Pozniak Boguslaw P, Cole Richard B
Department of Chemistry, University of New Orleans, New Orleans, Louisiana 70148, USA.
J Am Soc Mass Spectrom. 2007 Apr;18(4):737-48. doi: 10.1016/j.jasms.2006.11.012. Epub 2007 Jan 25.
A movable disc-like wire probe electrode placed inside the electrospray (ES) capillary was used to measure currents flowing within the ES device for the first time. Currents were measured between the wire probe and the ES capillary. Current maps revealing measured current versus wire probe position were generated for a variety of solution conditions in the positive and negative ion modes and are compared to potential maps. The electrospray device was found to subsist on highly stable total currents; this current regulator aspect of the ES device showed remarkable resiliency regardless of the proportion of current produced at the wire probe electrode versus the ES capillary. However, kinks observed in the current and potential maps are attributed to adsorbed air participating in electrochemical reactions, and turbulence in solution flow in the region of the Taylor cone. From differential electrospray emitter potential (DEEP) maps, current maps, and cyclic voltammetry experiments performed at different wire probe locations, evidence is provided for separate regimes of current flow in the bulk solution and in the thin "skin" of highly conductive electrolyte constituting the outer surface (air interface) of the Taylor cone. Current maps reveal that current is drawn more evenly along the length of the ES capillary when solutions are highly conductive, in agreement with previous results for DEEP maps. In less conductive solutions, the area close to the capillary exit contributes more heavily to current production. Evidence that contaminant participation in electrochemical processes occurring within the electrospray device can be largely responsible for production of the excess charge in ES droplets is also provided. These investigations complement previous DEEP mapping studies to further elucidate the details of the electrochemical processes occurring within the electrospray device.
首次使用置于电喷雾(ES)毛细管内部的可移动盘状金属丝探针电极来测量ES装置内流动的电流。电流是在金属丝探针和ES毛细管之间测量的。针对正负离子模式下的各种溶液条件,生成了显示测量电流与金属丝探针位置关系的电流图,并与电势图进行了比较。发现电喷雾装置依靠高度稳定的总电流维持运行;ES装置的这种电流调节特性显示出显著的弹性,无论在金属丝探针电极与ES毛细管处产生的电流比例如何。然而,在电流图和电势图中观察到的扭结归因于参与电化学反应的吸附空气以及泰勒锥区域内溶液流动的湍流。通过在不同金属丝探针位置进行的差分电喷雾发射极电势(DEEP)图、电流图和循环伏安法实验,为本体溶液和构成泰勒锥外表面(空气界面)的高导电电解质薄“表皮”中不同的电流流动区域提供了证据。电流图显示,当溶液具有高导电性时,电流沿ES毛细管长度方向的分布更均匀,这与之前DEEP图的结果一致。在导电性较差的溶液中,靠近毛细管出口的区域对电流产生的贡献更大。还提供了证据表明,污染物参与电喷雾装置内发生的电化学过程在很大程度上可能是ES液滴中过量电荷产生的原因。这些研究补充了之前的DEEP映射研究,以进一步阐明电喷雾装置内发生的电化学过程的细节。