A. Freeman ◽  
Akachukwu D. Obi ◽  
Haleigh R. Machost ◽  
Andrew Molino ◽  
Asa W. Nichols ◽  
...  

The reduction of the relatively inert carbon–oxygen bonds of CO<sub>2</sub> to access useful CO<sub>2</sub>-derived organic products is one of the most important fundamental challenges in synthetic chemistry. Facilitating this bond-cleavage using earth-abundant, non-toxic main group elements (MGEs) is especially arduous because of the difficulty in achieving strong inner-sphere interactions between CO<sub>2</sub> and the MGE. Herein we report the first successful chemical reduction of CO<sub>2</sub> at room temperature by alkali metals, promoted by a cyclic(alkyl)(amino) carbene (CAAC). One-electron reduction of CAAC-CO<sub>2</sub> adduct (<b>1</b>) with lithium, sodium or potassium metal yields stable monoanionic radicals clusters [M(CAAC–CO<sub>2</sub>)]<sub>n</sub>(M = Li, Na, K, <b> 2</b>-<b>4</b>) and two-electron alkali metal reduction affords open-shell, dianionic clusters of the general formula [M<sub>2</sub>(CAAC–CO<sub>2</sub>)]<sub>n </sub>(<b>5</b>-<b>8</b>). It is notable that these crystalline clusters of reduced CO<sub>2</sub> may also be isolated via the “one-pot” reaction of free CO<sub>2</sub> with free CAAC followed by the addition of alkali metals – a reductive process which does not occur in the absence of carbene. Each of the products <b>2</b>-<b>8</b> were investigated using a combination of experimental and theoretical methods.<br>


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