{"title":"双化学活化法制备具有分层结构的纳米多孔生物碳,用于二氧化碳捕集和超级电容器。","authors":"Vishnumaya Narayanan, Gurwinder Singh*, Ajanya M Ruban, Arun Baskar, Rohan Bahadur, Vibin Perumalsamy, Kavitha Ramadass, Jae-Hun Yang, Sanje Mahasivam, Vipul Bansal and Ajayan Vinu*, ","doi":"10.1021/acsami.5c09564","DOIUrl":null,"url":null,"abstract":"<p >Porous carbons are at the forefront of several applications, and their efficiency mainly depends on their overall porosity and surface area, with particular emphasis on the amount of microporous and mesoporous contents. In our current research, we present a facile technique of dual activation to fabricate hierarchically architectured nanoporous biocarbons (HNBCs) via an innovative synthetic interplay of KOH and ZnCl<sub>2</sub> as chemical activating agents. Using KOH activation, it was possible to develop HNBC with a specific surface area of 3070 m<sup>2</sup> g<sup>–1</sup> and a nearly equal proportion of micropores (53%) and mesopores (47%). The chemical treatment of this material with ZnCl<sub>2</sub> led to the expansion of micropores into mesopores, the ratio of which can be tuned by varying the amount of ZnCl<sub>2</sub> used. While this treatment significantly affected the content of micro- and mesopores, there was a negligible effect on the overall surface area, which proves that there is no compromise in overall porosity. When tested as a CO<sub>2</sub> adsorbent, the material HNBC-5K-Zn1, synthesized using 1 g of ZnCl<sub>2</sub>, adsorbed 4.36 and 38.12 mmol of CO<sub>2</sub> at 0 °C and 1 and 30 bar, respectively. For HNBC-5K-Zn1, a reasonably high specific capacitance of 247.6 F g<sup>–1</sup> at a current density of 0.5 A g<sup>–1</sup> was observed, which can be retained to 155 F g<sup>–1</sup> even at a higher current density of 10 A g<sup>–1</sup>. This material also exhibited a specific capacitance of 166.71 F g<sup>–1</sup> at 0.5 A g<sup>–1</sup> in a two-electrode system and further demonstrated reasonable energy and power densities of 33.342 Wh/kg and 666.63 W/kg (0.5 A g<sup>–1</sup>), respectively. In addition, the prepared material is highly stable even after 5000 cycles, with no significant loss of specific capacitance. The hierarchical porosity with the combination of micro- and mesopores obtained through the dual activation approach is responsible for this excellent performance.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":"17 27","pages":"39281–39290"},"PeriodicalIF":8.2000,"publicationDate":"2025-06-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hierarchically Architectured Nanoporous Biocarbons Prepared via Dual Chemical Activation for Applicability in CO2 Capture and Supercapacitors\",\"authors\":\"Vishnumaya Narayanan, Gurwinder Singh*, Ajanya M Ruban, Arun Baskar, Rohan Bahadur, Vibin Perumalsamy, Kavitha Ramadass, Jae-Hun Yang, Sanje Mahasivam, Vipul Bansal and Ajayan Vinu*, \",\"doi\":\"10.1021/acsami.5c09564\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Porous carbons are at the forefront of several applications, and their efficiency mainly depends on their overall porosity and surface area, with particular emphasis on the amount of microporous and mesoporous contents. In our current research, we present a facile technique of dual activation to fabricate hierarchically architectured nanoporous biocarbons (HNBCs) via an innovative synthetic interplay of KOH and ZnCl<sub>2</sub> as chemical activating agents. Using KOH activation, it was possible to develop HNBC with a specific surface area of 3070 m<sup>2</sup> g<sup>–1</sup> and a nearly equal proportion of micropores (53%) and mesopores (47%). The chemical treatment of this material with ZnCl<sub>2</sub> led to the expansion of micropores into mesopores, the ratio of which can be tuned by varying the amount of ZnCl<sub>2</sub> used. While this treatment significantly affected the content of micro- and mesopores, there was a negligible effect on the overall surface area, which proves that there is no compromise in overall porosity. When tested as a CO<sub>2</sub> adsorbent, the material HNBC-5K-Zn1, synthesized using 1 g of ZnCl<sub>2</sub>, adsorbed 4.36 and 38.12 mmol of CO<sub>2</sub> at 0 °C and 1 and 30 bar, respectively. For HNBC-5K-Zn1, a reasonably high specific capacitance of 247.6 F g<sup>–1</sup> at a current density of 0.5 A g<sup>–1</sup> was observed, which can be retained to 155 F g<sup>–1</sup> even at a higher current density of 10 A g<sup>–1</sup>. This material also exhibited a specific capacitance of 166.71 F g<sup>–1</sup> at 0.5 A g<sup>–1</sup> in a two-electrode system and further demonstrated reasonable energy and power densities of 33.342 Wh/kg and 666.63 W/kg (0.5 A g<sup>–1</sup>), respectively. In addition, the prepared material is highly stable even after 5000 cycles, with no significant loss of specific capacitance. 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引用次数: 0
摘要
多孔碳是几种应用的前沿,其效率主要取决于其整体孔隙率和表面积,特别强调微孔和介孔内容物的数量。在我们目前的研究中,我们提出了一种简单的双活化技术,通过KOH和ZnCl2作为化学活化剂的创新合成相互作用来制造分层结构的纳米多孔生物碳(hnbc)。利用KOH活化,可以制备出比表面积为3070 m2 g-1的HNBC,微孔(53%)和中孔(47%)的比例几乎相等。用ZnCl2对该材料进行化学处理,导致微孔扩展为介孔,其比例可以通过改变ZnCl2的用量来调节。虽然该处理显著影响了微孔和中孔的含量,但对总表面积的影响可以忽略不计,这证明了总体孔隙度没有受到影响。作为CO2吸附剂,以1g ZnCl2合成的材料HNBC-5K-Zn1在0℃、1和30 bar条件下分别吸附了4.36和38.12 mmol的CO2。在0.5 a g-1电流密度下,HNBC-5K-Zn1的比电容达到247.6 F -1,在10 a g-1电流密度下,比电容保持在155 F -1。在双电极系统中,该材料在0.5 a g-1下的比电容为166.71 F -1,并进一步证明了合理的能量密度和功率密度分别为33.342 Wh/kg和666.63 W/kg (0.5 a g-1)。此外,制备的材料即使在5000次循环后也高度稳定,没有明显的比电容损失。通过双活化方法获得的微孔和介孔相结合的分层孔隙度是这种优异性能的原因。
Hierarchically Architectured Nanoporous Biocarbons Prepared via Dual Chemical Activation for Applicability in CO2 Capture and Supercapacitors
Porous carbons are at the forefront of several applications, and their efficiency mainly depends on their overall porosity and surface area, with particular emphasis on the amount of microporous and mesoporous contents. In our current research, we present a facile technique of dual activation to fabricate hierarchically architectured nanoporous biocarbons (HNBCs) via an innovative synthetic interplay of KOH and ZnCl2 as chemical activating agents. Using KOH activation, it was possible to develop HNBC with a specific surface area of 3070 m2 g–1 and a nearly equal proportion of micropores (53%) and mesopores (47%). The chemical treatment of this material with ZnCl2 led to the expansion of micropores into mesopores, the ratio of which can be tuned by varying the amount of ZnCl2 used. While this treatment significantly affected the content of micro- and mesopores, there was a negligible effect on the overall surface area, which proves that there is no compromise in overall porosity. When tested as a CO2 adsorbent, the material HNBC-5K-Zn1, synthesized using 1 g of ZnCl2, adsorbed 4.36 and 38.12 mmol of CO2 at 0 °C and 1 and 30 bar, respectively. For HNBC-5K-Zn1, a reasonably high specific capacitance of 247.6 F g–1 at a current density of 0.5 A g–1 was observed, which can be retained to 155 F g–1 even at a higher current density of 10 A g–1. This material also exhibited a specific capacitance of 166.71 F g–1 at 0.5 A g–1 in a two-electrode system and further demonstrated reasonable energy and power densities of 33.342 Wh/kg and 666.63 W/kg (0.5 A g–1), respectively. In addition, the prepared material is highly stable even after 5000 cycles, with no significant loss of specific capacitance. The hierarchical porosity with the combination of micro- and mesopores obtained through the dual activation approach is responsible for this excellent performance.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.